Rho-Nitro, Rho-Nitro

Rho-Nitro

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Rho-Nitro pumpspray

How does this medication work? What will it do for me?

Nitroglycerin belongs to the class of medications called anti-anginals . Nitroglycerin is used to relieve acute attacks of angina (chest pain). Nitroglycerin relieves acute angina attacks by relaxing blood vessels and increasing the oxygen and blood supply to the heart.

This medication may be available under multiple brand names and/or in several different forms. Any specific brand name of this medication may not be available in all of the forms or approved for all of the conditions discussed here. As well, some forms of this medication may not be used for all of the conditions discussed here.

Your doctor may have suggested this medication for conditions other than those listed in these drug information articles. If you have not discussed this with your doctor or are not sure why you are taking this medication, speak to your doctor. Do not stop taking this medication without consulting your doctor.

Do not give this medication to anyone else, even if they have the same symptoms as you do. It can be harmful for people to take this medication if their doctor has not prescribed it.

How should I use this medication?

To use this medication, spray it once or twice (as directed by doctor) onto or under the tongue at the first sign of an angina attack. Do not inhale. The dose may be repeated twice with at least a five minute interval between each dose, or as directed by your doctor. If relief is still not obtained after three doses of nitroglycerin (i. e. 15 minutes), seek medical help immediately.

While using nitroglycerin spray, remain at rest in a sitting position and keep the container vertical with the nozzle head up. Place the opening in the nozzle head as close to the mouth as possible. Avoid getting the spray in your eyes.

Many things can affect the dose of a medication that a person needs, such as body weight, other medical conditions, and other medications. If your doctor has recommended a dose different from the ones listed here, do not change the way that you are taking the medication without consulting your doctor.

It is very important to use this medication exactly as prescribed by your doctor.

Store nitroglycerin spray at room temperature (15°C to 30°C) away from hot water, radiators, or other sources of heat. Do not incinerate the canister and do not attempt to open it. Keep it out of reach of children.

Do not dispose of medications in wastewater (e. g. down the sink or in the toilet) or in household garbage. Ask your pharmacist how to dispose of medications that are no longer needed or have expired.

What form(s) does this medication come in?

Each metered dose contains 0.4 mg of nitroglycerin. Nonmedicinal ingredients: ethanol anhydrous, medium chain partial glycerides, medium chain triglycerides, and peppermint oil.

Who should NOT take this medication?

Do not use nitroglycerin spray if you:

are allergic to nitroglycerin or to any of the ingredients of the medication

are allergic to other nitrates

have extremely low blood pressure

have severe anemia

have heart failure

have increased eye pressure (glaucoma)

have increased pressure within the head (e. g. after an accident)

are having a heart attack

are taking the medication riociguat

are taking phosphodiesterase 5 inhibitors (e. g. sildenafil, tadalafil, vardenafil)

People who use nitroglycerin regularly or intermittently should not use phosphodiesterase 5 inhibitors (e. g. sildenafil, tadalafil, or vardenafil) because a life-threatening lowering of blood pressure can result.

What side effects are possible with this medication?

Many medications can cause side effects. A side effect is an unwanted response to a medication when it is taken in normal doses. Side effects can be mild or severe, temporary or permanent. The side effects listed below are not experienced by everyone who takes this medication. If you are concerned about side effects, discuss the risks and benefits of this medication with your doctor.

The following side effects have been reported by at least 1% of people taking this medication. Many of these side effects can be managed, and some may go away on their own over time.

Contact your doctor if you experience these side effects and they are severe or bothersome. Your pharmacist may be able to advise you on managing side effects.

dizziness or lightheadedness, especially when getting up from a lying or sitting position

fast heartbeat

flushing of the face and neck

headache

nausea or vomiting

rash

restlessness

runny nose

sore throat or mouth

weakness

Although most of these side effects listed below don't happen very often, they could lead to serious problems if you do not check with your doctor or seek medical attention.

Check with your doctor as soon as possible if any of the following side effects occur:

blurred vision

dryness of mouth

fainting

headache (severe or prolonged)

signs of low blood pressure (e. g. dizziness, lightheadedness, fainting)

swelling of the ankles

tingling or pins and needles of the arms or legs

Contact a doctor at once if any of the following signs of overdose occur:

bluish-coloured lips, fingernails, or palms of the hands

convulsions (seizures)

dizziness (extreme) or fainting

feeling of extreme pressure in head

fever

shortness of breath

unusual tiredness or weakness

weak and fast heartbeat

Stop taking the medication and seek immediate medical attention if any of the following occur:

signs of a serious allergic reaction (e. g. abdominal cramps, difficulty breathing, nausea and vomiting, or swelling of the face and throat)

continued chest pain

Some people may experience side effects other than those listed. Check with your doctor if you notice any symptom that worries you while you are taking this medication.

Are there any other precautions or warnings for this medication?

Before you begin using a medication, be sure to inform your doctor of any medical conditions or allergies you may have, any medications you are taking, whether you are pregnant or breast-feeding, and any other significant facts about your health. These factors may affect how you should use this medication.

Dizziness: This treatment may cause temporary dizziness. Do not drive, operate machinery, or perform other hazardous tasks until you have determined how this medication affects you.

Low blood pressure: Headaches or symptoms of low blood pressure, such as weakness or dizziness, particularly when getting up suddenly from a lying or sitting position, may result from taking too much nitroglycerin. If these symptoms occur, your doctor may reduce the dose or stop the use of nitroglycerin. People who might be negatively affected by low blood pressure should use nitroglycerin spray with caution. People who take diuretics or have pre-existing low blood pressure may be at more risk of experiencing low blood pressure. Discuss any concerns you might have with your doctor.

Medical conditions: The benefits and safety of nitroglycerin spray for people who have an acute heart attack or congestive heart failure have not been established.

Tolerance: Nitroglycerin users may develop tolerance to the medication, resulting in it not working as well. Tolerance to other nitrates or nitrites can also happen, especially if long-acting nitrates are being used at the same time. As tolerance to nitroglycerin develops, the effect of fast-acting sublingual (under the tongue) nitroglycerin is somewhat reduced.

Pregnancy: This medication has not been studied for use by pregnant women. This medication should not be used during pregnancy unless the benefits outweigh the risks. If you become pregnant while taking this medication, contact your doctor immediately.

Breast-feeding: It is not known whether this medication passes into breast milk. If you are a breast-feeding mother and are taking this medication, it may affect your baby. Talk to your doctor about whether you should continue breast-feeding.

Children: The safety and effectiveness of this medication for children have not been established.

What other drugs could interact with this medication?

There may be an interaction between nitroglycerin and any of the following:

alcohol

alfuzosin

alteplase

barbiturates (e. g. butalbital, phenobarbital)

bromocriptine

cabergoline

canagliflozin

dapagliflozin

duloxetine

ergot alkaloids (e. g. dihydroergotamine, ergotamine, methylergonavine)

heparin

levodopa

medications that reduce blood pressure (e. g. vasodilators, calcium channel blockers, ACE inhibitors, beta-blockers, diuretics)

quetiapine

riociguat

risperidone

rosiglitazone

phosphodiesterase 5 inhibitors (e. g. sildenafil, tadalafil, vardenafil)

tizanidine

tricyclic antidepressants (e. g. amitriptyline, imipramine, nortriptyline)

If you are taking any of these medications, speak with your doctor or pharmacist. Depending on your specific circumstances, your doctor may want you to:

stop taking one of the medications,

change one of the medications to another,

change how you are taking one or both of the medications, or

leave everything as is.

An interaction between two medications does not always mean that you must stop taking one of them. Speak to your doctor about how any drug interactions are being managed or should be managed.

Medications other than those listed above may interact with this medication. Tell your doctor or prescriber about all prescription, over-the-counter (non-prescription), and herbal medications you are taking. Also tell them about any supplements you take. Since caffeine, alcohol, the nicotine from cigarettes, or street drugs can affect the action of many medications, you should let your prescriber know if you use them.

All material © 1996-2016 MediResource Inc. Terms and conditions of use. The contents herein are for informational purposes only. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition.

Buy Angilol Online, Order No Prescription Propranolol, Angilol

Buy Angilol (Propranolol) without Prescription

ANGILOL (PROPRANOLOL) INDICATIONS

Angilol is used for treating certain types of irregular heartbeat. Angilol is a beta-blocker. It works by decreasing the action of pacemaker cells and slowing certain impulses in the heart. This helps to control irregular heartbeat.

ANGILOL (PROPRANOLOL) INSTRUCTIONS

Use Angilol as directed by your doctor.

Take Angilol with a full glass of water.

Take Angilol on a regular schedule to get the most benefit from it. Taking Angilol at the same time each day will help you remember to take it.

Continue to take Angilol even if you feel well. Do not miss any dose.

Do not suddenly stop taking Angilol. You may have an increased risk of side effects. If you need to stop Angilol or add a new medicine, your doctor will gradually lower your dose.

If you miss a dose of Angilol, take it as soon as possible. If your next dose is less than 4 hours away, skip the missed dose and take the medicine at the next regularly scheduled time.

Ask your health care provider any questions you may have about how to use Angilol.

ANGILOL (PROPRANOLOL) STORAGE

Store Angilol between 68 and 77 degrees F (20 and 25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Angilol out of the reach of children and away from pets.

Do NOT use Angilol if:

you are allergic to any ingredient in Angilol

you have moderate to severe heart block, sick sinus syndrome, or a very slow heartbeat and you do not have a permanent pacemaker

you have uncontrolled heart failure, shock caused by serious heart problems, or very low blood pressure after a heart attack

you have asthma

the patient is a child with diabetes or heart failure

you are taking mibefradil.

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Angilol. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine (eg, medicines to treat colds or congestion), herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances, or are taking medicine for allergies

if you have a history of other heart problems (eg, angina, congestive heart failure, slow heartbeat)

if you have a history of liver or kidney problems, blood vessel disease, lung or breathing problems (eg, chronic bronchitis, emphysema, chronic obstructive pulmonary disease [COPD]), diabetes, low blood sugar, overactive thyroid, or glaucoma

if you have Wolff-Parkinson-White syndrome, Down syndrome, Raynaud syndrome, or an adrenal gland tumor (pheochromocytoma)

if you smoke or drink alcohol.

Some medicines may interact with Angilol. Tell your health care provider if you are taking any other medicines, especially any of the following:

Mibefradil because the risk of serious heart side effects may be increased

Many prescription and nonprescription medicines (eg, used for infections, inflammation, aches and pains, high blood pressure, heart problems, irregular heartbeat, diabetes, prostate problems, blood thinning, thyroid problems, depression, mental or mood problems, immune system suppression, allergic reactions, asthma, high cholesterol, seizures, local anesthesia), multivitamin products, and herbal or dietary supplements (eg, herbal teas, coenzyme Q10, garlic, ginseng, ginkgo, St. John's wort) may interact with Angilol, increasing the risk of side effects

This may not be a complete list of all interactions that may occur. Ask your health care provider if Angilol may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Angilol may cause drowsiness, dizziness, lightheadedness, or vision changes. These effects may be worse if you use it with alcohol or certain medicines. Use Angilol with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Check with your doctor before you drink alcohol while you are using Angilol; it may increase the risk of Angilol's side effects.

Do NOT use more than the recommended dose without checking with your doctor.

Patients who take medicine for high blood pressure often feel tired or run down for a few weeks after starting treatment. Be sure to take your medicine even if you may not feel "normal." Tell your doctor if you develop any new symptoms.

Tell your doctor or dentist that you use Angilol before you receive any medical or dental care, emergency care, or surgery.

If you have a history of any severe allergic reaction, talk with your doctor. You may be at risk of an even more severe allergic reaction if you come into contact with the substance that caused your allergy. Some medicines used to treat severe allergies may also not work as well while you are using Angilol.

Angilol may lower your blood sugar levels. This is most likely to happen in infants and children, or in patients who have diabetes or kidney problems. It may also occur after prolonged physical activity or during fasting. Low blood sugar may make you anxious, sweaty, weak, dizzy, drowsy, or faint. It may also make your heart beat faster; make your vision change; give you a headache, chills, or tremors; or make you more hungry. If this occurs, you should eat or drink a quick source of sugar like table sugar, honey, candy, orange juice, or non-diet soda. This will raise your blood sugar level quickly. Tell your doctor right away if this happens.

Diabetes patients - Angilol may hide signs of low blood sugar, such as a rapid heartbeat. Be sure to watch for other signs of low blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Angilol may interfere with certain lab tests, including glaucoma screening and dobutamine stress echocardiography. Be sure your doctor and lab personnel know you are using Angilol.

Lab tests, including blood pressure and heart function, may be performed while you use Angilol. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Angilol with caution in the elderly; they may be more sensitive to its effects.

Angilol should not be used in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Angilol while you are pregnant. Angilol is found in breast milk. If you are or will be breast-feeding while you use Angilol, check with your doctor. Discuss any possible risks to your baby.

If you stop taking Angilol suddenly, you may have withdrawal symptoms. These may include worsening chest pain along with possible heart attack.

All medicines may cause side effects, but many people have no, or minor, side effects.

Check with your doctor if any of these most common side effects persist or become bothersome:

Constipation; diarrhea; dizziness; drowsiness; fatigue; lightheadedness; mild pain, swelling, or redness at the injection site; nausea; stomach upset or cramping; trouble sleeping; vomiting; weakness.

Seek medical attention right away if any of these severe side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); chest pain; disorientation; fever with aching and sore throat; hallucinations; memory loss; mental or mood changes; numbness or tingling of the hands; persistent or severe vision changes; red, swollen, blistered, or peeling skin; severe dizziness; shortness of breath or wheezing; sudden, unusual weight gain; swelling of the hands, ankles, or feet; unusual bruising; unusually slow heartbeat; very cold or blue fingers or toes.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider.

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Zoman, Zoman

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What Is Sancuso® (Granisetron Transdermal System), Sancuso

What is SANCUSO?

SANCUSO is different because it is the first and only patch approved for the prevention of chemotherapy induced nausea and vomiting (CINV) in patients receiving moderately and or highly emetogenic chemotherapy. 1

When properly applied, it continuously delivers medication to help prevent CINV and can be worn for up to 7 days in a row. 1

How Do I Know if SANCUSO Is Right for Me?

Ask your healthcare professional if SANCUSO might be the right choice for you.

Some people treated for cancer experience difficulty swallowing pills, feel nauseated, and are unable to keep pills down. This can be caused by certain cancers or certain cancer treatments that may make it hard for you to swallow medicine that prevents chemotherapy induced nausea and vomiting (CINV). 5-7

Some cancer treatments may also reduce the ability of your intestines to absorb or retain the medicine in pills or tablets. 8

SANCUSO enters your system through your skin, not through intestinal absorption. 2

How Does SANCUSO Prevent Chemotherapy Induced Nausea and Vomiting (CINV)?

Some chemotherapy may irritate cells in the small intestine and/or in your brain.

Once irritated, cells in the small intestine send messages to the brain.

When irritated, cells in one area of the brain send messages to a different area of the brain.

Upon receiving these messages, the brain instructs the body to react through feelings of nausea and/or vomiting.

How SANCUSO helps prevent CINV 1

From the time that you apply the patch, SANCUSO slowly and continuously delivers granisetron through your skin and into your bloodstream until it's removed within 7 days. 1

Granisetron blocks cells in the small intestine from sending messages to the brain that trigger CINV. 1

Granisetron blocks cells in one area of the brain from sending messages to a different area of the brain that triggers CINV. 1

Because the brain does not receive these messages, feelings of nausea and/or vomiting are less likely to occur. 1

How Do I Get SANCUSO?

The first step is to talk to your healthcare professional. You can download and fill out this questionnaire to help you discuss if SANCUSO is right for you.

Download the questionnaire

You can only get SANCUSO with a prescription from your healthcare professional. Either fill the prescription at your local pharmacy, or have your doctor or nurse use our Patient Rx Solutions program to get SANCUSO mailed directly to your home.

Kyowa Kirin is committed to providing services and programs that help you gain access to and pay for the medications you need.

Patient Rx Solutions offers reimbursement assistance, a copay assistance card,* and SANCUSO patch replacement program.

Learn more about Patient Rx Solutions here

* The copay assistance offer is not valid for prescriptions under Medicaid, a Medicare drug benefit plan, Veterans Administration, DOD, Tricare, or other federal or state programs (such as medical assistance programs). If you are eligible for drug benefits under any such program, you cannot receive this offer. Program managed by PSKW, LLC on behalf of Kyowa Kirin, Inc. The parties reserve the right to amend or end this program at any time. Product dispensed pursuant to program rules and federal and state laws.

For more information, call 1-800-SANCUSO (1-800-726-2876)

INDICATION

SANCUSO ® (Granisetron Transdermal System) is indicated for the prevention of nausea and vomiting in patients receiving moderately and/or highly emetogenic chemotherapy regimens of up to 5 consecutive days duration.

IMPORTANT SAFETY INFORMATION FOR PATIENTS

Who should not use Sancuso?

Do not use Sancuso if you are allergic to granisetron or any of the other ingredients in Sancuso.

What should I tell my healthcare provider before using Sancuso?

Tell your healthcare provider about all your medical conditions, including if you:

if you are allergic to medical adhesive tape, adhesive dressings, or other skin patches

have pain or swelling in stomach area (abdomen).

are pregnant. It is not known if Sancuso will harm your unborn baby. Talk to your healthcare provider if you are pregnant or plan to become pregnant.

are breastfeeding, or plan to breastfeed. It is not known if Sancuso passes into your breast milk.

Tell your healthcare professional about all the medicines you take . including prescription and nonprescription medicines, vitamins, and herbal supplements. Other medicines may affect how Sancuso works. Sancuso may also affect how other medicines work.

How should Sancuso be used? Use Sancuso exactly as prescribed . See the detailed Patient Instructions for Applying Sancuso in the Patient Information leaflet.

What should I avoid while using Sancuso?

Do not apply any heat source over or near the Sancuso patch. For example,

a heating pad or heat lamp should not be used where the patch is applied.

You should also avoid extended exposure to heat as it may increase your granisetron blood levels during the time of heat exposure.

Avoid sunlight . The medicine in Sancuso (granisetron) may not work well and/or may affect your skin if exposed to direct sunlight and the light from sunlamps or tanning beds.

While wearing the patch keep it covered with clothing if you will be in sunlight or near a sunlamp, including tanning beds.

Keep the skin where Sancuso was applied covered for another 10 days after the patch is taken off to protect from exposure to direct sunlight.

What are the possible side effects of Sancuso?

Sancuso can cause serious side effects:

Using Sancuso may make it harder to identify certain stomach and bowel problems that are from other causes . Tell your healthcare provider if you have any stomach area (abdominal) pain or swelling while using Sancuso.

Skin reactions . Skin reactions can happen just at the patch application site or outside the patch application site. Tell your healthcare provider if you get any redness, rashes, bumps, blisters or itching at the patch application site, and especially if they spread outside the place where the patch was or if they appear outside the patch application site. You may need to stop using Sancuso.

You may see mild redness on the skin where the patch is removed. This redness should go away within three days. If redness continues, tell your healthcare professional.

The most common side effect of Sancuso is constipation.

This is not the only possible side effect of Sancuso. Tell your healthcare professional if you have any side effect that bothers you or that does not go away.

Sancuso is a prescription medicine used to prevent nausea and vomiting in people receiving some types of chemotherapy treatment.

For more information, ask your healthcare professional or pharmacist.

To report suspected side effects, contact Kyowa Kirin, Inc. at 1-800-SANCUSO or FDA at 1-800-FDA-1088 or: WWW. FDA. GOV/MEDWATCH.

Challenge Unlimited, Cuine

Challenge Unlimited, Inc. is a nonprofit organization established in 1959 to provide work related opportunities to individuals with disabilities, which enable them to achieve their highest level of independence. For over 50 years, Challenge has been committed to the inclusion of individuals with disabilities into mainstream society.

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Ekosetol, Ekosetol

Ekosetol

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Berlipril - Instructions For Use, Dosage, Analogs, Berlipril

Berlipril

Berlipril - a drug used to treat hypertension and heart failure.

Release form and composition

Berlipril available as tablets of 5, 10 and 20 mg, the main active ingredient of which is enalapril maleate.

As auxiliary substances Berliprile utilized: gelatin, lactose monohydrate, magnesium stearate, magnesium carbonate, colloidal silicon dioxide, sodium carboxymethyl starch, brown iron oxide pigment.

The tablets are available in blister packs of 20, 30, 50 and 100 pieces per pack.

Indications

According to the instructions, Berlipril used for:

Hypertension (including renovascular hypertension);

Asymptomatic left ventricular dysfunction as part of combination therapy;

Chronic heart failure.

Contraindications

Application Berlipril contraindicated in:

The increased sensitivity of the patient to the drug and other ACE inhibitors;

A history of angioedema caused by ACE inhibitor therapy;

Porphyry;

Pregnancy and lactation;

and in patients under 18 years of age.

According to the instructions, Berlipril cautiously prescribed for:

Primary hyperaldosteronism;

Stenosis of the artery to a solitary kidney;

Of bilateral renal artery stenosis;

Aortic stenosis;

hyperkalemia;

Mitral stenosis;

Condition after kidney transplantation;

Idiopathic hypertrophic subaortic stenosis;

Cerebrovascular diseases;

Connective tissue diseases;

Diabetes;

Coronary heart disease;

Kidney failure;

Hepatic Insufficiency;

Receiving immunosuppressants and saluretikov;

as well as in patients on hemodialysis, or a diet with salt restriction, in elderly patients and patients with reduced blood volume.

Dosage and Administration

According to the instructions, Berlipril intended for oral administration. Tablets are taken at any time regardless of the meal.

When hypertension as monotherapy - 5 mg 1 time per day; if the effect of this dosage is absent, 1-2 weeks the dose was raised to 5 mg. If there is a need and well tolerated by the patient, the dosage was increased to 40 mg per day (1-2 doses); then after 2-3 weeks the drug begin to take a maintenance dose of 10-40 mg per day (1-2 doses);

At moderate hypertension - average mg per day and 10, but not more than 40 mg per day. Thus it is necessary to cancel the diuretic therapy. If unable to cancel it or the patient has hyponatremia drug is given at a dose of 2.5 mg per day;

When renovascular hypertension - at 2.5-5 mg daily (initial dose), but not more than 20 mg per day;

In chronic heart failure - 2.5 mg per day with gradual increase in the dose of the day every 3-4 2.5-5 mg but not more than 40 mg per day. When Sad below 110 mm Hg, and in older patients the initial dosage of 1.25 mg; average maintenance dose is 5-20 mg per day (1-2 doses);

In asymptomatic left ventricular dysfunction - 2 times a day, 2.5 mg, with a gradual increase in dosage until the maximum tolerated.

Side effects

When using Berlipril may experience certain adverse reactions:

The nervous system and sensory organs: headache, dizziness, insomnia, fatigue, anxiety, fatigue, confusion, drowsiness, nervousness, paresthesia, depression, hearing loss, visual, vestibular, tinnitus;

The cardiovascular system and the blood system: Orthostatic hypotension, severe decrease in blood pressure, angina, myocardial infarction, arrhythmia, palpitations, heart pain, fainting, thromboembolic pulmonary artery branches, reduction of hemoglobin, anemia, increased erythrocyte sedimentation rate, neutropenia, agranulocytosis (with Berlipril use in patients with autoimmune diseases);

Respiratory: interstitial pneumonitis, dry nonproductive cough, dyspnea, bronchospasm, pharyngitis, rhinorrhea;

Gastrointestinal tract: anorexia, dyspepsia, intestinal obstruction, disorders of the liver, pancreatitis, hepatitis;

Genito-urinary system: proteinuria, violation of the kidney;

Allergic reactions: rash, angioedema extremity edema, face, tongue, lips, throat, dysphonia, exfoliative dermatitis, erythema multiforme, Stevens-Johnson syndrome, pemphigus, toxic epidermal necrolysis, urticaria, photosensitivity, vasculitis, serositis, arthralgia, myositis, arthritis, glossitis, stomatitis;

Laboratory findings: hyperbilirubinemia, hypercreatininemia, increased urea levels, hyperkalemia, hyponatremia, decreased hematocrit;

Other: flushing, decreased libido.

special instructions

When applying Berlipril should be borne in mind that:

The risk of anaphylaxis is increased when using vysokoprotochnyh dialysis membranes. Correction in the dosage of the free days of dialysis is performed depending on the blood pressure;

Before and after therapy Berliprilom should monitor blood pressure, blood and the level of protein in the urine;

It is necessary to refrain from road management and the performance of potentially hazardous activities related to the speed of psychomotor reactions, and high concentration of attention;

Before the drug simultaneously with NSAIDs may reduce the hypotensive effect of it;

Before the drug with potassium-sparing diuretics may develop hyperkalemia;

Before the drug together with lithium salts in lithium excretion is slowing down;

Berlipril teofillinsoderzhaschih reduces the effect of drugs;

The antihypertensive effect of the drug is enhanced with diuretics, beta-blockers, nitrates, methyldopa, hydralazine, BPC, prazosin;

Gematotoksichnosti drug increases immunosuppressants, cytostatics, allopurinol;

The risk of neutropenia or agranulocytosis increases bone drugs depressing marrow function;

Overdose Berliprilom shown a pronounced decrease in blood pressure (up to the collapse, acute cerebrovascular accident, myocardial infarction, thromboembolic complications), stupor, convulsions; to reduce the symptoms of overdose the patient provide a horizontal position with a low headboard. In mild overdose gastric lavage is used with the purpose of saline inside, in severe - shows measures to stabilize blood pressure.

Analogs Berlipril

Berlipril analogs are drugs such as Enap, ednit, Renitec, Enam.

Terms and conditions of storage

Berlipril stored at a temperature not exceeding 25? in areas with limited access of children less than 3 years.

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Estracombi Tts (Discontinued In The Uk - May To July 2009), Estracombi

Estracombi TTS (discontinued in the UK - May to July 2009)

What is it used for?

Hormone replacement therapy to relieve symptoms of the menopause .

Second-line option for preventing osteoporosis in postmenopausal women who are at high risk of fractures and cannot take other medicines licensed for preventing osteoporosis.

How does it work?

Estracombi TTS is a hormone replacement therapy (HRT) preparation. It consists of two types of patches: Estraderm TTS 50 patches, which contain estradiol (previously spelt oestradiol in the UK) and Estragest TTS patches, which contain estradiol and norethisterone acetate. These are forms of the main female sex hormones, oestrogen and progesterone. Estradiol is a naturally occuring form of oestrogen and norethisterone acetate is a synthetic form of progesterone.

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Womens' ovaries gradually produce less and less oestrogen in the period up to the menopause, and oestrogen blood levels decline as a result. The declining levels of oestrogen can cause distressing symptoms, such as irregular periods, hot flushes, night sweats, mood swings and vaginal dryness or itching.

Oestrogen (in this case in the form of estradiol) can be supplemented to replace the falling levels in the body and help reduce these distressing symptoms of the menopause. This is known as hormone replacement therapy (HRT). HRT is usually only required for short-term relief from menopausal symptoms and its use should be reviewed at least once a year with your doctor.

A progestogen (in this case in the form of norethisterone acetate) is needed as part of HRT for women who have not had a hysterectomy. This is because in women with an intact womb, oestrogen stimulates the growth of the womb lining (endometrium), which can lead to endometrial cancer if the growth is unopposed. A progestogen is given to oppose oestrogen's effect on the womb lining and reduce the risk of cancer, though it does not eliminate this risk entirely. This is known as combined HRT.

Estracombi TTS is known as a sequential form of combined HRT, which means that oestrogen is used on a continuous basis and progesterone is added for the last two weeks of each monthly cycle. It is more suitable for women who are still having irregular periods because it usually results in a monthly withdrawal bleed. The patches release the medicine through the skin into the bloodstream at a constant rate and are designed to be changed twice a week, ie a patch is worn for three to four days and then replaced with a new one. The Estraderm TTS 50 patches are used in the first two weeks and the Estragest TTS patches are used in the second two weeks of each monthly cycle. A withdrawal bleed usually occurs each month, towards the end of the Estragest TTS patches.

The declining level of oestrogen at menopause can also affect the bones, causing them to become thinner and more prone to breaking; a condition known as osteoporosis. Oestrogen can therefore also be supplemented to help prevent bone loss and fractures that may occur in women in the years after menopause.

However, in December 2003, a review of the available evidence on the risks and benefits of HRT by the Medicines and Healthcare products Regulatory Agency (MHRA) and the Committee on Safety of Medicines (CSM) in the UK, concluded that the risks of using HRT long-term to prevent osteoporosis in women aged over 50 years exceed the benefits. As a result this medicine should not be used as a first-line option for preventing postmenopausal osteoporosis in women over 50. However, it may be used as a second-line option for women at high risk of fractures who cannot take other medicines that are licensed for preventing osteoporosis.

Women considered to be at risk of developing fractures following the menopause include those who have had an early menopause, those with a family history of osteoporosis, those who have had recent prolonged corticosteroid therapy (eg prednisolone), those with a small thin frame, and smokers.

You can read more about the risks and benefits of HRT and other medicines for preventing osteoporosis in the factsheets about menopause and osteoporosis linked below.

Warning!

Estracombi TTS patches will be discontinued during May to July 2009. If you are using these patches you will need to make an appointment with your doctor to discuss alternative medicines.

Follow the instructions provided with your patches carefully. Each patch should be applied to a clean, dry, unbroken, non-irritated area of skin on the trunk below the waist, preferably the buttock or hip. Don't apply creams, lotions or other oily products before applying the patch as they will stop it sticking. The patch should be replaced with a new one twice a week (Estraderm TTS 50 patches for the first two weeks and Estragest TTS patches for the second two weeks of each monthly cycle). Each fresh patch should be applied to a slightly different area to avoid irritating the skin. Leave at least a week before applying a patch to the same site. Patches should NOT be applied on or near the breasts. They should not be exposed to sunlight.

You can shower and bath without removing the patch. If a patch falls off before you are due to change it, for example because you have been doing vigorous exercise, sweating excessively, or wearing clothes that rub the patch, you should replace it with a new one of the same type as the one that fell off. Change this new patch as you usually would on your normal patch change day.

Women taking any form of HRT should have regular medical and gynaecological check-ups. Your need for continued HRT should be reviewed with your doctor at least once a year.

It is important to be aware that all women using HRT have an increased risk of being diagnosed with breast cancer compared with women who don't use HRT. This risk needs to be weighed against the personal benefits to you of taking HRT. There is more detailed information about the risks and benefits associated with HRT in the factsheet about the menopause linked above. You should discuss these with your doctor before starting HRT. Women on HRT should have regular breast examinations and mammograms and should examine their own breasts regularly. Report any changes in your breasts to your doctor or nurse.

It is important to be aware that women using HRT have a slightly increased risk of stroke and of blood clots forming in the veins (eg deep vein thrombosis /pulmonary embolism ) compared with women who don't use HRT. The risk is higher if you have existing risk factors (eg personal or family history, smoking, obesity, certain blood disorders - see cautions below) and needs to be weighed against the personal benefits to you of taking HRT. There is more detailed information about the risks and benefits associated with HRT in the factsheet about the menopause linked above. Discuss these with your doctor before starting treatment.

The risk of blood clots forming in the veins (thromboembolism) while taking HRT may be temporarily increased if you experience major trauma, have surgery, or are immobile for prolonged periods of time (this includes travelling for over five hours). For this reason, your doctor may recommend that you stop taking HRT for a period of time (usually four to six weeks) prior to any planned surgery, particularly abdominal surgery or orthopaedic surgery on the lower limbs, or if you are to be immobile for long periods. The risk of blood clots during long journeys may be reduced by appropriate exercise during the journey and possibly by wearing elastic hosiery. Discuss this with your doctor.

Stop using this medicine and inform your doctor immediately if you experience any of the following symptoms while using this medicine: stabbing pains or swelling in one leg; pain on breathing or coughing; coughing up blood; breathlessness; sudden chest pain; sudden numbness affecting one side or part of the body; fainting; worsening of epilepsy; migraine or severe headaches; visual disturbances; severe abdominal complaints; increased blood pressure; itching of the whole body; yellowing of the skin or eyes (jaundice); or severe depression.

This medicine will usually cause a withdrawal bleed towards the end of the Estragest TTS patches. You may also experience spotting or breakthrough bleeding during the first few months of treatment. Spotting or breakthrough bleeding is more likely if you forget to change a patch on schedule. If any breakthrough bleeding or spotting continues after a few months of taking the medicine, or after stopping treatment, you should consult your doctor so that it can be investigated.

A woman is considered fertile for two years after her last menstrual period if she is under 50, or for one year if over 50. HRT does not provide contraception for women who fall within this group. If a potentially fertile women is taking HRT but also requires contraception, a non-hormonal method (eg condoms or contraceptive foam ) should be used.

Use with caution in

Close family history of breast cancer (eg mother, sister or grandmother has had the disease)

History of benign breast lumps (fibrocystic breast disease)

History of fibroids in the womb

History of endometriosis

History of overgrowth of the lining of the womb (endometrial hyperplasia)

Personal or family history of blood clots in the veins (venous thromboembolism, eg deep vein thrombosis or pulmonary embolism )

Blood disorders that increase the risk of blood clots in the veins, eg antiphospholipid syndrome. factor V Leiden

Women taking medicines to prevent blood clots (anticoagulants), eg warfarin

Long-term inflammation of skin and some internal organs (systemic lupus erythematosus)

Personal or family history of recurrent miscarriage

Severe obesity

Varicose veins

Smokers

History of high blood pressure (hypertension)

Raised levels of fats called triglycerides in the blood (hypertriglyceridaemia)

History of liver disease, eg liver cancer

Decreased kidney function

Heart failure

History of diabetes

History of gallstones

History of migraines or severe headaches

History of epilepsy

History of asthma

History of an ear disorder that may cause hearing loss (otosclerosis)

History of irregular brown patches appearing on the skin, usually of the face, during pregnancy or previous use of hormone preparations such as contraceptive pills (chloasma). Women with a tendency to this condition should minimise their exposure to the sun or UV light while taking HRT.

Not to be used in

Known, suspected, or past history of breast cancer

Known or suspected cancer in which growth of the cancer is stimulated by oestrogen, eg cancer of the lining of the womb (endometrial cancer)

Untreated overgrowth of the lining of the womb (endometrial hyperplasia)

Vaginal bleeding of unknown cause

Women with a blood clot in a vein of the leg (deep vein thrombosis ) or in the lungs (pulmonary embolism ), or a past history of these conditions where the cause is unknown

Women who have recently had a stroke caused by a blood clot

Women who have recently had a heart attack

Angina pectoris

Active liver disease

History of liver disease when liver function has not returned to normal

Hereditary blood disorders known as porphyrias

Pregnancy

Breastfeeding .

This medicine should not be used if you are allergic to one or any of its ingredients. Please inform your doctor or pharmacist if you have previously experienced such an allergy.

If you feel you have experienced an allergic reaction, stop using this medicine and inform your doctor or pharmacist immediately.

Pregnancy and Breastfeeding

Certain medicines should not be used during pregnancy or breastfeeding. However, other medicines may be safely used in pregnancy or breastfeeding providing the benefits to the mother outweigh the risks to the unborn baby. Always inform your doctor if you are pregnant or planning a pregnancy, before using any medicine.

This medicine should not be used by women who are pregnant or breastfeeding. You should stop taking this medicine and consult your doctor immediately if you get pregnant during treatment.

A woman is considered fertile for two years after her last menstrual period if she is under 50, or for one year if over 50. HRT does not provide contraception for women who fall within this group. If you could get pregnant while taking this HRT, you should use a non-hormonal method of contraception (eg condoms or contraceptive foam ). Seek medical advice from your doctor.

Side effects

Medicines and their possible side effects can affect individual people in different ways. The following are some of the side effects that are known to be associated with this medicine. Because a side effect is stated here, it does not mean that all people using this medicine will experience that or any side effect.

Redness, irritation and itching of skin at patch application site

Breakthrough bleeding/spotting

Breast discomfort

Nausea

Abdominal pain and bloating

Headache/migraine

Leg cramps

Premenstrual-like symptoms

Heavy menstrual bleeding

Dizziness

Excessive fluid retention in the body tissues, resulting in swelling (oedema)

Weight changes

Increase in blood pressure

Disturbance in liver function

Irregular brown patches on the skin, usually of the face (chloasma)

Blood clots in the blood vessels (eg, DVT, pulmonary embolism, heart attack, stroke - see warnings above)

The side effects listed above may not include all of the side effects reported by the drug's manufacturer.

For more information about any other possible risks associated with this medicine, please read the information provided with the medicine or consult your doctor or pharmacist.

How can this medicine affect other medicines?

It is important to tell your doctor or pharmacist what medicines you are already taking, including those bought without a prescription and herbal medicines, before you start treatment with this medicine. Similarly, check with your doctor or pharmacist before taking any new medicines while using this one, to ensure that the combination is safe .

The following medicines may potentially reduce the blood levels and effect of this medicine, which could result in recurrence of symptoms or irregular bleeding:

antiepileptic medicines such as carbamazepine, phenytoin, phenobarbital and primidone

barbiturates such as amobarbital

protease inhibitors for HIV infection such as ritonavir and nelfinavir

rifamycin antibiotics such as rifabutin and rifampicin

the herbal remedy St John's wort (Hypericum perforatum).

Oestrogens may increase the blood level of ropinirole used to treat Parkinson's disease.

Some women with diabetes may need small adjustments in their dose of insulin or antidiabetic tablets while taking this medicine. You should monitor your blood sugar and seek advice from your doctor or pharmacist if your blood sugar control seems to be altered after starting this medicine.

Other medicines containing the same active ingredients

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Buy Rebilex-Dsr (Aciphex) Online No Prescription, Rebilex-Dsr

Buy Rebilex-dsr (Aciphex) without Prescription

Rebilex-dsr Marketing Information

Rebilex-dsr Description

Generic Rebilex-dsr is a perfect remedy in struggle against heartburn or irritation of the esophagus caused by gastroesophageal reflux disease (GERD).

Generic Rebilex-dsr acts as by decreasing the amount of acid produced in the stomach. It is a proton pump inhibitor.

Generic name of Generic Rebilex-dsr is Rabeprazole.

Brand name of Generic Rebilex-dsr is Rebilex-dsr.

Rebilex-dsr Dosage

Generic Rebilex-dsr is available in:

10mg Low Dosage20mg Standard Dosage

Take Generic Rebilex-dsr orally with or without food.

Do not crush or chew it.

Do not stop taking it suddenly.

Rebilex-dsr Missing of dose

Do not take double dose. If you miss a dose you should take it as soon as you remember about your missing. If it is the time for the next dose you should continue your regular dosing schedule.

Rebilex-dsr Overdose

If you overdose Generic Rebilex-dsr and you don't feel good you should visit your doctor or health care provider immediately.

Rebilex-dsr Side effects

Generic Rebilex-dsr has its side effects. The most common are:

Less common but more serious side effects during taking Generic Rebilex-dsr:

allergy reactions (urticaria, breathing difficulties, rash, and eruption)chest painfast or irregular heartbeatfever, chills, or sore throatred, swollen, blistered, or peeling skinsevere or persistent stomach painunusual bruising or bleedingunusual tirednessvision changes

Side effects manifestations are not only depend on medicine you are taking but also depend on your health state and on the other factors.

Rebilex-dsr Contra-indications

Do not take Generic Rebilex-dsr if you are allergic to Generic Rebilex-dsr components.

Do not take Generic Rebilex-dsr if you're pregnant or you plan to have a baby, or you are a nursing mother. Generic Rebilex-dsr can harm your baby.

Generic Rebilex-dsr may interfere with certain lab tests.

Generic Rebilex-dsr should be used with extreme caution in Asian patients.

Generic Rebilex-dsr should be used with extreme caution in children younger than 12 years old. Safety and effectiveness in these children have not been confirmed.

Do not stop taking Generic Rebilex-dsr suddenly.

Rebilex-dsr Frequently asked questions

Q: What is the important Generic Rebilex-dsr information?

A: Generic Rebilex-dsr is a perfect remedy in struggle against heartburn or irritation of the esophagus caused by gastroesophageal reflux disease (GERD). Generic Rebilex-dsr may interfere with certain lab tests. Generic Rebilex-dsr should be used with extreme caution in Asian patients. Generic Rebilex-dsr should be used with extreme caution in children younger than 12 years old; safety and effectiveness in these children have not been confirmed. Do not take Generic Rebilex-dsr in case of allergy to this medicine or to its ingredients. Generic Rebilex-dsr cannot be taken if you're pregnant or you plan to have a baby, or you are a nursing mother. If you want to achieve most effective results it is better to avoid alcohol.

Q: What are Generic Rebilex-dsr side effects?

A: Generic Rebilex-dsr has its common side effects such as: diarrhea; headache. But in case of rejection of Generic Rebilex-dsr ingredients you can experience more serious side effects: allergic symptoms (difficulties with breathing, throat closing, swelling, rash, hives), chest pain; fast or irregular heartbeat; fever, chills, or sore throat; red, swollen, blistered, or peeling skin; severe or persistent stomach pain; unusual bruising or bleeding; unusual tiredness; vision changes.

Q: What are generic and brand names of Generic Rebilex-dsr?

A: Generic name of Generic Rebilex-dsr is Rabeprazole. Brand name of Generic Rebilex-dsr is Rebilex-dsr.

Dafiro Hct 5 Mg, Dafiro

Dafiro HCT 5 mg/160 mg/25 mg film-coated tablets

Dafiro HCT tablets contain three substances called amlodipine, valsartan and hydrochlorothiazide. All of these substances help to control high blood pressure.

Amlodipine belongs to a group of substances called “calcium channel blockers”. Amlodipine stops calcium from moving into the blood vessel wall, which stops the blood vessels from tightening.

Valsartan belongs to a group of substances called “angiotensin-II receptor antagonists”. Angiotensin II is produced by the body and makes the blood vessels tighten, thus increasing the blood pressure. Valsartan works by blocking the effect of angiotensin II.

Hydrochlorothiazide belongs to a group of substances called “thiazide diuretics”. Hydrochlorothiazide increases urine output, which also lowers blood pressure. As a result of all three mechanisms, the blood vessels relax and blood pressure is lowered.

Dafiro HCT is used to treat high blood pressure in adult patients who are already taking amlodipine, valsartan and hydrochlorothiazide and who may benefit from taking one tablet containing all three substances.

Do not take Dafiro HCT

if you are more than 3 months pregnant (It is also better to avoid Dafiro HCT in early pregnancy – see Pregnancy section).

if you are allergic (hypersensitive) to amlodipine, valsartan, hydrochlorothiazide, sulphonamide-derived medicines (medicines used to treat chest or urinary infections), or any of the other ingredients of Dafiro HCT (see section 6, “What Dafiro HCT contains”. If you think you may be allergic, do not take Dafiro HCT and talk to your doctor.

if you have liver problems, such as liver disorders and jaundice (cholestasis).

if you have severe kidney problems or if you are having dialysis.

if you are suffering from an inability to produce urine.

if the level of potassium or sodium in your blood is too low despite treatment.

if the level of calcium in your blood is too high despite treatment.

if you have gout (uric acid crystals in the joints). If any of the above applies to you, do not take Dafiro HCT and talk to your doctor .

Take special care with Dafiro HCT

if you have a low level of potassium, sodium or magnesium in your blood.

if you have a high level of calcium in your blood.

if you are taking medicines or substances that increase the amount of potassium in your blood. These include potassium supplements or salt substitutes containing potassium, potassium-sparing medicines and heparin. It may be necessary to check the amount of potassium in your blood at regular intervals.

if you have kidney problems, have had a kidney transplant or if you had been told that you have a narrowing of your kidney arteries.

if you have liver problems.

if you have or have had heart failure or coronary arterydisease, particularly if you are taking the maximum dose of Dafiro HCT (10 mg/320 mg/25 mg)

if your doctor has told you that you have a narrowing of the valves in your heart (called “aortic or mitral stenosis”) or that the thickness of your heart muscle is abnormally increased (called “obstructive hypertrophic cardiomyopathy”).

if you suffer from aldosteronism. This is a disease in which the adrenal glands make too much of the hormone aldosterone If this applies to you, the use of Dafiro HCT is not recommended.

if you suffer from a disease called systemic lupus erythematosus (also called “lupus” or “SLE”).

if you have diabetes (high blood sugar).

if you have high levels of cholesterol or triglycerides in your blood.

if you experience skin reactions such as rash after sun exposure

if you had an allergic reaction to other high blood pressure medicines or diuretics (a type of medicine also known as “water tablets”), especially if you suffer from asthma and allergies

if you have been sick (vomiting or diarrhoea).

if you experience dizziness and/or fainting during treatment with Dafiro HCT, tell your doctor as soon as possible. If any of these apply to you, talk to your doctor.

You must tell your doctor if you think that you are ( or might become ) pregnant. Dafiro HCT is not recommended in early pregnancy and must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if used at this stage (see section “Pregnancy and breast-feeding”).

The use of Dafiro HCT in children and adolescents under 18 years of age is not recommended.

Dafiro HCT and older people (age 65 years and older) Dafiro HCT can be used by people aged 65 years and over at the same dose as for other adults and in the same way as they have already taken the three substances called amlodipine, valsartan and hydrochlorothiazide. Elderly patients, particularly those taking the maximum dose of Dafiro HCT (10 mg/320 mg/25 mg), should have their blood pressure checked regularly.

Using other medicines Please tell your doctor or pharmacist if you are using or have recently used any other medicine, including medicines obtained without a prescription. Your doctor may need to change the dose or take other precautions. In some cases you may have to stop using one of the medicines. This is especially important if you are using any of the medicines listed below:

Do not take together with:

lithium (a medicine used to treat some types of depression);

medicines or substances that increase the amount of potassium in your blood. These include potassium supplements or salt substitutes containing potassium, potassium-sparing medicines and heparin.

Caution should be used with:

alcohol, sleeping pills and anaesthetics (medicines allowing patients to undergo surgery and other procedures);

allopurinol (anti-gout treatment);

amantadine (anti-Parkinson therapy, also used for influenza treatment);

anticholinergic agents (medicines used to treat a variety of disorders such as gastrointestinal cramps, urinary bladder spasm, asthma, motion sickness, muscular spasms, Parkinson's disease and as an aid to anaesthesia);

anticonvulsant medicines and mood-stabilising medicines used to treat epilepsy and bipolar disorder (e. g. carbamazepine, phenobarbital, phenytoin, fosphenytoin, primidone);

cholestyramine and colestipol (substances used mainly to treat high levels of lipids in the blood);

ciclosporin (a medicine used in transplantation to prevent organ rejection or for other conditions, e. g: rheumatoid arthritis or atopic dermatitis);

cortisone-like medicines, steroids;

curare derivatives (a medicine to relax the muscles which is used during operations);

cytotoxic medicines (used to treat cancer);

digoxin (a heart medicine);

medicines for the treatment of diabetes (oral agents such as metformin or insulins);

medicines to increase blood pressure (adrenaline, noradrenaline);

medicines used for HIV/AIDS (e. g. ritonavir) or for treatment of fungal infections (e. g. ketoconazole);

medicines used for oesophageal ulceration and inflammation (carbenoxolone);

medicines used to relieve pain or inflammation, especially non-steroidal anti-inflammatory agents;

nitroglycerin and other nitrates, or other substances called “vasodilators”;

other medicines to treat high blood pressure (beta blockers, diazoxides, methyldopa);

rifampicin (used, for example, to treat tuberculosis);

some medicines used to treat infections such as amphotericin, penicillin G, tetracycline;

St. John’s wort;

vitamin D and calcium salts. Talk to your doctor before drinking alcohol. Alcohol may make your blood pressure fall too much and/or increase the possibility of dizziness or fainting.

Taking Dafiro HCT with food and drink You can take Dafiro HCT with or without food.

Pregnancy and breast-feeding Pregnancy You must tell your doctor if you think you are ( or might become ) pregnant. Your doctor will normally advise you to stop taking Dafiro HCT before you become pregnant or as soon as you know you are pregnant and will advise you to take another medicine instead of Dafiro HCT. Dafiro HCT is not recommended in early pregnancy and must not be taken if you are more than 3 months pregnant, as it may cause serious harm to your baby if it is used after the third month of pregnancy.

Breast-feeding Tell your doctor if you are breast-feeding or about to start breast-feeding. Dafiro HCT is not recommended for mothers who are breast-feeding, and your doctor may choose another treatment for you if you wish to breast-feed, especially if your baby is a newborn, or was born prematurely.

Ask your doctor or pharmacist for advice before taking any medicine.

Driving and using machines As with many other medicines used to treat high blood pressure, this medicine may make you feel dizzy. If you experience this symptom, do not drive or use tools or machines.

Always take this medicine exactly as your doctor has told you. You should check with your doctor if you are not sure. This will help you get the best results and lower the risk of side effects.

The usual dose of Dafiro HCT is one tablet per day.

It is best to take the tablet at the same time each day. Morning is the best time.

Swallow the tablet whole with a glass of water.

You can take Dafiro HCT with or without food.

Depending on how you respond to the treatment, your doctor may suggest a higher or lower dose.

If you take more Dafiro HCT than you should If you have accidentally taken too many Dafiro HCT tablets, talk to a doctor immediately. You may require medical attention.

If you forget to take Dafiro HCT If you forget to take a dose of this medicine, take it as soon as you remember and then take the next dose at its usual time. If it is almost time for your next dose you should simply take the next tablet at the usual time. Do not take a double dose (two tablets at once) to make up for a forgotten tablet.

If you stop taking Dafiro HCT Stopping your treatment with Dafiro HCT may cause your disease to get worse. Do not stop taking your medecine unless your doctor tells you to.

Always take this medicine, even if you are feeling well People who have high blood pressure often do not notice any signs of the problem. Many feel normal. It is very important that you take this medicine exactly as your doctor tells you to get the best results and reduce the risk of side effects. Keep your appointments with the doctor even if you are feeling well.

If you have any further questions on the use of this product ask your doctor or pharmacist.

Like all medicines, Dafiro HCT can cause side effects, although not everybody gets them. These side effects may occur with certain frequencies, which are defined as follows: very common: affects more than 1 user in 10 common: affects 1 to 10 users in 100 uncommon: affects 1 to 10 users in 1,000 rare: affects 1 to 10 users in 10,000 very rare: affects less than 1 user in 10,000 not known: frequency cannot be estimated from the available data

Some side effects can be serious and need immediate medical attention:

You should see your doctor immediately if you experience any of the following symptoms: Common

dizziness

low blood pressure (feeling of faintness, light-headedness, sudden loss of consciousness) Uncommon

severely decreased urine output (decreased kidney function)

spontaneous bleeding

irregular heart beat

liver disorder Very rare

allergic reaction with symptoms such as rash, itching

angioedema: swelling of face or lips or tongue, difficulty of breathing

crushing/tight chest pain that gets worse or that does not go away

weakness, bruising, fever and frequent infections

stiffness

Other possible side effects of Dafiro HCT: Common . Stomach discomfort after meal; tiredness; swelling; low level of potassium in the blood; headache; frequent urination. Uncommon: Fast heart beat; spinning sensation; vision disorder; stomach discomfort; chest pain; increase of urea nitrogen, creatinine and uric acid in the blood; high level of calcium fat or sodium in the blood; decrease of potassium in the blood; breath odour; diarrhoea; dry mouth; nausea; vomiting; abdominal pain; weight increase; loss of appetite; disturbed sense of taste; back pain; joint swelling; muscle cramps/weakness/pain; pain in extremity; inability to either stand or walk in a normal manner; weakness; abnormal coordination; dizziness on standing up or after exercising; lack of energy; sleep disturbances; tingling or numbness; neuropathy; sleepiness; sudden, temporary loss of consciousness; low blood pressure on standing up; impotence; cough; breathlessness; throat irritation; excessive sweating; itching; swelling, reddening and pain along a vein; skin reddening; trembling. Not known . Changes in blood tests for kidney function, increase of potassium in your blood, low level of red blood cells.

Side effects reported with amlodipine or valsartan or hydrochlorothiazide alone, but not observed with Dafiro HCT or observed in a higher frequency:

Amlodipine Common: Palpitations; abdominal pain; nausea; sleepiness; hot flushes. Uncommon: Ringing noise in ears; change of bowel habit; pain; weight decrease; joint pain; trembling; mood swings; urination disorders; urination at night; breast enlargement in men; runny nose; hair loss; skin eruption; purple skin patches; rash; skin discoloration. Very rare . Low level of white blood cells and blood platelets; irregular heart beat; heart attack; inflammation of the stomach lining or of the pancreas, gingival overgrowth, abnormal liver function test; liver disorder which can occur together with yellow skin and eyes, or dark-coloured urine; allergic reaction including swelling deeper in the skin and difficulty breathing; high level of sugar in the blood; increased muscle stiffness; skin reaction with skin reddening and peeling, blistering of lips, eyes or mouth; itchy rash; inflammation of blood vessels. Not known . Stiff limbs and trembling hands.

Valsartan Not known: Abnormal red blood cell test; low level of a certain type of white blood cell and blood platelet; increase of potassium in the blood; increase of creatinine in the blood; abnormal liver function test; allergic reaction including swelling deeper in the skin and difficulty breathing; muscle pain; severely decreased urine output; itching; rash; inflammation of blood vessels.

Hydrochlorothiazide Common: Increase of lipids in the blood. Uncommon: Low level of magnesium in the blood; rash; itchy rash. Rare: Low level of blood platelets, sugar in the urine; high level of sugar in the blood; depression; irregular heart beat; abdominal discomfort; constipation; liver disorder which can occur together with yellow skin and eyes, or dark-coloured urine; increased sensitivity of skin to sun; purple skin patches.

Very rare . Lack or low level of white blood cells; haemolytic anaemia (abnormal breakdown of red blood cells either in the blood vessels or elsewhere in the body); inflammation of the pancreas; allergic reaction; difficulty breathing, breathlessness; inflammation of the lungs, lupus erythematosus; inflammation of blood vessels; severe skin disease that causes rash, red skin, blistering of the lips, eyes or mouth, skin peeling, fever.

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

Keep out of the reach and sight of children. Do not use Dafiro HCT after the expiry date which is stated on the carton and blister after EXP. The expiry date refers to the last day of that month. Do not store above 30°C. Store in the original package in order to protect from moisture. Do not use any Dafiro HCT pack that is damaged or shows signs of tampering.

Revibra, Revibra

Revibra

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Simovil Generic Name Simvastatin Online, Simovil

Simovil General Information

Simovil - Pharmacology:

The 6-membered lactone ring of simvastatin is hydrolyzed in vivo to generate mevinolinic acid, an active metabolite structurally similar to HMG-CoA (hydroxymethylglutaryl CoA). Once hydrolyzed, simvastatin competes with HMG-CoA for HMG-CoA reductase, a hepatic microsomal enzyme. Interference with the activity of this enzyme reduces the quantity of mevalonic acid, a precursor of cholesterol.

Simovil for patients

Patients should be advised about substances they should not take concomitantly with simvastatin and be advised to report promptly unexplained muscle pain, tenderness, or weakness. Patients should also be advised to inform other physicians prescribing a new medication that they are taking ZOCOR.

This description is suitable for active ingredient Simvastatin

Simovil Interactions

Simovil is metabolized by CYP3A4 but has no CYP3A4 inhibitory activity; therefore it is not expected to affect the plasma concentrations of other drugs metabolized by CYP3A4. Potent inhibitors of CYP3A4 (below) increase the risk of myopathy by reducing the elimination of simvastatin.

HIV protease inhibitors

Large quantities of grapefruit juice (>1 quart daily)

Interactions with lipid-lowering drugs that can cause myopathy when given alone

The risk of myopathy is increased by gemfibrozil and to a lesser extent by other fibrates and niacin (nicotinic acid) (1 g/day).

Other drug interactions

Danazol: The risk of myopathy/rhabdomyolysis is increased by concomitant administration of danazol particularly with higher doses of simvastatin

Amiodarone or Verapamil: The risk of myopathy/rhabdomyolysis is increased by concomitant administration of amiodarone or verapamil with higher doses of simvastatin

Propranolol: In healthy male volunteers there was a significant decrease in mean Cmax, but no change in AUC, for simvastatin total and active inhibitors with concomitant administration of single doses of ZOCOR and propranolol. The clinical relevance of this finding is unclear. The pharmacokinetics of the enantiomers of propranolol were not affected.

Digoxin: Concomitant administration of a single dose of digoxin in healthy male volunteers receiving simvastatin resulted in a slight elevation (less than 0.3 ng/mL) in digoxin concentrations in plasma (as measured by a radioimmunoassay) compared to concomitant administration of placebo and digoxin. Patients taking digoxin should be monitored appropriately when simvastatin is initiated.

Warfarin: In two clinical studies, one in normal volunteers and the other in hypercholesterolemic patients, simvastatin 20-40 mg/day modestly potentiated the effect of coumarin anticoagulants: the prothrombin time, reported as International Normalized Ratio (INR), increased from a baseline of 1.7 to 1.8 and from 2.6 to 3.4 in the volunteer and patient studies, respectively. With other reductase inhibitors, clinically evident bleeding and/or increased prothrombin time has been reported in a few patients taking coumarin anticoagulants concomitantly. In such patients, prothrombin time should be determined before starting simvastatin and frequently enough during early therapy to ensure that no significant alteration of prothrombin time occurs. Once a stable prothrombin time has been documented, prothrombin times can be monitored at the intervals usually recommended for patients on coumarin anticoagulants. If the dose of simvastatin is changed or discontinued, the same procedure should be repeated. Simovil therapy has not been associated with bleeding or with changes in prothrombin time in patients not taking anticoagulants.

Simovil Contraindications

Hypersensitivity to any component of this medication.

Active liver disease or unexplained persistent elevations of serum transaminases

Pregnancy and lactation. Atherosclerosis is a chronic process and the discontinuation of lipid-lowering drugs during pregnancy should have little impact on the outcome of long-term therapy of primary hypercholesterolemia. Moreover, cholesterol and other products of the cholesterol biosynthesis pathway are essential components for fetal development, including synthesis of steroids and cell membranes. Because of the ability of inhibitors of HMG-CoA reductase such as ZOCOR to decrease the synthesis of cholesterol and possibly other products of the cholesterol biosynthesis pathway, ZOCOR is contraindicated during pregnancy and in nursing mothers. ZOCOR should be administered to women of childbearing age only when such patients are highly unlikely to conceive. If the patient becomes pregnant while taking this drug, ZOCOR should be discontinued immediately and the patient should be apprised of the potential hazard to the fetus.

This description is suitable for active ingredient Simvastatin

Simovil tags categories:

Zoylex

Zoylex

Korea United Pharm. Inc provides wide range of pharmaceutical products which includes zoylex. It belongs to anti-infectives category. Indications and uses: herpes simplex virus infections of the skin and mucous membranes including initial and recurrent genital herpes, herpes zoster (shingles) infections, chicken pox (varicella) in children over the age of two years. Dosage and administration: treatment of herpes simplex infections: 200mg zoylex should be taken five times daily at approximately four hourly intervals omitting the night time dose. Contact us for more information.

Contact Korea United Pharm. Inc.

Korea United Pharm. Inc.

Bisocard - 10 Tanszych Zamiennikow Tego Leku, Bisocard

Znajdz tanszy, refundowany odpowiednik leku Bisocard

Bisocard (nazwa chemiczna bisoprololi fumaras ) jest jednym z najczesciej stosowanych w Polsce lekow kardiologicznych (na serce).

Bisocard jest lekiem generycznym czyli odtworczym leku oryginalnego Concoru . Od czasu kiedy Bisocard pojawil sie w aptekach minelo wiele czasu i powstaly liczne jego dokladne odpowiedniki (zamienniki).

Bisocard refundacja

Bisocard jest lekiem, ktory nie znajduje sie na liscie (urzedowym wykazie) lekow refundowanych, czyli jest dostepny w aptece na recepte, ale ze 100% odplatnoscia.

Bisocard ulotka informacyjna

Ulotka Biocardu dostepna w internecie (PDF).

Poniewaz obecnie dostepne sa tansze i refundowane zamienniki Bisocardu . to w aptece lub u lekarza mozemy poprosic o zmiane leku na dokladny odpowiednik, ktorego cena nizsza (tansza miesieczna kuracja). Ten lek bierze sie codziennie miesiacami, badz latami, wiec w ciagu roku mozna zaoszczedzic kilkadziesiat i wiecej zlotych.

Zobacz tez: Bisocard i jego refundowany zamiennik Coronal

10 tanszych, refundowanych odpowiednikow Bisocardu

Wazna uwaga! Leki oznaczone 100%, nie sa objete cenami urzedowymi i ich ostateczne ceny, w konkretnej aptece, moga sie roznic od podanych ponizej.

Odpowiedniki sa uszeregowane od najnizszego do najwyzszego kosztu miesiecznej terapii. a NIE ceny 1 opakowania.

Dawka 2,5 mg

Sobycor 30 szt. 100% 7,06 zl

Bibloc 30 szt. 100% 8,89 zl

Bisocard 60 szt. 100% 18,47 zl

Bilokord 30 szt. 100% 10,75 zl

Bisocard 2,5 mg 30 szt. 100% 11,26 zl

Concor COR 28 szt. 100% 19,50 zl

Concor COR 56 szt. 100% 23,50 zl

Dawka 5 mg

Bicardef 90 szt. ryczalt 3,20 zl

Bicardef 60 szt. ryczalt 4,80 zl

Coronal 5 60 szt. ryczalt 3,32 zl

Sobycor 60 szt. ryczalt 5,91 zl

Bisoprolol Actavis 30 szt. ryczalt 3,32 zl

Sobycor 30 szt. ryczalt 4,67 zl

Bisoratio 5 30 szt. ryczalt 4,70 zl

Coronal 5 30 szt. ryczalt 6,74 zl

Bisoprolol Aurobindo 30 szt. 100% 8,00 zl

Corectin 5 30 szt. 100% 8,20 zl

Bibloc 30 szt. 100% 8,90 zl

BisoHEXAL 5 30 szt. 100% 10,00 zl

Bilokord tabl. 30 szt. 100% 11,00 zl

Bisocard 5 mg 60 szt. 100% 18,60 zl

Bicardef 30 szt. 100% 10,23 zl

Bisoprolol Vitabalans 30 szt. 100% 11,66 zl

Bisoprolol VP 30 szt. 100% 12,70 zl

Bisocard 5 mg 30 szt. 100% 12,80 zl

Bisopromerck 5 30 szt. 100% 13,50 zl

Concor 5 50 szt. 100% 28,00 zl

Concor COR 5 56 szt. 100% 41,14 zl

Concor 5 30 szt. 100% 21,00 zl

Concor COR 5 28 szt. 100% 24,00 zl

Dawka 10 mg

Bicardef 90 szt. ryczalt 9,60 zl

Bicardef 60 szt. ryczalt 6,40 zl

Corectin 10 60 szt. ryczalt 6,40 zl

Coronal 10 60 szt. ryczalt 6,40 zl

Bisoprolol Actavis 30 szt. ryczalt 3,21 zl

Coronal 10 30 szt. ryczalt 3,22 zl

Bisoratio 10 30 szt. ryczalt 3,82 zl

Sobycor 60 szt. ryczalt 10,81 zl

Sobycor 30 szt. ryczalt 5,91 zl

Bisoprolol Aurobindo 30 szt. 100% 12,50 zl

Corectin 10 30 szt. 100% 12,50 zl

Bibloc 30 szt. 100% 13,30 zl

Bicardef 30 szt. 100% 13,40 zl

BisoHEXAL 10 30 szt. 100% 14,50 zl

Bisocard 10 mg 60 szt. 100% 28,80 zl

Bisopromerck 10 30 szt. 100% 16,20 zl

Bilokord 30 szt. 100% 16,40 zl

Bisoprolol Vitabalans 30 szt. 100% 17,00 zl

Bisoprolol VP 30 szt. 100% 17,30 zl

Bisocard 10 mg 30 szt. 100% 17,50 zl

Concor 10 50 szt. 100% 43,00 zl

Concor COR 10 56 szt. 100% 56,00 zl

Concor 10 30 szt. 100% 32,50 zl

Concor COR 10 28 szt. 100% 39,00 zl

Bisocard skutki uboczne

Jesli wlasciwie stosowany to zwykle Bisocard nie ma powaznych skutkow ubocznych.

Do waznych skutkow ubocznych naleza:

niskie tetno (puls np. ponizej 55 uderzen na minute)

pogorszenie problemow z chodzeniem (koniecznosc robienia "przystankow")

sinienie rak i stop,

za niskie cisnienie krwi

nasilenie dusznosci przy chodzeniu lub w nocy

bol serca

zawroty i bole glowy

pojawienie sie uczucie zmeczenia i oslabienie

problemy ze snem

uczucie depresji

u osob z astma nasilenie dusznosci

uczucie zimna w dloniach / stopach

biegunka, nudnosci bole brzucha

swedzenie skory

wysypka

problemy z potencja erekcja

Bisocard ulotka informacyjna

Bisocard i alkohol

Bisocardu nie nalezy pod zadnym pozorem laczyc ze spozyciem alkoholu ( uwaga! piwo to tez alkohol). Picie alkoholu przy zazywaniu Bisocardu grozi powaznymi konsekwencjami. Moze to byc spadek cisnienia lub spadek tetna, omdlenie lub zapasc. Odstep miedzy zazyciem leku a piciem alkoholu powinien wynosic minimum 24 godziny.

Epelin - Anticonvulsants, Atc N03ab02, Atc N03ab04, Atc N03ab05, Epelin

Epelin

Capsule (extended release); Liquid; Solution; Suspension; Tablet

Epelin Indication

For the control of generalized tonic-clonic (grand mal) and complex partial (psychomotor, temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery.

Epelin Pharmacology

Phenytoin is an antiepileptic drug which can be useful in the treatment of epilepsy. The primary site of action appears to be the motor cortex where spread of seizure activity is inhibited. Phenytoin reduces the maximal activity of brain stem centers responsible for the tonic phase of tonic-clonic (grand mal) seizures. Phenytoin acts to damp the unwanted, runaway brain activity seen in seizure by reducing electrical conductance among brain cells. It lacks the sedation effects associated with phenobarbital. There are some indications that phenytoin has other effects, including anxiety control and mood stabilization, although it has never been approved for those purposes by the FDA.

Epelin Absorption

Bioavailability 70-100% oral, 24.4% for rectal and intravenous administration. Rapid rate of absorption with peak blood concentration expected in 1½ to 3 hours.

Epelin side effects and Toxicity

Oral, mouse: LD 50 = 150 mg/kg; Oral, rat: LD 50 = 1635 mg/kg. Symptoms of overdose include coma, difficulty in pronouncing words correctly, involuntary eye movement, lack of muscle coordination, low blood pressure, nausea, sluggishness, slurred speech, tremors, and vomiting.

Epelin Patient Information

Patients taking phenytoin should be advised of the importance of adhering strictly to the prescribed dosage regimen, and of informing the physician of any clinical condition in which it is not possible to take the drug orally as prescribed, eg, surgery, etc.

Patients should also be cautioned on the use of other drugs or alcoholic beverages without first seeking the physician's advice.

Patients should be instructed to call their physician if skin rash develops.

The importance of good dental hygiene should be stressed in order to minimize the development of gingival hyperplasia and its complications.

Do not use capsules which are discolored.

Epelin Organisms Affected

Humans and other mammals

Opistan

Opistan

Tiap kapiet salut selaput mengandung :

Mefenamic Acid. 500 mg

CARA KERJA OBAT :

Mefenamic Acid merupakan kelompok anti-inflamasi non steroid, bekerja dengan cara menghambat sintesa prostaglandin dalam jaringan tubuh dengan menghambat enzim. siklooksigenase sehingga mempunyai efek analgesik, anti-inflamasi dan antipiretik.

Meredakan nyeri ringan sampai sedang sehubungan dengan sakit kepala, sakit gigi, dismenore primer, termasuk nyeri karena trauma, nyeri otot dan nyeri sesudah operasi.

- Pasien yang hipersensitif terhadap Mefenamic Acid.

- Penderita yang dengan Asetosal mengalami bronkospasme, rinitis alergis dan urtikaria.

- Penderita dengan tukak lambung dan usus.

- Penderita dengan gangguan ginjal yang berat.

- Sistem pencernaan. mual, muntah, diare dan rasa sakit abdominal.

- Sistem hematopoietik. leukopenia, eosinophilia, trombocytopenia, dan agranulo-cytopenia.

- Sistem saraf. rasa mengantuk, "pusing, penglihatan kabur dan insomnia.

PERINGATAN DAN PERHATIAN :

- Sebaiknya diminum sesudah makan.

- Hati-hati jika digunakan pada wanita hamil dan menyusui.

- Keamanan penggunaan pada anak-anak dibawah 14 tahun belum diketahui dengan pasti.

Penggunaan bersamaan dengan antikoagulan oral dapat memperpanjang waktu prothrombin.

Dewasa dan anak-anak > 14 tahun :

Dosis awal 500 mg, kemudian dianjurkan 250 mg tiap 6 jam sesuai dengan kebutuhan.

Jika terjadi overdosis maka pasien harus dirangsang muntah atau pasien diberi arang aktif (karbo absorben) untuk menyerap obat

Simpan pada suhu < 30°C, terlindung dari cahaya.

KEMASAN & NO. REGISTRASI :

OPISTAN®500 kapiet salut selaput. Box isi 10 strip @ 10 kaplet/DKL8818803909A1

HARUS DENGAN RESEP DOKTER

PT Otto Pharmaceutical Industries

Buy Prolertus Diclofenac Online Without Prescriptions, Prolertus

Diclofenac is used primarily for the treatment of inflammation and pain caused by conditions such as rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis. It is also effective in treating soft tissue inflammations due to tendinitis and bursitis, and treating dysmenorrhea (menstrual cramps). Diclofenac is an NSAID. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.

Use Diclofenac as directed by your doctor!

Take Diclofenac by mouth. It may be taken with food if it upsets your stomach. Taking it with food may not lower the risk of stomach or bowel problems (eg, bleeding, ulcers). Talk with your doctor or pharmacist if you have persistent stomach upset.

Take Diclofenac with a full glass of water (8 oz/240 mL) as directed by your doctor.

If you miss a dose of Diclofenac, take it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Diclofenac.

Store Diclofenac at 77 degrees F (25 degrees C). Brief storage at temperatures between 59 and 86 degrees F (15 and 30 degrees C) is permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do NOT use Diclofenac if:

you are allergic to any ingredient in Diclofenac or to bovine (cow) protein

you have had a severe allergic reaction (eg, severe rash, hives, trouble breathing, growths in the nose, dizziness) to aspirin or an NSAID (eg, ibuprofen, celecoxib)

you have recently had or will be having bypass heart surgery

you have severe kidney problems

you are in the last 3 months of pregnancy.

Contact your doctor or health care provider right away if this applies to you.

Some medical conditions may interact with Diclofenac. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of kidney or liver problems, diabetes, or stomach or bowel problems (eg, bleeding, perforation, ulcers)

if you have a history of swelling or fluid buildup, asthma, growths in the nose (nasal polyps), or mouth inflammation

if you have high blood pressure, blood disorders (eg, porphyria), bleeding or clotting problems, heart problems (eg, heart failure), or blood vessel disease, or if you are at risk for any of these diseases

if you have poor health, dehydration or low fluid volume, or low blood sodium levels, you smoke, drink alcohol, or have a history of alcohol abuse

if you are taking an antibiotic or an anti-seizure medicine. The risk of liver problems may be increased with some of these medicines.

Some medicines may interact with Diclofenac. Tell your health care provider if you are taking any other medicines, especially any of the following:

Anticoagulants (eg, warfarin), aspirin, clopidogrel, corticosteroids (eg, prednisone), heparin and other blood thinners (eg, dalteparin), or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of stomach bleeding may be increased

Acetaminophen because the risk of liver problems may be increased

Probenecid because it may increase the risk of Diclofenac's side effects

Cyclosporine, lithium, metformin, methotrexate, oral NSAIDs (eg, ibuprofen), or quinolones (eg, ciprofloxacin) because the risk of their side effects may be increased by Diclofenac

Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril) or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Diclofenac.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Diclofenac may interact with other medicines that you take. Check with your health care provider before you start, stop, or change the dose of any medicine.

Important safety information:

Diclofenac may cause dizziness or drowsiness. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possible unsafe tasks until you know how you react to it.

Serious stomach ulcers or bleeding can occur with the use of Diclofenac. Taking it in high doses, for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Diclofenac with food will NOT reduce the risk of these effects. If you have severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling, contact your doctor or emergency room right away.

Do NOT take more than the recommended dose or use for longer than prescribed without checking with your doctor.

Diclofenac is an NSAID. Before you start any new medicine, check the label to see if it has an NSAID (eg, ibuprofen) in it too. If it does or if you are not sure, check with your doctor or pharmacist.

Do not take aspirin while you are using Diclofenac unless your doctor tells you to.

Check with your doctor or pharmacist before you take acetaminophen while you are taking Diclofenac. The risk of liver problems may be increased.

Do not switch between different forms of Diclofenac (eg, enteric-coated tablets, immediate-release tablets, capsules) unless your doctor tells you to. They may not provide the same amount of medicine to your body.

Lab tests, including kidney function, liver function, blood electrolyte levels, complete blood cell counts, and blood pressure, may be performed while you use Diclofenac. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Diclofenac with caution in the elderly; they may be more sensitive to its effects, especially stomach bleeding and kidney problems.

Diclofenac should be used with extreme caution in children; safety and effectiveness in children have not been confirmed.

Pregnancy and breast-feeding: Diclofenac may cause harm to the fetus. Do not use it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breastfeed while taking Diclofenac.

Piriteze Allergy Tablets, Piriteze

PIRITEZE ALLERGY TABLETS

Transcript

Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Sotatic, Sotatic

Static-X

About Static-X

Static-X's roots trace to the Midwest, where vocalist/guitarist Wayne Static grew up in Michigan and drummer Ken Jay in Illinois. They ended up in Chicago separately and met at the record store where Jay worked, introduced to one another by Smashing Pumpkins vocalist Billy Corgan. Static and Jay decided to head west to California and start up a new band. Shortly after their arrival, Osaka native Koichi Fukada responded to the duo's ad and became their new guitarist, as well as programmer. Bassist Tony Campos, the only true Californian, was the final piece of the puzzle. Static-X's music combined aggressive metal and thrash with industrial overtones and techno pulse. Signed to Warner Brothers in February 1998, Static-X debuted with Wisconsin Death Trip a year later, and the album was eventually certified gold. Departing guitarist Fukada was replaced with Tripp Eisen (ex-Dope) for 2001's Machine, and drummer Jay left after the 2003 album Shadow Zone. If that weren't enough, personal issues forced Eisen to leave the band in 2004. Still, Static-X was undeterred. Static tapped Fukada to rejoin on guitar and programming, and touring drummer Nick Oshiro took over full-time.

In June 2005, a rejuvenated Static-X returned to recording with Start a War. Cannibal arrived in 2007, charting inside Billboard's Top 40. The band toured and released a CD/DVD document, Cannibal Killers Live, then settled into the recording of their sixth studio album, Cult of Static. Released in March 2009, it debuted inside the Top 20. The band broke up not long after finishing a lengthy tour, with Wayne Static announcing a renewed focus on his Pighammer side project, with contributions from his wife, Tera Wray. In 2011, Pighammer appeared as a solo album under his own name. A year later, he reformed Static-X -- minus any of the original members. The lineup, which basically consisted of his solo backing band, mounted a tour, but broke up by 2013, and a year later, Wayne Static was dead at the age of 48.

Josh Loehr, Rovi

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Static-X's roots trace to the Midwest, where vocalist/guitarist Wayne Static grew up in Michigan and drummer Ken Jay in Illinois. They ended up in Chicago separately and met at the record store where Jay worked, introduced to one another by Smashing Pumpkins vocalist Billy Corgan. Static and Jay decided to head west to California and start up a new band. Shortly after their arrival, Osaka native Koichi Fukada responded to the duo's ad and became their new guitarist, as well as programmer. Bassist Tony Campos, the only true Californian, was the final piece of the puzzle. Static-X's music combined aggressive metal and thrash with industrial overtones and techno pulse. Signed to Warner Brothers in February 1998, Static-X debuted with Wisconsin Death Trip a year later, and the album was eventually certified gold. Departing guitarist Fukada was replaced with Tripp Eisen (ex-Dope) for 2001's Machine, and drummer Jay left after the 2003 album Shadow Zone. If that weren't enough, personal issues forced Eisen to leave the band in 2004. Still, Static-X was undeterred. Static tapped Fukada to rejoin on guitar and programming, and touring drummer Nick Oshiro took over full-time. In June 2005, a rejuvenated Static-X returned to recording with Start a War. Cannibal arrived in 2007, charting inside Billboard's Top 40. The band toured and released a CD/DVD document, Cannibal Killers Live, then settled into the recording of their sixth studio album, Cult of Static. Released in March 2009, it debuted inside the Top 20. The band broke up not long after finishing a lengthy tour, with Wayne Static announcing a renewed focus on his Pighammer side project, with contributions from his wife, Tera Wray. In 2011, Pighammer appeared as a solo album under his own name. A year later, he reformed Static-X -- minus any of the original members. The lineup, which basically consisted of his solo backing band, mounted a tour, but broke up by 2013, and a year later, Wayne Static was dead at the age of 48.

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Warner Bros. Records

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Cult of Static (2009)

Cannibal Killers Live (2008)

Start a War (2005)

Beneath. Between. Beyond (2004)

Shadow Zone (2003)

Warner Bros. Records

Warner Bros. Records

Wisconsin Death Trip (1999)

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Nine Inch Nails

Type O Negative

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Buy Cipmox Cv 625 - (500 125)Mg From Online Pharmacy, Cipmox

Amoxicillin and Clavulanic acid is a combination product. This is a combination antibiotic that consists of two ingredients:

Amoxicillin trihydrate, a B-lactum antibiotic

Clavulanic acid. a B-lactamase inhibitor

The combination of these two products is used to treat various infections caused by bacteria. Antibiotics are not meant to fight viral infections like cold, flu etc. the bacterial infections such as that of ears, lungs, sinus, skin, and urinary tract etc. can be treated using this combination drug.

Understanding the drug:

This drug consists of a combination of two products amoxicillin and Clavulanic acid. Amoxicillin works by stopping the growth of bacteria. Amoxicillin is penicillin like antibiotic. While on the other hand Clavulanic acid works by stopping the bacteria from destroying the amoxicillin.

When should you avoid it?

You should not take this drug if you:

Are allergic to amoxicillin or penicillin or any other antibiotic or Clavulanic acid

Are pregnant or planning to have a baby

Are a breastfeeding mother

Have or ever had kidney problems or any kind of liver problems

Have asthma or hay fever

Are taking oral contraceptives as this drug may inhibit the action the oral contraceptives. So, consult your doctor about that too.

Are below 16 years of age

What are the strengths available?

The following strengths of the combination product are available:

Cipmox CV 625(500+125) mg

Augmentin 1000 ( 875-125 mg)

Augmentin 625 (500-125 mg)

Augmentin dry syrup 30 ml

Augmentin-375 (250/125 mg)

Who is the manufacturer?

Augmentin products are manufactured by GSK and the Cipmox is manufactured by Cipla, both leading pharmaceutical companies. The products are available in various pack sizes on our website.

Dosage depends upon your age, weight, medical condition and your response to the treatment. Hence doctor will decide your dose. Take the dose exactly as prescribed by the doctor. Never take two 250 mg tablets to substitute one 500 mg tablets.

The drug comes in various forms like chewable tablets, tablets and syrups. The drug is usually recommended to be taken with the meal or snack. The tablets can be swallowed easily with a glass of water; chewable tablets should be thoroughly chewed before they are swallowed. Syrup bottle should be properly shaken before each dose and should be carefully measured using a measuring device or spoon. Do not use household spoon as it may give incorrect measurements.

The doctor usually recommends it either three time a day after every eight hours or two times a day after every 12 hours. Take the dose as prescribed by him. It is recommends that the dose should be taken with the meal or snack or right after it.

For how long should it be taken?

You should take the dose until you finish the prescription. Do not change the dose or stop it even if you feel better. You should complete the dose.

What if you take too much (overdose)?

You may require urgent medical help in this situation. In such a case visit nearest healthcare center or call your doctor immediately.

What if you miss the dose?

In case you forget to take the dose, skip the dose and take the next dose on the recommended time period if it’s too late but if it’s less than 1 hour of the meal then go and take it. Do not double up the dose for the missed one.

What are the side effects?

Tell your doctor as soon as possible if you notice any of the following:

Severe skin rash

Mild skin rash

Itching

Vaginal itching and discharge

Hives

Vomiting

Diarrhea

Upset stomach

Yellowing of the skin or eyes

Difficulty breathing or swallowing

Wheezing

In above cases you must go for immediate medical help. Do not get alarmed by the list. You may /may not experience all of them. Tell your doctor immediately in the above situations.

Are there any possible drug interactions?

Certain other drugs can interact with amoxicillin and increase the risk of serious muscle problems. So it is necessary to consult your doctor about the following drugs such as:

BCG Vaccine Live

Demeclocycline

Doxycycline

Lymecycline

Minocycline

Mycophenolate

Oxytetracycline

Probenecid

Tetracycline

Typhoid Vaccine Live

What are the things to be taken care of?

Do not share this medicine with anyone else even if he has same symptoms as you do.

Do not use this medication for any other infection without referring to the doctor.

In case you do not feel comfort after completing the dose prescribed by the doctor then consult with your doctor immediately.

The safety and efficacy of this drug is not established in children below 16 years of age.

Do not freeze the medicine and store the medicine at room temperature.

Quick delivery (Posted on 6/20/15) I have been ordering all my medicines from All Day Chemist as I completely rely on their delivery speed. I decided to buy Cipmox 500 mg online from them and got it at a reasonable price. It has helped me get over my severe skin condition and given me relief from rashes. The medicine has ensured that I don't get the infection again and helped me regain my confidence. It is crucial to consume the exact dosage prescribed by the doctor to get the best results.

Review by Addison

Safe choice (Posted on 6/19/15) I have been struggling with urinary tract infections since a few years. I am glad that I decided to buy Cipmox 500 mg online as it helped me recover. UTIs can disrupt your life and daily activities to a great extent. It was very uncomfortable as it can get difficult to deal with for active women. Thankfully, the medicine worked, and I have been leading a healthy life since then. If you are looking for a cure for bacterial infections, this is a safe choice.

Review by Joshua

a big relief in my life (Posted on 6/19/15) I used to suffer from respiratory problems and failed to get an effective treatment that could make a difference. A friend of mine asked me to buy Cipmox 500 mg online as he had suffered from the same condition. I did not notice any harmful effects after consuming the medicine. I can now breathe properly, and it has reduced my stress immensely. This medicine has been a big relief in my life. I am a much happier and can concentrate completely at my workplace.

Review by Lillian

helped me tremendously to feel better (Posted on 6/19/15) I decided to buy Cipmox 500 mg online for my respiratory infection, and it has helped me tremendously to feel better. I also am very happy with the decision as I had to go through many bad treatments. Thankfully, this online store was offering the medicine at a discounted price, and I could not resist buying from them. The effects of the medicine have been great, and I would recommend everyone to trust the quality.

Review by Brookylin

cleared the itching (Posted on 6/19/15) It is very crucial to follow the instructions mentioned on the pack to avoid any side-effects. I am glad that I made the right choice and chose to buy Cipmox 500 mg online. I had a minor hearing problem because of the bacterial infection and needed to do something about it. My doctor had tried many other medications, and it was in vain. This medicine has worked wonders and has slowly cleared the itching I used to experience.

hassle-free experience from alldaychemist (Posted on 6/19/15) Initially, I was not sure about this medicine as I sometimes get side-effects with allopathic drugs. I took the decision eventually and decided to buy Cipmox 500 mg online as I had no choice. I have no regrets of having purchased it from All Day Chemist. I can hear better, and there is no irritation in my ears. The tablet helped me get rid of the excessive pus as well. I am looking forward to buying more medicines online as the experience has been hassle-free.

ensures better results (Posted on 6/19/15) I stumbled upon this product while browsing the internet and checking remedies for ENT infections. It is a combination of two products: Amoxicillin and Clavulanic acid. Being a medical student, I had a faint idea about its effectiveness and still consulted my doctor for the same. He too recommended the same medicine, and I decided to buy Cipmox 500 mg online. The doctor asked me to take it three times a day after every eight hours or twice a day after every 12 hours. The medicine ensures better results when consumed with food.

Review by Carter

Satisfied with this medication (Posted on 6/19/15) The medicine is more effective after it is taken immediately after or with the meal. In fact, I used to feel nauseated after taking it on an empty stomach. The tablets work by stopping the growth of bacteria. Clavulanic acid stops the bacteria from destroying the amoxicillin. The results are satisfying, and I don't get bacterial infections anymore. My skin looks much better, and there are no rashes. Thanks, All Day Chemist. My decision to buy Cipmox 500 mg online has been great.

Review by Hannah

Great effects (Posted on 6/19/15) My doctor had prescribed Cipmox 500 mg for my UTI, and I immediately decide to buy it online. It is a better alternative to many other products and also easy on the pocket. The tablets have worked in my favor and got me the best possible results. The effects are great, and I do not experience any burning during urination anymore. Guys, please ensure that you discuss your medical history with your doctor before taking this medication. It is crucial to inform your health practitioner if you are pregnant or planning to have a baby.

Items 1 to 10 of 16 total

Please note that not all medications, including any referenced on this page, are dispensed from our affiliated Indian pharmacy. The medications in your order may be filled and shipped from an approved International fulfilment center located in a country other than India. In addition to dispensing medications from our Indian pharmacy, medication orders are also filled and shipped from international fulfilment centers that are approved by the regulatory bodies from their respective countries.

Medication orders are filled and shipped from approved fulfilment centers around the world including, but not limited to, India, United Kingdom, New Zealand, Mauritius and the United States. The items in your order may be filled and shipped from any one of the above jurisdictions. The products are sourced from various countries as well as those listed above. All of our affiliated fulfilment centers have been approved by the regulatory bodies from their respective countries.

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Mebendazole Monograph For Professionals, Bendazol

Mebendazole

Warnings/Precautions

Warnings

Myelosuppression

Neutropenia (including agranulocytosis) and/or thrombocytopenia has been reported in patients receiving high dosages (e. g. 30–50 mg/kg daily) for treatment of extraintestinal infections. 103 107 111 113 120 Myelosuppression is usually reversible following discontinuance of the drug, but death has occurred rarely. 113

Monitor organ system function (including hematopoietic and hepatic) periodically during prolonged mebendazole therapy. 107

General Precautions

Minimal adverse effects associated with usual recommended dosages (i. e. 100–200 mg daily). Adverse effects appear to occur more frequently when higher dosages are used 103 104 109 111 113 114 116 120 121 and may be related to effects resulting from drug-induced killing of parasites. 104 107 108 109 114 116 121 122

Transient diarrhea 107 108 119 147 and abdominal pain 107 108 119 147 have occurred occasionally during treatment but usually have been associated with massive infections and expulsion of the helminths. 107

Specific Populations

Pregnancy

Embryotoxic and teratogenic in rats when given as a single oral dose as low as 10 mg/kg (approximately equal to the human dose on a mg/m 2 basis). 107 Use during pregnancy, especially during the first trimester, only when potential benefits justify possible risks to the fetus. 107

Lactation

Not known if distributed into milk; use with caution in nursing women. 107

Pediatric Use

Only limited experience in children <2 years of age; 107 use in this age group only when potential benefits justify possible risks. 107

Common Adverse Effects

Interactions for Mebendazole

Actions and Spectrum

Broad-spectrum anthelmintic agent. 107

Benzimidazole derivative structurally related to albendazole and thiabendazole. a

Inhibits formation of worms’ microtubules and causes glucose depletion in worms, leading to death of the parasite. 107 Has no effect on blood glucose concentrations in humans. a

Active against certain nematodes (roundworms) pathogenic to humans, including Ancylostoma duodenale (hookworm), Angiostrongylus cantonensis . Ascaris lumbricoides (roundworm), Capillaria philippinensis (Philippine threadworm), Enterobius vermicularis (pinworm), Gnathostoma spinigerum . Necator americanus (hookworm), Strongyloides stercoralis (threadworm), Trichinella spiralis (pork worm), and Trichuris trichiura (whipworm). Reported to be filaricidal against Mansonella perstans and Onchocerca volvulus . a

Active against certain cestodes (tapeworms), including Hymenolepis nana (dwarf tapeworm), Taenia saginata (beef tapeworm), T. solium (pork tapeworm), and Echinococcus granulosus (hydatid cyst). a

Advice to Patients

Advise patients that mebendazole may be taken with or without food and that the tablets may be chewed, swallowed whole, or crushed and mixed with food. 107

Importance of completing full course of therapy, even if feeling better after a few days. 107

Importance of good hygiene to minimize reinfection, such as washing hands with soap and cleaning under fingernails often during the day (especially before eating and after using the toilet). 107

When treating enterobiasis (pinworm infection), importance of following additional hygiene recommendations such as wearing tight underpants both day and night and changing them daily, cleaning the bedroom floor daily (avoiding dry sweeping that may stir up dust), washing bed linens and night clothes after treatment, and keeping toilet seats clean. 107

When treating hookworm, whipworm, or roundworm infections, importance of following additional hygiene recommendations such as washing all fruits and vegetables thoroughly or cooking them well, wearing shoes, and using the bathroom. 107

Importance of women informing clinicians if they are or plan to become pregnant or plan to breast-feed. 107

Importance of informing clinicians of existing or contemplated concomitant therapy, including prescription and OTC drugs, as well as any concomitant illnesses. 107

Importance of notifying clinician of persistent or worsening symptoms of infection.

Importance of informing patients of other important precautionary information. (See Cautions.)

Preparations

Excipients in commercially available drug preparations may have clinically important effects in some individuals; consult specific product labeling for details.

Please refer to the ASHP Drug Shortages Resource Center for information on shortages of one or more of these preparations.

AHFS DI Essentials. © Copyright, 2016, American Society of Health-System Pharmacists, Inc. 7272 Wisconsin Avenue, Bethesda, Maryland 20814. Review Date: September 06, 2016.

References

100. American Academy of Pediatrics. 2006 Red Book: Report of the Committee on Infectious Diseases. 27th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2006.

101. Luder PJ, Siffert B, Witassek F et al. Treatment of hydatid disease with high oral doses of mebendazole: long-term follow-up of plasma mebendazole levels and drug interactions. Eur J Clin Pharmacol . 1986; 31:443-8. [IDIS 224651] [PubMed 3816925]

102. Hansten PD. Carbamazepine (Tegretol) interactions. Drug Interact Newsl . 1987; 7(Updates):U9-10.

103. Levin MH, Weinstein RA, Axelrod JL et al. Severe, reversible neutropenia during high-dose mebendazole therapy for echinococcosis. JAMA . 1983; 249:2929-31. [IDIS 170845] [PubMed 6842806]

104. Murray-Lyon IM, Reynolds KW. Complication of mebendazole treatment for hydatid disease. Br Med J . 1979; 2:1111-2. [IDIS 104975] [PubMed 519316]

105. Seah SKK. Mebendazole in the treatment of helminthiasis. Can Med Assoc J . 1976; 115:777-9. [PubMed 974969]

106. Harris A. Pyrexia and mebendazole. Br Med J . 1979; 2:1365. [PubMed 519452]

107. Teva. Mebendazole tablets, USP prescribing information. Sellersville, PA; 2004 May.

108. Beard TC, Rickard MD. Medical treatment for hydatids. Med J Aust . 1978; 1:633-5. [IDIS 107257] [PubMed 683082]

109. Levin ML. Treatment of trichinosis with mebendazole. Am J Trop Med Hyg . 1983; 32:980-3. [PubMed 6625077]

110. Horstmann RD, Kern P, Volkmer KJ et al. Observations on mebendazole vs. thiabendazole in the treatment of human trichinellosis. Tropenmed Parasitol . 1982; 33:191-4. [PubMed 7135477]

111. Schantz PM, Van den Bossche H. Chemotherapy for larval echinococcosis in animals and humans: report of a workshop. Z Parasitenkd . 1982; 67:5-26. [PubMed 7041454]

112. Mittermayer T. The use of mebendazole in the treatment of trichinellosis in man. Folia Parasitol (Praha) . 1981; 28:235-42. [PubMed 7274835]

113. Wilson JF. Mebendazole and alveolar hydatid disease. Ann Trop Med Parasitol . 1982; 76:165-73. [PubMed 7092370]

114. Rivas-Alcala AR, Greene BM, Taylor HR et al. Chemotherapy of onchocerciasis: a controlled comparison of mebendazole, levamisole, and diethylcarbamazine. Lancet . 1981; 2:485-90. [IDIS 137126] [PubMed 6115246]

115. Rivas-Alcala AR, Greene BM, Taylor HR et al. 12 Month follow-up of mebendazole therapy for onchocerciasis. Lancet . 1981; 2:1043. [IDIS 140247] [PubMed 6118495]

116. Rivas-Alcala AR, Mackenzie CD, Gomez-Rojo F et al. The effects of diethylcarbamazine, mebendazole and levamisole on Onchocerca volvulus in vivo and in vitro. Tropenmed Parasitol . 1984; 35:71-7. [PubMed 6464189]

117. Kale OO. Further trials of mebendazole and metrifonate in the treatment of onchocerciasis. Bull World Health Organ . 1982; 60:109-13. [PubMed 7044588]

118. Hansten PD. Phenytoin (Dilantin) interactions. Drug Interact Newsl . 1987; 7(Updates):U10.

119. Pelletier LL Jr. Treatment failures following mebendazole therapy for chronic strongyloidiasis. J Infect Dis . 1987; 156:532-3. [IDIS 233794] [PubMed 3611840]

120. Miskovitz PF. Leukopenia associated with mebendazole therapy of hydatid disease. Am J Trop Med Hyg . 1980; 29:1356-8. [PubMed 7446825]

121. Kern P, Dietrich M. Chemotherapy of echinococcosis with mebendazole: clinical observations of 7 patients. Tropenmed Parasitol . 1979; 30:65-72. [PubMed 375511]

122. Anon. Medical treatment for hydatid disease? Br Med J . 1979; 2:563. Editorial.

123. Bekhti A. Mebendazole in toxocariasis. Ann Intern Med . 1984; 100:463. [IDIS 182246] [PubMed 6696379]

124. Keystone JS. Mebendazole. Ann Intern Med . 1979; 91:582-6. [PubMed 484964]

125. Petri WA Jr, Holsinger JR. Common-source outbreak of trichinosis associated with eating raw home-butchered pork. South Med J . 1988; 81:1056-8. [PubMed 3043686]

126. Brackmann T, Lang W. [Case report of florid trichinosis in otorhinolaryngology]. (German; with English abstract.) HNO . 1985; 33:409-12.

127. Blondheim DS, Klein R, Ben-Dror G et al. Trichinosis in southern Lebanon. Isr J Med Sci . 1984; 20:141-4. [PubMed 6706538]

128. Richard-Lenoble D, Kombila M, Burnier I et al. [Filariasis in Gabon: treatment with mebendazole of filariasis due to M. perstans and Loa loa .] (French; with English abstract.) Bull Soc Pathol Exot Fil . 1985; 78:485-91.

129. Almaviva M, Galli M, Rizzi M et al. Immune response in a symptomatic case of Tetrapetalonema perstans . Trans R Soc Trop Med Hyg . 1984; 78:489-91. [PubMed 6541380]

130. Wahlgren M. Treatment of Dipetalonema perstans infections with mebendazole. Trans R Soc Trop Med Hyg . 1983; 77:422-3. [PubMed 6684816]

131. Olumide YM. Dipetalonema perstans in a patient with chronic lymphoedema: case report. East Afr Med J . 1983; 60:186-9. [PubMed 6684545]

132. Wahlgren M. The successful treatment of Dipetalonema perstans filariasis with mebendazole. Ann Trop Med Parasitol . 1982; 76:557-9. [PubMed 6891576]

133. Bernberg HC, Clarke VV. The combined treatment with levamisole and mebendazole for a perstans-like filarial infection in Rhodesia. Trans R Soc Trop Med Hyg . 1979; 73:233-4. [PubMed 573005]

134. Goldsmid JM. A preliminary study on the treatment of filariasis due to Dipetalonema perstans . Cent Afr J Med . 1979; 25:51-2. [PubMed 571764]

135. Goldsmid JM. Studies on the diagnosis and treatment of human filariasis in Rhodesia. S Afr Med J . 1976; 50:1129-32. [PubMed 60784]

136. Maertens K. Effect of mebendazole and levamisole on Onchocerca volvulus and Dipetalonema perstans . Trans R Soc Trop Med Hyg . 1975; 69:359-60. [PubMed 1237183]

137. Newland HS, White AT, Greene BM et al. Effect of single-dose ivermectin therapy on human Onchocerca volvulus infection with onchocercal ocular involvement. Br J Ophthalmol . 1988; 72:561-9. [PubMed 3046657]

138. Albiez EJ, Newland HS, White AT et al. Chemotherapy of onchocerciasis with high doses of diethylcarbamazine or a single dose of ivermectin: microfilaria levels and side effects. Trop Med Parasitol . 1988; 39:19-24. [PubMed 3291074]

139. Larviere M, Vingtain P, Aziz M et al. Double-blind study of ivermectin and diethylcarbamazine in African onchocerciasis patients with ocular involvement. Lancet . 1985; 2:174-7. [IDIS 203198] [PubMed 2862370]

140. Greene BM, Taylor HR, Cupp EW et al. Comparison of ivermectin and diethylcarbamazine for the treatment of onchocerciasis. N Engl J Med . 1985; 313:133-8. [IDIS 201907] [PubMed 3892293]

141. Awadzi K, Dadzie KY, Shulz-Key H et al. The chemotherapy of onchocerciasis: X. An assessment of four single dose treatment regimes of MK-933 (ivermectin) in human onchocerciasis. Ann Trop Med Parasitol . 1985; 79:63-78. [PubMed 3838638]

142. Anon. Ivermectin in onchocerciasis. Lancet . 1984; 2:1021. [PubMed 6149402]

143. Ambu S, Kwa BH. Studies on the experimental chemotherapy of Angiostrongylus malaysiensis infection in rats with mebendazole and levamisole. Trans R Soc Trop Med Hyg . 1982; 76:458-62. [PubMed 6926760]

144. Ambu S, Kwa BH, Mak JW et al. Chemotherapy and chemoprophylaxis of Angiostrongylus malaysiensis infection in rats with levamisole and mebendazole. Folia Parasitol (Prague) . 1982; 29:361-4.

145. Fernandez-Banares F, Gonzalez-Huix F, Xiol X et al. Marrow aplasia during high-dose mebendazole treatment. Am J Trop Med Hyg . 1986; 35:350-1. [PubMed 3953948]

146. Braithwaite PA, Thomas RJS. Hydatid disease: the alveolar variety in Australia. A case report with comment on the toxicity of mebendazole. Aust NZ J Surg . 1985; 55:519-23.

147. Anon. Drugs for parasitic infections. Med Lett Drugs Ther . Aug 2004. From the Medical Letter website ().

148. Plorde JJ, Ramsey PG. Nematodes, cestodes, and hermaphroditic trematodes. In: Wilson JD, Braunwald E, Isselbacher KJ et al. eds. Harrison’s principles of internal medicine. 12th ed. New York: McGraw-Hill Company 1991:817-31.

149. Wilson M, Schantz P. Nonmorphologic diagnosis of parasitic infection. In: Balows A, Hausler WJ Jr. Herrmann KL et al. Manual of clinical microbiology. 5th ed. Washington, D. C: American Society for Microbiology; 1991:717-26.

150. Davis A, Pawlowski ZS, Dixon H. Multicentre clinical trials of benzimidazolecarbamates in human echinococcosis. Bulletin of the World Health Organization. 1986; 64:383-8.

151. Al-Waili NSD, Hasa NU. Mebendazole in giardial infection: a comparative study with metronidazole. J Infect Dis . 1992; 165:1170-1. [IDIS 297157] [PubMed 1583344]

152. Tsai HC, Liu YC, Kunin CM et al. Eosinophilic meningitis caused by Angiostrongylus cantonensis . report of 17 cases. Am J Med . 2001; 111:109-14. [IDIS 468785] [PubMed 11498063]

a. AHFS drug information 2007. McEvoy GK, ed. Mebendazole. Bethesda, MD: American Society of Health-System Pharmacists; 2007:[page 52].

Cerebryl, Cerebryl

cerebrum

cerebrum

the main portion of the brain. occupying the upper part of the cranial cavity; its two cerebral hemispheres. united by the corpus callosum. form the largest part of the central nervous system in humans. The term is sometimes extended to refer to the postembryonic forebrain and midbrain together or to the entire brain.

cer·e·brum

ce·re·bra

cer·e·brums

( ser'ĕ-brŭm, sĕ-rē'brŭm; - bră; - brŭmz ), [TA] Although the pronunciation of this word with stress on the first syllable is classically correct, the second syllable is often stressed in the U. S.

Term originally referring to the largest portion of the brain, including practically all parts within the skull except the medulla, pons, and cerebellum; it now usually refers only to those parts derived from the telencephalon and includes mainly the cerebral hemispheres (cerebral cortex and basal nuclei, also called basal ganglia).

cerebrum

/cer·e·brum/ ( ser?ĕ-brum ) ( sĕ-re?brum ) the main portion of the brain, occupying the upper part of the cranial cavity; its two hemispheres, united by the corpus callosum, form the largest part of the central nervous system in humans. The term is sometimes applied to the postembryonic forebrain and midbrain together or to the entire brain.

cerebrum

The large rounded structure of the brain occupying most of the cranial cavity, divided into two cerebral hemispheres that are joined at the bottom by the corpus callosum. It controls and integrates motor, sensory, and higher mental functions, such as thought, reason, emotion, and memory.

cerebrum

[ser′əbrəm, sərē′brəm] pl. cerebrums, cerebra

Etymology: L, brain

the largest and uppermost section of the brain, divided by a longitudinal fissure into the left and right cerebral hemispheres. At the bottom of the groove, the hemispheres are connected by the corpus callosum. The internal structures of the hemispheres merge with those of the diencephalon and further communicate with the brainstem through the cerebral peduncles. The surface of the cerebrum is called gyri. Each lobe bears the name of the bone under which it lies. The cerebrum performs sensory functions, motor functions, and less easily defined integration functions associated with various mental activities. It generates a variety of electrical waves that may be recorded as an electroencephalogram to localize areas of brain dysfunction, to identify altered states of consciousness, or to establish brain death. See also cerebral cortex, cerebral hemisphere. cerebral, adj.

brain

The epicentre of the central nervous system, which is located within the cranial vault and divided into the right and left hemispheres. The brain functions as a primary receiver, organiser and distributor of information for the body; it is the centre of thought and emotion, co-ordinates and controls bodily activities and interprets sensory visual, auditory, olfactory, tactile and other information.

cer·e·brum

pl. cerebra ( ser'ĕ-brŭm, - bră ) [TA]

Originally referred to the largest portion of the brain; it now usually refers only to the parts derived from the telencephalon and includes mainly the cerebral hemispheres (cerebral cortex and basal ganglia).

cerebrum

(sĕr′ĕ-brŭm) (sĕr-ē′brŭm) [L.]

The largest part of the brain, consisting of two hemispheres separated by a deep longitudinal fissure. The hemispheres are united by three commissures—the corpus callosum and the anterior and posterior hippocampal commissures. The surface of each hemisphere is thrown into numerous folds or convolutions called gyri, which are separated by furrows called fissures or sulci.

Embryology

The cerebrum develops from the telencephalon, the most anterior portion of the prosencephalon or forebrain.

Anatomy

Each cerebral hemisphere consists of three primary portions—the rhinencephalon or olfactory lobe, the corpus striatum, and the pallium or cerebral cortex. The cortex is a layer of gray matter that forms the surface of each hemisphere. The part in the rhinencephalon (phylogenetically the oldest) is called the archipallium; the larger nonolfactory cortex is called the neopallium. The cerebrum contains two cavities, the lateral ventricles (right and left) and the rostral portion of the third ventricle. The white matter of each hemisphere consists of three kinds of myelinated fibers: commissural fibers, which pass from one hemisphere to the other; projection fibers, which convey impulses to and from the cortex; and association fibers, which connect various parts of the cortex within one hemisphere.

Lobes: The principal lobes are the frontal, parietal, occipital, and temporal lobes and the central (the insula or island of Reil). Basal ganglia: Masses of gray matter are deeply embedded within each hemisphere. They are the caudate, lentiform, and amygdaloid nuclei and the claustrum. Fissures and sulci: These include the lateral cerebral fissure (of Sylvius), the central sulcus (of Rolando), the parieto-occipital fissure, the calcarine fissure, the cingulate sulcus, the collateral fissure, the sulcus circularis, and the longitudinal cerebral fissure. Gyri: These include the superior, middle, and inferior frontal gyri, the anterior and posterior central gyri, the superior, middle, and inferior temporal gyri, and the cingulate, lingual, fusiform, and hippocampal gyri.

Physiology

The cerebrum is concerned with sensations (the interpretation of sensory impulses) and all voluntary muscular activities. It is the seat of consciousness and the center of the higher mental faculties such as memory, learning, reasoning, judgment, intelligence, and the emotions. See: illustration

On the basis of function, several areas have been identified and located. Motor areas in the frontal lobes initiate all voluntary movement of skeletal muscles. Sensory areas in the parietal lobes are for taste and cutaneous senses, those in the temporal lobes are for hearing and smell, and those in the occipital lobes are for vision. Association areas are concerned with integration, analysis, learning, and memory.

cerebrum

The largest, and most highly developed, part of the brain. It contains the neural structures for memory and personality, cerebration, volition, speech, vision, hearing, voluntary movement, all bodily sensation, smell, taste and other functions.

cerebrum

that part of the forebrain which expands to form the CEREBRAL HEMISPHERES. found in all vertebrates except fishes.

cerebrum

cer·e·brum

pl. cerebra ( ser'ĕ-brŭm, - bră ) [TA]

Cerebral parts derived from the telencephalon; includes mainly the cerebral cortex and basal ganglia.

cerebrum (ser´əbrum, sərē´brum) ,

n the largest portion of the brain. Operating at the highest functional level and occupying the upper part of the cranium, it consists of two hemispheres united at the bottom by commissures of large bundles of nerve fibers. As with all parts of the nervous system, each part of it has highly specific functions (e. g. a specific outer cortical area controls voluntary mastication, whereas certain inner subcortical areas are involved in involuntary jaw posture).

cerebrum

the main portion of the brain, occupying the front part of the cranial cavity; its two cerebral hemispheres are united by the corpus callosum. The term is sometimes applied to the postembryonic forebrain and midbrain together or to the entire brain. See also brain .

Four major lobes of the cerebrum. By permission from Cunningham JG, Textbook of Veterinary Physiology, Saunders, 2002

cerebral

Did You Know?

English borrowed its word cerebrum directly from the Latin word for "brain," but the adjective cerebral took a slightly more circuitous route into our language, reaching English by way of French cerebral. Cerebrum has been used in our language as a name for the brain since the early 1600s, though the more specific scientific sense, referring just to the large upper part of the brain, didn't develop until later. Cerebral has been appearing in print in English since at least 1816. Other brainy descendants of cerebrum in English include cerebellum (the part of the brain between the brain stem and the back of the cerebrum) and cerebrate, which arrived in English in 1915 with the meaning "to use the mind" or "to think."

Origin and Etymology of cerebral

French cerebral, from Latin cerebrum brain; akin to Old High German hirni brain, Greek kara head, keras horn, Sanskrit siras head — more at horn

First Known Use: 1816

cerebral Synonyms

Synonyms

Antonyms

Other Anatomy Terms

CEREBRAL Defined for Kids

cerebral

adjective ce·re·bral s?-?re-br?l, ?ser-?-br?l

Definition of cerebral for Students

1 : of or relating to the brain or mind

2 : of, relating to, or affecting the cerebrum

Medical Dictionary

cerebral

adjective ce·re·bral s?-?re-br?l, ?ser-?-

Medical Definition of cerebral

1 : of or relating to the brain or the intellect

2 : of, relating to, affecting, or being the cerebrum < cerebral blood flow> < cerebral toxoplasmosis>

Learn More about cerebral

Thesaurus: All synonyms and antonyms for cerebral Spanish Central: Translation of cerebral Nglish: Translation of cerebral for Spanish speakers Britannica English: Translation of cerebral for Arabic speakers

Cerebryl

Important Notice: The Drugs. com international database is in BETA release. This means it is still under development and may contain inaccuracies. It is not intended as a substitute for the expertise and judgement of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that the use of any medication in any country is safe, appropriate or effective for you. Consult with your healthcare professional before taking any medication.

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Acheter Anesderm Lidocaine En Ligne Sans Prescriptions, Dequaspra

Lidocaine injection is used to numb an area of your body to help reduce pain or discomfort caused by invasive medical procedures such as surgery, needle punctures, or insertion of a catheter or breathing tube.

Lidocaine injection is also given in an epidural (spinal block) to reduce the discomfort of contractions during labor.

Lidocaine injection is sometimes used to treat irregular heart rhythms that may signal a possible heart attack.

Lidocaine injection may also be used for other purposes not listed in this medication guide.

Lidocaine is given as an injection through a needle placed into a vein or directly into the body area to be numbed. Your doctor, nurse, or other healthcare provider will give you this injection. Your breathing, blood pressure, oxygen levels, and other vital signs will be watched closely while you are receiving lidocaine injection in a hospital setting.

To treat irregular heart rhythms, you may be shown how to use your medicine at home. Do not self-inject this medicine if you do not fully understand how to give the injection and properly dispose of needles and other items used in giving the medicine.

The LidoPen auto-injector is a prefilled automatic injection device to be used in an emergency. Keep the device with you at all times. Your doctor will describe the signs and symptoms to watch for when deciding when it's time to use the injection. Never use the LidoPen auto-injector without first calling your doctor.

Do not use the auto-injector in or near a vein or into your buttocks. Inject the medication only in your upper thigh or upper arm.

With the LidoPen auto-injector you will also receive a CardioBeeper. This device is used to transmit your heart rate and rhythm to your doctor over a telephone. Read all provided instructions and practice using the CardioBeeper so you will be able to quickly use it in an emergency.

Use Lidocaine as directed by your doctor

Store the LidoPen auto-injector at room temperature away from moisture and extreme hot or cold.

Active ingredient: Lidocaine

You should not receive this medication if you are allergic to lidocaine or any other type of numbing medicine.

If you have any of these other conditions, you may need a dose adjustment or special tests to safely use lidocaine injection:

coronary artery disease, circulation problems; or

a history of malignant hyperthermia.

FDA pregnancy category B. This medication is not expected to be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. It is not known whether lidocaine injection passes into breast milk or if it could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Important safety information

There may be other drugs that can interact with lidocaine injection. Tell your doctor about all the prescription and over-the-counter medications you use. This includes vitamins, minerals, herbal products, and drugs prescribed by other doctors. Do not start using a new medication without telling your doctor.

Get emergency medical help if you have any of these signs of an allergic reaction: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Tell your caregivers at once if you have any of these serious side effects:

feeling anxious, shaky, dizzy, restless, or depressed;

drowsiness, vomiting, ringing in your ears, blurred vision;

confusion, twitching, seizure (convulsions);

fast heart rate, rapid breathing, feeling hot or cold;

weak or shallow breathing, slow heart rate, weak pulse; or

feeling like you might pass out.

Less serious side effects include:

mild bruising, redness, itching, or swelling where the medication was injected;

numbness in places where the medicine is accidentally applied.

This is not a complete list of side effects and others may occur.

Call your doctor for medical advice about side effects.

Les clients qui ont achete ce produit ont egalement achete

Lidocaine €27.47 Par unite Plus d'information Phenergan €0.34 Par unite Plus d'information Nimotop €0.93 Par unite Plus d'information Periactin €0.45 Par unite Plus d'information Benemid €0.74 Par unite Plus d'information Prednisone €0.29 Par unite Plus d'information

Buy Woman S Health - Eyeclof (Brand Name Diclofenac) Online - Order Diclofenac - Purchase Woman S He

Diclofenac is used to treat pain or inflammation caused by arthritis or ankylosing spondylitis. Diclofenac may also be used for purposes other than those listed in this medication guide.

Use Diclofenac as directed by your doctor.

Take Diclofenac by mouth with or without food. Ask your health care provider any questions you may have about how to use Diclofenac.

Drug Class and Mechanism

Diclofenac is in a group of drugs called nonsteroidal anti-inflammatory drugs (NSAIDs). Diclofenac works by reducing hormones that cause inflammation and pain in the body.

If you miss a dose of Diclofenac, use it as soon as possible. If it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

Store Diclofenac at room temperature between 68 and 77 degrees F (20 and 25 degrees C) in a tightly closed container. Brief periods at temperatures of 59 to 86 degrees F (15 to 30 degrees C) are permitted. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Diclofenac out of the reach of children and away from pets.

Do not use Diclofenac if:

you are allergic to any ingredient in Diclofenac; you have had a severe allergic reaction (e. g. severe rash, hives, breathing difficulties, dizziness) to another NSAID (e. g. ibuprofen, naproxen, celecoxib) or aspirin. Contact your doctor or health care provider right away if any of these apply to you.

Important : Diclofenac may cause dizziness or blurred vision. These effects may be worse if you take it with alcohol or certain medicines. Use Diclofenac with caution. Do not drive or perform other possibly unsafe tasks until you know how you react to it. Before you start any new medicine, check the label to see if it has Eyeclof or another nonsteroidal anti-inflammatory drug (NSAID) medicine in it too. If it does or if you are not sure, check with your doctor or pharmacist. Diclofenac should not be used in children; safety and effectiveness in children have not been confirmed. Pregnancy and breast-feeding: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Diclofenac while you are pregnant. It is not known if Diclofenac is found in breast milk. Do not breast-feed while using Diclofenac.

Possible Side Effects

Check with your doctor if any of these most common side effects persist or become bothersome:

burning or stinging; discharge; eye redness, irritation, or itching. Seek medical attention right away if any of these severe side effects occur:

severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); blurred or distorted vision; eye infection; eyelid swelling or redness; sensitivity to glare or light.

Diclofenac is to be used only by the patient for whom it is prescribed. Do not share it with other people. If your symptoms do not improve or if they become worse, check with your doctor.

Compound S, Compound S

compound 1

Grammar. of or relating to a compound sentence or compound-complex sentence.

consisting of two or more parts that are also bases, forming a compound noun, compound adjective, compound verb, or compound preposition, as housetop, many-sided, playact, or upon.

consisting of any two or more parts that have identifiable meaning, as a base and a noninflectional affix ( return, follower ), a base and a combining form ( biochemistry ), two combining forms ( ethnography ), or a combining form and a noninflectional affix ( aviary, dentoid ).

(of a verb tense) consisting of an auxiliary verb and a main verb, as are swimming, have spoken, or will write (opposed to simple ).

Botany. composed of several similar parts that combine to form a whole:

a compound fruit.

Zoology. composed of a number of distinct individuals that are connected to form a united whole or colony, as coral.

Music. of or relating to compound time.

Machinery. noting an engine or turbine expanding the same steam or the like in two successive chambers to do work at two ranges of pressure.

something formed by compounding or combining parts, elements, etc.

Chemistry. a pure substance composed of two or more elements whose composition is constant.

a compound word, especially one composed of two or more words that are otherwise unaltered, as moonflower or rainstorm.

verb (used with object)

to put together into a whole; combine:

to compound drugs to form a new medicine.

to make or form by combining parts, elements, etc.; construct:

to compound a new plan from parts of several former plans.

to make up or constitute:

all the organs and members that compound a human body.

to settle or adjust by agreement, especially for a reduced amount, as a debt.

Law. to agree, for a consideration, not to prosecute or punish a wrongdoer for:

to compound a crime or felony.

to pay (interest) on the accrued interest as well as the principal:

My bank compounds interest quarterly.

to increase or add to:

The misery of his loneliness was now compounded by his poverty.

Electricity. to connect a portion of the field turns of (a direct-current dynamo) in series with the armature circuit.

verb (used without object)

to make a bargain; come to terms; compromise.

to settle a debt, claim, etc. by compromise.

Colic Drops Oral Uses, Side Effects, Interactions, Pictures, Warnings - Dosing, Dentinox

Colic Drops

Uses

This product is used to relieve symptoms of extra gas caused by air swallowing or certain foods/infant formulas. Simethicone helps break up gas bubbles in the gut.

How to use Colic Drops

Shake the container well before each use. Give this product by mouth as needed, usually after meals and at bedtime. or as directed by the doctor. Follow all directions on the product package. If you are uncertain about any of the information, consult the doctor or pharmacist.

Fill the dropper to the correct dosage and squeeze the liquid slowly into the baby's mouth. towards the inner cheek. You can also measure the correct dosage with the dropper and mix it in 1 ounce of cool water, infant formula, or juice. Mix well and give the solution to your baby. The proper dosage is based on your child's age and weight .

If you are treating the child yourself (without direction from a doctor), do not use more than 12 doses of simethicone per day.

Clean the dropper well after each use and close the bottle tightly.

If your child's condition persists or worsens, or if you think there may be a serious medical problem, seek immediate medical attention.

Side Effects

There are no reports of any side effects due to this medication. However, tell the doctor if your child experiences any unpleasant effects while taking this medication.

A very serious allergic reaction to this product is rare. However, seek immediate medical attention if you notice any of the following symptoms of a serious allergic reaction. rash. itching /swelling (especially of the face/tongue /throat), severe dizziness. trouble breathing .

This is not a complete list of possible side effects. If you notice other effects not listed above, contact your doctor or pharmacist.

Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088 or at www. fda. gov/medwatch.

In Canada - Call your doctor for medical advice about side effects. You may report side effects to Health Canada at 1-866-234-2345.

Precautions

Before giving simethicone, tell your doctor or pharmacist if your child is allergic to it; or if your child has any other allergies. This product may contain inactive ingredients, which can cause allergic reactions or other problems. Talk to your pharmacist for more details.

Interactions

If you are giving this product under your doctor's direction, your doctor or pharmacist may already be aware of possible drug interactions and may be monitoring for them. Do not start, stop, or change the dosage of any medicine before checking with your doctor or pharmacist first.

Tell your doctor of any prescription or nonprescription medication your child may use, including any antacids or digestive medications since some combination products may also contain simethicone.

Simethicone can decrease the absorption of thyroid medications (such as levothyroxine ). If you take thyroid medication, take it at least 4 hours before or after products that contain simethicone.

Keep a list of all your medications with you, and share the list with your doctor and pharmacist.

Overdose

If overdose is suspected, contact a poison control center or emergency room right away. US residents can call their local poison control center at 1-800-222-1222. Canada residents can call a provincial poison control center.

Notes

Keep all regular medical and laboratory appointments.

Missed Dose

If your child is taking this product on a regular schedule and misses a dose, give it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume the usual dosing schedule. Do not double the dose to catch up.

Storage

Store at room temperature between 59-86 degrees F (15-30 degrees C) away from moisture, heat, and light. Do not freeze. Do not store in the bathroom. Refer to storage information printed on the package. If you have any questions about storage, ask your pharmacist. Keep all medicines away from children and pets.

Do not flush medications down the toilet or pour them into a drain unless instructed to do so. Properly discard this product when it is expired or no longer needed. Consult your pharmacist or local waste disposal company for more details about how to safely discard your product.

Information last revised October 2015. Copyright(c) 2015 First Databank, Inc.

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Selected from data included with permission and copyrighted by First Databank, Inc. This copyrighted material has been downloaded from a licensed data provider and is not for distribution, expect as may be authorized by the applicable terms of use.

CONDITIONS OF USE: The information in this database is intended to supplement, not substitute for, the expertise and judgment of healthcare professionals. The information is not intended to cover all possible uses, directions, precautions, drug interactions or adverse effects, nor should it be construed to indicate that use of a particular drug is safe, appropriate or effective for you or anyone else. A healthcare professional should be consulted before taking any drug, changing any diet or commencing or discontinuing any course of treatment.

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Dinac Tablets, Dinac

DINAC®

diclofenac sodium 25 mg & 50 mg enteric coated tablets

Consumer Medicine Information

What is in this leaflet

This leaflet answers some of the common questions about DINAC. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist.

All medicines have risks and benefits. Your doctor has weighed the risks of you taking DINAC against the benefits they expect it will have for you.

If you have any concerns about taking this medicine, ask your doctor or pharmacist. Keep this leaflet with the medicine. You may want to read it again.

What DINAC Tablets are used for

The name of your medicine is DINAC. It contains the active ingredient diclofenac sodium.

DINAC is used for treating the symptoms of inflammatory and degenerative forms of rheumatism, rheumatoid arthritis and osteoarthritis. It is also used to relieve states of acute or chronic pain in which there is an inflammatory component, as well as for the symptomatic treatment of dysmenorrhoea (heavy, painful periods).

Your doctor may have prescribed DINAC for another reason. Ask your doctor if you have any questions about why DINAC was prescribed for you.

DINAC belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). It also has analgesic and antipyretic properties.

Diclofenac acts by reducing pain (at rest and on movement), morning stiffness and swelling of the joints associated with rheumatic diseases, as well as improving function.

In addition, it has been shown to relieve pain in dysmenorrhoea.

There is no evidence that DINAC is addictive.

Before you take DINAC Tablets

When you must not take DINAC Tablets

DINAC tablets should not be used by children. In adults, they should not be taken if:

You are allergic to the active ingredient or any of the inactive ingredients mentioned at the end of this leaflet under Product Description.

You have had allergic reactions (such as asthma, itchy rash or severe hay fever) after taking aspirin or any other NSAIDs.

You suffer from a stomach ulcer, bleeding from the stomach or bowel.

It has passed its expiry date or the packaging appears to have been tampered with.

You are pregnant or breast feeding, or if there is a possibility that pregnancy may occur.

Before you start to take DINAC Tablets

Tell your doctor if you plan on becoming pregnant or will be breast feeding while you are using DINAC.

Tell your doctor if you have any medical conditions, especially the following:

problems with your heart, liver or kidney function.

any infection.

a stomach ulcer, severe attacks of indigestion, or any other stomach or bowel disorder in the past.

Taking other medicines

Tell your doctor if you are taking any other medicines, including medicines you buy without a prescription from a pharmacy, supermarket or health food shop.

In particular, tell your doctor if you take any of the following:

Lithium, a medicine used to treat some types of depression

Digoxin, a heart tablet

Diuretics, also called fluid or water tablets

Medicines which lower blood pressure

Aspirin or any other anti-inflammatory (NSAID or COX-2 inhibitor) medications

Anticoagulants, tablets for thinning the blood

Antidiabetic agents, for diabetes

Methotrexate, a medicine used for treatment of rheumatoid arthritis, as well as some types of cancers

Cyclosporin, a medicine used after organ transplants, as well as in the treatment of rheumatoid arthritis

Glucocorticoids, a group of anti-inflammatory medications

These medicines may be affected by DINAC, or may affect how well it works. You may need to use different amounts of your medicine, or you may need to take different medicines. Your doctor will advise you.

Tell your doctor or pharmacist if you are currently taking a diuretic and other medicine(s) to help lower blood pressure at the same time. Sometimes diuretics and certain blood pressure lowering drugs are combined in the one product. If you are taking these drug combinations, your doctor may advise a blood test to check your kidney function before you start to take DINAC.

How to take DINAC Tablets

The daily dose should generally be prescribed in two or three divided doses. The prescribed dose should be swallowed whole with a glass of water. You may take it with or immediately after food in order to reduce the chance of stomach upset.

The dosage and duration of treatment will be determined for you by your doctor.

If you forget to take your dose

Take your dose as soon as you remember, and continue to take it as you would normally.

If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to.

Do not take a double dose to make up for the dose you missed.

If you are not sure what to do, ask your doctor or pharmacist.

If you have trouble remembering when to take your medicine, ask your pharmacist for some hints.

If you take too much

Immediately telephone your doctor or Poisons Information Centre (telephone 13 11 26) or go to accident and emergency at your nearest hospital, if you think that you or anyone else has taken too much DINAC.

Do this even if there are no signs of discomfort or poisoning.

While you are using DINAC Tablets

Things you must do

Always follow your doctor's instructions carefully.

Tell your doctor if you become pregnant while taking DINAC.

If you are about to start taking a new medicine, tell your doctor and pharmacist that you are taking DINAC.

Things you must not do

Do not use DINAC to treat any other complaint unless your doctor says so.

Do not give this medication to anyone else, even if their symptoms seem similar to yours.

Things to be careful of

Be careful driving or operating machinery until you know how DINAC affects you. DINAC may cause dizziness or light-headedness in some people.

Side effects

All medicines can have unwanted effects. Sometimes they are serious, most of the time they are not. Do not be alarmed by this list of possible side effects. You may not experience any of them.

The most common side effects seen in patients taking diclofenac preparations are:

stomach pain

nausea, vomiting, diarrhoea

abdominal cramps

flatulence

anorexia

rashes

dizziness

headache

vertigo

These are the more common side effects of DINAC. Mostly, these are mild and short-lived.

If any of the following happen, stop taking DINAC, and tell your doctor immediately, or go to accident and emergency at your nearest hospital:

swelling of the face, lips, mouth or throat which may cause difficulty in swallowing or breathing

peptic ulceration and gastrointestinal bleeding.

If you feel unusually weak and tired, or notice blood in your faeces, together with severe stomach pain, stop taking the tablets and see your doctor immediately.

These are very serious side effects. You may need urgent medical attention or hospitalisation.

Other side effects not listed above may also occur in some people. Tell your doctor if you notice any other effects.

After using DINAC

Storage

Keep DINAC in the original packaging until you need to take it.

Store below 25 de C in a dry place, out of the reach of children.

Disposal

Return any unused or out of date medicine to your pharmacist.

Product Description

What DINAC Tablets look like

DINAC 25 mg: round, brown-yellow film coated tablets. They are available in bottles of 50 tablets.

DINAC 50 mg: round, brown-yellow film coated tablets. They are available in bottles of 50 tablets.

Ingredients

Active Ingredient is diclofenac sodium. DINAC also contains some inactive ingredients. These are lactose, calcium hydrogen phosphate, microcrystalline cellulose, maize starch, sodium starch glycollate, magnesium stearate, colloidal silicon dioxide, methacrylic acid copolymer, triethyl citrate, talc, titanium dioxide and yellow ferric oxide.

Supplier

DINAC is supplied in Australia by:

Douglas Pharmaceuticals Australia Ltd 3/10 Inglewood Place Norwest Business Park BAULKHAM HILLS NSW 2153

Australian Registration Numbers:

25 mg tablets: Bottles - AUST R 68941

50 mg tablets: Bottles - AUST R 68943

Date of leaflet preparation: 20 April 2005

Published by MIMS December 2005

Consumers should be aware that the information provided by the Consumer Medicines Information (CMI) search (CMI Search) is for information purposes only and consumers should continue to obtain professional advice from a qualified healthcare professional regarding any condition for which they have searched for CMI. CMIs are provided by MIMS Australia. CMI is supplied by the relevant pharmaceutical company for each consumer medical product. All copyright and responsibility for CMI is that of the relevant pharmaceutical company. MIMS Australia uses its best endeavours to ensure that at the time of publishing, as indicated on the publishing date for each resource (e. g. Published by MIMS/myDr January 2007), the CMI provided was complete to the best of MIMS Australia's knowledge. The CMI and the CMI Search are not intended to be used by consumers to diagnose, treat, cure or prevent any disease or for any therapeutic purpose. Cirrus Media Pty Limited, its servants and agents shall not be responsible for the continued currency of the CMI, or for any errors, omissions or inaccuracies in the CMI and/or the CMI Search whether arising from negligence or otherwise or from any other consequence arising there from.

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Dinac Tablets

DINAC®

diclofenac sodium 25 mg & 50 mg enteric coated tablets

Consumer Medicine Information

What is in this leaflet

This leaflet answers some of the common questions about DINAC. It does not contain all the available information. It does not take the place of talking to your doctor or pharmacist.

All medicines have risks and benefits. Your doctor has weighed the risks of you taking DINAC against the benefits they expect it will have for you.

If you have any concerns about taking this medicine, ask your doctor or pharmacist. Keep this leaflet with the medicine. You may want to read it again.

What DINAC Tablets are used for

The name of your medicine is DINAC. It contains the active ingredient diclofenac sodium.

DINAC is used for treating the symptoms of inflammatory and degenerative forms of rheumatism, rheumatoid arthritis and osteoarthritis. It is also used to relieve states of acute or chronic pain in which there is an inflammatory component, as well as for the symptomatic treatment of dysmenorrhoea (heavy, painful periods).

Your doctor may have prescribed DINAC for another reason. Ask your doctor if you have any questions about why DINAC was prescribed for you.

DINAC belongs to a group of medicines called non-steroidal anti-inflammatory drugs (NSAIDs). It also has analgesic and antipyretic properties.

Diclofenac acts by reducing pain (at rest and on movement), morning stiffness and swelling of the joints associated with rheumatic diseases, as well as improving function.

In addition, it has been shown to relieve pain in dysmenorrhoea.

There is no evidence that DINAC is addictive.

Before you take DINAC Tablets

When you must not take DINAC Tablets

DINAC tablets should not be used by children. In adults, they should not be taken if:

You are allergic to the active ingredient or any of the inactive ingredients mentioned at the end of this leaflet under Product Description.

You have had allergic reactions (such as asthma, itchy rash or severe hay fever) after taking aspirin or any other NSAIDs.

You suffer from a stomach ulcer, bleeding from the stomach or bowel.

It has passed its expiry date or the packaging appears to have been tampered with.

You are pregnant or breast feeding, or if there is a possibility that pregnancy may occur.

Before you start to take DINAC Tablets

Tell your doctor if you plan on becoming pregnant or will be breast feeding while you are using DINAC.

Tell your doctor if you have any medical conditions, especially the following:

problems with your heart, liver or kidney function.

any infection.

a stomach ulcer, severe attacks of indigestion, or any other stomach or bowel disorder in the past.

Taking other medicines

Tell your doctor if you are taking any other medicines, including medicines you buy without a prescription from a pharmacy, supermarket or health food shop.

In particular, tell your doctor if you take any of the following:

Lithium, a medicine used to treat some types of depression

Digoxin, a heart tablet

Diuretics, also called fluid or water tablets

Medicines which lower blood pressure

Aspirin or any other anti-inflammatory (NSAID or COX-2 inhibitor) medications

Anticoagulants, tablets for thinning the blood

Antidiabetic agents, for diabetes

Methotrexate, a medicine used for treatment of rheumatoid arthritis, as well as some types of cancers

Cyclosporin, a medicine used after organ transplants, as well as in the treatment of rheumatoid arthritis

Glucocorticoids, a group of anti-inflammatory medications

These medicines may be affected by DINAC, or may affect how well it works. You may need to use different amounts of your medicine, or you may need to take different medicines. Your doctor will advise you.

Tell your doctor or pharmacist if you are currently taking a diuretic and other medicine(s) to help lower blood pressure at the same time. Sometimes diuretics and certain blood pressure lowering drugs are combined in the one product. If you are taking these drug combinations, your doctor may advise a blood test to check your kidney function before you start to take DINAC.

How to take DINAC Tablets

The daily dose should generally be prescribed in two or three divided doses. The prescribed dose should be swallowed whole with a glass of water. You may take it with or immediately after food in order to reduce the chance of stomach upset.

The dosage and duration of treatment will be determined for you by your doctor.

If you forget to take your dose

Take your dose as soon as you remember, and continue to take it as you would normally.

If it is almost time for your next dose, skip the dose you missed and take your next dose when you are meant to.

Do not take a double dose to make up for the dose you missed.

If you are not sure what to do, ask your doctor or pharmacist.

If you have trouble remembering when to take your medicine, ask your pharmacist for some hints.

If you take too much

Immediately telephone your doctor or Poisons Information Centre (telephone 13 11 26) or go to accident and emergency at your nearest hospital, if you think that you or anyone else has taken too much DINAC.

Do this even if there are no signs of discomfort or poisoning.

While you are using DINAC Tablets

Things you must do

Always follow your doctor's instructions carefully.

Tell your doctor if you become pregnant while taking DINAC.

If you are about to start taking a new medicine, tell your doctor and pharmacist that you are taking DINAC.

Things you must not do

Do not use DINAC to treat any other complaint unless your doctor says so.

Do not give this medication to anyone else, even if their symptoms seem similar to yours.

Things to be careful of

Be careful driving or operating machinery until you know how DINAC affects you. DINAC may cause dizziness or light-headedness in some people.

Side effects

All medicines can have unwanted effects. Sometimes they are serious, most of the time they are not. Do not be alarmed by this list of possible side effects. You may not experience any of them.

The most common side effects seen in patients taking diclofenac preparations are:

stomach pain

nausea, vomiting, diarrhoea

abdominal cramps

flatulence

anorexia

rashes

dizziness

headache

vertigo

These are the more common side effects of DINAC. Mostly, these are mild and short-lived.

If any of the following happen, stop taking DINAC, and tell your doctor immediately, or go to accident and emergency at your nearest hospital:

swelling of the face, lips, mouth or throat which may cause difficulty in swallowing or breathing

peptic ulceration and gastrointestinal bleeding.

If you feel unusually weak and tired, or notice blood in your faeces, together with severe stomach pain, stop taking the tablets and see your doctor immediately.

These are very serious side effects. You may need urgent medical attention or hospitalisation.

Other side effects not listed above may also occur in some people. Tell your doctor if you notice any other effects.

After using DINAC

Storage

Keep DINAC in the original packaging until you need to take it.

Store below 25 de C in a dry place, out of the reach of children.

Disposal

Return any unused or out of date medicine to your pharmacist.

Product Description

What DINAC Tablets look like

DINAC 25 mg: round, brown-yellow film coated tablets. They are available in bottles of 50 tablets.

DINAC 50 mg: round, brown-yellow film coated tablets. They are available in bottles of 50 tablets.

Ingredients

Active Ingredient is diclofenac sodium. DINAC also contains some inactive ingredients. These are lactose, calcium hydrogen phosphate, microcrystalline cellulose, maize starch, sodium starch glycollate, magnesium stearate, colloidal silicon dioxide, methacrylic acid copolymer, triethyl citrate, talc, titanium dioxide and yellow ferric oxide.

Supplier

DINAC is supplied in Australia by:

Douglas Pharmaceuticals Australia Ltd 3/10 Inglewood Place Norwest Business Park BAULKHAM HILLS NSW 2153

Australian Registration Numbers:

25 mg tablets: Bottles - AUST R 68941

50 mg tablets: Bottles - AUST R 68943

Date of leaflet preparation: 20 April 2005

CMI provided by MIMS Australia, December 2014  

Related information - Dinac Tablets

07 Nov 2014 – Information on medicines available in Australia containing diclofenac sodium (anti-inflammatory medicines (NSAIDs)), including our latest evidence-based information and resources for health professionals and consumers. The active ingredient is the chemical in a medicine that makes it work. Medicines that contain the same active ingredient can be available under more than one brand name. Brands include both active ingredients and inactive ingredients. You'll find information about brands of medicines that contain diclofenac sodium (anti-inflammatory medicines (NSAIDs)) below, including their consumer medicine information (CMI) leaflets.

09 Nov 2012 – Find reliable, independent information about painful periods. You’ll find resources for consumers and health professionals about this health condition and any related treatments, medicines and medical tests. painful periods is also known as dysmenorrhoea and painful menstruation.

02 Nov 2012 – Find reliable, independent information about arthritis. You’ll find resources for consumers and health professionals about this health condition and any related treatments, medicines and medical tests. arthritis is also known as osteoarthritis and OA (osteoarthritis).

02 Nov 2012 – Find reliable, independent information about rheumatoid arthritis. You’ll find resources for consumers and health professionals about this health condition and any related treatments, medicines and medical tests. rheumatoid arthritis is also known as RA (rheumatoid arthritis).

Nilol Tablet Intas Use, Composition, Dosage, Side Effect, Price And Review - Tablet Tree, Nilol

Nilol

Nilol Tablet - Uses, Composition, Dosage, Side Effects & Reviews

The older we get, the more infections we get, the more likely it is that doctors will treat us with multiple, intravenously administered (IV) antibiotics. These life-saving medications can interact with common drugs. Nilol is manufactured by intas that contain two active ingredients, nifedipine a calcium channel blocker and atenolol a beta blocker type of medication used to treat hypertension. It is usually taken orally 1 to 2 times per day or as directed by a doctor. The tablets should be swallowed whole and not chewed, crushed or split to prevent too much of the medication from being released at one time. It is recommended to avoid consuming grapefruits and grapefruit juice as it can increase the level of nifedipine in the blood and increase the chance of side effects. It is not always suitable for all patients. Always consult your health care provider prior to using this medication.

Nilol tablets can be used to prevent chest pain (angina) and treat high blood pressure (hypertension) which can reduce the risk of heart attacks, strokes, and kidney diseases. Make it available at your doorsteps by buying it online from Tablet Tree at discounted price.

Nilol Tablet Uses

Atenolol is the cardioselective beta blocker. It dialates the blood vessels and increases the blood flow to the heart. Amlodipine is calcium channel blocker that relaxes blood vessels and improves blood flow. Nifedipine is calcium channel blockers that act by widening the blood vessels to allow easy blood flow, which lowers the blood pressure and reduces chest pain. It is used to treat high blood pressure or chest pain and other conditions caused by coronary artery disease. The combination of these two drugs leads to antihypertensive action. It improves blood and oxygen supply to the heart muscles.

Nilol Tablet Composition

Atenolol……………50 mg

Nifedipine…………20 mg

Nilol Tablet Dosage

Hypertension, Angina pectoris

Adult: Per capsule contains atenolol 50 mg and nifedipine (sustained release) 20 mg: 1 capsule once or twice daily.

Elderly: Per capsule contains atenolol 50 mg and nifedipine (sustained release) 20 mg: 1 capsule once daily.

The correct dosage and prescription commonly depend on the patient and the condition being treated. Do not adjust your dosage without the approval of your healthcare provider. Please consult your doctor and follow his or her recommendations. Please do not self medicate.

Nilol Tablet Side Effects

Central Nervous System - Headache, fatigue, dizziness, hallucinations, confusion and sleep disturbances

Heart - Slow heart rate and heart failure

Gastrointestinal - Diarrhea and nausea

Respiratory - Wheezing and shortness of breath

Other Information on Nilol Tablet:

Pharmaceutical Form

Indications

Hypertension

Angina pectoris

Myocardial infarction

Precautions

Caution should be exercised in patients with the history of asthma or other lung disease, diabetes, any allergy, overactive thyroid, neuroendocrine tumor, heart failure, slow heart rate, poor blood circulation, heart or kidney disease, any allergy, who are taking other medications, elderly, children, during pregnancy and breastfeeding.

It may cause dizziness or drowsiness, do not drive a car or operate machinery and get up slowly from bed while taking this medication.

It may affect platelet counts; avoid injury or bruising.

Patient may develop with increased risk of allergic reaction, if it so consult with your doctor.

Drug – Drug Interaction

This medication is known to interact with the following drugs and increase or decrease its own potency:

Decreased effect with aluminum and calcium salts, barbiturates, cholestyramine, NSAIDs, ampicillin, rifampicin

Potentially Fatal: May increase effects of drugs which slow AV conduction (digoxin, verapamil, diltiazem)

Overdose

If you think there is an overdose, here are the general symptoms of such an overdose:

Symptoms: Rapid heartbeats, severe dizziness, and fainting Management: Seek emergency medical attention if you think you have taken too much of this medicine

Contraindications

Significant aortic stenosis

Sinoatrial node disease

Hypersensitivity to dihydropyridines

Cardiogenic shock

Unstable angina

Storage

Store this medicine at 20-25°C

Manufacturer

Sunya Publishing, Sunya

Sunya®

The Magic and Wonder

of Math and Science

For Home, School, and Homeschool

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meets superior educational standards as a game for children and their parents/grandparents to play together;

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fun family game for children and adults

For reviews from families who have played Sunya® click on "Reviews" at right .

When learning the rules follow the Quick Start Instructions mentioned on the "More Than A Game" page at right.

1) Sunya® ? the Magic and Wonder of Math and Science Adding & Subtracting ?- Ages 7 to Adult?

extraordinary game book for Sunya® Adding & Subtracting

sixty custom Sunya® ? Adding & Subtracting playing cards

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thirty amazing math and science fact and riddle cards ( all different facts and riddles than those with Sunya® Multiplying & Dividing)?

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extraordinary game book for Sunya® Multiplying & Dividing?

sixty custom Sunya®? Multiplying & Dividing playing cards

the Sunya®? Multiplying & Dividing Number Line Tool

thirty amazing math and science fact and riddle cards ( all different facts and riddles than those with Sunya Adding & Subtracting)?

Dolium - One-Way Pet Kegs, Dolium

Dolium ® Overview

Dolium ® one-way PET kegs are designed for a single trip from filler to consumer, ideal for opening or growing export markets, increasing sales capacity without investments, and for peak sales periods. Dolium ® one-way PET kegs are available in two sizes: 20L and 30L. We supply D, S, A and G type connectors which make the Dolium ® one-way PET kegs compatible to existing filling lines. Dolium ® one-way PET kegs are produced in a clean room environment and are delivered dry, clean, sterile, CO 2- flushed, pre-pressurized and ready to fill. With Dolium ® one-way PET kegs there is no need to clean, recover or repair stainless steel kegs. Dolium ® one-way PET kegs are safe, easy to use and 100% recyclable.

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You have to upload your prescription to buy medicines after you click on Add to Cart.

LAMUZID

Brief Info About Medicine

All Information published below is from public sources and cannot be used as expert's opinion. We request you to consult your doctor for more information

1 Why Is it Used ?

MEROPENEM :

Adult: IV Susceptible infections 0.5-1 g 8 hrly. Meningitis 2 g 8 hrly. Cystic fibrosis Up to 2 g 8 hrly. Skin infections 500 mg 8 hrly. Diabetic foot; Intra-abdominal infections 1 g 8 hrly.

2 What are the Side Effects ?

MEROPENEM :

Diarrhoea, nausea, vomiting, abdominal pain; headache; constipation; rash, pruritus, uticaria; apnoea; phlebitis, thrombophlebitis, swelling and pain at inj site; disturbances in LFTs (may cause increases in serum transaminases, alkaline phosphatase, lactic dehydrogenase). Rarely: erythema multiforme; eosinophilia, thrombocytopenia, leucopenia, neutropenia; seizures and CNS effects reported in patients with underlying CNS disorders or renal impairment. Potentially Fatal: Anaphylaxis; pseudomembranous colitis; Stevens-Johnsons sydrome.

3 What Precautions should be taken ?

MEROPENEM :

History of hypersensitivity to carbapenem, pencillins or other ?-lactam antibiotics; infants LAMDA Z

1 TAB in Single Unit

Cadila Pharmaceuticals Ltd.

Metronidazole Side Effects In Detail, Metrolag

Metronidazole Side Effects

Other dosage forms:

In addition to its needed effects, some unwanted effects may be caused by metronidazole. In the event that any of these side effects do occur, they may require medical attention.

Major Side Effects

You should check with your doctor immediately if any of these side effects occur when taking metronidazole:

More common:

Agitation

back pain

blindness

blurred vision

burning, numbness, tingling, or painful sensations in the hands or feet

changes in speech patterns

confusion

convulsions

decreased vision

depression

dizziness

drowsiness

eye pain

fever

hallucinations

headache

irritability

lack of coordination

nausea

seizures

shakiness and unsteady walk

slurred speech

stiff neck or back

trouble speaking

unsteadiness, trembling, or other problems with muscle control or coordination

unusual tiredness or weakness

vomiting

weakness in the arms, hands, legs, or feet

Less common:

Black, tarry stools

blood in the urine or stools

body aches or pain

chills

clumsiness or unsteadiness

difficulty with breathing

ear congestion

feeling of pelvic pressure

frequent or painful urination

loss of voice

nasal congestion

pinpoint red spots on the skin

runny nose

skin rash, hives, redness, or itching

sneezing

stomach and back pain (severe)

unusual bleeding or bruising

vaginal irritation, discharge, or dryness not present before taking the medicine

Rare

Bleeding gums

bloating

chest pain

constipation

cough

dark-colored urine

fast heartbeat

indigestion

loss of appetite

painful or difficult urination

pains in the stomach, side, or abdomen, possibly radiating to the back

sore throat

sores, ulcers, or white spots on the lips or in the mouth

swollen glands

yellow eyes or skin

Incidence not known:

Blistering, peeling, or loosening of the skin

bloody or cloudy urine

burning while urinating

continuing diarrhea

continuing stomach pain

diarrhea

feeling of warmth

increased volume of pale, dilute urine

joint or muscle pain

loss of bladder control

red skin lesions, often with a purple center

red, irritated eyes

redness of the face, neck, arms, and occasionally, upper chest

redness of the skin

Minor Side Effects

Some of the side effects that can occur with metronidazole may not need medical attention. As your body adjusts to the medicine during treatment these side effects may go away. Your health care professional may also be able to tell you about ways to reduce or prevent some of these side effects. If any of the following side effects continue, are bothersome or if you have any questions about them, check with your health care professional:

More common:

Abdominal or stomach cramps

dizziness or lightheadedness

feeling of constant movement of self or surroundings

heartburn

sensation of spinning

trouble sleeping

weight loss

Less common or rare:

Change in taste sensation

congestion

dry mouth

pain or tenderness around the eyes and cheekbones

tender, swollen glands in the neck

trouble with swallowing

unpleasant or sharp metallic taste

voice changes

Incidence not known:

Decreased interest in sexual intercourse

inability to have or keep an erection

loss in sexual ability, desire, drive, or performance

painful sexual intercourse

For Healthcare Professionals

Applies to metronidazole: compounding powder, intravenous powder for injection, intravenous solution, oral capsule, oral tablet, oral tablet extended release

General

The most serious side effects reported with metronidazole have included convulsive seizures, encephalopathy, aseptic meningitis, optic and peripheral neuropathy (primarily characterized by numbness or paresthesia of an extremity). Persistent peripheral neuropathy has been reported with prolonged oral administration of metronidazole. [Ref ]

Nervous system

Headache (18%) and dizziness (4%) were reported in patients using the extended-release tablet formulation. Headaches were considered severe in 10% of these patients.

A rare but serious side effect of metronidazole was peripheral neuropathy which was thought to be related to dose and duration of therapy. Most cases occurred after doses of 1000 to 2400 mg per day for at least 30 days, or a total dose of 50 grams. Neuropathy was generally located in the lower extremities and presented with numbness, tingling, and paresthesias. Patients should be advised to discontinue metronidazole if they experience these effects. Neuropathy may be persistent despite discontinuation of metronidazole. Seizures associated with metronidazole were rare, but did occur.

Several cases of MRI abnormalities of the dentate nuclei associated with symptoms of ataxia and dysarthria have been reported. The symptoms and dentate nuclei lesions resolved several weeks after discontinuation of metronidazole. These symptoms and metronidazole-induced lesions in the brain stem and cerebellar nuclei have also been described in rat studies. [Ref ]

Very common (10% or more): Headache Common (1% to 10%): Dizziness Frequency not reported: Encephalopathy, aseptic meningitis, peripheral neuropathy (characterized mainly by numbness or paresthesia of an extremity), convulsive seizures, vertigo, syncope, incoordination, ataxia, confusion, dysarthria, weakness, reversible abnormalities in the cerebellar dentate nuclei [Ref ]

Gastrointestinal

Very common (10% or more): Nausea Common (1% to 10%): Taste perversion (metallic taste), abdominal pain, diarrhea, dry mouth Rare (less than 0.1%): Pseudomembranous colitis, pancreatitis Frequency not reported: Sharp unpleasant metallic taste, vomiting, abdominal discomfort, epigastric distress, abdominal cramping, constipation, proctitis, coating of the tongue (furry tongue), glossitis, stomatitis, taste of alcoholic beverages modified [Ref ]

Nausea (10%), taste perversion (metallic taste; 9%), abdominal pain (4%), diarrhea (4%), and dry mouth (2%) in patients using the extended-release tablet formulation. Nausea was considered severe in less than 2% of these patients.

Furry tongue, glossitis, and stomatitis may be associated with sudden overgrowth of Candida.

Although metronidazole has been used to treat pseudomembranous colitis, it has rarely also been implicated as a causative agent. These rare cases have been successfully treated with vancomycin. [Ref ]

Genitourinary

Very common (10% or more): Vaginitis Common (1% to 10%): Genital pruritus, abnormal urine, dysmenorrhea, urinary tract infection Rare (less than 0.1%): Darkened urine Frequency not reported: Dysuria, cystitis, polyuria, incontinence, vulvovaginal candidiasis, vaginal itching, dyspareunia, sense of pelvic pressure [Ref ]

Vaginitis (15%), genital pruritus (5%), abnormal urine (3%), dysmenorrhea (3%), and urinary tract infection (2%) were reported in patients using the extended-release tablet formulation.

Instances of darkened urine have been investigated. The pigment responsible has not been positively identified; however, it is most likely a metabolite of metronidazole and appears to have no clinical significance. [Ref ]

Other

Bacterial infection (7%), influenza-like symptoms (6%), and moniliasis (3%) were reported in patients using the extended-release tablet formulation.

A disulfiram-like reaction has been reported in some patients drinking ethanol while taking metronidazole. Patients have experienced abdominal distress, vomiting, flushing, nausea, headache, and hypotension. Patients should be advised to refrain from all forms of ethanol while taking metronidazole and for at least 72 hours after the last dose. [Ref ]

Common (1% to 10%): Bacterial infection, influenza-like symptoms, moniliasis Frequency not reported: Fever, overgrowth of Candida, disulfiram-like reaction (abdominal distress, nausea, vomiting, flushing, hypotension, or headache) with ethanol [Ref ]

Respiratory

Upper respiratory tract infection (4%), rhinitis (4%), sinusitis (3%), and pharyngitis (3%) were reported in patients using the extended-release tablet formulation.

Common (1% to 10%): Upper respiratory tract infection, rhinitis, sinusitis, pharyngitis

Hypersensitivity

Metronidazole has rarely been associated with a serum sickness-like reaction which presented as arthralgias, malaise, fever, chills, pruritus, and rash. [Ref ]

Rare (less than 0.1%): Serum sickness-like reaction Frequency not reported: Hypersensitivity (including urticaria, erythematous rash, Stevens-Johnson syndrome, toxic epidermal necrolysis, flushing, nasal congestion, dryness of the mouth [or vagina or vulva], fever), fixed drug eruptions, cross-sensitivity to other nitroimidazole derivatives [Ref ]

Hematologic

Rare (less than 0.1%): Reversible thrombocytopenia Frequency not reported: Reversible neutropenia (leukopenia) [Ref ]

Cardiovascular

Frequency not reported: Flattening of the T-wave in ECG tracings

Dermatologic

Frequency not reported: Erythematous rash, pruritus

Local

Frequency not reported: Thrombophlebitis (after IV infusion)

Thrombophlebitis can be minimized or avoided by avoiding prolonged use of indwelling IV catheters.

Psychiatric

Frequency not reported: Irritability, depression, decreased libido, insomnia, disorientation, agitation, hallucinations

Ocular

Frequency not reported: Optic neuropathy

Metabolic

Frequency not reported: Anorexia

Musculoskeletal

Frequency not reported: Fleeting joint pains (sometimes resembling "serum sickness")

Oncologic

Breast and colon cancer have been reported in Crohn's disease patients treated with high doses of metronidazole for extended periods of time.

Frequency not reported: Breast cancer, colon cancer

References

1. Rosenblatt JE, Edson RS "Metronidazole." Mayo Clin Proc 62 (1987): 1013-7

2. Koch-Weser J "Metronidazole." N Engl J Med 303 (1980): 1212-8

3. Stahlberg D, Barany F, Einarsson K, Ursing B, Elmquist D, Persson A "Neurophysiologic studies of patients with Crohn's disease on long-term treatment with metronidazole." Scand J Gastroenterol 26 (1991): 219-24

4. Wienbren M, Perinpanayagam RM, Camba L, Lee CA "Convulsions and encephalopathy in a patient with leukaemia after treatment with metronidazole." J Clin Pathol 38 (1985): 1076

5. Learned-Coughlin S "Peripheral neuropathy induced by metronidazole." Ann Pharmacother 28 (1994): 536

6. Lawford R, Sorrell TC "Amebic abscess of the spleen complicated by metronidazole-induced neurotoxicity: case report." Clin Infect Dis 19 (1994): 346-8

7. Boyce EG, Cookson ET, Bond WS "Persistent metronidazole-induced peripheral neuropathy." DICP 24 (1990): 19-21

8. Beloosesky Y, Grosman B, Marmelstein V, Grinblat J "Convulsions induced by metronidazole treatment for Clostridium difficile-associated disease in chronic renal failure." Am J Med Sci 319 (2000): 338-9

9. Schentag JJ, Ziemniak JA, Greco JM, Rainstein M, Buckley RJ "Mental confusion in a patient treated with metronidazole: a concentration-related effect." Pharmacotherapy 2 (1982): 384-7

10. Kusumi RK, Plouffe JF, Wyatt RH, Fass RJ "Central nervous sytem toxicity associated with metronidazole therapy." Ann Intern Med 93 (1980): 59-60

11. Juillerat P, Pittet V, Felley C, et al. "Drug safety in Crohn's disease therapy." Digestion 76 (2007): 161-8

12. Ahmed A, Laes DJ, Bressler EL "Reversible magnetic resonance imaging findings in metronidazole-induced encephalopathy." Neurology 45 (1995): 588-9

13. Bonkowsky JL, Sondrup C, Benedict SL "Acute reversible cerebellar lesions associated with metronidazole therapy." Neurology 68 (2007): 180

14. Schreiber W, Spernal J "Metronidazole-induced psychotic disorder." Am J Psychiatry 154 (1997): 1170-1

15. Woodruff BK, Wijdicks EF, Marshall WF, et al. "Reversible metronidazole-induced lesions of the cerebellar nuclei." N Engl J Med 346 (2002): 68-9

16. Gerding DN, Muto CA, Owens RC Jr "Treatment of Clostridium difficile infection." Clin Infect Dis 46 Suppl 1 (2008): S32-42

17. Finegold SM "Therapy for infections due to anaerobic bacteria: an overview." J Infect Dis 135 Suppl (1977): S25-9

18. Duffy LF, Daum F, Fisher SE, et al "Peripheral neuropathy in Crohn's disease patients treated with metronidazole." Gastroenterology 88 (1985): 681-4

19. Whyte CA, Shivdat-Nanhoe R, Kramer P "A Case of Amoxicillin-Induced Meningitis." Clin Infect Dis 46 (2008): 642

20. Alvarez RS, Richardson DA, Bent AE, Ostergard DR "Central nervous system toxicity related to prolonged metronidazole therapy." Am J Obstet Gynecol 145 (1983): 640-1

21. Schwebke JR, Desmond RA "A Randomized Trial of the Duration of Therapy with Metronidazole plus or minus Azithromycin for Treatment of Symptomatic Bacterial Vaginosis." Clin Infect Dis 44 (2007): 213-9

22. Sura ME, Heinrich KA, Suseno M "Metronidazole-associated pancreatitis." Ann Pharmacother 34 (2000): 1152-5

23. Saginur R, Hawley CR, Bartlett JG "Colitis associated with metronidazole therapy." J Infect Dis 141 (1980): 772-4

24. Eland IA, van Puijenbroek EP, Sturkenboom MJ, Wilson JH, Stricker BH "Drug-associated acute pancreatitis: twenty-one years of spontaneous reporting in The Netherlands." Am J Gastroenterol 94 (1999): 2417-22

25. Friedman GD, Selby JV "How often does metronidazole induce pancreatitis." Gastroenterology 98 (1990): 1702-3

26. Lagrotteria D, Holmes S, Smieja M, Smaill F, Lee C "Prospective, Randomized Inpatient Study of Oral Metronidazole versus Oral Metronidazole and Rifampin for Treatment of Primary Episode of Clostridium difficile-Associated Diarrhea." Clin Infect Dis 43 (2006): 547-52

27. Daly JJ, Chowdary KV "Pseudomembranous colitis secondary to metronidazole." Dig Dis Sci 28 (1983): 573-4

28. Loulergue P, Mir O "Metronidazole-induced pancreatitis during HIV infection." AIDS 22 (2008): 545-6

29. Bingley PJ, Harding GM "Clostridium difficile colitis following treatment with metronidazole and vancomycin." Postgrad Med J 63 (1987): 993-4

30. Giannini AJ, DeFrance DT "Metronidazole and alcohol: potential for combinative abuse." J Toxicol Clin Toxicol 20 (1983): 509-15

31. Harries DP, Teale KF, Sunderland G "Metronidazole and alcohol: potential problems." Scott Med J 35 (1990): 179-80

32. Alexander I "Alcohol-antabuse syndrome in patients receiving metronidazole during gynaecological treatment." Br J Clin Pract 39 (1985): 292-3

33. Shelley WB, Shelley ED "Fixed drug eruption due to metronidazole." Cutis 39 (1987): 393-4

34. Helms DJ, Mosure DJ, Secor WE, Workowski KA "Management of Trichomonas vaginalis in women with suspected metronidazole hypersensitivity." Am J Obstet Gynecol 198 (2008): 370. e1-7.

35. Knowles S, Choudhury T, Shear NH "Metronidazole hypersensitivity." Ann Pharmacother 28 (1994): 325-6

36. Hermida MD, Consalvo L, Lapadula MM, Della Giovanna P, Cabrera HN "Bullous fixed drug eruption induced by intravaginal metronidazole ovules, with positive topical provocation test findings." Arch Dermatol 147 (2011): 250-1

37. Mishra D, Mobashir M, Zaheer MS "Fixed drug eruption and cross-reactivity between tinidazole and metronidazole." Int J Dermatol 29 (1990): 740

38. White CM, Price JJ, Hunt KM "Bone marrow aplasia associated with metronidazole." Br Med J 280 (1980): 647

39. Weart CW, Hyman LC "Serum sickness associated with metronidazole." South Med J 76 (1983): 410-1

40. Smith JA "Neutropenia associated with metronidazole therapy." Can Med Assoc J 123 (1980): 202

Not all side effects for metronidazole may be reported. You should always consult a doctor or healthcare professional for medical advice. Side effects can be reported to the FDA here .

Feeling - Definition Of Feeling By The Free Dictionary, Fealin

feeling

c. ( impression ) → senso. impressione f a feeling of security/isolation → un senso di sicurezza /di isolamento my feeling is that. → ho l'impressione che. I have a (funny) feeling that. → ho la (strana) sensazione che. I got the feeling that. → ho avuto l'impressione che. there was a general feeling that. → il sentimento generale era che.

feel

( fi?l ) – past tense, past participle felt (felt) – verb

1. to become aware of (something) by the sense of touch. She felt his hand on her shoulder. voel ????? усещам sentir (u)citit fuhlen fole; m?rke ??????????. ????? sentir tundma ??? ???? tuntea sentir ????????? ????? ???? osjecati erez merasakan finna sentire ??? (?????) ???? jausti []just merasakan voelen fole. kjenne. merke czuc ???????? ?????? ??? ????? ??? ???? ?? ??? ?? ?????? ??? ?? ?????? ????? ???: ????? ??? ???? ???? ??? ??? ???? ????? ??? ??? ?????? ? ?????? sentir a simti чувствовать citit cutiti osetiti kanna ????????? hissetmek. farketmek ?? відчувати ??? ??? ?? ??? ?? ?? ?? ??????? ?? ????? ???? c?m th?y ??

2. to find out the shape, size, texture etc of something by touching, usually with the hands. She felt the parcel carefully. voel, bevoel ???????? ?????????? напипвам apalpar ohmatat befuhlen fole; m?rke ?????? tocar. palpar kompima ??? ???? ?? ?? ??? ???? ????? ???? tunnustella palper ?????? ?????? ?? ????? ???? opipati (meg)tapint meraba ?reifa, snerta tastare ??? ??? ??? (ap)ciupineti []taustit merasa voelen fole. kjenne macac ??? ????? ??? ??? apalpar a pipai ощупывать ohmatat otipati opipati kanna pa ?????? yoklamak, yoklayarak bakmak ? мацати ??? ?? ??? ??? ?? ??? ???? ????? ?? ?????? ????? s? mo ?

3. to experience or be aware of (an emotion, sensation etc ). He felt a sudden anger. ondervind, ervaar ??????? ??? ??????? ?? (по)чуствам sentir pocitit spuren fole; m?rke ????? sentir tundma ?? ???? tuntea ressentir ?????? ????? ???? osjetiti, iskusiti erzekel merasa finna, upplifa sentire. provare ???? (?? ???) ??? pajusti izjust merasa gevoelen fole. kjenne czuc ??????? sentir a simti ощущать pocitit obcutiti osetiti kanna, erfara, fornimma ?????????? hissetmek. hissi duymak ?? відчувати ??? ???? ?? ????? ???? co c?m giac; c?m th?y ??

4. to think (oneself) to be. She feels sick; How does she feel about her work? voel ??????? чуствам се sentir-se citit se fuhlen fole sig ?????????? sentirse. encontrarse tunduma, end tundma ????? ???? tuntea sentir. penser de ????????? ????? osjecati se vel berpikir li?a; finnast sentirsi ??? (…? ??? ???) ??? jaustis justies berfikir zich voelen foles, kjennes, fole/kjenne seg czuc sie ??????? sentir-se a (se) simti; a crede (despre) чувствовать citit sa pocutiti se, meniti osecati se kanna sig, ma ??? dusunmek. hissetmek ?? почувати себе; сприймати ??? ?? ??? ????? ???? c?m th?y ??

5. to believe or consider. She feels that the firm treated her badly. meen, dink, voel ?????????? ??????? ?? смятам achar mit pocit glauben fole ????? creer tunduma ???? ???? uskoa avoir l'impressiom ?????? ??????? ???? smatrati, misliti gondol yakin finnast credere ?? ?? manyti, laikyti uzskatit yakin vinden fole. synes. tenke uwazac ?????? achar a avea senzatia (ca) сознавать mat pocit imeti obcutek smatrati tycka, mena ??????????????? inanmak ; dusunmek ?? вважати ???? ??? ????? tin; cho r?ng ??

(in certain animals, insects etc ) an organ for touching, especially one of the two thread-like parts on an insect's head. voeler, tasorgaan ?????? ????? антена antena tykadlo der Fuhler folehorn; antenne ?????? antena. tentaculo katsesarv ???? tuntosarvi antenne ???? ????? ???? ???? ?????-??????? ?? ???? ?? ???, ???? ??? ?? ??? ???? ticalo, pipak tapogato, csap sungut falmari antenna ?? ??? ciuptuvelis [] tausteklis sesungut voeler folehorn czulek ??? ?? (??? ?? ????? ?????? ?? ?????? ???? ?? ??? ???? ??? ??????? ?? ????? ?????? ??????? ???????? ????? ?????? ???? antena antena щупальце ; усик tykadlo tipalka pipak kanselsprot, antenn, tentakel ?????????????????? duyarga. anten ??,?? щупальце; вусик ???? ??? ???? rau; rau s?; xuc tu ??,??

1. power and ability to feel. I have no feeling in my little finger. gevoel, sensasie ????? осезание sensacao cit das Gefuhl folelse ??????? sensibilidad tundlikkus ?? tuntoaisti sensation ????? ??? osjecaj, osjet erzekeles perasaan tilfinning sensibilita ?? ?? jautrumas sajuta perasaan gevoel folelse. fornemmelse czucie ?? sensacao simt чувствительность cit obcutljivost osecaj kansel ?????????? his. duyu ?? відчуття ????? ???? ?? ???? ?? ???? ?????? c?m giac ??

2. something that one feels physically. a feeling of great pain. gevoel, sensasie ?????? усещане sensacao pocit das Gefuhl folelse ???????. ??????? sensacion tunne ????? tuntemus sensation ????? ????? osjecaj erzet rasa tilfinning, kennd sensazione ?? ?? pojutis sajuta rasa gevoel folelse uczucie ????? sensacao senzatie ощущение pocit obcutek osecaj kansla, fornimmelse ???????????????????? duygu. his ?? відчуття ?????? ????? s? c?m th?y; c?m giac ??

3. ( usually in plural ) something that one feels in one's mind. His angry words hurt my feelings; a feeling of happiness. gevoelens ??????? чувства sentimento city; pocit das Gefuhl folelse ??????? sentimiento tunne, tundmus ????? tunteet sentiment ????? ??????????? osjecaj erzes perasaan tilfinningar sentimento ?? ?? jausmas jutas; emocijas perasaan gevoel folelse uczucie ????? sentimento sentiment чувства; чувство city; pocit(y) obcutek, custvo osecanje kansla, kanslor ?????????????????? duyarl?k, hassasiyet ?? почуття ?????? ?? ?????? tinh c?m ??

4. an impression or belief. I have a feeling that the work is too hard. gevoel, vermoede. mening ???????? ????? впечатление pressentimento dojem, pocit das Gefuhl folelse; fornemmelse ???????? impresion mulje ????? kasitys impression ??? ????? osjecaj, misljenje erzes kesan tilfinning; hugbo?; sko?un senzazione ?? ??, ?? ispudis, nuomone nojauta; izjuta merasakan idee folelse wrazenie ????? pressentimento impresie впечатление. мнение dojem vtis osecaj kansla ???????; ????????? sezis, sezme ?? погляд; враження ???? ?? ???? ???? c?m giac ??

5. affection. He has no feeling for her now. gevoelens ???????? ????? страст afeicao cit, sympatie das Gefuhl folelse ?????????. ??????? ??????? afecto hoolivus ????? tunteet sentiment ???????? ??????, ?????, ??????? naklonost, osjecaj erzelem perasaan tilfinning sentimento ?? ?? meile, simpatija lidzjutiba; simpatijas perasaan affectie kj?rlig folelse, sans for uczucie ??? afeicao sen­timent симпатия sympatia nagnjenje emocija kanslor ??????? sevgi. yak?nl?k ?? почуття ???? yeu m?n; thuong ??

6. emotion. He spoke with great feeling. gevoel, gevoelvol ?????? ????? ????? емоция emocao vzruseni das Gefuhl folelse ?????????. ????? emocion. sentimiento tunne ??? tunne emotion ??? ??????, ???, ???? emocija erzelem emosi ge?shr?ring, uppnam; tilfinningasemi emozione ?? ??? susijaudinimas satraukums; uzbudinajums emosi emotie folelse emocja. wzruszenie ?????? ????? emocao emo­tie волнение vzrusenie ginjenost emocija kansla ?????? duygu. ihtiras ?? почуття, емоція ???? s? c?m d?ng; s? xuc d?ng ??

feel as if / as though

to have the sensation (physical or mental) or feeling that. I feel as if I am going to be sick; She feels as though she has known him for years. voel asof ??????? ???????? чуствам се сякаш sentir como se mit pocit, ze/jako kdyby das Gefuhl haben, als ob fole det som om ?????????? ??? ?? sentir como si, tener la impresion de tundub, nagu ????? ???? tuntea avoir l'impression de ????? ?????? ???? imati odreden osjecaj, osjecati se kao da. ugy gondolja, mintha merasa finnast; hafa a tilfinningunni sentirsi come se ~??????? …?? ???? kam nors rodytis/pasirodyti lyg skist, ka merasa zich voelen alsof fole det som om. ha pa folelsen czuc sie jak gdyby ??????? sentir como se/. que? a avea impresia (ca) казаться mat pocit, ze imeti obcutek, da osecati kao da kannas som om ???????????????; ???????????? sanmak, hissine kap?lmak. gibi duymak ???? здаватися, ніби ??? ????? ???? co ho?c dem l?i c?m giac r?ng ????

1. to have the feelings that one would have if one were. I feel like a princess in this beautiful dress; He felt like an idiot (= He felt very foolish). voel soos ??????? ????? чуствам се като sentir-se como citit se jako sich fuhlen wie fole som ????? sentirse como end (kellenagi) tundma ??? ?? ??? ??? ???? tuntea olevansa sentir ?????? ?????? ???? osjecati se kao, poput (vmilyennek) erzi magat merasa seperti li?a (eins og) sentirsi ~???????????. ? ??? ?? jaustis kaip justies ka merasa seperti zich voelen als kjenne/fole seg som czuc sie jak ??????? sentir-se como/como? a se simti ca чувствовать себя как citit sa ako pocutiti se (kot) osecati se poput kanna sig som ????????????????. gibi hissetmek ???. ?? почувати себе ??? ?? ??? ?? ??? ????? ???? c?m th?y gi?ng nhu (ai) ???. ??

2. to feel that one would like to (have, do etc ). I feel like a drink; Do you feel like going to the cinema? voel soos, is lus vir ???????? ??????? ???????? прави ми се нещо ter vontade de mit chut Lust haben auf/zu have lyst til ??? ??????? ??? apetecer algo, tener ganas de algo meeldiks (midagi teha) ??? ????? haluta avoir envie ??????????? ?????? ????? misliti, zeljeti kedve van vmihez ingin langa i avere voglia ~???. ? ?? ?? noreti, buti linkusiam just velesanos (kaut ko darit) ingin zin hebben in ha lyst pa/til miec ochote na ????? ter vontade de/apetecer a-si dori хотеть mat chut zeleti si biti raspolozen za kanna for ????; ??????? can? istemek ?? бути схильним до ???? ????? ???? nghi r?ng ai s? (lam /co) cai gi; mu?n (lam) cai gi ??

to find one's way by feeling. I had to feel my way to the door in the dark. jou pad voel ?????? ???????? ??????????? ?????? проправям си път andar as apalpadelas jit poslepu/tapave tasten fole sig frem ??????? ????????? andar a tientas teed kobama ??? ?????? ? ??? ???? tunnustella avancer a tatons ??????? ?????? tapkanjem i pipanjem traziti put tapogatodzva halad meraba-raba ?reifa sig afram/a? andare a tentoni ?????? ???? ?? apgraibomis eiti iet taustoties berjalan meraba-raba op de tast gaan fole seg fram isc po omacku ??? ????? andar as apalpadelas a inainta bajbaind идти ощупью ist opatrne pretipati se napipati put ?????? sag? solu yoklayarak yolunu bulmak, yavas yavas ilerlemek ???? іти помацки ?? ?? ??? ????? do d?m ????

get the feel of

to become accustomed to. to get the feel of a new job. kry die gevoel van ???????? ???? свиквам acostumar-se zvyknout si ein Gefuhl bekommen fur v?nne sig til ????????????? ?? acostumbrarse a harjuma ?? ????? paasta sisalle se faire a ????? ??? ???? naviknuti se belejon membiasakan diri venjast, na tokum a abituarsi a ?????? ????? priprasti prie, pajusti skoni apgut kaut ko membiasakan diri ergens bekend mee raken bli kjent med/vant til przyzwyczaic sie do ?? ??? acostumar-se a se obisnui осваиваться zvyknut si navaditi se naviknuti se fa kansla (ratta kanslan) for ??????? al?smak ??? освоювати ??? ??? ?? ????? ???? s? d?ng thanh th?o cai gi ???

feeling

feel·ing

n. sensacion; [ emotion ] sentimiento, emocion, sensibilidad.

feeling

n ( sensation ) sensación f; (emotion ) sentimiento, emoción f; (sense of touch ) sensibilidad f ; feeling of warmth . sensación de calor… strong feelings sentimientos fuertes… Have you lost feeling in your feet? . ¿Ha perdido la sensibilidad en los pies?

He knew my father years ago, and he sent me a polite note this afternoon, saying he hoped I would allow him to express his friendly feeling toward my children by sending them a few trifles in honor of the day.

In their feeling for the boys under their charge such men are not unlike the finer sort of women in their love of men.

No suspicious flourishes now of apology or concern; it was the language of real feeling towards Mrs.

And all this series of calamities from one little accident in the process of Feeling .

Upon my word," said Caderousse, from whose mind the friendly treatment of Dantes, united with the effect of the excellent wine he had partaken of, had effaced every feeling of envy or jealousy at Dantes' good fortune, -- "upon my word, Dantes is a downright good fellow, and when I see him sitting there beside his pretty wife that is so soon to be.

Goodbye, Makar Alexievitch, for I have come to the end of all I had to say, and am feeling too unwell to write more.

She paused, and saw with no slight indignation that he was listening with an air which proved him wholly unmoved by any feeling of remorse.

When Arthur Donnithorne landed at Liverpool and read the letter from his Aunt Lydia, briefly announcing his grand-father's death, his first feeling was, "Poor Grandfather

And so the days passed on: I witnessed Bertha's engagement and heard her marriage discussed as if I were under a conscious nightmare--knowing it was a dream that would vanish, but feeling stifled under the grasp of hard-clutching fingers.

I can enjoy feeling melancholy, and there is a good deal of satisfaction about being thoroughly miserable; but nobody likes a fit of the blues.

It is a passive feeling capable of being roused for any object, as the vine can grow on any tree; and the wisdom of the world recognises its strength when it urges a girl to marry the man who wants her with the assurance that love will follow.

It was a great affection that he felt for her, and he liked her company; it was curiously soothing; and he had a feeling for her which seemed to him ridiculous to entertain towards a shop-girl of nineteen: he respected her.

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Loss of appetite and poor eating habits, Anorexia after a brief illness. Patients experiencing loss of appetite during convalescence following surgery or after any major illness.

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Additional Information

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Prozac Side Effects In Detail, Prozamel

Prozac Side Effects

Note: This page contains side effects data for the generic drug fluoxetine. It is possible that some of the dosage forms included below may not apply to the brand name Prozac.

In Summary

Common side effects of Prozac include: weakness, anxiety, drowsiness, tremor, diarrhea, dyspepsia, nausea, nervousness, insomnia, headache, xerostomia, decreased libido, anorexia, and decreased appetite. Other side effects include: bulimia nervosa, dizziness, skin rash, and diaphoresis. See below for a comprehensive list of adverse effects.

For the Consumer

Applies to fluoxetine: oral capsule, oral capsule delayed release, oral solution, oral syrup, oral tablet

As well as its needed effects, fluoxetine (the active ingredient contained in Prozac) may cause unwanted side effects that require medical attention.

Major Side Effects

If any of the following side effects occur while taking fluoxetine, check with your doctor immediately:

More common:

Hives, itching, or skin rash

inability to sit still

restlessness

Less common:

Chills or fever

joint or muscle pain

Rare

Anxiety

cold sweats

confusion

convulsions (seizures)

cool pale skin

diarrhea

difficulty with concentration

drowsiness

dryness of the mouth

excessive hunger

fast or irregular heartbeat

headache

increased sweating

increased thirst

lack of energy

mood or behavior changes

overactive reflexes

purple or red spots on the skin

racing heartbeat

shakiness or unsteady walk

shivering or shaking

talking, feeling, and acting with excitement and activity you cannot control

trouble with breathing

unusual or incomplete body or facial movements

unusual tiredness or weakness

Incidence not known:

Abdominal or stomach pain

agitation

back or leg pains

bleeding gums

blindness

blistering, peeling, or loosening of the skin

bloating

blood in the urine or stools

bloody, black or tarry stools

blue-yellow color blindness

blurred vision

chest pain or discomfort

clay-colored stools

constipation

continuing vomiting

cough or dry cough

dark urine

decreased urine output

decreased vision

depression

difficulty with breathing

difficulty with swallowing

dizziness or lightheadedness

eye pain

fainting

fast, pounding, or irregular heartbeat or pulse

general body swelling

high fever

hives, itching, puffiness or swelling of the eyelids or around the eyes, face, lips, or tongue

hostility

indigestion

irregular or slow heart rate

irritability

large, hive-like swelling on the face, eyelids, lips, tongue, throat, hands, legs, feet, or sex organs

light-colored stools

loss of appetite

loss of bladder control

muscle twitching

nausea

nightmares

noisy breathing

nosebleeds

pain in the ankles or knees

painful, red lumps under the skin, mostly on the legs

pains in the stomach, side, or abdomen, possibly radiating to the back

pinpoint red spots on the skin

rapid weight gain

red or irritated eyes

red skin lesions, often with a purple center

redness, tenderness, itching, burning, or peeling of the skin

severe muscle stiffness

severe sleepiness

slurred speech

sore throat

sores, ulcers, or white spots on the lips or in the mouth

stopping of heart

sudden shortness of breath or troubled breathing

sudden weakness in the arms or legs

sudden, severe chest pain

swelling of the face, ankles, or hands

swollen or painful glands

thoughts of killing oneself

tightness in the chest

tiredness

twitching, twisting, or uncontrolled repetitive movements of the tongue, lips, face, arms, or legs

unconsciousness

unpleasant breath odor

unusual bleeding or bruising

unusual drowsiness, dullness, tiredness, weakness, or feeling of sluggishness

unusually pale skin

use of extreme physical or emotional force

vomiting of blood

yellow eyes or skin

Minor Side Effects

Some fluoxetine side effects may not need any medical attention. As your body gets used to the medicine these side effects may disappear. Your health care professional may be able to help you prevent or reduce these side effects, but do check with them if any of the following side effects continue, or if you are concerned about them:

More common:

Decreased appetite

Less common or rare:

Abnormal dreams

breast enlargement or pain

change in sense of taste

changes in vision

feeling of warmth or heat

flushing or redness of the skin, especially on face and neck

frequent urination

hair loss

increased appetite

increased sensitivity of the skin to sunlight

menstrual pain

stomach cramps, gas, or pain

unusual secretion of milk, in females

weight loss

yawning

Incidence not known:

Cracks in the skin

loss of heat from the body

painful or prolonged erections of the penis

scaly skin

swelling of the breasts or breast soreness in both females and males

unusual milk production

For Healthcare Professionals

Applies to fluoxetine: compounding powder, oral capsule, oral delayed release capsule, oral solution, oral tablet

General

The most common side effects that have been associated with the discontinuation of placebo-controlled clinical trials were anxiety, nervousness, nausea, rash, pruritus, insomnia, asthenia, and headache.

The side effect profile appears generally similar between adults, children, and adolescents. Treatment-emergent side effects reported in pediatric patients that were reported at an incidence of at least 2% or more for fluoxetine (the active ingredient contained in Prozac) and greater than placebo included thirst, hyperkinesia, agitation, personality disorder, epistaxis, urinary frequency, and menorrhagia. The most common side effect associated with treatment discontinuation in children and adolescents was mania/hypomania. [Ref ]

Psychiatric

Antidepressants may have a role in inducing worsening of depression and the emergence of suicidality in certain patients during the early phases of treatment. An increased risk of suicidal thinking and behavior in children, adolescents, and young adults (aged 18 to 24 years) with major depressive disorder (MDD) and other psychiatric disorders has been reported with short-term use of antidepressant drugs.

Adult and pediatric patients receiving antidepressants for MDD, as well as for psychiatric and nonpsychiatric indications, have reported symptoms that may be precursors to emerging suicidality, including anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia, hypomania, and mania. Causality has not been established. [Ref ]

Very common (10% or more): Anxiety, insomnia, nervousness Common (1% to 10%): Abnormal dreams, disturbance in attention, emotional lability, feeling abnormal, restlessness, sleep disorder, tension, thinking abnormal Uncommon (0.1% to 1%): Akathisia, apathy, bruxism, depersonalization, elevated mood, euphoria, hostility, intentional overdose, manic reaction, neurosis, paranoid reaction, personality disorder, psychomotor hyperactivity, psychosis, suicide attempt Rare (less than 0.1%): Agitation, antisocial reaction, delusions, hallucinations, hypomania, intentional injury, mania, panic attacks, stupor Frequency not reported: Dysphemia, suicidal thoughts and behavior Postmarketing reports: Confusion, violent behaviors [Ref ]

Nervous system

Very common (10% or more): Dizziness, headache, somnolence, tremor Common (1% to 10%): Amnesia, paresthesia, taste perversion Uncommon (0.1% to 1%): Abnormal gait, acute brain syndrome, ataxia, balance disorder, CNS depression, CNS stimulation, dyskinesia, hyperkinesia, hypesthesia, hypertonia, incoordination, migraine, myoclonus, neuralgia, neuropathy, seizures, syncope, vascular headache Rare (0.01% to 0.1%): Abnormal EEG, cerebral embolism, cerebral ischemia, circumoral paresthesia, convulsion, decreased reflexes, dysarthria, dystonia, extrapyramidal syndrome, foot drop, hyperesthesia, neuritis, paralysis, taste loss Very rare (less than 0.01%): Serotonin syndrome (neuroleptic malignant syndrome-like effects) Postmarketing reports: Cerebrovascular accident, memory impairment, movement disorders, oculogyric crisis, tardive dyskinesia [Ref ]

One retrospective study of 23 outpatients with Parkinson's disease treated with 40 mg of fluoxetine a day reported that three patients experienced worsening of parkinsonism, two patients experienced improvement of parkinsonism, and 18 patients experienced no change. Another small study reported a series of four patients who experienced worsening of parkinsonism during treatment with fluoxetine.

Potentially life-threatening serotonin syndrome has been reported with SSRIs and SNRIs as monotherapy, but particularly with concomitant use of other serotonergic drugs and drugs that impair the metabolism of serotonin.

A number of case reports have implicated fluoxetine in causing seizures. Twelve of 6000 patients experienced convulsions during pre-marketing testing.

A case of dose-dependent exacerbation of preexisting, mild restless legs syndrome (which ultimately required discontinuation of fluoxetine) has been reported. [Ref ]

Cardiovascular

One placebo-controlled study has suggested that fluoxetine (the active ingredient contained in Prozac) has no effects on intraventricular conduction. Other case reports have suggested that fluoxetine may rarely provoke dysrhythmias. Other conflicting case reports have suggested that fluoxetine may have a propensity to provoke and alleviate vasoconstriction. Several cases of unexpected death occurring shortly after initiation of fluoxetine therapy have been reported in elderly patients with multiple medical problems.

In one case report, QTc prolongation and torsades de pointes developed in an elderly woman 6 months after starting therapy with fluoxetine 20 mg daily. The QTc interval returned to normal following discontinuation of fluoxetine. Four additional cases suggesting fluoxetine associated QTc prolongation or torsades de pointes have been reported. [Ref ]

Common (1% to 10%): Chest pain, flushing, hypertension, palpitations, vasodilatation Uncommon (0.1% to 1%): Angina pectoris, arrhythmia, congestive heart failure, generalized edema, hypotension, myocardial infarct, peripheral edema, postural hypotension Rare (less than 0.1%): Bradycardia, extrasystoles, heart block, pallor, peripheral vascular disorder, phlebitis, shock, thrombophlebitis, thrombosis, vasculitis, vasospasm, ventricular extrasystoles, ventricular fibrillation Postmarketing reports: Atrial fibrillation, heart arrest, QT-interval prolongation and ventricular arrhythmia including torsades de pointes [Ref ]

Gastrointestinal

A study of 26,005 antidepressant users has reported 3.6 times more upper GI bleeding episodes with the use of SSRIs relative to the population who did not receive antidepressant medications. Upper gastrointestinal tract bleeding was observed in 3.9 times more frequently in patients receiving fluoxetine (the active ingredient contained in Prozac) [Ref ]

Very common (10% or more): Diarrhea, dry mouth, nausea Common (1% to 10%): Abdominal pain, constipation, dyspepsia, flatulence, increased appetite, vomiting Uncommon (0.1% to 1%): Aphthous stomatitis, buccoglossal syndrome, cholelithiasis, colitis, dysphagia, eructation, esophagitis, gastritis, gastroenteritis, glossitis, gum hemorrhage, hyperchlorhydria, increased salivation, melena, mouth ulcerations, stomach ulcer, stomatitis, thirst Rare (less than 0.1%): Acute abdominal syndrome, biliary pain, bloody diarrhea, cholecystitis, duodenal ulcer, enteritis, esophageal pain, esophageal ulcer, fecal incontinence, gastrointestinal hemorrhage, hematemesis, intestinal obstruction, pancreatitis, peptic ulcer, salivary gland enlargement, stomach ulcer hemorrhage, tongue edema Postmarketing reports: Gastrointestinal bleeding [Ref ]

Metabolic

Numerous cases of hyponatremia have been reported following treatment with an SSRI. Risk factors for the development of SSRI associated hyponatremia including advanced age, female gender, concomitant use of diuretics, low body weight, and lower baseline serum sodium levels have been identified. Hyponatremia tends to develop within the first few weeks of treatment (range 3 to 120 days) and typically resolves within 2 weeks (range 48 hours to 6 weeks) after therapy has been discontinued with some patients requiring treatment. The proposed mechanism for the development of hyponatremia involves the syndrome of inappropriate secretion of antidiuretic hormone (SIADH) via release of antidiuretic hormone.

Decreased weight gain has been observed in association with the use of fluoxetine (the active ingredient contained in Prozac) in children and adolescent patients. [Ref ]

Very common (10% or more): Anorexia Common (1% to 10%): Weight loss Uncommon (0.1% to 1%): Decreased appetite, dehydration, gout, hypocholesteremia, hyperlipemia, hypokalemia Rare (less than 0.1%): Alcohol intolerance, creatine phosphokinase increased, diabetes mellitus, hyperkalemia, hyperuricemia, hypocalcemia, hyponatremia Postmarketing reports: Hypoglycemia [Ref ]

Other

Very common (10% or more): Fatigue (including asthenia) Common (1% to 10%): Accidental injury, chills, ear pain, feeling jittery, fever, infection, pain, tinnitus Uncommon (0.1% to 1%): Face edema, feeling hot/cold, malaise, vertigo Rare (less than 0.1%): Deafness, hyperacusis, hypothermia Frequency not reported: Mucosal hemorrhage Postmarketing reports: Malignant hyperthermia [Ref ]

Genitourinary

Common (1% to 10%): Decreased libido, ejaculation disorder, erectile dysfunction, gynecological bleeding, impotence, urinary frequency Uncommon (0.1% to 1%): Abortion, albuminuria, amenorrhea, anorgasmia, breast enlargement, breast pain, cystitis, dysuria, female lactation, fibrocystic breast, hematuria, impaired urination, Increased libido, leukorrhea, menorrhagia, metrorrhagia, nocturia, pelvic pain, polyuria, sexual dysfunction (occasionally persisting after treatment discontinuation), urinary incontinence, urinary retention, urinary urgency, vaginal hemorrhage Rare (less than 0.1%): Breast engorgement, galactorrhea, glycosuria, hypomenorrhea, kidney pain, oliguria, priapism, uterine fibroids, uterine hemorrhage Postmarketing reports: Enlarged clitoris, gynecomastia, vaginal bleeding [Ref ]

Urinary retention and galactorrhea have been reported with other SSRIs.

The estimates of the incidence of untoward sexual experience and performance may underestimate their actual incidence, partly because patients and physicians may be reluctant to discuss this issue. In placebo-controlled clinical trials ejaculation disorder (primarily ejaculation delay) was reported as a treatment-emergent side effect at an incidence of 6% and at least twice the incidence in placebo-treated male patients. [Ref ]

Dermatologic

Common (1% to 10%): Pruritus, rash, sweating, urticaria Uncommon (0.1% to 1%): Acne, alopecia, cold sweat, contact dermatitis, ecchymosis, eczema, increased tendency to bruise, maculopapular rash, skin discoloration, skin ulcer Rare (less than 0.1%): Angioedema, furunculosis, hirsutism, petechia, photosensitivity reaction, psoriasis, purpura, purpuric rash, seborrhea Postmarketing reports: Epidermal necrolysis, erythema multiforme, erythema nodosum, exfoliative dermatitis, Stevens Johnson syndrome, thrombocytopenic purpura [Ref ]

Approximately 3% of treated patients have been reported to develop a skin reaction. [Ref ]

Endocrine

Uncommon (0.1% to 1%): Hypothyroidism Rare (less than 0.1%): Diabetic acidosis, hyperprolactinemia Postmarketing reports: Inappropriate secretion of antidiuretic hormone [Ref ]

Hematologic

Uncommon (0.1% to 1%): Anemia Rare (less than 0.1%): Blood dyscrasia, hypochromic anemia, leukopenia, lymphedema, lymphocytosis, thrombocythemia, iron deficiency anemia Very rare (less than 0.01%): Thrombocytopenia Postmarketing reports: Aplastic anemia, eosinophilia, immune-related hemolytic anemia, pancytopenia [Ref ]

Hepatic

Uncommon (0.1% to 1%): Abnormal liver function tests Rare (less than 0.1%): Alkaline phosphatase increased, hepatitis, liver fatty deposit, SGPT increased Postmarketing reports: Aggravation of hepatic damage, cholestatic jaundice, hepatic failure/necrosis, idiosyncratic hepatitis [Ref ]

Hypersensitivity

Common (1% to 10%): Allergic reaction Rare (less than 0.1%): Anaphylactoid reaction, serum sickness [Ref ]

Immunologic

Common (1% to 10%): Flu syndrome Uncommon (0.1% to 1%): Herpes zoster [Ref ]

Musculoskeletal

Epidemiological studies, primarily in patients aged 50 years or older, have shown an increased risk of bone fractures in patients receiving SSRIs or TCAs. [Ref ]

Common (1% to 10%): Arthralgia, twitching Uncommon (0.1% to 1%): Arthritis, bone pain, bursitis, leg cramps, tenosynovitis Rare (less than 0.1%): Arthrosis, chondrodystrophy, myasthenia, myopathy, myositis, osteomyelitis, osteoporosis, rheumatoid arthritis Frequency not reported: Myalgia [Ref ]

Ocular

Common (1% to 10%): Abnormal vision, vision blurred Uncommon (0.1% to 1%): Conjunctivitis, dry eyes, mydriasis, photophobia Rare (less than 0.1%): Blepharitis, diplopia, exophthalmos, glaucoma, iritis, scleritis, strabismus, visual field defect Frequency not reported: Angle-closure glaucoma, eye pain Postmarketing reports: Cataract, optic neuritis [Ref ]

Renal

Rare (less than 0.1%): BUN increased Postmarketing reports: Kidney failure [Ref ]

Respiratory

Very common (10% or more): Pharyngitis, rhinitis Common (1% to 10%): Epistaxis, yawn Uncommon (0.1% to 1%): Asthma, dyspnea, hiccup, hyperventilation Rare (less than 0.1%): Apnea, atelectasis, decreased cough, emphysema, hemoptysis, hypoventilation, hypoxia, larynx edema, lung edema, parosmia, pneumothorax, stridor, Frequency not reported: pulmonary events (inflammatory processes of varying histopathology and/or fibrosis) Postmarketing reports: Eosinophilic pneumonia, pulmonary embolism, pulmonary hypertension [Ref ]

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It is possible that some side effects of Prozac may not have been reported. These can be reported to the FDA here. Always consult a healthcare professional for medical advice.

Altisben, Altisben

Product Description Common use Sertraline belongs to a class of selective serotonin reuptake inhibitors (SSRIs). This medication is used to treat major depression associated with mood disorders. It is also applied in the treatment of body dysmorphic disorder and anxiety.

Dosage and direction Take Zoloft by mouth with a glass of water, with or without food. Avoid cutting, crushing or chewing this medicine. Do not take the medicine more often than it is prescribed. Do not give up taking it except on the advice of your doctor. It may need time for the medicine to help. Consult your doctor concerning proper dose for you.

Precautions Before taking Sertraline tell your doctor or chemist if you are allergic to it; or if you have other allergies. Inform your doctor or chemist if you have bipolar confusion, eye, liver or kidney problems. Aged people can be more sensitive to side effects of the medicine. During pregnancy this treatment should be used only in case of strong necessity. As this medicament can be absorbed by skin, women who are pregnant or may become pregnant should not manipulate this medicine.

Contraindications Prozac should not be used by pregnant/nursing women or children as well as by the patients having demonstrated a reaction of hypersensitivity to Sertraline.

Possible side effect The most common side effects are quick and irregular pulse, tremor, anxiety, blurred vision, vomiting, fever, diarrheia, etc. A very serious allergic reaction occurs very seldom. A majority of people who use this medicine do not have serious side effects. Turn to your doctor or pharmacist for more details. In case you notice the effects not listed here, contact your doctor or pharmacist.

Drug interaction Tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use before taking this medication. Sertraline can interact with: * MAO inhibitors: Furazolidone, Isocarboxazid, Linezolid, Moclobemide Tranylcypromine, etc. * Antiarrhythmic drugs: Propafenone, Quinidine, etc * Serotonin-norepinephrine reuptake inhibitors (SNRIs): Desvenlafaxine, Duloxetine, Milnacipram, Venlafaxine. * Antipsychotics (also called neuroleptics): Fluphenazine, etc. * H2-receptor antagonists: Cimetidine, Ranitidine, Famotidine, Nizatidine, etc. Turn to your doctor or pharmacist for more details.

Missed dose If you have missed your dose, take it as soon as you remember. If you see that it is near the time for the next dose, skip the missed dose and resume your usual dosing schedule. Do not take your dose twice.

Overdose If you think you have used too much of this medicine, seek emergency medical attention right away. The symptoms of overdose usually include chest pain, nausea, irregular heartbeat, and feeling light-headed or fainting.

Storage Store your medicines at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Do not store your drugs in the bathroom. Keep all drugs away from reach of children and pets.

We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Sertraline belongs to a class of selective serotonin reuptake inhibitors (SSRIs). This medication is used to treat major depression associated with mood disorders. It is also applied in the treatment of body dysmorphic disorder and anxiety.

Dosage and direction Take Zoloft by mouth with a glass of water, with or without food. Avoid cutting, crushing or chewing this medicine. Do not take the medicine more often than it is prescribed. Do not give up taking it except on the advice of your doctor. It may need time for the medicine to help. Consult your doctor concerning proper dose for you.

Precautions Before taking Sertraline tell your doctor or chemist if you are allergic to it; or if you have other allergies. Inform your doctor or chemist if you have bipolar confusion, eye, liver or kidney problems. Aged people can be more sensitive to side effects of the medicine. During pregnancy this treatment should be used only in case of strong necessity. As this medicament can be absorbed by skin, women who are pregnant or may become pregnant should not manipulate this medicine.

Contraindications Prozac should not be used by pregnant/nursing women or children as well as by the patients having demonstrated a reaction of hypersensitivity to Sertraline.

Possible side effect The most common side effects are quick and irregular pulse, tremor, anxiety, blurred vision, vomiting, fever, diarrheia, etc. A very serious allergic reaction occurs very seldom. A majority of people who use this medicine do not have serious side effects. Turn to your doctor or pharmacist for more details. In case you notice the effects not listed here, contact your doctor or pharmacist.

Drug interaction Tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use before taking this medication. Sertraline can interact with: * MAO inhibitors: Furazolidone, Isocarboxazid, Linezolid, Moclobemide Tranylcypromine, etc. * Antiarrhythmic drugs: Propafenone, Quinidine, etc * Serotonin-norepinephrine reuptake inhibitors (SNRIs): Desvenlafaxine, Duloxetine, Milnacipram, Venlafaxine. * Antipsychotics (also called neuroleptics): Fluphenazine, etc. * H2-receptor antagonists: Cimetidine, Ranitidine, Famotidine, Nizatidine, etc. Turn to your doctor or pharmacist for more details.

Missed dose If you have missed your dose, take it as soon as you remember. If you see that it is near the time for the next dose, skip the missed dose and resume your usual dosing schedule. Do not take your dose twice.

Overdose If you think you have used too much of this medicine, seek emergency medical attention right away. The symptoms of overdose usually include chest pain, nausea, irregular heartbeat, and feeling light-headed or fainting.

Storage Store your medicines at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Do not store your drugs in the bathroom. Keep all drugs away from reach of children and pets.

We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Product Description Common use Sertraline belongs to a class of selective serotonin reuptake inhibitors (SSRIs). This medication is used to treat major depression associated with mood disorders. It is also applied in the treatment of body dysmorphic disorder and anxiety.

Dosage and direction Take Zoloft by mouth with a glass of water, with or without food. Avoid cutting, crushing or chewing this medicine. Do not take the medicine more often than it is prescribed. Do not give up taking it except on the advice of your doctor. It may need time for the medicine to help. Consult your doctor concerning proper dose for you.

Precautions Before taking Sertraline tell your doctor or chemist if you are allergic to it; or if you have other allergies. Inform your doctor or chemist if you have bipolar confusion, eye, liver or kidney problems. Aged people can be more sensitive to side effects of the medicine. During pregnancy this treatment should be used only in case of strong necessity. As this medicament can be absorbed by skin, women who are pregnant or may become pregnant should not manipulate this medicine.

Contraindications Prozac should not be used by pregnant/nursing women or children as well as by the patients having demonstrated a reaction of hypersensitivity to Sertraline.

Possible side effect The most common side effects are quick and irregular pulse, tremor, anxiety, blurred vision, vomiting, fever, diarrheia, etc. A very serious allergic reaction occurs very seldom. A majority of people who use this medicine do not have serious side effects. Turn to your doctor or pharmacist for more details. In case you notice the effects not listed here, contact your doctor or pharmacist.

Drug interaction Tell your doctor or pharmacist of all prescription and nonprescription/herbal products you may use before taking this medication. Sertraline can interact with: * MAO inhibitors: Furazolidone, Isocarboxazid, Linezolid, Moclobemide Tranylcypromine, etc. * Antiarrhythmic drugs: Propafenone, Quinidine, etc * Serotonin-norepinephrine reuptake inhibitors (SNRIs): Desvenlafaxine, Duloxetine, Milnacipram, Venlafaxine. * Antipsychotics (also called neuroleptics): Fluphenazine, etc. * H2-receptor antagonists: Cimetidine, Ranitidine, Famotidine, Nizatidine, etc. Turn to your doctor or pharmacist for more details.

Missed dose If you have missed your dose, take it as soon as you remember. If you see that it is near the time for the next dose, skip the missed dose and resume your usual dosing schedule. Do not take your dose twice.

Overdose If you think you have used too much of this medicine, seek emergency medical attention right away. The symptoms of overdose usually include chest pain, nausea, irregular heartbeat, and feeling light-headed or fainting.

Storage Store your medicines at room temperature between 68-77 degrees F (20-25 degrees C) away from light and moisture. Do not store your drugs in the bathroom. Keep all drugs away from reach of children and pets.

We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information at the site cannot be used for self-treatment and self-diagnosis. Any specific instructions for a particular patient should be agreed with your health care adviser or doctor in charge of the case. We disclaim reliability of this information and mistakes it could contain. We are not responsible for any direct, indirect, special or other indirect damage as a result of any use of the information on this site and also for consequences of self-treatment.

Prams - Large Selection Very Low Prices, Pram

Quick guide to the perfect pram

Combi prams, baby prams, designer prams, buggies, 3 wheeler joggers, double twin prams, triple and multiple prams – if you are faced with the decision which pram to buy for the first time, you may well feel a bit lost and confused. The sheer mass of different models, makes and pram designs is enormous and can seem overwhelming.

But in fact, it's not that hard to find your way through this jungle of choices, provided you think carefully about what you and your family wants to get out of the pram. The following overview is intended as a brief guide on how to find your dream pram more easily.

The Advantages: Which pram for which purpose

At first glance, you may only notice the different designs of the various prams, but when choosing the suitable vehicle for your child, other criteria should take priority. Here are the most important questions you need to ask to find the right pram.

? Baby pram . buggy or combi pram

The "gold standard" these days is the combi pram, i. e. a complete set of chassis, carrycot and seat unit. If you want an even more complete service, you can choose an "all-in-one" travel system that also includes a baby car seat. As an alternative, you can use a reclining buggy with a carrycot, because this can also be used from birth.

Still relatively new but increasingly popular: prams with a buggy seat that can be converted to a carrycot. Then, there is also the classic baby pram, often in retro-style and with modern technology.

? Buggy . baby buggy . lightweight buggy . joggers

Not all buggies are the same, so you should consider what you want to use the buggy for. A baby buggy, particularly in combination with a carrycot, can function as fully fledged pram system. A lightweight buggy or travel buggy is particularly light and compact, so it fits into most car trunks and can also be taken on planes or public transport. Shoppers and shopping buggies are ideal for the city and town, often they already have a cupholder. 3 wheeler buggies or joggers are ideal for sporty parents who want to go jogging with the pram or walk in off-road terrain. The main features are large rear wheels and a good suspension.

? Tandem or Twin Pram

Tandem or twin prams are a special form of pram. Twin prams are for two children of the same age, tandem prams for two children of different ages. Plus, there are modular pram systems that can be used either for one child or for two – by adding a second seat or reclining unit.

Important: What to watch out for when buying

Again, the same applies: there is not just one pram that's perfect for every family and situation. So you need to consider carefully which pram or pram set is best for your personal circumstances. Here are some aspects that you should think about:

? How much pram would you like? Do you only need a pram or rather a whole set, including changing diaper bag, rain cover and the like?

? The question of quality. You should not compromise in this respect. After all, the health and safety of your child is at stake. So in terms of noxious substances and safety standards, you should never lower your sights.

Planning Ahead: When to Buy?

The pram should be towards the top of your shopping list for accessories for your child – directly next to the cot and first set of clothing. After all, you will want to take your child for a walk in the first few days after your little treasure is born – it's fun and will do the baby as much good as the new mom.

Prams & Buggies

Flodol - Pain Relief Cold Gel And Heating Cream, Flodol

ALTA CARE Laboratoires is a privately owned independent multinational company founded in France with the European Union as the main market. With over twenty years of experience in professional consultancy in all the stages required for manufacturing and branding, over the years ALTA CARE Laboratoires has produced products for other multinational companies. ALTA CARE Laboratoires research and development department has handed over many innovative formulations of pharmaceutical quality to other companies throughout the years. ALTA CARE Laboratoires is now also well known worldwide for being specialised in the registration of dossiers in the European Union. ALTA CARE Laboratoires immediately expanded its know-how in the manufacture of cosmeceuticals, food supplements, nutriceuticals and biotechnology to produce an exclusively innovative line of products to complement the existing line of pharmaceuticals.

ALTA CARE Laboratoires owns 16 brands and today it produces over 300 products that are distributed in pharmacies of 27 countries. Dermastir is the luxury skincare brand owned by Alta Care Laboratoires that is also sold in medical spas as well as in pharmacies.

ALTA CARE Laboratoires is directly and completely involved in the daily management of the company's business affairs, centralised at the head office in a historic building on the Avenue des Champs-Élysées, in Paris, with its very luxurious facilities. ALTA CARE Laboratoires operations and the sales and marketing office is based in central Rome in a 5-storey head office overlooking the most famous square for luxury in Italy, Piazza di Spagna. Training centres, medical spas, beauty centres in association with spas and the INSTITUT ALTA CARE and other universities have also been set up in France and Italy. Alta Care Laboratoires annually participates as exhibitor in more than 20 fairs and congresses.

ALTA CARE Laboratoires is also a major international player in the branding of products on printed media, television, international trade fairs and cinema. ALTA CARE Laboratoires owns 11 websites that are taken care of internally by a multilingual press office.

Today ALTA CARE Laboratoires is recognized as a specialist in the luxury market of derma-cosmeceuticals. Luxury vacuum airless technology jars have been created to protect ingredients from heat, light, oxygen and contamination. Hydrophilic serums and lipophilic serums are used during the aesthetic treatments in licensed Dermastir Beauty Spas. ALTA CARE Laboratoires has also produced 14 aesthetic machines that are used to compliment the Dermastir products during facial and body treatments.

ALTA CARE Laboratoires will not only be remembered as a pharmaceutical consultancy company but also as an independent multinational company with its vision and its own brands.

"ALTA CARE Laboratoires will continue to be a leader and promoter of development, research and the change that is necessary to improve the quality of the world of well-being. The company will invest a lot of its resources in order to cope with the ever more regulated and fast environment and to set up an organisation capable of anticipating an ever-changing future in this field, unlike other companies that seem to think that this environment will not change much and that people will continue to use their products. ALTA CARE Laboratoires will always maintain that its first responsibility is to satisfy both the professionals recommending our products and the customers benefiting from them".

Disclosure

Eating means coping with a fundamental need of the organism: with food we introduce into the body all that is necessary for living, energy and nutritive principles.

The organism uses energy for all the activities necessary for its survival: the only source of energy that our body is in a position to use is the one supplied from nourishment.

The calorie is the unit measure that quantifies energy. The nutritive principles, or nourishments, are substances that carry out specific functions within the human body, favouring and guaranteeing in some way the growth, the proper functioning and the health of the organism. Nutriments are substances classified in groups based on determined chemical characteristics: proteins, carbohydrates, fats, vitamins, minerals and water. Various nutritive principles are present in different quantities in all the food: no nourishment contains them all in the required quantities and, therefore there is no nourishment that alone can satisfy all our nutritive needs. For this an adequate and correct diet requires the intake of various foods, so as to ensure the daily required nutritive intake to our organism. The nutritive substances that carry calories are the carbohydrates, the proteins and the fats; vitamins, minerals and water are not a source of energy, but are equally indispensable for the human organism. Let’s analyse quickly the functions of the different nutritive substances:

PROTEINS: thanks to the extreme variability of their structure, are substances able to carry out a high number of biological functions: they are the main constituents of tissues, enzymes, some hormones and other substances that govern important processes of our organism. Proteins are present in many food of animal and vegetable origin (meat, eggs, milk, vegetables). Once ingested, they are broken down by the protease enzymes in their constituent parts, the AMINO ACIDS, which, once absorbed, are carried by the blood to the tissues in need of them. Out of the twenty amino acids that constitute proteins, eight, the so called essential amino acids, must be taken in the right proportions, with food, since the organism is not able to synthetise them; a deficiency of even one of these, may harm the general health of the organism.

CARBOHYDRATES: are substances of great biological importance, such as glucose, saccharose, starch, cellulose, etc.. They supply the most consistent portion of energy, representing especially a type of energy immediately available. In food, carbohydrates are present in forms that differ from a chemical point of view: there are in fact complex carbohydrates, with an elevated nutritive power, and simple sugars. Amongst the latter, glucose is certainly the source of energy preferred by the organism.

FATS: also called lipids, constitute the energy reservefor the organism. During the digestive phase they are broken down into fatty acids: they are distinguished in saturate fatty acids (especially of animal origin) and insaturate fatty acids (mostly present in food of vegetal origin) depending on their different chemical structures and their different nutritional properties.

MINERALS: are substances of an inorganic nature that must be taken with food because they are necessary for a series of functions of the organism: the formation of tissues, enzymatic reactions, muscular contraction, transmission of nervous impulses, etc.. They are subdivided in two classes: the macroelements (chlorine, calcium, phosphorus, magnesium, potassium, sodium, sulphur) and the oligoelements (chromium, iron, iodine, fluorine, copper, etc..).

VITAMINS: are compounds of an organic nature that take part in various physiological processes. They are classified according to their solubility in water or fats, in liposoluble vitamins (vit. A, vit. D, vit. E, vit. K if administered in excess, are accumulated in the liver and in adipose tissues) and hydrosoluble vitamins (vit. C, vit. B1, vit. B2, vit. B6, vit. B12, niacin, folic acid, pantothenic acid, biotin; these vitamins must be administered daily).

Disclosure

01 - Flodol Ice Massage Cryogel

Flodol Ice Cryogel is a massage cryogel that gives a long lasting cold effect. Flodol Ice improves flexibility and movement of the muscular skeletal system. The cold effect of Flodol Ice Cryogel improves the penetration of active ingredients that has the advantage of not acting only in an anti-inflammatory manner for pain relief.

Flodol Ice Cryogel has the advantage of having a large volume of 120 ml which is quite large when compared to its competitors.

• 2 in 1, pain relief and muscle-relaxant

• Massage cryogel that gives a cold effect to improve micro-circulation

• Large volume of 120 ml

• Good value for money

• Does not stain and is not greasy

• Immediate cold effect and long lasting

• Paraben free

> Alcohol Denat. and menthol → Cold effect • N-acetyl glucosamine → Improve the flexibility and mobility of the cartilage 0 Chamomile Recutita Flower → Soothes ♦ Glycyrrhiza Glabra Root Extract → Anti-inflammatory

People suffering from muscular and skeletal pain including lower and upper back pain, stiff necks, muscle cramps, joint pain, sport injuries, contusions, and arthritis.

DIRECTIONS FOR USE

Apply as often as required by rubbing in and leave in for the cold effect relief. Do not apply on irritated skin or on wounds.

Disclosure

Buy Teobid - Theophylline - Online Without Prescriptions, Teobid

Quibron-t (Teobid)

Preventing and treating symptoms and blockage of airway due to asthma or other lung diseases (eg, emphysema, bronchitis). It may also be used for other conditions as determined by your doctor.

Quibron-T is a xanthine derivative. It works by relaxing the muscle around the airways in the lungs, which allows them to widen and makes breathing easier. It also improves contraction of the diaphragm (the major breathing muscle) and decreases the response of the airways to irritants.

Use Quibron-T as directed by your doctor. Check the label on the medicine for exact dosing instructions. This medicine may be taken on an empty stomach or with food. Try to take this medicine every day at evenly spaced times. If you have questions about the best time to take it, ask your pharmacist.

Some foods may change the effectiveness or increase the side effects of Quibron-T. Talk to your doctor about how you should take Quibron-T with regard to food. Do not suddenly change your diet or eating habits without first checking with your doctor. Take Quibron-T at evenly spaced times throughout the day. Taking Quibron-T at the same time each day will help you remember to take it. Contact your doctor with any questions or concerns about the best way to take Quibron-T. If you miss a dose of Quibron-T, skip the missed dose and go back to your regular dosing schedule. Do not take 2 doses at once.

Ask your health care provider any questions you may have about how to use Quibron-T.

Use Quibron-T as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Store at room temperature away from sunlight and moisture.

Active Ingredient: Theophylline

Do NOT use Quibron-T if:

you are allergic to any ingredient in Quibron-T, similar medicines (eg, aminophylline), or xanthines (eg, caffeine, chocolate)

you are using large amounts of other products that contain xanthine (such as chocolate or caffeinated drinks)

you are taking dipyridamole intravenously (IV), febuxostat, halothane, or St. John's wort

Contact your doctor or health care provider right away if any of these apply to you.

Some medical conditions may interact with Quibron-T. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:

if you are pregnant, planning to become pregnant, or are breast-feeding

if you are taking any prescription or nonprescription medicine, herbal preparation, or dietary supplement

if you have allergies to medicines, foods, or other substances

if you have a history of heart problems (eg, congestive heart failure, cor pulmonale), an irregular heartbeat, liver problems (eg, cirrhosis, hepatitis), viral infection, thyroid problems, increased acid levels in the body, brain or nerve problems, or seizures (eg, epilepsy)

if you are in shock or have a fever, an ulcer, a severe infection, cystic fibrosis, or fluid in the lungs (pulmonary edema)

if you smoke, are stopping or starting smoking, or are exposed to the smoke from cigarettes or marijuana

if you are in the last 3 months of pregnancy

Important safety information:

Drinking alcohol may increase the risk of side effects of Quibron-T. Talk to your doctor before drinking alcohol while you are taking Quibron-T.

Tell your doctor or dentist that you take Quibron-T before you receive any medical or dental care, emergency care, or surgery.

Do not take more than the recommended dose or use more often than prescribed without checking with your doctor. If your symptoms become worse, contact your doctor.

Carry an ID card at all times that says you take Quibron-T.

Avoid large amounts of food or drink that have caffeine (eg, coffee, tea, cocoa, cola, chocolate).

Notify your doctor if you develop a new illness, especially if it is accompanied by fever; if a chronic illness becomes worse; or if you start or stop smoking cigarettes or marijuana.

Tell your doctor if another doctor prescribes a new medicine or tells you to stop using a medicine that you have already been taking. Tell your doctor if you start or stop any medicine, either prescription or over the counter.

Quibron-T will not stop an asthma attack once one has started. Be sure to always carry appropriate rescue medicine (eg, bronchodilator inhaler) with you in case of an asthma attack.

If you have more than one doctor, be sure to tell each of your doctors that you are taking Quibron-T.

Diabetes patients - Quibron-T may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Quibron-T may interfere with certain lab tests. Be sure your doctor and lab personnel know you are taking Quibron-T.

Lab tests, including blood theophylline levels, may be performed while you use Quibron-T. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

Use Quibron-T with caution in the ELDERLY; they may be more sensitive to its effects.

Caution is advised when using Quibron-T in CHILDREN, especially children younger than 1 year old; they may be more sensitive to its effects. Children may be more likely to experience mild, temporary behavior changes.

PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor.

You will need to discuss the benefits and risks of using Quibron-T while you are pregnant. Quibron-T is found in breast milk. If you are or will be breast-feeding while you use Quibron-T, check with your doctor. Discuss any possible risks to your baby.

All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:

Irritability; mild, temporary caffeine-like effects (eg, headache, nausea, diarrhea, trouble sleeping); mild, temporary changes in behavior; restlessness; temporary increased urination.

Seek medical attention right away if any of these SEVERE side effects occur:

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); confusion; dizziness; fast breathing; fast or irregular heartbeat; heart rhythm problems; seizures; severe or persistent nausea, diarrhea, or headache; sleeplessness; tremors; vomiting.

This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects.

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