Blackstrap Molasses For Nephrotic Syndrome-Kidney Cares Community, Molasic

Blackstrap Molasses for Nephrotic Syndrome

Blackstrap Molasses is a dark, thick liquid extracted during the process of refining sugar and has legion health benefits, so blackstrap molasses is a good source of nutrition for people. However, for patients with Nephrotic Syndrome . because of special illness condition, they can not eat foods as casually as others. They need to pay extra attention to their daily diet, so as to protect their residual kidney function. Well then, can Nephrotic Syndrome patients eat Blackstrap Molasses?

Health benefits of Blackstrap Molasses

Blackstrap Molasses is nutritious and it benefits Nephrotic Syndrome patients in may ways:

1. Energy production

Blackstrap molasses can offer Nephrotic Syndrome patients a temporary energy boost by providing carbohydrates which can be converted into energy quickly in the body. What is more, it can help to replenish the body’s storage of iron which plays an important role in energy production. Also, sufficient iron storage in blood helos to avoid anemia which occurs easily when Nephrotic Syndrome runs to kidney failure stage.

2. Antioxidant protection

Blackstrap molasses contain lots of manganese which can help Nephrotic Syndrome patients protect their cells and DNA from being damaged by free radical. Also, foods with great antioxidant protection are helpful in preventing cancer and heart problems.

3. Abundant trace elements and vitamin

Blackstrap molasses is an excellent source of trace elements and vitamin like potassium, calcium, vitamin B6 and so on which are essential for a healthy body.

4. Help to treat digestive problems

Blackstrap Molasses show great treatment effects in remitting stomach and digestive problems like stomach aches, constipation and diarrhea and so on.

Can I eat Blackstrap Molasses with Nephrotic Syndrome?

Blackstrap Molasses is health-beneficial, and good for Nephrotic Syndrome in some ways. However, because of impaired kidney function, Nephrotic Syndrome patients may need to adjust intake of trace elements. Usually, they need to limit potassium, sodium and phosphorus and ingest much more vitamin and calcium. In this light, whether Nephrotic Syndrome patients can eat Blackstrap Molasses or not depends on their specific illness condition. They need to consult their doctor firstly before they eat Blackstrap Molasses, so as to protect residual kidney function from being damaged.

Shi Jia Zhuang Kidney Disease Hospital

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Disinfecting Wipes For Multi-Surface Cleaning, Clorix

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Why are Clorox® Disinfecting Wipes better to use than paper towels, sponges and dish rags?

Clorox's answer:

Clorox® Disinfecting Wipes clean and disinfect at the same time. When you use a sponge, dishrag or even paper towel, you can spread bacteria from one surface to another. Instead of killing germs, you are pushing them around and possibly increasing the contaminated area.

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Do Clorox® Disinfecting Wipes have a clear-drying formula?

Clorox's answer:

Yes, Clorox® Disinfecting Wipes have a unique clear-drying formula, so they are great for cleaning and disinfecting shiny surfaces like glass tables, bathroom mirrors, and metal fixtures. (Use as directed)

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Do Clorox® Disinfecting Wipes kill cold and flu viruses?

Clorox's answer:

Yes. Clorox® Disinfecting Wipes kill 99.9% of germs including viruses that cause colds and flu.* Clorox® Disinfecting Wipes are also effective against common bacteria such as Staphylococcus aureus (Staph), Salmonella enterica, and E. coli. * Rhinovirus and Influenza A2

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Ingredients & Safety (3)

Can I use Clorox® Disinfecting Wipes as a hand wipe or for personal use?

Clorox's answer:

No. Clorox® Disinfecting Wipes should not be used for personal cleansing. Do not use them as baby wipes.

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Do Clorox® Disinfecting Wipes contain bleach?

Clorox's answer:

No. Clorox® Disinfecting Wipes are made with a bleach-free formula that’s available in different scents so they leave a light, clean smell every time you wipe down a surface.

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Can I safely use Clorox® Disinfecting Wipes around children, pets and pregnant women?

Clorox's answer:

Yes. Used as directed, Clorox® Disinfecting Wipes shouldn’t pose hazards to your pets, children or pregnant women. In general, it's a good idea to remove pets and children from an area when cleaning it and to follow label precautionary instructions. When out of use, as with many household cleaners, you should keep it out of the reach of children and pets.

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Usage & Packaging (5)

Where can I buy Clorox® Disinfecting Wipes?

Clorox's answer:

You can find stores near you that sell Clorox® Disinfecting Wipes on our Shop Now page. It's a good idea to call the store before going, to make sure they have it in stock. If you have any trouble finding it at a nearby store, you can also buy it online.

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Can I use Clorox® Disinfecting Wipes on different surfaces - like glass, mirrors, wood, kids toys, outdoors, etc.?

Clorox's answer:

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Can Clorox® Disinfecting Wipes be flushed down the toilet?

Clorox's answer:

No. Dispose of wipes in the trash after use. We don't recommend putting them in your septic system.

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Where can I get coupons for Clorox® Disinfecting Wipes?

Clorox's answer:

Check the Offers page to see if there are coupons available for Clorox® Disinfecting Wipes. And sign up for the Clorox® newsletter to find out about new coupons via e-mail.

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Are Clorox® Disinfecting Wipes canisters recyclable?

Clorox's answer:

Yes. Our regular Clorox® Disinfecting Wipes canisters are made from recyclable number 2 class of HDPE (High Density Polyethylene). Check with your local recycling company for a list of the materials it accepts for reprocessing.

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Rated 4.8 out of 5 by 27475 reviewers.

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Rated 5 out of 5 by Curious Clorox disinfectant This one also is fabulous! Cleans cabinet and bathroom area very well. Just grab a wipe and clean a quick mess up. September 15, 2016

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Rated 5 out of 5 by Birmingham37 I would recommend this to any one that wants a germ free bathroom and kitchen area. they are also good to disinfect your door knobs I think these are the best thing Clorox ever came out with there handy for just about everything you need to clean and disinfect. Like when one of your of your kids or family member has a stomach bug these wipes are the best to help the germs to a bare minimum. and I love that. August 15, 2016

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2016-09-18 T09:05:29.057-05:00

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Buy Zoleptil (Zotepine), Cheap Brand Zoleptil, Online (Zotepine), Discount Zoleptil - Pharmacy Rx Wo

Zoleptil (Zotepine) and/or alternatives

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General Information On Zoleptil

Zoleptil is used for the treatment of schizophrenia, a mental condition in which the patient experiences mood changes, behavior changes, delusions, and hallucinations. The generic name of this drug is zotepine, and it belongs to the class of drugs termed as anti-psychotic drugs. You can buy Zoleptil in the form of oral tablets. It works by blocking the brain receptors and regulating the transmission of signals between the nerve cells. In this way, negative symptoms such as lack of emotions, loneliness, depression, and the desire to be alone are relieved.

Side Effects for Zoleptil

Patients taking Zoleptil may commonly experience constipation, weight gain, stiffness, dizziness, uncontrolled body movements, indigestion, increase in saliva or a dry mouth, difficulty sleeping, blurred vision, headache, weakness, mood changes, anxiety, irritation, sweating, and fast heartbeat. Most of these symptoms are short-lived and get better on their own as your body gets used to the drug. However, if any of these persist or worsen, you should stop taking Zoleptil and contact your doctor. Sometimes, this medication may also lead to a decrease in the blood cell count and palpitations.

An allergic reaction to Zoleptil can be identified by difficulty in breathing, swollen face, tongue, throat or lips, hives and rashes. If you develop any of these symptoms after taking Zoleptil, you should stop taking it and seek medical help immediately.

Precautions

Before you buy Zoleptil, you should inform your doctor if you have a heart, kidney, or liver disease, prostate problem, epilepsy, difficulty urinating, glaucoma, or gout. This medicine may cause dizziness, blurred vision, and drowsiness in the patient. Therefore, you should avoid doing activities that require clear vision and complete alertness, such as driving a vehicle or operating a machine. Avoid alcohol, as it may worsen the side effect of dizziness. If you are going to have a surgical procedure or dental treatment, you should inform the surgeon or dentist that you are on Zoleptil treatment. In order to minimize lightheadedness and dizziness, rise from a sitting or lying position slowly. As this drug may cause a dry mouth, sucking on ice, sugar-free sweets, or chewing gum can be of help. In order to prevent excessive sweating, avoid getting overheated during hot weather or exercise, as it may lead to dehydration.

Zoleptil Dosage

Zoleptil 25mg, Zoleptil 50mg, and Zoleptil 100mg tablets are available in the market. The dosage recommended to you depends on your medical condition, response to treatment, other medical conditions you are suffering from, other medicinal products you are using at present, and your age.

Interactions

Zoleptil can adversely react with other medicines like CNS depressants and high dose anti-psychotics. It should also not be given if a patient is going to be administered anesthesia. You should inform your surgeon that you are taking Zoleptil before undergoing a surgery. Also do not take hypotensive agents along with Zoleptil, in addition to drugs that cause QTc prolongation. As this drug causes dizziness, do not take it with other drugs that cause the same effect. Such medicines may include sedatives, sleeping pills, tranquilizers, narcotic pain relievers, anti-anxiety and anti-seizure medicines, and antidepressants. It is important to make your doctor and pharmacist aware of all medications you are taking before you start Zoleptil.

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What is a "Generic" medication/drug?

Generic drugs are medications that have comparable medicinal ingredients as the original brand name drug, but which are generally cheaper in price. Nearly 1 in 3 drugs dispensed are "generic". They undergo testing to ensure that they are similar to their "brand" counterparts in:

Active Ingredient (e. g. "Pravastatin" is the active ingredient in brand name Pravachol)

Dosage (e. g. 10 mg of the active ingredient)

Safety (e. g. same or similar side effects, drug interactions)

Strength

Quality

Performance (e. g. 10 mg of a "generic" can be substituted for 10 mg of the "brand" and have the same therapeutic result)

Intended use (e. g. both "generic" and "brand" would be prescribed for the same conditions)

What this means is that "generic" medications can be used as a substitute of their brand equivalents with the comparable therapeutic results. There are a few exceptions (examples are outlined at the end of this page) and as always you should consult your physician before switching from a brand name medications to a generic or vice versa.

What differences are there between generic and brand?

While generics and brand equivalent drugs contain the same active ingredients, they may be different in the following ways:

The color, shape and size of the medication come from the fillers that are added to the active ingredients to make the drug. These fillers that are added to the drug have no medical use and do not to change the effectiveness of the final product. A generic drug must contain comparable active ingredients and must have a comparable strength and dosage as the original brand name equivalent. Generic drugs can be more cost effective than purchasing the brand name.

Why do generics cost less than the brand name equivalents?

When a new drug is "invented", the company that discovered it has a patent on it that gives them the exclusive production rights for this medication. Once the patent expires in a country, other companies can bring the product to market under their own name. This patent prevents other companies from copying the drug during that time so they can earn back their Research and Development costs through being the exclusive supplier of the product. After the patent expires however, other companies can develop a "generic" version of the product. These versions generally are offered at much lower prices because the companies do not have the same development costs as the original company who developed the medication.

The main thing to realize here though is that the two products are therapeutically equivalent. They may look different, and be called something different.

How are Generic drugs tested to ensure quality and efficacy?

Generally speaking, the two most generally accepted methods to prove the safety of a generic version of a drug are to either repeat most of the chemistry, animal and human studies originally done, or to show that the drug performs comparably with the original brand name drug. This second option is called a "comparative bioavailability" study. During this type of study, volunteers are given the original drug, and then separately later the generic drug. The rates at which the drug is delivered to the patient (into their blood stream or otherwise absorbed) are measured to ensure they are the same. Because the same active ingredient is used the major concern is just that it delivers the common chemical(s) at the same rate so that they have the same effect. Please note that the methods that the manufacturers use may vary from country to country.

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Chloramphenicol (Chloramphenicol), Xantervit

chloramphenicol

Chloramphenicol is used for treating serious infections caused by certain bacteria. Chloramphenicol is an antibiotic. It works by killing or slowing the growth of sensitive bacteria.

Use Chloramphenicol as directed by your doctor.

Take Chloramphenicol by mouth with or without food.

If you miss a dose of Chloramphenicol, use it as soon as possible. Then use your doses at evenly spaced times as directed by your doctor. Do not use 2 doses at once.

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

Store Chloramphenicol at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Chloramphenicol out of the reach of children and away from pets.

Do NOT use Chloramphenicol if:

you are allergic to any ingredient in Chloramphenicol

you have previously had serious side effects from Chloramphenicol

you have a low white or red blood cell count or decreased blood platelets

you have a minor infection such as a cold, flu, throat infection, or you are using Chloramphenicol to prevent a bacterial infection

you are taking other medicines that may decrease your bone marrow (eg, cancer chemotherapy); check with your doctor or pharmacist if you are unsure if any of your other medicines may decrease your bone marrow.

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

Some medical conditions may interact with Chloramphenicol. 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 anemia, bone marrow problems, liver disease, or kidney problems.

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

Anticoagulants (eg, warfarin) because side effects, including risk of bleeding, may be increased

Hydantoins (eg, phenytoin) or sulfonylureas (eg, glyburide) because the actions and side effects of these medicines may be increased.

Medicines that may decrease your bone marrow (eg, cancer chemotherapy ) because the risk of serious side effects, such as low blood platelet levels and low white blood cell counts, may be increased; check with your doctor or pharmacist if you are unsure if any of your medicines may decrease your bone marrow.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Chloramphenicol 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:

Do not exceed the recommended dose or use Chloramphenicol for longer than prescribed without checking with your doctor.

Chloramphenicol is effective only against bacteria. It is not effective for treating viral infections (eg, the common cold).

It is important to use Chloramphenicol for the full course of treatment. Failure to do so may decrease the effectiveness of Chloramphenicol and increase the risk that the bacteria will no longer be sensitive to Chloramphenicol and will not be able to be treated by this or certain other antibiotics in the future.

Long-term or repeated use of Chloramphenicol may cause a second infection. Your doctor may want to change your medicine to treat the second infection. Contact your doctor if signs of a second infection occur.

If symptoms of "gray syndrome" (swelling of the abdomen, pale or blue skin color, vomiting, shock, difficulty breathing, refusal to suck, loose green stools, limp muscles, low temperature) occur in a newborn or infant, contact your doctor. Death may occur within hours of the onset of symptoms. Stopping use of Chloramphenicol when symptoms first appear increases the chance for a complete recovery.

Chloramphenicol may lower your body's ability to fight infection. Prevent infection by avoiding contact with people with colds or other infections. Notify your doctor of any signs of infection, including fever, sore throat, rash, or chills.

Chloramphenicol may reduce the number of clot-forming cells (platelets) in your blood. To prevent bleeding, avoid situations in which bruising or injury may occur. Report any unusual bleeding, bruising, blood in stools, or dark, tarry stools to your doctor.

Diabetes patients - Chloramphenicol may affect your blood sugar. Check blood sugar levels closely and ask your doctor before adjusting the dose of your diabetes medicine.

LAB TESTS, including complete blood cell counts, may be performed to monitor your progress or check for side effects. Be sure to keep all doctor and lab appointments.

Use Chloramphenicol with extreme caution in children younger 1 year. Safety and effectiveness in this age group have not been confirmed.

Use Chloramphenicol with extreme caution in children younger 10 years who have diarrhea or a stomach or bowel infection.

Use Chloramphenicol with extreme caution in premature and full-term infants because they may be more sensitive to the effects of Chloramphenicol, especially the risk of "gray syndrome."

Pregnancy and breast-feeding: If you become pregnant while taking Chloramphenicol, discuss with your doctor the benefits and risks of using Chloramphenicol during pregnancy. Chloramphenicol should be used with extreme caution during full-term pregnancy and labor because the fetus may experience severe side effects. Chloramphenicol is excreted in breast milk. Do not breastfeed while taking Chloramphenicol.

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:

Mild diarrhea, nausea, or vomiting.

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; dark urine; delirium; depression; headache; fever, chills, or sore throat; pain, redness, or swelling at the injection site; symptoms of "gray syndrome" in an infant (swelling of the abdomen, pale or blue skin color, vomiting, shock, difficulty breathing, refusal to suck, loose green stools, limp muscles, low temperature); unusual bleeding or bruising; unusual tiredness; vision changes.

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.

Restwell Mattress, Restwel

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Trusted Mattress Factory

Restwell Mattress Factory in Eden Prairie, MN offers factory made, hand-crafted beds that we sell at a much lower price than other mattress retailers because we make them ourselves. We are a family owned and operated business delivering value for money since 1945. We have been handcrafting high quality mattresses and adjustable beds for more than 70 years. We have a team of friendly, knowledgeable staff members who are committed to help ensure that each customer gets a peaceful night’s sleep. Along with our tremendously skilled staff, we also have a full time service manager to ensure that all requirements of every customer are met and that bed delivery goes smoothly.

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8229 Highway 7 St. Louis Park, MN 55426 Across from Knollwood Mall

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Hours of Operation

Monday to Friday: 10:00 AM – 9:00 PM Saturday: 9:00 AM – 5:00 PM Sunday: 12:00 PM – 5:00 PM

Atenolol (Tenormin) Uses, Dosage, Side Effects, Atenomel

Atenolol

Atenolol (Tenormin) is in a group of drugs called beta-blockers. Beta-blockers affect the heart and circulation (blood flow through arteries and veins).

Atenolol is used to treat angina (chest pain) and hypertension (high blood pressure). It is also used to treat or prevent heart attack.

Atenolol may also be used for purposes other than those listed in this medication guide.

Important information

Do not stop taking atenolol without first talking to your doctor. Stopping suddenly may make your condition worse.

If you need to have any type of surgery, you may need to temporarily stop using atenolol. Be sure the surgeon knows ahead of time that you are using atenolol.

Atenolol can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol, which could increase drowsiness and dizziness while you are taking atenolol.

Atenolol is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

If you are being treated for high blood pressure, keep using this medication even if you feel fine. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

Store atenolol at room temperature away from moisture and heat.

What should I discuss with my healthcare provider before taking atenolol?

You should not use this medication if you are allergic to atenolol, or if you have certain heart conditions such as slow heartbeats, or heart block.

Before taking atenolol, tell your doctor if you have:

asthma, bronchitis, emphysema;

low blood pressure;

a heart problem such as heart block, sick sinus syndrome, slow heart rate, or congestive heart failure;

problems with circulation (such as Raynaud's syndrome).

If you have any of these conditions, you may need a dose adjustment or special tests to safely take this medication.

FDA pregnancy category D. This medication can cause harm to an unborn baby. Do not use atenolol if you are pregnant. Tell your doctor if you become pregnant during treatment. Use an effective form of birth control while you are using this medication. Atenolol can pass into breast milk and may harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

How should I take atenolol?

Take atenolol exactly as it was prescribed for you. Do not take the medication in larger amounts or for longer than recommended by your doctor. Follow the directions on your prescription label.

Take this medication with a full glass of water.

Take atenolol at the same time every day.

Do not skip doses or stop taking atenolol without first talking to your doctor. Stopping suddenly may make your condition worse.

To be sure this medication is helping your condition, your blood pressure will need to be checked on a regular basis. Do not miss any visits to your doctor.

If you need to have any type of surgery, tell the surgeon that you are using atenolol. You may need to briefly stop using atenolol before having surgery.

Atenolol is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

If you are being treated for high blood pressure, keep using atenolol even if you feel fine. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

Store atenolol at room temperature away from moisture and heat.

What happens if I miss a dose?

Take the missed dose as soon as you remember. If your next dose is less than 8 hours away, skip the missed dose and take the medicine at the next regularly scheduled time. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention if you think you have used too much of this medicine.

Overdose symptoms may include uneven heartbeats, shortness of breath, bluish-colored fingernails, dizziness, weakness, fainting, or seizure (convulsions).

What should I avoid?

Atenolol can cause side effects that may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be awake and alert. Avoid drinking alcohol, which could increase drowsiness and dizziness while you are taking atenolol.

Atenolol side effects

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. Call your doctor at once if you have any of these serious side effects:

slow or uneven heartbeats;

feeling light-headed, fainting;

feeling short of breath, even with mild exertion;

swelling of your ankles or feet;

nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

cold feeling in your hands and feet.

Less serious atenolol side effects may include:

decreased sex drive, impotence, or difficulty having an orgasm;

sleep problems (insomnia);

tired feeling; or

Side effects other than those listed here may also occur. Talk to your doctor about any side effect that seems unusual or that is especially bothersome.

What other drugs will affect atenolol?

Before taking atenolol, tell your doctor if you are using:

allergy treatments (or if you are undergoing allergy skin-testing);

amiodarone (Cordarone, Pacerone);

digoxin (digitalis, Lanoxin);

an MAO inhibitor such as isocarboxazid (Marplan), tranylcypromine (Parnate), phenelzine (Nardil), or selegiline (Eldepryl, Emsam);

a diabetes medication such as insulin, glyburide (Diabeta, Micronase, Glynase), glipizide (Glucotrol), chlorpropamide (Diabinese), or metformin (Glucophage);

a heart medication such as nifedipine (Procardia, Adalat), reserpine (Serpasil), verapamil (Calan, Verelan, Isoptin), diltiazem (Cartia, Cardizem);

medicine for asthma or other breathing disorders, such as albuterol (Ventolin, Proventil), bitolterol (Tornalate), metaproterenol (Alupent), pirbuterol (Maxair), terbutaline (Brethaire, Brethine, Bricanyl), and theophylline (Theo-Dur, Theolair); or

cold medicines, stimulant medicines, or diet pills.

If you are using any of these drugs, you may not be able to take atenolol, or you may need dosage adjustments or special tests during treatment.

There may be other drugs not listed that can affect atenolol. 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.

More about atenolol

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about atenolol.

What does my medication look like?

Atenolol is available with a prescription under the brand name Tenormin. Other brand or generic forms may also be available. Ask your pharmacist any questions you have about this medication, especially if it is new to you.

Tenormin 25 mg - round, flat, white, uncoated

Tenormin 50 mg - round, flat, white, uncoated

Tenormin 100 mg - round, flat, white, uncoated

Disclaimer: Every effort has been made to ensure that the information provided is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects.

Copyright 1996-2016 Cerner Multum, Inc. Version: 8.03. Revision Date: 4/12/2009 4:22:13 PM.

Buy Heart Disease - Metoprogamma (Brand Name Toprol Xl) Online - Order Cheap Metoprolol - Purchase H

Toprol XL, a type of medication known as a beta blocker, is used in the treatment of high blood pressure, angina pectoris (chest pain, usually caused by lack of oxygen to the heart due to clogged arteries), and heart attack. When prescribed for high blood pressure, it is effective when used alone or in combination with other high blood pressure medications. Beta blockers decrease the force and rate of heart contractions, thereby reducing the demand for oxygen and lowering blood pressure.

Take Toprol XL exactly as prescribed by your doctor.

Do not take in larger or smaller amounts or for longer than recommended. Follow the directions on your prescription label.

Take Toprol XL at the same time every day.

Toprol XL should be taken with food or just after a meal. A Toprol XL tablet can be divided in half if your doctor has told you to do so. The half tablet should be swallowed whole, without chewing or crushing. Chewing or crushing the pill could cause too much of the drug to be released at one time.

Do not skip doses or stop taking Toprol XL without first talking to your doctor. Stopping suddenly may make your condition worse.

Your blood pressure will need to be checked often. Visit your doctor regularly.

If you need surgery, tell the surgeon ahead of time that you are using Toprol XL.

Toprol XL is only part of a complete program of treatment for hypertension that may also include diet, exercise, and weight control. Follow your diet, medication, and exercise routines very closely if you are being treated for hypertension.

If you are being treated for high blood pressure, keep using this medication even if you feel well. High blood pressure often has no symptoms. You may need to use blood pressure medication for the rest of your life.

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

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

Store Toprol XL at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Toprol XL out of the reach of children and away from pets.

Active Ingredient: Metoprolol succinate.

Do NOT use Toprol XL if:

you are allergic to any ingredient in Toprol XL or to another beta-blocker

you have a very slow heart rate (eg, bradycardia), certain types of irregular heartbeat (eg, atrioventricular [AV] block, sick sinus syndrome), moderate to severe heart failure, very low systolic blood pressure (less than 100 mm Hg), or severe blood circulation problems.

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

Some medical conditions may interact with Toprol XL. 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 an adrenal gland tumor (pheochromocytoma), have an overactive thyroid, or are scheduled to have surgery

if you have low blood pressure or a history of heart attack, slow or irregular heartbeat, heart failure, or other heart problems; chest pain or angina; blood circulation problems; or liver problems

if you have diabetes mellitus, chronic obstructive pulmonary disease (COPD), bronchitis, breathing problems, or a history of asthma.

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

digoxin (digitalis, Lanoxin);

clonidine (Catapres);

ritonavir (Norvir);

terbinafine (Lamisil);

a diuretic (water pill);

cold medicines, stimulant medicines, or diet pills;

anti-malaria medications such as chloroquine (Aralen) or hydroxychloroquine (Plaquenil, Quineprox);

medicine to treat depression or mental illness, such as bupropion (Wellbutrin, Zyban), fluoxetine (Prozac, Sarafem), paroxetine (Paxil), thioridazine (Mellaril), and others;

an MAO inhibitor such as isocarboxazid (Marplan), tranylcypromine (Parnate), phenelzine (Nardil), or selegiline (Eldepryl, Emsam);

a diabetes medication such as insulin, glyburide (Diabeta, Micronase, Glynase), glipizide (Glucotrol), chlorpropamide (Diabinese), or metformin (Glucophage);

a heart medication such as nifedipine (Procardia, Adalat), quinidine (Quinaglute, Quinidex), propafenone (Rythmol), reserpine (Serpasil), verapamil (Calan, Verelan, Isoptin), diltiazem (Cartia, Cardizem); or

medicine for asthma or other breathing disorders, such as albuterol (Ventolin, Proventil), bitolterol (Tornalate), metaproterenol (Alupent), pirbuterol (Maxair), terbutaline (Brethaire, Brethine, Bricanyl), and theophylline (Theo-Dur, Theolair).

This may not be a complete list of all interactions that may occur. Ask your health care provider if Toprol XL 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:

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

Toprol XL may cause dizziness, lightheadedness, or fainting; alcohol, hot weather, exercise, or fever may increase these effects. To prevent them, sit up or stand slowly, especially in the morning. Sit or lie down at the first sign of any of these effects.

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.

Do not suddenly stop using Toprol XL without first talking your doctor. If your doctor decides you should no longer use Toprol XL, you will need to stop Toprol XL gradually according to your doctor's instructions.

If your doctor has instructed you to check your blood pressure and heart rate regularly, be sure to do so.

Do not take any medicines used to treat colds or congestion without first consulting with your doctor or pharmacist.

Diabetes patients - Toprol XL may hide signs of low blood sugar, such as rapid heartbeat. Be sure to watch for other signs or low blood sugar. Low blood sugar may make you anxious, sweaty, weak, dizzy, drowsy, or faint. It may also make your vision change; give you a headache, chills, or tremors; or make you more hungry. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

Tell your doctor or dentist that you take Toprol XL 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 for 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 Toprol XL.

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

Toprol XL should be used with extreme caution 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 Toprol XL while you are pregnant. Toprol XL is found in breast milk. If you are or will be breast-feeding while you use Toprol XL, check with your doctor. Discuss any possible risks to your baby.

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.

Call your doctor at once if you have any of these serious side effects:

chest pain, pounding heartbeats or fluttering in your chest;

feeling light-headed, fainting;

feeling short of breath, even with mild exertion;

swelling of your hands or feet;

nausea, upper stomach pain, itching, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

easy bruising, unusual bleeding (nose, mouth, vagina, or rectum), purple or red pinpoint spots under your skin;

wheezing, trouble breathing;

depression, confusion, memory problems, hallucinations; or

cold feeling in your hands and feet.

Less serious side effects may include:

dry mouth, constipation, heartburn, vomiting, diarrhea;

decreased sex drive, impotence, or difficulty having an orgasm;

headache, drowsiness, tired feeling;

sleep problems (insomnia); or

anxiety, nervousness.

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

Benzoyt, Benzoyt

Benzoyl peroxide has an antibacterial effect. It also has a mild drying effect, which allows excess oils and dirt to be easily washed away from the skin.

Use exactly as directed on the label, or as prescribed by your doctor. Do not use in larger or smaller amounts or for longer than recommended. Wash your hands before and after applying this medication. Shake the lotion well just before each use.

Clean and pat dry the skin to be treated. Apply benzoyl peroxide in a thin layer and rub in gently. Do not cover the treated skin area unless your doctor has told you to.

Benzoyl peroxide topical is usually applied one to three times daily. Follow your doctor's instructions.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

It may take several weeks before your symptoms improve. Keep using the medication as directed and tell your doctor if your symptoms do not improve.

If you miss a dose - use the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not use extra medicine to make up the missed dose.

Store this medicine at room temperature in a tightly-closed container, away from heat and light.

Avoid getting this medication in your mouth or eyes. If it does get into any of these areas, rinse with water. Do not use benzoyl peroxide topical on sunburned, windburned, dry, chapped, irritated, or broken skin. Also avoid using benzoyl peroxide topical on wounds or on areas of eczema. Wait until these conditions have healed before using this medication.

Avoid using skin products that can cause irritation, such as harsh soaps, shampoos, or skin cleansers, hair coloring or permanent chemicals, hair removers or waxes, or skin products with alcohol, spices, astringents, or lime. Do not use other medicated skin products unless your doctor has told you to.

Do not use benzoyl peroxide topical while you are also using tretinoin (Altinac, Avita, Renova, Retin-A, Tretin-X). Using these medications together could cause severe skin irritation. FDA pregnancy category C. It is not known whether benzoyl peroxide topical will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medication. It is not known whether benzoyl peroxide 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.

Benzoyl peroxide may bleach hair or fabrics. Avoid allowing this medication to come into contact with your hair or clothing.

Do NOT use Benzac if you are allergic to any ingredient in Benzac.

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

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. Stop using benzoyl peroxide and call your doctor at once if you have severe stinging or burning of your skin.

Less serious side effects may include:

mild stinging or burning;

itching or tingly feeling;

skin dryness, peeling, or flaking; or

redness or other irritation.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects.

Ceralide-P; Tablet, Arvincare Healthcare(Unikid Healthcare), Ceralide-P

CERALIDE-P - Tablet, Arvincare Healthcare(Unikid Healthcare)

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Talopam, Talopam

Topiramate

Click for further information on drug naming conventions and International Nonproprietary Names .

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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Cefaxine, Cefaxine

Product Description Common use Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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 Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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 Cephalexin is attributed as antibiotic of cephalosporins group which acts against bacteria preventing formation of their cell walls. It is enough resistant to penicillinases of gram positive microorganisms but can be destroyed by beta-lactamases of gram negative ones. It shows broad spectrum activity against gram positive microorganisms such as Staphylococcus, Staphylococcus epidermidis; Streptococcus, Corynebacterium diphtheriae, Clostridium, Actinomyces israelii, Bacillus anthracis, gram negative microorganisms like Escherichia coli, Klebsiella, Proteus mirabilis, Neisseria gonorrhoeae, Neisseria meningitidis, Shigella, Salmonella. Common infections that are treated with Cephalexin include infections of the middle ear, tonsils, throat, larynx (laryngitis), bronchi (bronchitis) and pneumonia as well as in urinary tract, skin, and bones.

Dosage and directions The dose of Cephalexin for adults is 1 to 4 grams in divided doses. The interval between doses may be 6 or 12 hours depending on the infection.

Precautions Before using Cephalexin, tell your doctor if you are allergic to any drugs (especially penicillins), have kidney or liver disease, a stomach or intestinal disorder such as colitis, and diabetes.

Contraindications Hypersensitivity to Cephalexin, cephalosporins (Ceclor, Duricef, Omnicef, Spectracef, Suprax, Cefzil, Fortaz, Ceftin) and beta-lactamase antibiotics. Cautiousness should be exercised in patients with kidney disorder, pseudomembranous colitis, pregnancy, breastfeeding and babies younger than 6 month.

Possible side effect

Most common side effects may include signs of allergy (hives, rash, swelling of face and tongue), seizure, fever, sore throat, and headache with a severe blistering, peeling, and red skin rash, pale or yellowed skin, dark colored urine, fever, hallucinations, confusion or weakness, easy bruising or bleeding, unusual weakness, confusion, agitation, decreased or absent urination. In case of serious and persistent side effects listed above seek immediate medical help.

Drug interaction Inform your doctor about all medications you take and especially about live vaccines, probenecid. Cephalexin may decrease the effectiveness of combination-type contraceptive pills. This medication is able to show false positive results with certain diabetic urine testing products. Cephalexin increases effects of indirect anticoagulants, polphenilbutazone, furocemide. Salicylates and indomethacin slow excretion of cephalolexin by kidneys. Medications decreasing secretion in renal tubules increase concentration of the medication blood serum and slow down its excretion.

Missed dose If you missed a dose take it as soon as you remember. If it is almost time of your next dose just skip it and return to your regular schedule. Never double the dose of this medication.

Overdose In case of serious and persistent symptoms of nausea, vomiting, stomach pain, diarrhea, and blood in your urine consult your doctor about medical attention.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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.

Kelnor Medical Facts From, Kelnor

Kelnor

What is Kelnor (ethinyl estradiol and ethynodiol diacetate)?

Ethinyl estradiol and ethynodiol diacetate is a combination birth control pill that contains female hormones to prevent ovulation (the release of an egg from an ovary). This medication also causes changes in your cervical mucus and uterine lining, making it harder for sperm to reach the uterus and harder for a fertilized egg to attach to the uterus.

Ethinyl estradiol and ethynodiol diacetate is used to prevent pregnancy.

Ethinyl estradiol and ethynodiol diacetate may also be used for purposes not listed in this medication guide.

What is the most important information I should know about birth control pills?

Do not use birth control pills if you are pregnant or if you have recently had a baby.

You should not take birth control pills if you have any of the following conditions: uncontrolled high blood pressure, heart disease, a blood-clotting disorder, circulation problems, diabetic problems with your eyes or kidneys, unusual vaginal bleeding, liver disease or liver cancer, severe migraine headaches, if you smoke and are over 35, or if you have ever had breast or uterine cancer, jaundice caused by birth control pills, a heart attack, a stroke, or a blood clot.

Taking birth control pills can increase your risk of blood clots, stroke, or heart attack, especially if you have certain other conditions, or if you are overweight.

Smoking can greatly increase your risk of blood clots, stroke, or heart attack. You should not take birth control pills if you smoke and are over 35 years old.

What should I discuss with my healthcare provider before taking birth control pills?

Taking birth control pills can increase your risk of blood clots, stroke, or heart attack. You are even more at risk if you have high blood pressure, diabetes, high cholesterol, or if you are overweight. Your risk of stroke or blood clot is highest during your first year of taking birth control pills. Your risk is also high when you restart birth control pills after not taking them for 4 weeks or longer.

Smoking can greatly increase your risk of blood clots, stroke, or heart attack. Your risk increases the older you are and the more you smoke. You should not take combination birth control pills if you smoke and are over 35 years old.

Do not use if you are pregnant. Stop taking this medicine and tell your doctor if you become pregnant, or if you miss two menstrual periods in a row. If you have recently had a baby, wait at least 4 weeks before taking birth control pills.

You should not take birth control pills if you have:

untreated or uncontrolled high blood pressure;

heart disease (coronary artery disease, uncontrolled heart valve disorder, history of heart attack, stroke, or blood clot);

a blood-clotting disorder or circulation problems;

problems with your eyes, kidneys or circulation caused by diabetes;

a history of hormone-related cancer such as breast or uterine cancer;

unusual vaginal bleeding that has not been checked by a doctor;

liver disease or liver cancer;

severe migraine headaches (with aura, numbness, weakness, or vision changes), especially if you are older than 35;

a history of jaundice caused by pregnancy or birth control pills; or

if you smoke and are over 35 years old.

To make sure birth control pills are safe for you, tell your doctor if you have:

high blood pressure, varicose veins;

high cholesterol or triglycerides;

a history of depression;

underactive thyroid, gallbladder disease;

seizures or epilepsy;

a history of irregular menstrual cycles;

a history of fibrocystic breast disease, an abnormal mammogram, or an abnormal pap smear.

The hormones in birth control pills can pass into breast milk and may harm a nursing baby. This medication may also slow breast milk production. Do not use if you are breast-feeding a baby.

How should I take birth control pills?

Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

You will take your first pill on the first day of your period or on the first Sunday after your period begins. You may need to use back-up birth control, such as condoms or a spermicide, when you first start using this medication. Follow your doctor's instructions.

Take one pill every day, no more than 24 hours apart. When the pills run out, start a new pack the following day. You may get pregnant if you do not take one pill daily. Get your prescription refilled before you run out of pills completely.

The 28-day birth control pack contains seven "reminder" pills to keep you on your regular cycle. Your period will usually begin while you are using these reminder pills.

You may have breakthrough bleeding, especially during the first 3 months. Tell your doctor if this bleeding continues or is very heavy.

Use a back-up birth control if you are sick with severe vomiting or diarrhea.

If you need surgery or medical tests or if you will be on bed rest, you may need to stop using this medication for a short time. Any doctor or surgeon who treats you should know that you are using birth control pills.

While taking birth control pills, you will need to visit your doctor regularly.

Store this medication at room temperature away from moisture and heat.

What happens if I miss a dose?

Follow the patient instructions provided with your medicine. Ask your doctor or pharmacist if you do not understand these instructions. Missing a pill increases your risk of becoming pregnant.

If you miss one active pill, take two pills on the day that you remember. Then take one pill per day for the rest of the pack.

If you miss two active pills in a row in Week 1 or 2, take two pills per day for two days in a row. Then take one pill per day for the rest of the pack. Use back-up birth control for at least 7 days following the missed pills.

If you miss two active pills in a row in Week 3, throw out the rest of the pack and start a new pack the same day if you are a Day 1 starter. If you are a Sunday starter, keep taking a pill every day until Sunday. On Sunday, throw out the rest of the pack and start a new pack that day.

If you miss three active pills in a row in Week 1, 2, or 3, throw out the rest of the pack and start a new pack on the same day if you are a Day 1 starter. If you are a Sunday starter, keep taking a pill every day until Sunday. On Sunday, throw out the rest of the pack and start a new pack that day.

If you miss two or more pills, you may not have a period during the month. If you miss a period for two months in a row, call your doctor because you might be pregnant.

If you miss a reminder pill, throw it away and keep taking one reminder pill per day until the pack is empty. You do not need back-up birth control if you miss a reminder pill.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.

What should I avoid while taking birth control pills?

Do not smoke while taking birth control pills, especially if you are older than 35 years of age.

Birth control pills will not protect you from sexually transmitted diseases--including HIV and AIDS. Using a condom is the only way to protect yourself from these diseases.

Birth control pills side effects

Get emergency medical help if you have signs of an allergic reaction . hives; difficult breathing; swelling of your face, lips, tongue, or throat.

Stop using birth control pills and call your doctor at once if you have:

signs of a stroke--sudden numbness or weakness (especially on one side of the body), sudden severe headache, slurred speech, problems with vision or balance;

signs of a blood clot in the lung--chest pain, sudden cough, wheezing, rapid breathing, coughing up blood;

signs of a blood clot in your leg--pain, swelling, warmth, or redness in one or both legs;

heart attack symptoms--chest pain or pressure, pain spreading to your jaw or shoulder, nausea, sweating;

liver problems--severe stomach pain, fever, tired feeling, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes);

a change in the pattern or severity of migraine headaches;

swelling in your hands, ankles, or feet;

a breast lump; or

symptoms of depression--sleep problems, weakness, tired feeling, mood changes.

Common side effects may include:

light vaginal bleeding or spotting;

problems with contact lenses;

nausea, vomiting, bloating;

changes in weight or appetite;

breast tenderness or swelling;

freckles or darkening of facial skin, increased hair growth, loss of scalp hair;

vaginal itching or discharge;

changes in your menstrual periods.

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

What other drugs will affect birth control pills?

Many drugs can interact with birth control pills and make them less effective, which may result in pregnancy. This includes prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

More about Kelnor 1/35 (ethinyl estradiol / ethynodiol)

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about ethinyl estradiol and ethynodiol diacetate.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2012 Cerner Multum, Inc. Version: 9.01. Revision Date: 2016-02-04, 7:16:28 AM.

Fenamin Generic Name Amphetamine Online, Fenamin

Fenamin General Information

Fenamin - Pharmacology:

Fenamins stimulate the release of norepinephrine from central adrenergic receptors. At higher dosages, they cause release of dopamine from the mesocorticolimbic system and the nigrostriatal dopamine systems. Fenamin may also act as a direct agonist on central 5-HT receptors and may inhibit monoamine oxidase (MAO). In the periphery, amphetamines are believed to cause the release of noradrenaline by acting on the adrenergic nerve terminals and alpha - and beta-receptors. Modulation of serotonergic pathways may contribute to the calming affect.

Fenamin for patients

Fenamins may impair the ability of the patient to engage in potentially hazardous activities such as operating machinery or vehicles; the patient should therefore be cautioned accordingly.

This description is suitable for active ingredient Amphetamine

Fenamin Interactions

Acidifying agents - Gastrointestinal acidifying agents (guanethidine, reserpine, glutamic acid HCl, ascorbic acid, fruit juices, etc.) lower absorption of amphetamines. Urinary acidifying agents -(ammonium chloride, sodium acid phosphate, etc.) Increase the concentration of the ionized species of the amphetamine. Primary excretion - Both Groups of agents lower blood levels and efficacy of amphetamines. Adrenergic blockers - Adrenergic blockers are inhibited by amphetamines. Alkalinizing agents - Gastrointestinal alkalinizing agents (sodium bicarbonate, etc.)increase absorption of amphetamines. Urinary alkalinizing agents (acetazolamide, some thiazides) increase the concentration of the non-ionized species of the amphetamine molecule, thereby decreasing urinary excretion. Both groups of agents increase blood levels and therefore potentate the actions of amphetamines. Antidepressants, tricyclic - Fenamins may enhance the activity of tricyclic or sympathomimetic agents; d-amphetamine with desipramine or protriptyline and possibly other tricyclics cause striking and sustained increases in the concentration of d-amphetamine in the brain; cardiovascular effects can be potentiated. MAO inhibitors - MAO antidepressants, as well as a metabolite of furazolidone, slow amphetamine metabolism. This slowing potentiates amphetamines, increasing their effect on the release of norepinephrine and other monoamines from adrenergic nerve endings, this can cause headaches and other signs of hypertensive crisis. A variety of neurological toxic effects and malignant hyperpyrexia can occur, sometimes with fatal results. Antihistamines - Fenamins may counteract the sedative effect of antihistamines. Antihypertensives - Fenamins may antagonize the hypotensive effects of antihypertensives. Chlorpromazine - Chlorpromazine blocks dopamine and norepinephrine receptors, thus inhibiting the central stimulant effects of amphetamines, and can be used to treat amphetamine poisoning. Ethosuximide - Fenamins may delay intestinal absorption of ethosuximide. Haloperidol - Haloperidol blocks dopamine receptors, thus inhibiting the central stimulant effects of amphetamines. Lithium carbonate - The anorectic and stimulatory effects of amphetamines may be inhibited by lithium carbonate. Meperidine - Fenamins pone the analgesic effect of meperidine. Methenamine therapy - Urinary excretion of amphetamines is increased, and efficacy is reduced, by acidifying agents used in methenamine therapy. Norepinephrine - Fenamins enhance the adrenergic effect of norepinephrine. Phenobarbital - Fenamins may delay intestinal absorption of phenobarbital; co-administration of phenobarbital may produce a synergistic anticonvulsant action. Phenytoin - Fenamins may delay intestinal absorption of phenytoin; co-administration of phenytoin may produce a synergistic anticonvulsant action. Propoxyphene - In cases of propoxyphene overdose, amphetamine CNS stimulation is potentiated and fatal convulsions can occur. Veratrum alkaloids - Fenamins inhibit the hypotensive effect of veratrum alkaloids. Drug/Laboratory Test Interactions Fenamins can cause a significant elevation in plasma corticosteroid levels. This increase is greatest in the evening. Fenamins may interfere with urinary steroid determinations.

Fenamin Contraindications

Advanced arteriosclerosis, symptomatic cardiovascular disease, moderate to severe hypertension, hyperthyroidism, known hypersensitivity or idiosyncrasy to the sympathomimetic amines, glaucoma. Agitated states. Patients with a history of drug abuse. During or within 14 days following the administration of monoamine oxidase inhibitors (hypertensive crises may result).

This description is suitable for active ingredient Amphetamine

Generic name, Overdose, Half Life Fenamin, Food Interactions, Chemical, etc..

Tricomin Solution Follicle Therapy Spray Discount Price Secure Order, Tricofin

" width="10" height="7"> Tricomin Solution Follicle Spray 6 oz 178ml US$68; 3 x 178ml US$204, 6 x 237ml US$408, 12 x 237ml US$816

" width="10" height="7"> Tricomin Restructuring Conditioner 237ml US$29; 3 x 237ml US$87, 6 x 237ml US$174, 12 x 237ml US$348

" width="10" height="7"> Tricomin Revitalizing Shampoo 237ml US$25; 2 x 237ml US$50, 3 x 237ml US$75, 6 x 237ml US$150, 12 x 237ml US$300

" width="10" height="7"> Tricomin Conditioning Shampoo 237ml US$31; 3 x 237ml US$91. 6 x 237ml US$179, 12 x 237ml US$355

" width="10" height="7"> Tricopack Value Pack 1 (shampoo, conditioner, follicle spray) US$122

" width="10" height="7"> Tricopack Value Pack 2 (shampoo, follicle spray) US$96

It is a ProCyte SOD product and it has its bases in the Iamin discovery by Dr. Loren Pickart.

It is a spray liquid bottle 180 ml (6 fl. oz).

It is also used 1 ml / day (6 months of provisioning).

Here are some components:

deionezed water, SD alcol 40B, amodimetlcotone, nonoxynol-10, pantenolo, poliquaternium-11, polisorbato 60, tallowtrimonium chloride, acido citrico, dimetil laurimine isosterate, linoleaminodopropyl etil dimonium etosolfato, triamino copper nutritional complex (alanina/istidina/lisina rame polipeptide HCL), metilparaben, benzetonium chloride, mentolo.

This product is the result of scientific searches on the copper and on the relations with the skin health.

A meaningful increase of hair in anagen phase has been measured in a 6 month-old clinical study using a copper peptide topical solution.

The preliminary studies have shown that:

(NON VELLUS HAIR COUNT) AT 4 MONTHS

It stimulates the fibroplastis, the collagen synthesis and the enzymatic system which are important for the skin and hair health.

Other characteristic would be to repair the skin around the follicle and to improve therefore the function of the follicle.

When properly formulated with specific aminoacidis, the copper can have brought directly to the follicles.

The SOD in tricomin solution is a "Blue copper peptide".

Tricomin solution can be used with effectiveness as supplement to other treatments as Rogaine and Propecia.

Have other source from SOD together with Dr. Proctor products and to the Folligen!

Is Copper Better Than Propecia? for Blocking DHT Production?

Copper ion is more effective in inhibiting the type 1 form which primarily produce the DHT that damages follicles and can be administered locally to the skin. Sugimoto et al (Sugimito 1995) found that copper ion is a potent inhibitor of 5-alpha reductase. inhibiting both types of 5-alpha reductase (both type 1 and type 2) that produce DHT and is the only metal to do so. Copper ion inhibits (50% reduction in activity) type 1 alpha reductase at 1.9 micromolar (0.12 micrograms copper ion per milliliter) and type 2 alpha reductase at 19.2 microM (1.2 micrograms copper ion per milliliter). No other metal has these effects.

The application of copper-peptides may provide sufficient copper ion into the hair follicle area to block DHT production in the scalp. Metabolically active copper ion (that is, copper ion free to block 5-alpha reductase) in the human body exists at about 1 microgram per milliliter in the blood and less in the skin. While the uptake of ionic copper from copper-peptides applied to the scalp is very low, human experiments by Prof. John Sorenson (University of Arkansas) have found that they can raise copper ion levels in the skin to the effective level of 1 microgram per millimiter.

Effects on baldness

Q: Did you know that your body and your hair require copper to be at their best? A: It?s true ? and scientifically proven. Tricomin line involved copper and amino acids. Copper is linked to these important biological processes critical to the health of your skin and hair:

? Melanin production (pigmentation)

? Scavenging of damaging free radicals

? Crosslinking of collagen and elastin

? Inhibition of 5-alpha reductase (the enzyme that reduces testosterone to DHT ? its active metabolite reponsible for androgenetic alopecia)

Q: Did you know that your hair is relatively rich in copper? A: Also true. Compared to most other parts of your body, your hair has a natural affinity to copper. It is also interesting to know that copper levels in the body tend to decrease as you get older, just when you may need it more!

Q: Did you realize that your hair follicles cycle between growth periods and resting periods? A: True again! In fact, hair thinning and loss can result from changes in the hair cycle resulting in a process known as miniaturization.

Tricomin story is Growing!! Studies have demonstrated the positive effects of Triamino Copper Nutritional Complex? on hair follicles! During the growth phase, the base of the follicle (dermal papilla) is richly endowed with substances such as collagen and various proteins. These substances are virtually absent during the resting phase. Copper has been shown to stimulate the cells responsible of production of these substances! As shown, Tricomin products target delivery of copper to the base of the follicle.

The Tricomin Advantage

In addition to copper, other components of the Tricomin products (such as panthenol) add desirable structural qualities to the hair, building its body and adding it shine. While Tricomin?s cosmetic benefits will be realized in a short-term, the added benefits of the Triamino Copper Nutritional Complex? may require a longer using period.

As the centerpiece of the product line, Tricomin Solution ? Follicle Therapy Spray combines the highest concentration of copper peptide with an excellent leave-in conditioner framework. Tricomin products can be used effectively with other hair treatments including Rogaine? and Propecia?, providing additional benefit to the hair follicle and surrounding environment.

Rosuvastatin Medlineplus Drug Information, Dosavastatin

Rosuvastatin

Why is this medication prescribed?

Rosuvastatin is used together with diet, weight-loss, and exercise to reduce the risk of heart attack and stroke and to decrease the chance that heart surgery will be needed in people who have heart disease or who are at risk of developing heart disease. Rosuvastatin is also used to decrease the amount of cholesterol such as low-density lipoprotein (LDL) cholesterol ('bad cholesterol') and triglycerides in the blood and to increase the amount of high-density lipoprotein (HDL) cholesterol ('good cholesterol') in the blood. Rosuvastatin may also be used to decrease the amount of cholesterol and other fatty substances in the blood in children and teenagers 10 to 17 years of age who have familial heterozygous hypercholesterolemia (an inherited condition in which cholesterol cannot be removed from the body normally). Rosuvastatin is in a class of medications called HMG-CoA reductase inhibitors (statins). It works by slowing the production of cholesterol in the body to decrease the amount of cholesterol that may build up on the walls of the arteries and block blood flow to the heart, brain, and other parts of the body.

Accumulation of cholesterol and fats along the walls of your arteries (a process known as atherosclerosis) decreases blood flow and, therefore, the oxygen supply to your heart, brain, and other parts of your body. Lowering your blood level of cholesterol and fats with rosuvastatin has been shown to prevent heart disease, angina (chest pain), strokes, and heart attacks.

How should this medicine be used?

Rosuvastatin comes as a tablet to take by mouth. It is usually taken once a day with or without food. Take rosuvastatin at around the same time every day. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Take rosuvastatin exactly as directed. Do not take more or less of it or take it more often than prescribed by your doctor.

Your doctor will probably start you on a low dose of rosuvastatin and gradually increase your dose, not more than once every 2 to 4 weeks.

Continue to take rosuvastatin even if you feel well. Do not stop taking rosuvastatin without talking to your doctor.

Other uses for this medicine

1, 1-Dimethylbiguanide Hydrochloride - 97%, Dimethylbiguanid

1,1- Dimethylbiguanide hydrochloride

Description

Biochem/physiol Actions

Metformin is an antidiabetic agent that reduces blood glucose levels and improves insulin sensitivity. Its metabolic effects, including the inhibition of hepatic gluconeogenesis, are mediated at least in part by activation of the LKB1-AMPK (AMP-activated protein kinase) pathway. Activation of this pathway also appears to be involved in the antiproliferative and proapoptotic actions of metformin in cancer cell lines.

Price and Availability

Buy Bitensil - Bitensil Without A Prescription Drug At, Bitensil

How to buy Bitensil online? FAQ. 1. Q. How I can pay Bitensil? A. Now we accept payment for Bitensil credit card Visa only. We do not use checks and other methods of payment.

2. Q. Through what time I shall receive the Bitensil order? A. Each Bitensil order sends us within current or next day avia-mail. Standard delivery by avia-mail makes 9-27 days from the date of departure.

3. Q. Why sometimes name Bitensil happens in brackets? A. We are outside of the United States, and Bitensil can be issued under other name. Actually is too the medicine made by the same company under other name or a generic drug, made by other pharmaceutical company.

4. Q. Can I trace my Bitensil order? A. After sending the Bitensil order, you receive the letter confirming shipment. Delivery Bitensil by avia-mail does not provide dialogue procaking from our party.

5. Q. Whether the Bitensil prescription is necessary for me? A. No, you do not need the Bitensil prescription. We work under laws of the country from which we send the order.

6. Q. You give full medical consultation on the Bitensil drug? A. To each our client before use Bitensil we recommend to consult at the doctor. We do not do consultations in any form.

7. Q. Do you guarantee Bitensil delivery? A. Yes - we guarantee it. If Bitensil to you it will not be delivered within 27 days, we shall repeat sending or we shall return to you your money. It is our rule.

8. Q. In what countries you can sell Bitensil? A. We sell Bitensil almost in all the countries of the world (the USA, England, France, Spain, Italy and others). To a regret, we do not sell to Germany and Canada.

9. Q. How many there is delivery Bitensil? A. Delivery Bitensil is free-of-charge. All charges on transfer is paid by us.

10. A. Bitensil Order arrive in discrete unmarked parcels.

Lipofib 160 Mg, Lipofib

Medicament cu pret maximal stabilit de Ministerul Sanatatii

Denumirea comerciala: LIPOFIB 160 mg Denumirea comuna internationala: FENOFIBRATUM Forma farmaceutica: capsule Bucati: 30 capsule Doza (concentratia): 160mg Forma de prezentare: cutie x 3 blist. al/pvc x 10 capsule Firma: TERAPIA SA Tara: Romania

Cod ATC: C10AB05 C – sistem cardiovascular C10 – hipolipemiante C10AB – fibrati

Acest pret este PRET mediu de RAFT al medicamentului LIPOFIB 160 mg capsule (pret necompensat)

PRET LIPOFIB 160 mg capsule: VEZI PRET

VEZI AICI pretul medicamentului si al inlocuitorilor

Vezi pret medicamente care contin aceeasi substanta activa:

Atentie! Informatiile privind medicamantul LIPOFIB 160 mg capsule au caracter informativ. Nu folositi informatiile prezentate in scopul diagnosticarii sau tratarii unei probleme de sanatate.

Lipomed Ag, Santuril

Santuril®

(500 mg probenecid containing tablets)

Probenecid, (4-(dipropylsulfamoyl) benzoic acid inhibits the organic anion-transport across cell membranes by binding to to the relevant membrane transporter polypeptides thereby increasing urinary uric acid excretion while decreasing renal excretion and increasing plasma levels of drugs (ATC-Code: M04AB01).

Santuril ® (500 mg Probenecid containing tablets) is an uricosuric agent.

Santuril ® (500 mg Probenecid containing Tablets) is registered and available in packs of 30 and 100 tablets each in the following countries:

Product Information

For further information, please contact LIPOMED .

Ordering Information

Comprar Barato Online Molargesico, Molargesico

Comprar Molargesico

Das weibliche Becken unterscheidet sich genetisch vom mannlichen Becken. Durch den Einfluss der weiblichen Sexualhormone werden die Unterschiede in der Pubertat verstarkt.

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Bruxzir Solid Zirconia - Crowns - Bridges - Dental Zirconia, Brux

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An Authorized BruxZir Laboratory is a dental laboratory that uses authentic BruxZir Solid Zirconia for the fabrication of solid zirconia dental restorations. BruxZir Solid Zirconia is one of the most prescribed brands of full-contour zirconia restorations, a status owed to the countless dental and laboratory professionals who have adopted the material into their workplaces. The tremendous effort put forth by the continually growing list of authorized laboratories ensures that dentists have access to authentic BruxZir Solid Zirconia globally. Find a BruxZir Authorized Lab

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What Is Ashwagandha, Ashvagandha

What Is Ashwagandha?

Ashwagandha, one of the most powerful herbs in Ayurvedic healing, has been used since ancient times for a wide variety of conditions, and is most well-known for its restorative benefits. In Sanskrit Ashwagandha means “the smell of a horse,” indicating that the herb imparts the vigor and strength of a stallion, and has traditionally been prescribed to help people strengthen their immune system after an illness.

Ashwagandha is frequently referred to as “Indian ginseng” because of its rejuvenating properties, even though botanically, ginseng and Ashwagandha are unrelated.

Belonging to the same family as the tomato, Ashwagandha is a plump shrub with oval leaves and yellow flowers. It bears red fruit about the size of a raisin. The herb is native to the dry regions of India, northern Africa, and the Middle East, and today is also grown in more mild climates, including the United States.

Why Use Ashwagandha?

Do any of these common symptoms sound familiar?

Stress

Fatigue

Lack of energy

Difficulty concentrating

The use of the Ayurvedic herb, Ashwagandha can help alleviate these symptoms and support an energetic and rejuvenating sense of wellbeing.

Benefits and Healing Effects

Ashwagandha contains many useful medicinal chemicals, including withanolides (steroidal lactones), alkaloids, choline, fatty acids, amino acids, and a variety of sugars. While the leaves and fruit have valuable therapeutic properties, the root of the Ashwagandha plant is the part most commonly used in Western herbal remedies.

Medical researchers have been studying Ashwagandha for years with great interest and have completed more than 200 studies on the healing benefits of this botanical. Some key examples of the healing effects of Ashwagandha are:

Protects the immune system

Helps combat the effects of stress

Improves learning, memory, and reaction time

Reduces anxiety and depression without causing drowsiness

Helps reduce brain-cell degeneration

Stabilizes blood sugar

Helps lower cholesterol

Offers anti-inflammatory benefits

Contains anti-malarial properties

Enhances sexual potency for both men and women

Ashwagandha as an Adaptogenic Herb

In Ayurveda, there are specific herbs with adaptogenic benefits, Ashwagandha is one of them. Adaptogens are substances (a combination of amino acids, vitamins, and herbs) that modulate your response to stress or a changing environment. Adaptogens help the body cope with external stresses such as toxins in the environment and internal stresses such as anxiety and insomnia.

How to Add Ashwagandha to Your Daily Diet

According to Ayurveda, our bodies are woven from food. The nutrients we ingest are metabolized into the energy and information that form our cells, tissues, and organs. Every day our bodies need essential vitamins, minerals, and other nutrients to maintain our body’s delicate balance. Taking an Ashwagandha supplement is a highly effective way to create that balance.

Ashwagandha is typically ingested in capsule form. Ashwagandha is included in the single Ayurvedic herb collection of at the Chopra Center Marketplace. The typical recommended dose is 600 to 1,000 mg. twice daily. For people who suffer from insomnia and anxiety, having a cup of hot milk that contains a teaspoon of powdered Ashwagandha before bedtime is beneficial.

Medical Caution: Always consult with your healthcare practitioner before using Chopra Center signature supplements if you have any health conditions. Ashwagandha is not recommended for women who are pregnant.

Certified Instructor: Yoga; Meditation

Jenna found yoga as a student at Virginia Tech where she attended yoga classes at the on-campus gym. She moved to San Diego from the east coast after her graduation in 2008 and has grown to love the practice of yoga. Through her practice she discovered the healing benefits of yoga both on and off of the mat and hopes to help students learn about yoga beyond the physical asana practice. She completed a 200 hour teacher training with YogaWorks in April 2012 and the Seven Spiritual Laws of Yoga 200 hour teacher training with The Chopra Center in November 2014. Jenna is passionate about living a healthy. Read more

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Acromon, Acromon

acromion

Etymology: Gk, akron + omos, shoulder

the lateral extension of the spine of the scapula, forming the highest point of the shoulder and connecting with the clavicle at a small oval surface in the middle of the spine. It gives attachment to the deltoid and trapezius muscles. Also called acromion process. Compare coracoid process. acromial, adj.

Acromion

The flattened lateral, vaguely triangular projection of the spine of the scapula that forms the highest point of the shoulder and articulates with the clavicle. The acromion forms the point of attachment for the trapezius and deltoid muscles; medially, the acromion articulates with the lateral end of the clavicle, immediately behind the attachment of the coracoacromial ligament, the latter of which, in conjunction with the acromion and the coracoid process, forms an arch over the glenohumeral joint, preventing its upward dislocation and limiting the upward rotation of the humerus. The acromion is recognised by its thickened lateral border, which is a palpable subcutaneous mass.

ac·ro·mi·on

The lateral end of the spine of the scapula, which projects as a broad flattened process overhanging the glenoid fossa; it articulates with the clavicle and gives attachment to parts of the deltoid and trapezius muscles. Synonym(s): acromial process.

[G. akrōmion, fr. akron, tip, + ōmos, shoulder]

acromion

The outermost extremity of the spine of the shoulder-blade. The acromion is joined to the outer tip of the collar bone (clavicle) in the acromioclavicular joint.

acromion

the ventral prolongation of the spine of the shoulder blade or SCAPULA.

acromion

the prominence at the distal end of the spine of the scapula.

acromion

Etymology: Gk, akron + omos, shoulder

the lateral extension of the spine of the scapula, forming the highest point of the shoulder and connecting with the clavicle at a small oval surface in the middle of the spine. It gives attachment to the deltoid and trapezius muscles. Also called acromion process. Compare coracoid process. acromial, adj.

Acromion

The flattened lateral, vaguely triangular projection of the spine of the scapula that forms the highest point of the shoulder and articulates with the clavicle. The acromion forms the point of attachment for the trapezius and deltoid muscles; medially, the acromion articulates with the lateral end of the clavicle, immediately behind the attachment of the coracoacromial ligament, the latter of which, in conjunction with the acromion and the coracoid process, forms an arch over the glenohumeral joint, preventing its upward dislocation and limiting the upward rotation of the humerus. The acromion is recognised by its thickened lateral border, which is a palpable subcutaneous mass.

ac·ro·mi·on

The lateral end of the spine of the scapula, which projects as a broad flattened process overhanging the glenoid fossa; it articulates with the clavicle and gives attachment to parts of the deltoid and trapezius muscles. Synonym(s): acromial process.

[G. akrōmion, fr. akron, tip, + ōmos, shoulder]

acromion

The outermost extremity of the spine of the shoulder-blade. The acromion is joined to the outer tip of the collar bone (clavicle) in the acromioclavicular joint.

acromion

the ventral prolongation of the spine of the shoulder blade or SCAPULA.

acromion

the prominence at the distal end of the spine of the scapula.

Lengout (As), Lengout

Search CMI

What is in this leaflet

This leaflet answers some common questions about Lengout. 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 Lengout 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 need to read it again.

What Lengout is used for

Lengout contains colchicine as the active ingredient. Lengout is used for the relief of pain in acute attacks of gout. It is not an analgesic and does not provide relief from other types of pain.

Lengout has a preventative effect that helps to reduce the incidence of acute attacks. It will not reduce the amount of uric acid in the body.

Lengout belongs to a group of medicines called antigout drugs.

Ask your doctor if you have any questions about why Lengout has been prescribed for you.

Your doctor may have prescribed it for another reason.

This medicine is only available with a doctor's prescription.

There is no evidence that it is addictive.

Before you take it

When you must not take it

Do not take Lengout if you have an allergy to:

any medicine containing colchicine

any of the ingredients listed at the end of this leaflet.

Some of the symptoms of an allergic reaction may include shortness of breath, wheezing or difficulty breathing; swelling of the face, lips or tongue; skin rash, itching or hives.

Do not give this medicine to children.

This medication may be dangerous to children. It is important that it is kept out of reach of children at all times.

Do not take Lengout if you have:

combined kidney and liver disease

serious kidney or liver disease

serious heart disease

severe stomach disorder

a blood disorder.

Do not take this medicine after the expiry date (EXP) printed on the pack.

If you take this medicine after the expiry date has passed, it may not work as well.

Do not take this medicine if the bottle shows signs of having been tampered with.

If you are not sure whether you should start taking this medicine, talk to your doctor.

Before you start to take it

Tell your doctor if you are allergic to any other medicines or any foods, preservatives or dyes.

Tell your doctor if you have or have had any of the following medical conditions:

kidney or liver disease

Tell your doctor if you are pregnant or plan to become pregnant.

Lengout may affect your developing baby if you take it during pregnancy.

Tell your doctor if you are breast-feeding or plan to breastfeed.

Your doctor will discuss the risks and benefits of you taking Lengout when breast-feeding.

If you have not told your doctor about any of the above, tell them before you start taking Lengout.

Taking other medicines

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

Some medicines may interfere with Lengout. These include:

cyclosporin - a medicine used to suppress the immune system

erythromycin, clarithromycin and telithromycin - antibiotics used to treat bacterial infection

protease inhibitors, including atazanavir, indinavir, nelfinavir, ritonavir and saquinavir, used to treat HIV and other viral infections

ketoconazole and itraconazole, used to treat certain fungal infections

nefazodone, used to treat depression

acidifying and alkalinising agents, such as ammonium chloride, ascorbic acid (vitamin C), sodium bicarbonate

medicines to help you sleep

NSAIDs or aspirin - anti-inflammatory drugs used to treat pain

medicines used to treat cancer including radiation therapy

anticoagulants such as coumarin, heparin

These medicines may be affected by Lengout or may affect how well it works. You may need to take different amounts of your medicines or you may need to take different medicines. Your doctor or pharmacist has a more complete list of medicines to be careful with or avoid while taking Lengout.

Use in elderly or debilitated patients

Elderly or debilitated patients may be more sensitive to the effects or side effects of this medicine.

How to take it

Follow all directions given to you by your doctor carefully.

They may differ from the information contained in this leaflet.

If you do not understand the instructions on the bottle, ask your doctor or pharmacist for help.

How much to take

Your doctor will tell you how much Lengout to take.

Do not take more than your doctor tells you to.

Do not take more than 12 tablets in total over 4 days.

How to take it

Swallow the tablet whole with a full glass of water.

When to take it

Lengout may be taken before or after food.

How long to take it

Continue taking your medicine for as long as your doctor tells you.

This will depend on your condition and your response to the treatment.

Lengout helps to control your condition but does not cure it.

Immediately stop taking Lengout at the first sign of stomach pain, nausea, vomiting or diarrhoea. Do this even if your symptoms have not been relieved.

If you forget to take it

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 that you missed.

This may increase the chance of you getting an unwanted side effect.

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

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

If you take too much (overdose)

Immediately telephone your doctor or the Poisons Information Centre (telephone 13 11 26) for advice, or go to Accident and Emergency at the nearest hospital if you think that you or anyone else may have taken too much Lengout. Do this even if there are no signs of discomfort or poisoning.

You may need urgent medical attention.

Symptoms of an overdose may include:

severe nausea, vomiting, stomach pain and diarrhoea

burning feeling or rawness in the mouth and throat

difficulty in breathing or swallowing

mental confusion, delirium, convulsions.

While you are taking it

Things you must do

Immediately stop taking Lengout at the first sign of stomach pain, nausea, vomiting or diarrhoea. Do this even if your symptoms have not been relieved.

Remember to take note of the number of tablets you took before the onset of these symptoms so that you can take fewer tablets during subsequent attacks.

Tell any other doctors, dentists, and pharmacists who are treating you that you are taking this medicine, especially if you are being started on any new medicines.

Tell your doctor, surgeon or anaesthetist that you are taking Lengout if you are about to undergo surgery or an operation.

Tell your doctor immediately if you become pregnant while taking Lengout.

If you are about to have any blood tests, remind your doctor that you are taking Lengout.

It may interfere with the results of some tests.

Keep all of your doctor's appointments so that your progress can be checked.

Your doctor may do some tests from time to time to make sure the medicine is working and to prevent unwanted side effects.

Things you must not do

Do not take Lengout to treat any other complaints unless your doctor tells you to.

Do not give your medicine to anyone else, even if they have the same condition as you.

Things to be careful of

Be careful driving or operating machinery until you know how Lengout affects you.

Check with your doctor or pharmacist before drinking alcohol while you are taking Lengout.

If you drink alcohol while taking this medicine, you may develop stomach problems.

This medication may be dangerous to children. It is important that it is kept out of reach of children at all times.

Side effects

Tell your doctor or pharmacist as soon as possible if you do not feel well while you are taking Lengout.

This medicine helps most people with gout, but it may have unwanted side effects in a few people. All medicines can have side effects. Sometimes they are serious, most of the time they are not. You may need medical treatment if you get some of the side effects.

If you are elderly you may have an increased chance of getting side effects.

Ask your doctor or pharmacist to answer any questions you may have.

Immediately stop taking Lengout at the first sign of stomach pain, nausea, vomiting or diarrhoea. Do this even if your symptoms have not been relieved.

The above list includes the more common side effects of your medicine.

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

loss of appetite

The above list includes more serious side effects which may require medical attention.

Tell your doctor immediately, or go to Accident and Emergency at your nearest hospital if you notice any of the following symptoms:

burning feeling in the stomach or throat

severe stomach pain, nausea, vomiting

severe diarrhoea with bloody or black tarry stools

itchy skin, skin rash, hives, unusual bleeding or bruising under the skin

difficulty in passing urine or blood in urine

numbness or weakness in the fingers and toes.

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

Tell your doctor or pharmacist if you notice anything else that is making you feel unwell.

Some people may get other side effects while taking Lengout.

Some of these side effects (e. g. changes in thyroid function or in the blood) can only be found when your doctor does tests from time to time to check your progress.

Do not be alarmed by this list of possible side effects.

You may not experience any of them.

After taking it

Storage

Keep your tablets in the bottle until it is time to take them.

If you take the tablets out of the bottle they may not keep well.

Keep your tablets in a cool dry place where the temperature stays below 30°C.

Do not store Lengout or any other medicine in the bathroom or near a sink. Do not leave it on a window sill or in the car.

Heat and dampness can destroy some medicines.

Keep it where children cannot reach it.

A locked cupboard at least one-and-a-half metres above the ground is a good place to store medicines.

Disposal

If your doctor tells you to stop taking Lengout or the expiry date has passed, ask your pharmacist what to do with any medicine that is left over.

Product description

What it looks like

Lengout tablets are round, white tablets and are available in bottles of 30.

Ingredients

Bumex - Fda Prescribing Information, Side Effects And Uses, Bomox

Bumex

Bumex ® brand of bumetanide TABLETS

Bumex (bumetanide) is a potent diuretic which, if given in excessive amounts, can lead to a profound diuresis with water and electrolyte depletion. Therefore, careful medical supervision is required, and dose and dosage schedule have to be adjusted to the individual patient's needs (see DOSAGE AND ADMINISTRATION ).

Bumex Description

Bumex ® (bumetanide) is a loop diuretic, available as scored tablets, 0.5 mg (light green), 1 mg (yellow) and 2 mg (peach) for oral administration; each tablet also contains lactose, magnesium stearate, microcrystalline cellulose, cornstarch and talc, with the following dye systems: 0.5 mg—D&C Yellow No. 10 and FD&C Blue No. 1; 1 mg—D&C Yellow No. 10; 2 mg—red iron oxide.

Chemically, bumetanide is 3-(butylamino)-4-phenoxy-5-sulfamoylbenzoic acid. It is a practically white powder having a calculated molecular weight of 364.41, and the following structural formula:

Bumex - Clinical Pharmacology

Bumex is a loop diuretic with a rapid onset and short duration of action. Pharmacological and clinical studies have shown that 1 mg Bumex has a diuretic potency equivalent to approximately 40 mg furosemide. The major site of Bumex action is the ascending limb of the loop of Henle.

The mode of action has been determined through various clearance studies in both humans and experimental animals. Bumex inhibits sodium reabsorption in the ascending limb of the loop of Henle, as shown by marked reduction of free-water clearance (CH 2 O) during hydration and tubular free-water reabsorption (T C H 2 O) during hydropenia. Reabsorption of chloride in the ascending limb is also blocked by Bumex, and Bumex is somewhat more chloruretic than natriuretic.

Potassium excretion is also increased by Bumex, in a dose-related fashion.

Bumex may have an additional action in the proximal tubule. Since phosphate reabsorption takes place largely in the proximal tubule, phosphaturia during Bumex induced diuresis is indicative of this additional action. This is further supported by the reduction in the renal clearance of Bumex by probenecid, associated with diminution in the natriuretic response. This proximal tubular activity does not seem to be related to an inhibition of carbonic anhydrase. Bumex does not appear to have a noticeable action on the distal tubule.

Bumex decreases uric acid excretion and increases serum uric acid. Following oral administration of Bumex the onset of diuresis occurs in 30 to 60 minutes. Peak activity is reached between 1 and 2 hours. At usual doses (1 mg to 2 mg) diuresis is largely complete within 4 hours; with higher doses, the diuretic action lasts for 4 to 6 hours. Diuresis starts within minutes following an intravenous injection and reaches maximum levels within 15 to 30 minutes.

Several pharmacokinetic studies have shown that bumetanide, administered orally or parenterally, is eliminated rapidly in humans, with a half-life of between 1 and 1½ hours. Plasma protein-binding is in the range of 94% to 96%.

Oral administration of carbon-14 labeled Bumex to human volunteers revealed that 81% of the administered radioactivity was excreted in the urine, 45% of it as unchanged drug. Urinary and biliary metabolites identified in this study were formed by oxidation of the N-butyl side chain. Biliary excretion of Bumex amounted to only 2% of the administered dose.

Pediatric Pharmacology

Elimination of bumetanide appears to be considerably slower in neonatal patients compared with adults, possibly because of immature renal and hepatobiliary function in this population. Small pharmacokinetic studies of intravenous bumetanide in preterm and full-term neonates with respiratory disorders have reported an apparent half-life of approximately 6 hours, with a range up to 15 hours and a serum clearance ranging from 0.2 to 1.1 mL/min/kg. In a population of neonates receiving bumetanide for volume overload, mean serum clearance rates were 2.17 mL/min/kg in patients less than 2 months of age and 3.8 mL/min/kg in patients aged 2 to 6 months. Mean serum half-life of bumetanide was 2.5 hours and 1.5 hours in patients aged less than 2 months and those aged 2 to 6 months, respectively. Elimination half-life decreased considerably during the first month of life, from a mean of approximately 6 hours at birth to approximately 2.4 hours at 1 month of age.

In preterm neonates, mean serum concentrations following a single 0.05 mg/kg dose ranged from 126 mcg/L at 1 hour to 57 mcg/L at 8 hours. In another study, mean serum concentrations following a single 0.05 mg/kg dose were 338 ng/mL at 30 minutes and 176 ng/mL after 4 hours. A single dose of 0.1 mg/kg produced mean serum levels of 314 ng/mL at 1 hour, and 195 ng/mL at 6 hours. Mean volume of distribution in neonates and infants has been reported to range from 0.26 L/kg to 0.39 L/kg.

The degree of protein binding of bumetanide in cord sera from healthy neonates was approximately 97%, suggesting the potential for bilirubin displacement. A study using pooled sera from critically ill neonates found that bumetanide at concentrations of 0.5 to 50 mcg/mL, but not 0.25 mcg/mL, caused a linear increase in unbound bilirubin concentrations.

In 56 infants aged 4 days to 6 months, bumetanide doses ranging from 0.005 mg/kg to 0.1 mg/kg were studied for pharmacodynamic effect. Peak bumetanide excretion rates increased linearly with increasing doses of drug. Maximal diuretic effect was observed at a bumetanide excretion rate of about 7 mcg/kg/hr, corresponding to doses of 0.035 to 0.040 mg/kg. Higher doses produced a higher bumetanide excretion rate but no increase in diuretic effect. Urine flow rate peaked during the first hour after drug administration in 80% of patients and by 3 hours in all patients.

Geriatric Pharmacology

In a group of ten geriatric subjects between the ages of 65 and 73 years, total bumetanide clearance was significantly lower (1.8 ± 0.3 mL/min·kg) compared with younger subjects (2.9 ± 0.2 mL/min·kg) after a single oral bumetanide 0.5 mg dose. Maximum plasma concentrations were higher in geriatric subjects (16.9 ± 1.8 ng/mL) compared with younger subjects (10.3 ± 1.5 ng/mL). Urine flow rate and total excretion of sodium and potassium were increased less in the geriatric subjects compared with younger subjects, although potassium excretion and fractional sodium excretion were similar between the two age groups. Nonrenal clearance, bioavailability, and volume of distribution were not significantly different between the two groups.

Indications and Usage for Bumex

Bumex is indicated for the treatment of edema associated with congestive heart failure, hepatic and renal disease, including the nephrotic syndrome.

Almost equal diuretic response occurs after oral and parenteral administration of bumetanide. Therefore, if impaired gastrointestinal absorption is suspected or oral administration is not practical, bumetanide should be given by the intramuscular or intravenous route.

Successful treatment with Bumex following instances of allergic reactions to furosemide suggests a lack of cross-sensitivity.

Contraindications

Bumex is contraindicated in anuria. Although Bumex can be used to induce diuresis in renal insufficiency, any marked increase in blood urea nitrogen or creatinine, or the development of oliguria during therapy of patients with progressive renal disease, is an indication for discontinuation of treatment with Bumex. Bumex is also contraindicated in patients in hepatic coma or in states of severe electrolyte depletion until the condition is improved or corrected. Bumex is contraindicated in patients hypersensitive to this drug.

Warnings

Volume and Electrolyte Depletion

The dose of Bumex should be adjusted to the patient's need. Excessive doses or too frequent administration can lead to profound water loss, electrolyte depletion, dehydration, reduction in blood volume and circulatory collapse with the possibility of vascular thrombosis and embolism, particularly in elderly patients.

Hypokalemia

Hypokalemia can occur as a consequence of Bumex administration. Prevention of hypokalemia requires particular attention in the following conditions: patients receiving digitalis and diuretics for congestive heart failure, hepatic cirrhosis and ascites, states of aldosterone excess with normal renal function, potassium-losing nephropathy, certain diarrheal states, or other states where hypokalemia is thought to represent particular added risks to the patient, ie, history of ventricular arrhythmias.

In patients with hepatic cirrhosis and ascites, sudden alterations of electrolyte balance may precipitate hepatic encephalopathy and coma. Treatment in such patients is best initiated in the hospital with small doses and careful monitoring of the patient's clinical status and electrolyte balance. Supplemental potassium and/or spironolactone may prevent hypokalemia and metabolic alkalosis in these patients.

Ototoxicity

In cats, dogs and guinea pigs, bumetanide has been shown to produce ototoxicity. In these test animals bumetanide was 5 to 6 times more potent than furosemide and, since the diuretic potency of bumetanide is about 40 to 60 times furosemide, it is anticipated that blood levels necessary to produce ototoxicity will rarely be achieved. The potential exists, however, and must be considered a risk of intravenous therapy, especially at high doses, repeated frequently in the face of renal excretory function impairment. Potentiation of aminoglycoside ototoxicity has not been tested for bumetanide. Like other members of this class of diuretics, bumetanide probably shares this risk.

Allergy to Sulfonamides

Patients allergic to sulfonamides may show hypersensitivity to Bumex.

Thrombocytopenia

Since there have been rare spontaneous reports of thrombocytopenia from postmarketing experience, patients should be observed regularly for possible occurrence of thrombocytopenia.

Precautions

General

Serum potassium should be measured periodically and potassium supplements or potassium-sparing diuretics added if necessary. Periodic determinations of other electrolytes are advised in patients treated with high doses or for prolonged periods, particularly in those on low-salt diets.

Hyperuricemia may occur; it has been asymptomatic in cases reported to date. Reversible elevations of the BUN and creatinine may also occur, especially in association with dehydration and particularly in patients with renal insufficiency. Bumex may increase urinary calcium excretion with resultant hypocalcemia.

Diuretics have been shown to increase the urinary excretion of magnesium; this may result in hypomagnesemia.

Laboratory Tests

Studies in normal subjects receiving Bumex revealed no adverse effects on glucose tolerance, plasma insulin, glucagon and growth hormone levels, but the possibility of an effect on glucose metabolism exists. Periodic determinations of blood sugar should be done, particularly in patients with diabetes or suspected latent diabetes.

Patients under treatment should be observed regularly for possible occurrence of blood dyscrasias, liver damage or idiosyncratic reactions, which have been reported occasionally in foreign marketing experience. The relationship of these occurrences to Bumex use is not certain.

Drug Interactions

Drugs With Ototoxic Potential (see WARNINGS)

Especially in the presence of impaired renal function, the use of parenterally administered bumetanide in patients to whom aminoglycoside antibiotics are also being given should be avoided, except in life-threatening conditions.

Drugs With Nephrotoxic Potential

There has been no experience with the concurrent use of Bumex with drugs known to have a nephrotoxic potential. Therefore, the simultaneous administration of these drugs should be avoided.

Lithium should generally not be given with diuretics (such as Bumex) because they reduce its renal clearance and add a high risk of lithium toxicity.

Pretreatment with probenecid reduces both the natriuresis and hyperreninemia produced by Bumex. This antagonistic effect of probenecid on Bumex natriuresis is not due to a direct action on sodium excretion but is probably secondary to its inhibitory effect on renal tubular secretion of bumetanide. Thus, probenecid should not be administered concurrently with Bumex.

Indomethacin blunts the increases in urine volume and sodium excretion seen during Bumex treatment and inhibits the bumetanide-induced increase in plasma renin activity. Concurrent therapy with Bumex is thus not recommended.

Bumex may potentiate the effect of various antihypertensive drugs, necessitating a reduction in the dosage of these drugs.

Interaction studies in humans have shown no effect on digoxin blood levels.

Interaction studies in humans have shown Bumex to have no effect on warfarin metabolism or on plasma prothrombin activity.

Carcinogenesis, Mutagenesis and Impairment of Fertility

Bumex was devoid of mutagenic activity in various strains of Salmonella typhimurium when tested in the presence or absence of an in vitro metabolic activation system. An 18-month study showed an increase in mammary adenomas of questionable significance in female rats receiving oral doses of 60 mg/kg/day (2000 times a 2-mg human dose). A repeat study at the same doses failed to duplicate this finding.

Reproduction studies were performed to evaluate general reproductive performance and fertility in rats at oral dose levels of 10, 30, 60 or 100 mg/kg/day. The pregnancy rate was slightly decreased in the treated animals; however, the differences were small and not statistically significant.

Pregnancy

Pregnancy Category C. Bumex is neither teratogenic nor embryocidal in mice when given in doses up to 3400 times the maximum human therapeutic dose.

Bumex has been shown to be nonteratogenic, but it has a slight embryocidal effect in rats when given in doses of 3400 times the maximum human therapeutic dose and in rabbits at doses of 3.4 times the maximum human therapeutic dose. In one study, moderate growth retardation and increased incidence of delayed ossification of sternebrae were observed in rats at oral doses of 100 mg/kg/day, 3400 times the maximum human therapeutic dose. These effects were associated with maternal weight reductions noted during dosing. No such adverse effects were observed at 30 mg/kg/day (1000 times the maximum human therapeutic dose). No fetotoxicity was observed at 1000 to 2000 times the human therapeutic dose.

In rabbits, a dose-related decrease in litter size and an increase in resorption rate were noted at oral doses of 0.1 and 0.3 mg/kg/day (3.4 and 10 times the maximum human therapeutic dose). A slightly increased incidence of delayed ossification of sternebrae occurred at 0.3 mg/kg/day; however, no such adverse effects were observed at the dose of 0.03 mg/kg/day. The sensitivity of the rabbit to Bumex parallels the marked pharmacologic and toxicologic effects of the drug in this species.

Bumex was not teratogenic in the hamster at an oral dose of 0.5 mg/kg/day (17 times the maximum human therapeutic dose). Bumetanide was not teratogenic when given intravenously to mice and rats at doses up to 140 times the maximum human therapeutic dose.

There are no adequate and well-controlled studies in pregnant women. A small investigational experience in the United States and marketing experience in other countries to date have not indicated any evidence of adverse effects on the fetus, but these data do not rule out the possibility of harmful effects. Bumex should be given to a pregnant woman only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

It is not known whether this drug is excreted in human milk. As a general rule, nursing should not be undertaken while the patient is on Bumex since it may be excreted in human milk.

Pediatric Use

Safety and effectiveness in pediatric patients below the age of 18 have not been established.

In vitro studies using pooled sera from critically ill neonates have shown bumetanide to be a potent displacer of bilirubin (see CLINICAL PHARMACOLOGY: Pediatric Pharmacology ). The administration of bumetanide could present a particular concern if given to critically ill or jaundiced neonates at risk for kernicterus.

Geriatric Use

Clinical studies of Bumex did not include sufficient numbers of subjects aged 65 and over to determine whether they responded differently from younger subjects. Other reported clinical experience has not identified differences in responses between the elderly and younger patients. In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal function.

Adverse Reactions

The most frequent clinical adverse reactions considered probably or possibly related to Bumex are muscle cramps (seen in 1.1% of treated patients), dizziness (1.1%), hypotension (0.8%), headache (0.6%), nausea (0.6%) and encephalopathy (in patients with preexisting liver disease) (0.6%). One or more of these adverse reactions have been reported in approximately 4.1% of patients treated with Bumex.

Less frequent clinical adverse reactions to Bumex are impaired hearing (0.5%), pruritus (0.4%), electrocardiogram changes (0.4%), weakness (0.2%), hives (0.2%), abdominal pain (0.2%), arthritic pain (0.2%), musculoskeletal pain (0.2%), rash (0.2%) and vomiting (0.2%). One or more of these adverse reactions have been reported in approximately 2.9% of patients treated with Bumex.

Other clinical adverse reactions, which have each occurred in approximately 0.1% of patients, are vertigo, chest pain, ear discomfort, fatigue, dehydration, sweating, hyperventilation, dry mouth, upset stomach, renal failure, asterixis, itching, nipple tenderness, diarrhea, premature ejaculation and difficulty maintaining an erection.

Laboratory abnormalities reported have included hyperuricemia (in 18.4% of patients tested), hypochloremia (14.9%), hypokalemia (14.7%), azotemia (10.6%), hyponatremia (9.2%), increased serum creatinine (7.4%), hyperglycemia (6.6%), and variations in phosphorus (4.5%), CO 2 content (4.3%), bicarbonate (3.1%) and calcium (2.4%). Although manifestations of the pharmacologic action of Bumex, these conditions may become more pronounced by intensive therapy.

Also reported have been thrombocytopenia (0.2%) and deviations in hemoglobin (0.8%), prothrombin time (0.8%), hematocrit (0.6%), WBC (0.3%) and differential counts (0.1%). There have been rare spontaneous reports of thrombocytopenia from postmarketing experience.

Diuresis induced by Bumex may also rarely be accompanied by changes in LDH (1.0%), total serum bilirubin (0.8%), serum proteins (0.7%), SGOT (0.6%), SGPT (0.5%), alkaline phosphatase (0.4%), cholesterol (0.4%) and creatinine clearance (0.3%). Increases in urinary glucose (0.7%) and urinary protein (0.3%) have also been seen.

Overdosage

Overdosage can lead to acute profound water loss, volume and electrolyte depletion, dehydration, reduction of blood volume and circulatory collapse with a possibility of vascular thrombosis and embolism. Electrolyte depletion may be manifested by weakness, dizziness, mental confusion, anorexia, lethargy, vomiting and cramps. Treatment consists of replacement of fluid and electrolyte losses by careful monitoring of the urine and electrolyte output and serum electrolyte levels.

Bumex Dosage and Administration

Dosage should be individualized with careful monitoring of patient response.

Oral Administration

The usual total daily dosage of Bumex is 0.5 mg to 2 mg and in most patients is given as a single dose.

If the diuretic response to an initial dose of Bumex is not adequate, in view of its rapid onset and short duration of action, a second or third dose may be given at 4- to 5-hour intervals up to a maximum daily dose of 10 mg. An intermittent dose schedule, whereby Bumex is given on alternate days or for 3 to 4 days with rest periods of 1 to 2 days in between, is recommended as the safest and most effective method for the continued control of edema. In patients with hepatic failure, the dosage should be kept to a minimum and, if necessary, dosage increased very carefully.

Because cross-sensitivity with furosemide has rarely been observed, Bumex can be substituted at approximately a 1:40 ratio of Bumex to furosemide in patients allergic to furosemide.

Parenteral Administration

Bumetanide injection may be administered parenterally (IV or IM) to patients in whom gastrointestinal absorption may be impaired or in whom oral administration is not practical.

Parenteral treatment should be terminated and oral treatment instituted as soon as possible.

How is Bumex Supplied

Tablets, 0.5 mg (light green), bottles of 100 (NDC 0004-0125-01) and 5000 (NDC 0004-0125-11); 1 mg (yellow), bottles of 100 (NDC 0004-0121-01), 500 (NDC 0004-0121-14) and 5000 (NDC 0004-0121-11); 2 mg (peach), bottles of 100 (NDC 0004-0162-01) and 5000 (NDC 0004-0162-11).

Imprint on tablets: 0.5 mg–ROCHE Bumex 0.5; 1 mg–ROCHE Bumex 1; 2 mg–ROCHE Bumex 2.

Store tablets at 59° to 86°F (15° to 30°C).

Copyright © 1997-2003 by Roche Laboratories Inc. All rights reserved.

Kop Resporito (Trandate) Utan Recept, Resporito

Kopa Resporito (Trandate) Natet Utan Recept

Resporito (Trandate) Forklaring

Resporito ar egentligen en medicin som ofta anvands nar det galler att hantera hypertoni. Det verkligen ar forknippat med karvedilol (Coreg). Nervtradar som ar del av de adrenerga nerver besoker majoriteten av arteriella blodkarlen varhelst dessa manniskor starta en bra adrenerga kemiskt amne noradrenalin. Sjalva noradrenalin ansluter for att smarta i muskelvavnad fran arteriella blodkarlen leda till muskel for att avtalet, vilket minskar den verkliga arteriella blodkarlen, samt okande blod stress. Resporito forhindrar smarta fran de adrenerga nerver. Nar Resporito ansluter for att liksom forhindrar sjalva smartan, den verkliga arteriella muskler vila, och aven den arteriella blodkarlen okar, skapar tillsammans med lagt blodtryck.

Allmant titeln i samband med Resporito ar faktiskt Labetalol.

Resporito kan ocksa kallas Labetalol, Normodyne.

Brand i samband med Resporito ar faktiskt Resporito.

Resporito (Trandate) Dose

Resporito kommer in:

50 mg lagre dos friktionsmaterial

100mg Regular Dos friktionsmaterial

200mg Forbattrad Dos friktionsmaterial

Utnyttja detta lakemedel tillsammans med maltider eller ens mejeri.

Om du vill astadkomma basta resultaten brukar inte sluta med Resporito helt plotsligt.

Resporito (Trandate) I brist forknippas med doserings

Vanligtvis far inte dubbel dos. Om du hoppar over dosen du behover for att bara den nar du kom ihag nar det galler din saknas. Nar det ar dags for dosering du behover bara pa din egen normal dosering rutin.

Resporito (Trandate) Overdosering

Om du overdoserar Resporito och du undviker ocksa stor att du behover kolla din lakare eller ens lakare omedelbart.

Resporito (Trandate) Lagringsutrymme

Shop i rymden temperaturer mellan 10 och 30 nivaer D (59 samt 86 nivaer F) fran fukt, belysning samt temperatur. Behall text ordentligt stangd. Starka nagon form av orord medicinering efter utgangen dagen. Behall fran uppna barnen.

Resporito (Trandate) Negativa effekter

Resporito erbjuder de negativa effekterna. Den mest typiska tenderar att vara:

utmattning friktionsmaterial

illamaende eller krakningar friktionsmaterial

Tingley fran huvudet eller ens porer och huden friktionsmaterial

Mycket mindre typiska och allvarliga negativa effekter i hela anvander Resporito:

allergiska reaktion reaktioner (urtikaria, andas in och andas problem, allergi, samt utbrott) friktionsmaterial

svimning friktionsmaterial

underben obehag friktionsmaterial

forbattrad svett friktionsmaterial

forbattrades peeing friktionsmaterial

ovanlig onskan friktionsmaterial

langvarig brist pa hunger friktionsmaterial

magen obehag friktionsmaterial

langvarig vark tonsiller eller jamn temperatur friktionsmaterial

enkla blodforlust eller ens stoter friktionsmaterial

synformaga andringar friktionsmaterial

problem peeing friktionsmaterial

psykologiska eller ens kanner modifieringar friktionsmaterial

morkt kissa friktionsmaterial

gulfargning ogon eller ens porer och huden friktionsmaterial

Negativa effekter indikationer beroende av medicin du kanske anvander men dessutom lita pa ditt valbefinnande skick och annan aspekter.

Resporito (Trandate) Kontraindikationer

Vanligtvis inte far Resporito om du ar kanslig for att Resporito element.

Var forsiktig tillsammans med Resporito om du vantar annars du tanker ha ett barn, annars ar du verkligen en medicinsk mamma.

Var forsiktig tillsammans med Resporito for dem som har en kort historia i samband med fragor som lever orgel, hjartfragor, feokromocytom, diabetes, nagon form av allergiska reaktioner.

Vanligtvis inte far Resporito for dem som har brost sjukdom (astma, KOL), overlagsen hjart forhindra allvarlig bradykardi, allvarlig kardiovaskular misslyckas, efter CABG kirurgisk behandling.

P-piller kan gora en person yr i huvudet i ungefar tre timmar direkt efter det verkligen tillhandahalls. Du maste halla benagna under denna period tidsperiod for att kunna undvika droppar.

Du behover uppat gradvis nar okar fran sammantradet eller liggande plats.

Bli forsiktig om du reser ordning.

Forhindra alkoholhaltiga drycker.

Diabetiker bor vara forsiktig tillsammans med Resporito.

Vanligtvis inte sluta anvanda Resporito helt plotsligt.

Resporito (Trandate) Vanliga fragor

Queen: Vad exakt ar Resporito?

Resporito anvands for att behandla allvarlig hypertoni (hogt blodtryck). Minskande hypertoni Resporito hjalper till att forebygga gungor, kardiovaskulara misshandel samt renal issues. A

Queen: Exakt hur ska jag fa Resporito?

Resporito kommer i piller (50 milligram, hundra milligram, tva hundra mg). Dra nytta av detta lakemedel tillsammans med maltider eller ens mejeri. Om du vill uppna basta resultat brukar inte sluta med Resporito helt sudden. A

Queen: Exakt vad ska jag fag situationen i samband med overdos?

Vanligtvis inte fa Resporito piller i stora mangder. Vid Resporito mer an dos, maste du kolla in lakare eller ens lakare instantly. A

Queen: Kan man verkligen konsumera alkohol?

Absolut ingen, det ar verkligen oacceptabelt uppskattar alkoholhaltiga beverages. A

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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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Blood Pressure Buy Lisinopril At, Tensinop

Blood Pressure

Lisinopril (Tensinop)

Lisinopril is used for treating high blood pressure alone or with other medicines. It is used along with other medicines to manage heart failure or improve survival after a heart attack. Lisinopril is an angiotensin-converting enzyme (ACE) inhibitor. It works by relaxing blood vessels. This helps to lower blood pressure.

Use Lisinopril as directed by your doctor.

Take Lisinopril by mouth with or without food.

If you miss a dose of Lisinopril, 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 Lisinopril.

Store Lisinopril at room temperature, between 59 and 86 degrees F (15 and 30 degrees C). Do not freeze. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Lisinopril out of the reach of children and away from pets.

Do NOT use Lisinopril if:

you are allergic to any ingredient in Lisinopril

you have a history of angioedema (swelling of the hands, face, lips, eyes, throat, or tongue; difficulty swallowing or breathing; or hoarseness), including angioedema caused by treatment with an ACE inhibitor

you are in your second or third trimester of pregnancy

the patient is a child with severe kidney problems.

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

Some medical conditions may interact with Lisinopril. 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 are able to become pregnant

if you have a history of heart problems (eg, heart failure, aortic stenosis), blood vessel problems, blood flow problems, bone marrow problems, kidney problems, or diabetes

if you have a history of stroke, recent heart attack, or kidney transplant

if you have an autoimmune disease (eg, rheumatoid arthritis, lupus, scleroderma)

if you are dehydrated or have low blood volume

if you have high blood potassium levels, low blood sodium levels, or are on a low salt (sodium) diet

if you are on dialysis or are scheduled to have major surgery.

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

Diuretics (eg, furosemide, hydrochlorothiazide) because the risk of low blood pressure may be increased

Aldosterone blockers (eg, eplerenone), potassium-sparing diuretics (eg, spironolactone, triamterene), or potassium supplements because the risk of high blood potassium levels may be increased

Insulin, sulfonylureas (eg, glipizide), or other oral diabetes medicines (eg, metformin) because the risk of low blood sugar may be increased

Gold-containing medicines (eg, auranofin) because flushing, nausea, vomiting, and low blood pressure may occur

Nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, indomethacin, celecoxib) or salicylates (eg, aspirin) because they may decrease Lisinopril's effectiveness

Lithium or thiopurines (eg, azathioprine) because the risk of their side effects may be increased by Lisinopril.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Lisinopril 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:

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

Lisinopril may cause a serious side effect called angioedema. Contact your doctor at once if you develop swelling of the hands, face, lips, eyes, throat, or tongue; difficulty swallowing or breathing; or hoarseness.

Lisinopril may not work as well in black patients. They may also be at greater risk of side effects. Contact your doctor if your symptoms do not improve or if they become worse.

Dehydration, excessive sweating, vomiting, or diarrhea may increase the risk of low blood pressure. Contact your health care provider at once if any of these occur.

Rarely, Lisinopril may lower the ability of your body to fight infection. This risk may be greater if you have certain other health problems (eg, kidney problems, collagen vascular disease). Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

Check with your doctor before you use a salt substitute or a product that has potassium in it.

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

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.

If you have high blood pressure, do not use nonprescription products that contain stimulants. These products may include diet pills or cold medicines. Contact your doctor if you have any questions or concerns.

Diabetes patients - Lisinopril may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

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

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

Lisinopril should not be used in children younger 6 years; safety and effectiveness in these children have not been confirmed.

Pregnancy and breast-feeding: Lisinopril may cause birth defects or fetal death if you take it while you are pregnant. If you think you may be pregnant, contact your doctor right away. It is not known if Lisinopril is found in breast milk. Do not breastfeed while taking Lisinopril.

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:

Cough; diarrhea; dizziness; headache; tiredness.

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 hands, eyes, mouth, face, lips, or tongue; hoarseness); chest pain; dark urine; decreased urination; difficulty swallowing; infection (eg, fever, chills, persistent sore throat); irregular or slow heartbeat; stomach pain (with or without nausea or vomiting); symptoms of low blood pressure (eg, fainting, severe dizziness, lightheadedness); yellowing of the skin or eyes.

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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Lipitor - Cholesterol Lowering, Inflammide

Common use Atorvastatin is a cholesterol-lowering used to treat high cholesterol or to lower the risk of stroke, heart attack or other heart complications in patients with coronary heart disease or second type of diabetes. Atorvastatin helps to clear harmful low-density lipoprotein cholesterol out of the blood and by limiting the body's ability to form new LDL cholesterol. Thus it can help prevent hardening of the arteries and heart disease, conditions that can lead to vascular disease, heart attack, stroke.

Dosage and direction Take it orally once a day with or without food. Atorvastatine should be taken with full glass of water. The common dose for adults is 10 mg once daily. The common dose for children from 10 to 17 years of age is 10 mg once daily. Using Atorvastatin in children less than 10 years of age is not recommended and dose must be determined by your family doctor.

Note: this instruction presented here just for review. It's very necessary to consult with your doctor before using. It help you to get best results.

Precautions People with diabetes, underactive thyroid glands, kidney disease, or muscle disease sometimes need additional tests before or during atorvastatin therapy since dosage adjustments may be required. Do not use large amounts of alcohol while taking this drug because it can worsen the adverse effects of this medicine on the liver. Atorvastatin should not be used during pregnancy, becoming pregnant or lactating without doctor's advice. Do not use Atorvastatin before breast-feeding without doctor's permission.

Contraindications Atorvastatin is not allowed to people who have liver problems or unexplained abnormal liver function tests. Do not use it if you are taking an HIV protease inhibitor (eg, ritonavir), itraconazole, or mibefradil. Also Atorvastatin contraindicated if you are hypersensitive to any components of this medication, pregnancy or breast-feeding.

Possible side effect They may include all types of an allergic reaction. Also the most possible side effects include: muscle pain, tenderness, or weakness with fever or flu symptoms; or nausea, clay-colored stools, stomach pain, low fever, jaundice, loss of appetite, dark urine. Less serious include: mild nausea or stomach pain, stomach upset, heartburn; constipation, bloating, gas; stuffy nose; itching, skin rash; headache. If you experience one of them stop using Atorvastatin and tell your doctor as soon as possible. Also consult with your doctor about any side effect that seems unusual.

Drug interaction Atrovastatin interact with the following drugs: digoxin; erythromycin or clarithromycin; gemfibrozil or fenofibrate; niacin; an antifungal medication such as itraconazole, fluconazole, or ketoconazole; drugs that weaken your immune system such as cancer medicine or steroids, cyclosporine, sirolimus, tacrolimus, and others; HIV or AIDS medication such as indinavir, nelfinavir, ritonavir, lopinavir-ritonavir, or saquinavir. Also note that interaction between two medications does not always mean that you must stop taking one of them. As usual it affects the the effect of drugs, so consult with your doctor about how it interactions are being managed or should be managed.

If you forgot to take your dose in time, please do it as soon as you remember. But do not take if it is too late or almost time for your next dose. Do not increase your recommended dose. Take your usually dose next day in the same regularly time.

Symptoms of Atorvastatin are not known well but most possible of them include a severe drop in blood pressure and a faster heartbeat. If you experience one of them or any unusual symptoms, call your doctor immediately.

Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

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.

Suprasone Ohne Rezept, Suprasone

Betnovate ohne rezept

Betnovate is used to help relieve redness, itching, swelling, or other discomfort caused by skin conditions. This medicine is a corticosteroid (cortisone-like medicine or steroid).

Use Betnovate as directed by your doctor.

Betnovate is for use on the skin only. Do not get it in your eyes.

Wash your hands with soap and water before and after using this medicine.

Apply a thin layer of this medicine to the affected area of the skin. Rub it in gently.

Do not use cosmetics or other skin care products on the treated areas.

Do not bandage or otherwise wrap the skin being treated unless directed to do so by your doctor.

If the medicine is applied to the diaper area of an infant, do not use tight-fitting diapers or plastic pants unless directed to do so by your doctor.

If your doctor ordered an occlusive dressing or airtight covering to be applied over the medicine, make sure you know how to apply it. Occlusive dressings increase the amount of medicine absorbed through your skin, so use them only as directed. If you have any questions about this, check with your doctor.

Using too much of this medicine or using it for a long time may increase your risk of having adrenal gland problems.

If you miss a dose of Betnovate, skip the missed dose and go back to your regular dosing schedule. Do not use 2 doses at once.

The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.

The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.

For redness, itching, and swelling of the skin:

Adults: Apply to the affected area of the skin one to three times per day.

Children: Use and dose must be determined by your doctor.

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

Store Betnovate at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Keep Betnovate out of the reach of children and away from pets.

Active Ingredient: Betamethasone.

Do NOT use Betnovate if:

you are allergic to any ingredient in Betnovate

you are taking mifepristone

you have a systemic fungal infection

you are scheduled to have a smallpox vaccine

you have a certain bleeding disorder (idiopathic thrombocytopenic purpura).

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

Some medical conditions may interact with Betnovate. 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 bleeding problems, heart problems (eg, congestive heart failure [CHF]), heart attack, high blood pressure, kidney problems, liver problems, diabetes, seizures, an underactive thyroid, adrenal gland problems, any mental or mood problems, or low blood potassium levels

if you have or have recently had a bacterial, fungal, malarial, viral, or other type of infection; herpes infection of the eye; chickenpox; measles; shingles; or a head or brain injury

if you have HIV infection or tuberculosis (TB), or if you have ever had a positive TB skin test

if you have any stomach problems (eg, ulcers), intestinal problems (eg, blockage, perforation, infection, unexplained diarrhea, diverticulitis, ulcerative colitis), recent intestinal surgery, or inflammation of the esophagus

if you have weak bones (eg, osteoporosis) or muscle problems (eg, myasthenia gravis)

if you have had any recent vaccinations (eg, smallpox)

if you have a history of joint surgery or any joint problems (eg, fracture, infection).

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

Aprepitant, clarithromycin, cyclosporine, diltiazem, erythromycin, itraconazole, ketoconazole, or troleandomycin because side effects, such as adrenal gland or nervous system problems (eg, seizures), may occur

Barbiturates (eg, phenobarbital), carbamazepine, hydantoins (eg, phenytoin), lithium, or rifampin because they may decrease Betnovate's effectiveness

Aspirin, live vaccines, mifepristone, or ritodrine because the risk of their side effects may be increased by Betnovate.

This may not be a complete list of all interactions that may occur. Ask your health care provider if Betnovate 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:

Betnovate may lower the ability of your body to fight infection. Avoid contact with people who have colds or infections. Tell your doctor if you notice signs of infection like fever, sore throat, rash, or chills.

If you have not had chickenpox, shingles, or measles, avoid contact with anyone who does.

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

Diabetes patients - Betnovate may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

If you use Betnovate for an extended period of time, your body may not produce enough natural steroids for up to several months after you stop using it. Severe symptoms may occur if you experience injury, surgery, infection, or loss of blood electrolytes. Contact your doctor immediately if you experience any of these events. You may need to begin taking additional corticosteroids.

If you have had Betnovate injected into a joint and you experience increased pain along with swelling, decreased joint movement, fever, and general feeling of being unwell, contact your doctor.

Talk with your doctor before you receive any vaccine while you are using Betnovate.

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

Betnovate may have benzyl alcohol in it. Do not use it in newborns or infants. It may cause serious and sometimes fatal nervous system problems and other side effects.

Corticosteroids may affect growth rate in children and teenagers in some cases. They may need regular growth checks while they use Betnovate.

Betnovate should be used with extreme caution 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 Betnovate while you are pregnant. Betnovate is found in breast milk. If you are or will be breast-feeding while you use Betnovate, check with your doctor. Discuss any possible risks to your baby.

If you suddenly stop taking Betnovate, you may have withdrawal symptoms, These may include unbalanced hormones (in both men and women).

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:

Acne; clumsiness; dizziness; facial flushing; general body discomfort; headache; increased appetite; increased sweating; lightheadedness; nausea; nervousness; sleeplessness; upset stomach.

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); black, tarry stools; changes in body fat; changes in menstrual periods; changes in skin color; chest pain; easy bruising or bleeding; irregular heartbeat; mental or mood changes (eg, depression); muscle pain, wasting, or weakness; seizures; severe nausea or vomiting; sudden severe dizziness or headache; swelling of feet or legs; symptoms of infection (eg, chills, fever, sore throat); tendon or bone pain; thinning of the skin; unusual skin sensation; unusual weight gain; vision changes or other eye problems; vomit that looks like coffee grounds.

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.

Dom Lagana To Make Nitro Fc Debut At Englishtown, Nitrodom

Veteran driver Dom Lagana will add a new line to his resume this weekend.

The Scarsdale, N. Y. native is making his nitro Funny Car debut at NHRA’s Summernationals Thursday through Sunday at Englishtown, N. J.

“We had a match race this past weekend (at Martin, Mich.) with our dragster and we were going to run just Englishtown with the dragster,” Lagana said. “Then, we were going to have a week off and switch everything over because Paul Lee’s driving the Funny Car at Bristol (Tenn. June 19-21), and the match race got postponed (May 26) due to a bad forecast. We saw the car count was kind of low (at Englishtown, 17 cars), and if we take the Funny Car to Englishtown, then we will just take it to Epping (N. H. June 12-14) because then we can go right to Bristol with Paul Lee without having to swap anything over.”

Lagana acknowledged making his maiden nitro Funny Car runs at Old Bridge Township Raceway Park will be special.

“It will be pretty cool to run at Englishtown with the Funny Car with our dad’s history of having Funny Cars there,” Lagana said. “I was going to Englishtown when I was in my mom’s stomach. I’m pretty excited about racing there. Unfortunately my dad isn’t here to see it, but he will be watching because a Funny Car is something he always wanted us to get. He probably only dreamed that I would drive one, one day, so it’s pretty cool to get to do this for him. All his old school buddies will be out at the track. They will be walking around the pits expecting to see the dragster, and when they see the Funny Car I’m sure they will get excited.”

Bobby Lagana, Sr. the patriarch of the Lagana family died Sept. 5, 2013. Dom said he also will be piloting the Funny Car at Epping.

Dom is driving the Funny Car owned by he and his brother Bobby as well as Aaron Brooks and John Stewart. Stewart will be the crew chief at Englishtown. Dom said the Funny Car was bought in December. The Funny Car was originally built as a back-up car for Melanie Troxel when she was driving the In-N-Out Burger Funny Car for Roger Burgess’ R2B2Racing team. Troxel last drove the In-N-Out Burger Funny Car in 2011, finishing 15th in the point standings.

According to Dom, Nitro Ninja, a T-shirt and apparel company owned by he and his brother Bobby, will be the sponsor on the side of the Funny Car. Dom licensed in the nitro Funny Car March 30 at zMax Dragway in Charlotte, N. C. making two hits.

“The main thing for us at Englishtown is to look good and try not make any mistakes with the car,” Dom said. “The car, in testing in Charlotte, is literally just a full run away from running a 4.10 or 4.15. Obviously we are going to play the conditions and see what the track is like, and if we can leave the weekend running a 4.20 full run I would be happy, and if that happens to get us qualified that would be awesome. We are going to have to come out and learn with the car, and I need to get some more seat time, and as long as we can keep the car safe and everybody can have a good time, and we can run a 4.20 that would be cool.”

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Vartalon Duo Para Que Sirve, Vartalon

VARTALON DUO

No usar VARTALON DUO con lactantes.

Revise siempre que no sea alergico a ninguno de los componentes de VARTALON DUO . podria poner en peligro su salud

Recuerda antes de tomar este medicamento consultar siempre con su medico, la informacion que ofrecemos es orientativa y no sustituye en ningun caso la de su medico u otro profesional de la salud.

Prospecto e indicaciones

?Que es vartalon-duo?

El vartalon-duo es un medicamento que viene en presentacion de capsulas o tambien en sobres. Este medicamento esta elaborado con compuestos como lo son el Condroitin Sulfato Sodico, tambien contiene Sulfato de D - Glucosamina y Glucosamina Policristalina.

Dentro de las presentaciones de capsulas se encuentra las de 30 y tambien las de tratamiento de 60. En los el caso de las presentaciones en sobres viene de 15 y tambien de 30.

?Para que sirve y como tomar vartalon-duo?

Los ingredientes de este medicamento hacen que el efecto que este tiene sobre el cuerpo sea relacionado con el tratamiento para los procesos que intervienen en la degeneracion o dano del cartilago.

Asi el vartalon-duo es un medicamento que se receta y funciona en el cuerpo como antiartrosico y tambien como condroprotector.

Este medicamento puede ser usado en los momentos primarios y tambien secundarios de la presencia degenerativa de los cartilagos.

La forma de tomar este medicamento debe estar guiada de acuerdo a las indicaciones medicas aunque lo que normalmente se recomienda es tomar un sobre de este medicamento diariamente.

Efectos adversos y alergias

En los efectos adversos que podemos encontrar con este medicamento estan:

La hipersensibilidad a alguno de los componentes del medicamento.

Asi mismo puede presentase alergia a alguno de estos componentes.

• Asi mismo se recomienda no consumir en estado de gestacion y tampoco en la lactancia ya que no se han realizado suficientes estudios sobre la influencia del medicamento en el desarrollo del feto o el bebe.

Composicion

Capsulas: cada capsula contiene: Condroitin Sulfato Sodico 400 mg, Sulfato de D-Glucosamina (como sulfato de Glucosamina policristalino 628 mg) 500 mg. Sobres: cada sobre contiene Sulfato de Glucosamina Policristalina (equivalente a 1500 mg de sulfato

Presentaciones

Capsulas: envases conteniendo 30 y 60 capsulas. Sobres: envases conteniendo 15 y 30 sobres.

Para Que Sirve

Microvibrate, Microvibrate

Product Description Common use Doxycyline is a synthetic broad-spectrum antibiotic derived from tetracycline and used to treat many different bacterial infections, such as infections of urinary tract, acne, gonorrhea, chlamydiosis, periodontitis (gum disease), blemishes, bumps, and acne-like lesions caused by rosacea.

Dosage and directions This medication should be taken after a meal with a big glass of water to decrease irritation of esophagus. Daily dose should be taken as a single dose or divided in two (12 hours between each one). Do not take it in larger amounts or continue to take it after the administered period. Certain brands of this medication cannot be used with dairy products. Do not crush, break, or open a delayed-release capsule, eat the pill whole. If it is an oral suspension shake it before use and measure with special measuring spoon. Never take this drug if it is expired as it may damage your kidney.

Precautions Usage of Doxycycline during growth of teeth may result in their permanent color change. Avoid exposure of your body to prolonged UV radiation during treatment and 4-5 days after it. If long treatment with this medication is prescribed a regular monitoring of peripheral blood cell content, liver function tests and determination of nitrogen and urea in serum are required.

Contraindications Hypersensitivity to Doxycycline and tetracyclines, pregnancy (second half of the term), breastfeeding, infancy (for children younger than 9 y. o.), leucopenia, porphyria, severe liver failure.

Possible side effect Side effects caused by Doxycycline may appear as headache, dizziness, blurred vision, fever, chills, body aches, red skin rash, pale or yellowed skin, dark colored urine, severe pain in upper stomach, loss of appetite, jaundice, easy bruising or bleeding. Contact your doctor if you experience severe effects listed above.

Drug interaction Co-administration with aluminum, magnesium, or calcium based antacids is not recommended as Doxycyline absorption maybe slowered. Minerals (such as calcium or iron) or with bismuth subsalicylate have the same effect. Doxycycline is reported to enhance the activity of warfarin. Phenytoin (Dilantin), carbamazepine (Tegretol), and barbiturates (such as phenobarbital) may enhance the metabolism of Doxycycline.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose just skip the missed portion and continue to take the medicine according to the schedule.

Overdose In case of serious and persistent nausea, vomiting, and diarrhea consult your doctor.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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 Doxycyline is a synthetic broad-spectrum antibiotic derived from tetracycline and used to treat many different bacterial infections, such as infections of urinary tract, acne, gonorrhea, chlamydiosis, periodontitis (gum disease), blemishes, bumps, and acne-like lesions caused by rosacea.

Dosage and directions This medication should be taken after a meal with a big glass of water to decrease irritation of esophagus. Daily dose should be taken as a single dose or divided in two (12 hours between each one). Do not take it in larger amounts or continue to take it after the administered period. Certain brands of this medication cannot be used with dairy products. Do not crush, break, or open a delayed-release capsule, eat the pill whole. If it is an oral suspension shake it before use and measure with special measuring spoon. Never take this drug if it is expired as it may damage your kidney.

Precautions Usage of Doxycycline during growth of teeth may result in their permanent color change. Avoid exposure of your body to prolonged UV radiation during treatment and 4-5 days after it. If long treatment with this medication is prescribed a regular monitoring of peripheral blood cell content, liver function tests and determination of nitrogen and urea in serum are required.

Contraindications Hypersensitivity to Doxycycline and tetracyclines, pregnancy (second half of the term), breastfeeding, infancy (for children younger than 9 y. o.), leucopenia, porphyria, severe liver failure.

Possible side effect Side effects caused by Doxycycline may appear as headache, dizziness, blurred vision, fever, chills, body aches, red skin rash, pale or yellowed skin, dark colored urine, severe pain in upper stomach, loss of appetite, jaundice, easy bruising or bleeding. Contact your doctor if you experience severe effects listed above.

Drug interaction Co-administration with aluminum, magnesium, or calcium based antacids is not recommended as Doxycyline absorption maybe slowered. Minerals (such as calcium or iron) or with bismuth subsalicylate have the same effect. Doxycycline is reported to enhance the activity of warfarin. Phenytoin (Dilantin), carbamazepine (Tegretol), and barbiturates (such as phenobarbital) may enhance the metabolism of Doxycycline.

Missed dose Never take a double dose of this medication. If it is almost time of the next dose just skip the missed portion and continue to take the medicine according to the schedule.

Overdose In case of serious and persistent nausea, vomiting, and diarrhea consult your doctor.

Storage Store at room temperature between 59-77 degrees F (15-25 degrees C) away from light and moisture, kids and pets. Do not use after expiration term.

Disclaimer We provide only general information about medications which does not cover all directions, possible drug integrations, or precautions. Information on 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.

Manipulator

Our 3D printed Manipulator allows you to precisely place your electrodes or probes on tiny things like cockroach leg hairs, a worm nerve fiber, or a fly muscle.

Product Details

Your hands only have so much control and microvibrate to boot. For very fine work, you need our Manipulator. Each ships fully assembled and features 4 degrees of freedom: up/down, left/right, forward/backward, and electrode angle of attack. We also attach four rare earth magnets on the bottom of the manipulator so that you can firmly attach it to any metal work surface. When you place your order, we then print the pieces on our own in-house MakerBot 3D printer, assemble the pieces, and then ship it to you. If you have your own 3D printer we offer the open-source schematic so that you can make it yourself. With a MakerBot Replicator, you can load the. x3g file directly on your machine and push print!

August 2013 update . We 1) added a stronger clamping mechanism on the electrode holder, 2) now ship with two different holder types (our original and adjustable width version), 3) added a small notch on the knobs so you can count turns easily, and 4) added knobs to both sides of x-axis for Completo compatibility.

Note: In the pictures to the left, you will see we also have an adaptor for a Hamilton syringe. Let us know if you want us to add this adaptor to your manipulator, and also if you have any custom adaptor design requests. We'll try to accommodate you!

Video of Manipulator

Technical Specs

Made of durable ABS Plastic

Offers 4 degrees of freedom for electrode placement

Occupies a total volume (without electrode attached) of 10.5 cm (4.1 inch) long by 7.9 cm (3.1 inch) wide by 9.5 cm (3.8 inch) high

Each full turn of a knob moves an axis 0.8 mm (0.03 inch)

Range of Motion of x-axis = 37 mm (

1.4 inch)

Range of Motion of y-axis = 32 mm (

1.2 inch)

Range of Motion of z-axis = 18 mm (

0.7 inch)

Range of Motion of Angle of Attack = 135 degrees

Comes with bottom mounted magnets for firm staying power

1x Manipulator electrode

1x Manipulator

Brixonax, Brixonax

Tag Archives: Brixonax

Naproxen (Naprosyn)

is a medicine that is widely prescribed in the treatment of pain and inflammation that can be caused by a variety of medical conditions:

Ankylosing Spondylitis

Aseptic Necrosis

Back Pain

Bursitis

Chronic Myofascial Pain

Costochondritis

Diffuse Idiopathic Skeletal Hyperostosis

Dysautonomia

Fever

Frozen Shoulder

Gout – Acute

Headache

Juvenile Rheumatoid Arthritis

Muscle Pain

Osteoarthritis

Pain

Period Pain

Radiculopathy

Rheumatoid Arthritis

Sciatica

Spondylolisthesis

Tendonitis

Transverse Myelitis

It is also used for the treatment of primary dysmenorrhea.

Brand Names : Adco-Naproxen, Adin N, Aflamax, Aflaxil, Aksen Fort, ALACETAN NNA, Aleve, Aleve, Aleve-D Sinus & Cold (Naproxen and Pseudoephedrine), Alevetabs, Alidase, Alidase, Alpoxen, Alpron, Anaflex, Anaflex SR, Analgen, Anapran, Anapran Neo, Anaprox, Anaprox DS, Anex, Annoxen-S, A-Nox, Antalgin, Ao Pu Li, Apain, Apo-Napro, Apo-Napro-Na, Apo-Naproxen, Apralgin Forte, Apraljin, Apranax, Apranax, Apraxin, Aprodent, Aprol, Apromed, Apronax, Apronax, Apron-F, Aprowell, Aproxen, Aproxil, Armanaks, Artagen, Arthopan (Naproxen and Pantoprazole), Arthrox, Aspen Naproxen, Assonax, Atac, Aterpin (Naproxen and Paracetamol), Bai Tong, Beckanflam, Bei Li, Bifardol (Naproxen and Paracetamol), Bloxen, Bonmin, Bonyl, Boots Period Pain Relief, Boots Pharmacy Period Pain Relief, Brax (Naproxen and Paracetamol), Bremol (Naproxen and Paracetamol), Brixonax, Brunadol (Naproxen and Paracetamol), Brunadol (Naproxen and Paracetamol), Bruproxen, Bumaflex N, Chemists’ Own Period Pain Tablets, Colfem Forte (Naproxen and Scopolamine), Congex, Cudeprox, Dafloxen, Dafloxen F (Naproxen and Paracetamol), Debril, Deflamox Plus (Naproxen and Paracetamol), Deproxen, Desinflam, Deucoval, Deucoval Forte, Diproxen, Diproxen CR, Dolo Apranax (Naproxen and Paracetamol), Dolofleximax, Dolomes, Dolormin mit Naproxen, Dolotandax (Naproxen and Paracetamol (veterinary use)), Doprox, Dozin, Dropsen, Dysmenalgit, EC-Naprosyn, Emox, Emoxen, Equiproxen (veterinary use), Eurogesic, Eurogesic, Eurogesic Forte, Exvile, Fabralgina, Febrax (Naproxen and Paracetamol), Feminax Ultra, Femynass, Flanax, Flogotone, Fluconazinn, Gao Di (Naproxen and Pseudoephedrine), Gen-Naproxen EC, Gerinap, Gynestrel, Honlow, Hui Ke, Improstan, Inflamax, Inza, Iraxen, Jia Dan, Jie Jie, Jinkangpuli, Kapnax, Karoksen, Laser, Lexinax, Licorax, Liotondol Action, Lumbal Lafrancol (Naproxen and Caffeine), Lundiran, Mafidol Compuesto (Naproxen and Paracetamol), Mai Er, Maxiflam, Mednap, Melgar, Messelxen, Miranax, Mobilat, Momendol, Momendol, Momendol (Naproxen and Sulodexide), Monarit, Monochroton, Movibon, Mylan Naproxen, Na Pu Xing, Nafar, Nafasol, Nafxen, Naixan, Nalgesin, Nalgesin, Nalgesin Forte, Nalgesin Forte, Nalgesin S, Nalgesin S, Naloxen, Napec, Napflam, Napmel, Naponal, Naposin, Napoton, Napoxen, Napradol, Napratec (Naproxen and Misoprostol), Napreben, Naprelan, Napren-E, Naprind, Naprius, Napro, Napro Itedal, Napro-A, Naprobene, Naprocet, Naprocop Compuesto (Naproxen and Paracetamol), Naprodel, Naprodev, Naprodom (Naproxen and Domperidone), Naprofidex, Naproflam, Naproflex, Naprogen, Naprogesic, Naprogesic Forte, Naproksen, Naproksens, Napromed, Naprometin, Naprontag, Napro-Pac (Naproxen and Lansoprazole), Napropain, Naprophar, Naprophar Duo (Naproxen and Paracetamol), Naprorex, Naprosian, Naproson, Naprossene Eg, Naprosyn, Naprosyn, Naprosyn CR, Naprosyn EC, Naprosyn Entero, Naprosyn SR, Naprosyne, Naproval, Naproven, Naprovite, Naprox, Naproxen, Naproxen – 1 A Pharma, Naproxen – Shyndec Pharm, Naproxen A, Naproxen Actavis, Naproxen Aflofarm, Naproxen AL, Naproxen Alphapharm, Naproxen Amneal, Naproxen Apotex, Naproxen Apotex, Naproxen Aristo, Naproxen Astar, Naproxen Aurobindo, Naproxen BasicPharma, Naproxen beta, Naproxen BMM Pharma, Naproxen CF, Naproxen Community Pharm, Naproxen CP, Naproxen Dava, Naproxen Delayed Release, Naproxen Disphar, Naproxen Douglas Pharm, Naproxen EB, Naproxen Emo, Naproxen FLX, Naproxen Genericon, Naproxen GenRx, Naproxen Glenmark, Naproxen Hasco, Naproxen HEXAL, Naproxen InvaGen, Naproxen IPS, Naproxen Johnson, Naproxen Lagap, Naproxen Li Ta, Naproxen Lindopharm, Naproxen Marksans Pharma, Naproxen Merck, Naproxen Merck NM, Naproxen Mylan, Naproxen Mylan-E, Naproxen Natrium-B, Naproxen New Chemical, Naproxen Orifarm, Naproxen PCH, Naproxen Perrigo, Naproxen Pharmacin, Naproxen Pliva, Naproxen Polfarmex, Naproxen ratiopharm, Naproxen Roxane, Naproxen Royal, Naproxen Sandoz, Naproxen Sandoz, Naproxen Schworer, Naproxen Sinphar, Naproxen Sinton, Naproxen Siu Guan, Naproxen Sodium Amneal, Naproxen Sodium and Pseudoephedrine Hydrochloride Dr. Reddy’s (Naproxen and Pseudoephedrine), Naproxen Sodium and Pseudoephedrine Hydrochloride Perrigo (Naproxen and Pseudoephedrine), Naproxen Sodium Aurobindo, Naproxen Sodium Banner, Naproxen Sodium CPC, Naproxen Sodium Dr. Reddy’s, Naproxen Sodium Glenmark, Naproxen Sodium Granules India, Naproxen Sodium Hikma, Naproxen Sodium Marksans Pharma, Naproxen Sodium Perrigo, Naproxen Sodium Ranbaxy, Naproxen Sodium Sandoz, Naproxen Sodium Shou Chan, Naproxen Sodium Teva, Naproxen Sodium Watson, Naproxen STADA, Naproxen Teva, Naproxen Teva, Naproxen Tiofarma, Naproxen Watson, Naproxen West-Ward, Naproxen Yang Sheng, Naproxen Yung Chi, Naproxen Zydus, Naproxen-C-Dragon Pharmacy, Naproxen-CT, Naproxen-CT, Naproxene EG, Naproxene Germed, Naproxen-E Mylan, Naproxene sodico DOC, Naproxene sodico Dorom, Naproxene Sodique EG, Naproxene Sodique Teva, Naproxene-Eurogenerics, Naproxen-Mepha, Naproxennatrium Apotex, Naproxennatrium Ceft, Naproxennatrium DA, Naproxennatrium Disphar, Naproxennatrium HTP, Naproxennatrium Leidapharm, Naproxennatrium Nordic, Naproxennatrium Sandoz, Naproxeno, Naproxeno, Naproxeno + Paracetamol (Naproxen and Paracetamol), Naproxeno + Paracetamol (Naproxen and Paracetamol), Naproxeno Andromaco, Naproxeno Base Nifa, Naproxeno Cinfa, Naproxeno Gel Nifa, Naproxeno Generis, Naproxeno Genfar, Naproxeno Germed, Naproxeno La Sante, Naproxeno MK, Naproxeno Normon, Naproxeno Pharma Genexx, Naproxeno Ratiopharm, Naproxeno Sodico, Naproxeno Sodico, Naproxeno Sodico L. CH. 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Tobrex - Fda Prescribing Information, Side Effects And Uses, Tobrafen

Tobrex

Tobrex ® (tobramycin ophthalmic solution) 0.3% is a sterile topical ophthalmic antibiotic formulation prepared specifically for topical therapy of external ophthalmic infections.

Each mL of Tobrex ® solution contains: Active: tobramycin 0.3% (3 mg). Preservative: benzalkonium chloride 0.01% (0.1 mg). Inactives: boric acid, sodium sulfate, sodium chloride, tyloxapol, sodium hydroxide and/or sulfuric acid (to adjust pH) and purified water. Tobrex ® (tobramycin ophthalmic solution) 0.3% has a pH range between 7.0 and 8.0 and an osmolality of 260-320 mOsm/kg.

Tobramycin is a water-soluble aminoglycoside antibiotic active against a wide variety of gram-negative and gram-positive ophthalmic pathogens.

The chemical structure of tobramycin is:

Molecular Weight = 467.52

Molecular Formula: C 18 H 37 N 5 O 9

CLINICAL PHARMACOLOGY

In Vitro Data: In vitro studies have demonstrated tobramycin is active against susceptible strains of the following microorganisms: Staphylococci, including S. aureus and S. epidermidis (coagulase-positive and coagulase-negative), including penicillin-resistant strains.

Streptococci, including some of the Group A-beta-hemolytic species, some nonhemolytic species, and some Streptococcus pneumoniae .

Pseudomonas aeruginosa, Escherichia coli, Klebsiella pneumoniae, Enterobacter aerogenes, Proteus mirabilis, Morganella morganii. most Proteus vulgaris strains, Haemophilus influenzae and H. aegyptius, Moraxella lacunata. Acinetobacter calcoaceticus and some Neisseria species. Bacterial susceptibility studies demonstrate that in some cases, microorganisms resistant to gentamicin retain susceptibility to tobramycin.

INDICATIONS AND USAGE

Tobrex ® (tobramycin ophthalmic solution) 0.3% is a topical antibiotic indicated in the treatment of external infections of the eye and its adnexa caused by susceptible bacteria. Appropriate monitoring of bacterial response to topical antibiotic therapy should accompany the use of Tobrex ®. Clinical studies have shown tobramycin to be safe and effective for use in children.

CONTRAINDICATIONS

Tobrex ® (tobramycin ophthalmic solution) 0.3% is contraindicated in patients with known hyper sensitivity to any of its components.

WARNINGS

FOR TOPICAL OPHTHALMIC USE ONLY. NOT FOR INJECTION INTO THE EYE. Sensitivity to topically applied aminoglycosides may occur in some patients. If a sensitivity reaction to Tobrex ® (tobramycin ophthalmic solution) 0.3% occurs, discontinue use.

PRECAUTIONS

General

As with other antibiotic preparations, prolonged use may result in overgrowth of nonsusceptible organisms, including fungi. If superinfection occurs, appropriate therapy should be initiated. Cross-sensitivity to other aminoglycoside antibiotics may occur; if hypersensitivity develops with this product, discontinue use and institute appropriate therapy. Patients should be advised not to wear contact lenses if they have signs and symptoms of bacterial ocular infection.

Information For Patients

Do not touch dropper tip to any surface, as this may contaminate the solution.

Pregnancy Category B

Reproduction studies in three types of animals at doses up to thirty-three times the normal human systemic dose have revealed no evidence of impaired fertility or harm to the fetus due to tobramycin. There are, however, no adequate and well-controlled studies in pregnant women. Because animal studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.

Nursing Mothers

Because of the potential for adverse reactions in nursing infants from Tobrex ®. a decision should be made whether to discontinue nursing the infant or discontinue the drug, taking into account the importance of the drug to the mother.

Pediatric Use

Safety and effectiveness in pediatric patients below the age of 2 months has not been established.

Geriatric Use

No overall differences in safety or effectiveness have been observed between elderly and younger patients.

ADVERSE REACTIONS

The most frequent adverse reactions to Tobrex ® Ophthalmic Solution are hypersensitivity and localized ocular toxicity, including lid itching and swelling, and conjunctival erythema. These reactions occur in less than three of 100 patients treated with Tobrex ®. Similar reactions may occur with the topical use of other aminoglycoside antibiotics. Other adverse reactions have not been reported from Tobrex ® (tobramycin ophthalmic solution) 0.3% therapy; however, if topical ocular tobramycin is administered concomitantly with systemic aminoglycoside antibiotics, care should be taken to monitor the total serum concentration.

OVERDOSAGE

Clinically apparent signs and symptoms of an overdose of Tobrex ® (tobramycin ophthalmic solution) 0.3% (punctate keratitis, erythema, increased lacrimation, edema and lid itching) may be similar to adverse reaction effects seen in some patients.

DOSAGE AND ADMINISTRATION

In mild to moderate disease, instill one or two drops into the affected eye(s) every four hours. In severe infections, instill two drops into the eye(s) hourly until improvement, following which treatment should be reduced prior to discontinuation.

HOW SUPPLIED

5 mL sterile solution is packaged in a 8 mL low density polyethylene white DROP-TAINER ® bottle and natural dispensing plug and white polypropylene closure (NDC 0065-0643-05) containing tobramycin 0.3% (3 mg/mL).

Storage: Store at 2° - 25°C (36° - 77°F).

Rx Only © 2000-2003, 2012 Novartis Revised: June 2012

ALCON LABORATORIES, INC. Fort Worth, Texas 76134 USA Printed in USA

PRINCIPAL DISPLAY PANEL

Tobrex ® (tobramycin ophthalmic solution) 0.3%

Ulcesep Generic Name Omeprazole Online, Ulcesep

Ulcesep General Information

Ulcesep - Pharmacology:

Ulcesep is a proton pump inhibitor that suppresses gastric acid secretion by specific inhibition of the H + /K + - ATPase in the gastric parietal cell. By acting specifically on the proton pump, omeprazole blocks the final step in acid production, thus reducing gastric acidity.

Ulcesep for patients

PRILOSEC Delayed-Release Capsules should be taken before eating. Patients should be cautioned that the PRILOSEC Delayed-Release Capsule should not be opened, chewed or crushed, and should be swallowed whole.

For patients who have difficulty swallowing capsules, the contents of a PRILOSEC Delayed-Release Capsule can be added to applesauce. One tablespoon of applesauce should be added to an empty bowl and the capsule should be opened. All of the pellets inside the capsule should be carefully emptied on the applesauce. The pellets should be mixed with the applesauce and then swallowed immediately with a glass of cool water to ensure complete swallowing of the pellets. The applesauce used should not be hot and should be soft enough to be swallowed without chewing. The pellets should not be chewed or crushed. The pellets/applesauce mixture should not be stored for future use.

This description is suitable for active ingredient Omeprazole

Ulcesep Interactions

Ulcesep can prolong the elimination of diazepam, warfarin and phenytoin, drugs that are metabolized by oxidation in the liver. Although in normal subjects no interaction with theophylline or propranolol was found, there have been clinical reports of interaction with other drugs metabolized via the cytochrome P-450 system ( e. g., cyclosporine, disulfiram, benzodiazepines). Patients should be monitored to determine if it is necessary to adjust the dosage of these drugs when taken concomitantly with omeprazole.

Because of its profound and long lasting inhibition of gastric acid secretion, it is theoretically possible that omeprazole may interfere with absorption of drugs where gastric pH is an important determinant of their bioavailability ( e. g., ketoconazole, ampicillin esters, and iron salts). In the clinical trials, antacids were used concomitantly with the administration of omeprazole.

Combination Therapy with Clarithromycin

Co-administration of omeprazole and clarithromycin may result in increases in plasma levels of ompeprazole, clarithromycin, and 14-hydroxy-clarithromycin.

Concomitant administration of clarithromycin with cisapride, pimozide, or terfenadine is contraindicated.

There have been reports of an intereaction between erythromycin and astemizole resulting in QT prolongation and torsades de points. Concomitant administration of erythromycin and astemizole is contraindicated. Because clarithromycin is also metabolized by cytochrome P450, concomitant administration of clarithromycin with astemizole is not recommended.

Ulcesep Contraindications

Imdur Uses, Dosage - Side Effects, Imbun

Imdur

Imdur (isosorbide mononitrate) belongs to a group of drugs called nitrates. Isosorbide mononitrate dilates (widens) blood vessels, making it easier for blood to flow through them and easier for the heart to pump.

Imdur is used to prevent angina attacks (chest pain).

Imdur will not treat an angina attack that has already begun.

Important information

Do not use Imdur if you are taking medicine to treat erectile dysfunction or pulmonary arterial hypertension (PAH). This includes sildenafil (Viagra, Revatio), avanafil (Stendra), tadalafil (Cialis, Adcirca), vardenafil (Levitra, Staxyn), and riociguat (Adempas). Serious, life-threatening side effects may occur.

You should not use Imdur if you have early signs of a heart attack (chest pain or heavy feeling, pain spreading to the arm or shoulder, nausea, sweating, general ill feeling).

Imdur will not treat an angina attack that has already begun.

Imdur can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use the medication. Do not stop taking Imdur. Ask your doctor before using any headache pain medication.

Use this medicine regularly to prevent an angina attack. Get your prescription refilled before you run out of medicine completely.

Do not stop taking Imdur suddenly. Stopping suddenly could cause a severe angina attack.

Before taking this medicine

Do not use Imdur if you are taking medicine to treat erectile dysfunction or pulmonary arterial hypertension (PAH). This includes sildenafil (Viagra, Revatio), avanafil (Stendra), tadalafil (Cialis, Adcirca), vardenafil (Levitra, Staxyn), and riociguat (Adempas). Serious, life-threatening side effects may occur.

You should not use Imdur if:

you are allergic to isosorbide mononitrate, isosorbide dinitrate, or nitroglycerin; or

you have early signs of a heart attack (chest pain or pressure, pain spreading to your jaw or shoulder, nausea, sweating).

To make sure Imdur is safe for you, tell your doctor if you have:

congestive heart failure;

low blood pressure; or

kidney disease (or if you are on dialysis);

if you take a diuretic or "water pill"; or

if you are on a low salt diet.

FDA pregnancy category C. It is not known whether Imdur will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant while using this medicine.

It is not known whether isosorbide mononitrate passes into breast milk or if it could harm a nursing baby. Tell your doctor if you are breast-feeding a baby.

How should I take Imdur?

Take Imdur exactly as prescribed by your doctor. Follow all directions on your prescription label. Your doctor may occasionally change your dose to make sure you get the best results. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Not all brands and forms of isosorbide mononitrate are taken the same number of times per day. You may need to take the medicine only once daily, in the morning after getting out of bed. Or you may need a second dose later in the day. Follow your doctor's dosing instructions very carefully.

If possible, try to rest or stay seated when you use this medicine. Imdur can cause dizziness or fainting.

Do not crush, chew, or break an extended-release tablet . Swallow it whole.

You may have very low blood pressure while taking this medicine. Call your doctor if you are sick with vomiting or diarrhea, or if you are sweating more than usual. Prolonged illness can lead to a serious electrolyte imbalance, making it dangerous for you to use Imdur.

Use Imdur regularly to prevent an angina attack. Get your prescription refilled before you run out of medicine completely.

You should not stop using Imdur suddenly if you take this medicine to prevent angina. Stopping suddenly may cause you to have a severe attack of angina.

Do not change brands of isosorbide mononitrate without the approval of your doctor.

Store at room temperature away from moisture, heat, and light. Keep the bottle tightly closed when not in use.

What happens if I miss a dose?

Take the missed dose as soon as you remember. Skip the missed dose if it is almost time for your next scheduled dose. Do not take extra medicine to make up the missed dose.

What happens if I overdose?

Seek emergency medical attention or call the Poison Help line at 1-800-222-1222. An overdose of isosorbide mononitrate can be fatal.

Overdose symptoms may include a severe throbbing headache, fever, confusion, severe dizziness, fast or pounding heartbeats, vision problems, nausea, vomiting, stomach pain, bloody diarrhea, trouble breathing, sweating, cold or clammy skin, fainting, and seizure (convulsions).

What should I avoid while taking Imdur?

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert.

Avoid getting up too fast from a sitting or lying position, or you may feel dizzy. Get up slowly and steady yourself to prevent a fall.

Drinking alcohol can increase certain side effects of Imdur.

Imdur side effects

Get emergency medical help if you have any of these signs of an allergic reaction to Imdur: hives; difficulty breathing; swelling of your face, lips, tongue, or throat.

Call your doctor at once if you have:

a light-headed feeling, like you might pass out;

worsening angina pain;

fast or slow heart rate; or

pounding heartbeats or fluttering in your chest.

Imdur can cause severe headaches, especially when you first start using it. These headaches may gradually become less severe as you continue to use this medicine. Do not stop taking this medicine to avoid headaches. Ask your doctor before using any headache pain medication.

Common Imdur side effects may include:

flushing (warmth, redness, or tingly feeling).

This is not a complete list of side effects and others may occur. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.

Imdur dosing information

Usual Adult Dose for Angina Pectoris Prophylaxis:

30-60 mg orally once a day

Usual Adult Dose for Congestive Heart Failure:

30-60 mg orally once a day.

What other drugs will affect Imdur?

Other drugs may interact with Imdur, including prescription and over-the-counter medicines, vitamins, and herbal products. Tell each of your health care providers about all medicines you use now and any medicine you start or stop using.

More about Imdur (isosorbide mononitrate)

Consumer resources

Professional resources

Related treatment guides

Where can I get more information?

Your pharmacist can provide more information about Imdur.

Remember, keep this and all other medicines out of the reach of children, never share your medicines with others, and use this medication only for the indication prescribed.

Disclaimer: Every effort has been made to ensure that the information provided by Cerner Multum, Inc. ('Multum') is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. Multum information has been compiled for use by healthcare practitioners and consumers in the United States and therefore Multum does not warrant that uses outside of the United States are appropriate, unless specifically indicated otherwise. Multum's drug information does not endorse drugs, diagnose patients or recommend therapy. Multum's drug information is an informational resource designed to assist licensed healthcare practitioners in caring for their patients and/or to serve consumers viewing this service as a supplement to, and not a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. Multum does not assume any responsibility for any aspect of healthcare administered with the aid of information Multum provides. The information contained herein is not intended to cover all possible uses, directions, precautions, warnings, drug interactions, allergic reactions, or adverse effects. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

Copyright 1996-2016 Cerner Multum, Inc. Version: 12.01. Revision Date: 2014-11-17, 9:49:38 AM.

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