Norflex Indications, Side Effects, Warnings, Norilet

Norflex

Short-term treatment of painful muscle conditions. It is used along with rest and physical therapy. It may also be used for other conditions as determined by your doctor.

Norflex is a skeletal muscle relaxant. It works by helping to decrease pain, which helps muscles to relax.

Do NOT use Norflex if:

you are allergic to any ingredient in Norflex

you have glaucoma, stomach or intestinal blockage, a stomach ulcer, a blockage of your bladder, certain esophagus problems (eg, blockage or trouble swallowing), enlargement of the prostate, or myasthenia gravis

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

Before using Norflex:

Some medical conditions may interact with Norflex. 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 (eg, sulfites)

if you have a history of heart problems (eg, fast or irregular heartbeat), stomach or bowel problems (eg, inflammation, enlarged colon), kidney or liver problems, increased eye pressure, or porphyria

if you have trouble urinating

Some MEDICINES MAY INTERACT with Norflex. Tell your health care provider if you are taking any other medicines, especially any of the following:

Potassium tablets or capsules because they may not be able to move through the stomach and bowel as well when taken with Norflex

Propoxyphene because confusion, anxiety, or tremors may occur

Phenothiazines (eg, chlorpromazine) because their effectiveness may be decreased by Norflex

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

How to use Norflex:

Use Norflex as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Norflex is usually given as an injection at your doctor's office, hospital, or clinic. If you will be using Norflex at home, a health care provider will teach you how to use it. Be sure you understand how to use Norflex. Follow the procedures you are taught when you use a dose. Contact your health care provider if you have any questions.

If Norflex contains particles or is discolored, or if the vial is cracked or damaged in any way, do not use it.

Keep this product, as well as syringes and needles, out of the reach of children and pets. Do not reuse needles, syringes, or other materials. Ask your health care provider how to dispose of these materials after use. Follow all local rules for disposal.

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

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

Important safety information:

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

If dizziness occurs, sit up or stand slowly, especially in the morning. Also, sit or lie down at the first sign of dizziness, lightheadedness, or weakness.

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

Some of these products contain sulfites, which can cause allergic reactions in certain individuals (eg, asthma patients). If you have previously had allergic reactions to sulfites, contact your pharmacist to determine if the product you are taking contains sulfites.

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

Use Norflex with caution in the ELDERLY; they may be more sensitive to its effects, especially confusion.

Norflex is not recommended for use in CHILDREN; safety and effectiveness have not been confirmed.

PREGNANCY and BREAST-FEEDING: If you become pregnant while taking Norflex, contact your doctor. You will need to discuss the benefits and risks of using Norflex while pregnant. It is not known if this medicine is found in breast milk. If you are or will be breast-feeding while you are using Norflex, check with your doctor. Discuss any possible risks to your baby.

Possible side effects of Norflex:

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:

Blurred vision; constipation; dizziness or lightheadedness; drowsiness; dry mouth; headache; nausea; stomach irritation or upset; vomiting; weakness.

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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); agitation, chills, fever, or sore throat; confusion; fainting; fast or irregular heartbeat; hallucinations; pain, swelling, or redness the injection site; severe or persistent tiredness or weakness; tremor; trouble urinating or inability to urinate; unusual bruising or bleeding; 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. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA .

If OVERDOSE is suspected:

Contact 1-800-222-1222 (the American Association of Poison Control Centers), your local poison control center. or emergency room immediately. Symptoms may include fainting; irregular heart rate; loss of consciousness; seizures.

Proper storage of Norflex:

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

General information:

If you have any questions about Norflex, please talk with your doctor, pharmacist, or other health care provider.

Norflex is to be used only by the patient for whom it is prescribed. Do not share it with other people.

If your symptoms do not improve or if they become worse, check with your doctor.

Check with your pharmacist about how to dispose of unused medicine.

This information should not be used to decide whether or not to take Norflex or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about Norflex. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to Norflex. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using Norflex.

Review Date: August 8, 2016

Disclaimer: This information should not be used to decide whether or not to take this medicine or any other medicine. Only your health care provider has the knowledge and training to decide which medicines are right for you. This information does not endorse any medicine as safe, effective, or approved for treating any patient or health condition. This is only a brief summary of general information about this medicine. It does NOT include all information about the possible uses, directions, warnings, precautions, interactions, adverse effects, or risks that may apply to this medicine. This information is not specific medical advice and does not replace information you receive from your health care provider. You must talk with your healthcare provider for complete information about the risks and benefits of using this medicine.

More about Norflex (orphenadrine)

Buy Toraseptol - Fda Approved Prescription Drug At, Toraseptol

FAQ. How to buy Toraseptol without Prescription Drugs? Q. Where is your drugstore situated? A. We have branches all over the world: in the south of the Pacific ocean, Europe and Middle East. All will depend on Toraseptol which you have ordered, manufacturer and from the wholesale seller who delivers Toraseptol.

Q. How long it will take to get my Toraseptol order? A. All Toraseptol orders are sent by air mail. It is the most reliable kind of post transfer. Usually it takes about 9-26 days to receive the order. If the order is not received by you within 29 days, address us and we shall send the order again.

Q. Do I need a Toraseptol prescription to order a medicine? A. No, you do not. The recipe on Toraseptol is not necessary for you. We work under the laws of those countries from which we make dispatches.

Q. Do you guarantee the delivery of the Toraseptol order? A. We guarantee the delivery of all Toraseptol orders. If do not receive the Toraseptol order within 29 days (about 1 % of orders will be lost at the post office), we shall send a new order free of charge.

Q. What countries do you not send Toraseptol in? A. Now we do not send Toraseptol orders to Germany, Canada and Australia.

Q. Whether my signature is necessary at the receipt of the order? A. Yes. Your signature is required when the Toraseptol order is delivered. We also advise to you to get reliable post-box.

Q. Why are the prices on Toraseptol so low? A. We buy big sets of prescription drugs from the manufacturers or very large distributors. We have a great volume of sales and it allows us to hold our low price level. Therefore we have made a reliable and free of charge transfer of medicines.

Q. How can I Toraseptol order? A. It is very simple. Find a product which you want to order and press the button "To add in a basket ". Then fill in the information on your credit card and write your address. We shall check up the details of your credit card and then the Toraseptol order will be sent to you. We guarantee 100 % safety of the information of your credit card. We can deliver Toraseptol to any address. You will receive e-mail after we have sent your order.

Provanax Reviewed Does Provanax Work, Pravanox

ProVanax Reviewed: Does ProVanax Work?

ProVanax Overview

ProVanx is an all natural herbal. ProVanax is formulated from “safe and clinically shown” ingredients. This supplement is sold and promoted through its official website where a large number of user experience stories are currently featured. However, determining the price of this supplement is difficult, since the price is not prominently displayed on this website.

ProVanax The Product Details

ProVanax is made up of herbs, vitamins, and amino acids. ProVanax contains the following ingredients in its all natural formula: Magnesium oxide, Phenibut, 5-HTP 5 Hydroxytryptophan, St. John’s Wort, Passion Flower, L-Theanine, Valerian, Inositol, L-Taurine, Kava Kava Extract 10:1 Extract, GABA (Gamma-Amino-Butyric Acid), plant-derived cellulose gelatin, rice flour, magnesium stearate, silicon, and water.

The recommended dosage for ProVanax is also dependent upon its intended use, and consumers can find details about this on the official product website.

Strengths of ProVanax

There are many positive user reviews for this supplement.

A timeline for when results should be expected is provided online.

All of the ingredients are featured on the product’s website.

ProVanax is a relatively fast-acting supplement.

This product is endorsed by a satisfaction protection plan.

Weaknesses of ProVanax

Pricing information could not be easily determined through the ProVanax homepage.

Clinical studies do not appear to have been conducted on ProVanax itself.

ProVanax The Bottom Line

While ProVanax might very well be an excellent supplement, the fact that pricing information is not easily locatable on the official product website is very frustrating. Without this information it is impossible to determine the overall value of ProVanax — an issue that is a huge factor in determining whether or not ProVanax should be recommended as an ideal supplement.

A note to our readers: LegitScript was sourced in the gathering of information for this product overview. LegitScript is a verification and monitoring service that has found that this product may be the subject of regulatory action or marketed by unsupported claims.

**This is a subjective assessment based on the strength of the available information and our estimation of efficacy.

*Results may vary. If you are pregnant, nursing, have a serious medical condition, or have a history of heart conditions we suggest consulting with a physician before using any supplement. The information contained in this website is provided for general informational purposes only. It is not intended to diagnose, treat*, cure, or prevent any disease and should not be relied upon as medical advice. Always consult your doctor before using any supplements.

Disclosure of Material Connection: Some of the links in the post above are "associate sales links." This means if you click on the link and purchase an item, we will receive a commission. Regardless, we only recommend products or services which we use personally and/or believe will add value to our readers. We are disclosing this in accordance with the Federal Trade Commission’s 16 CFR, Part 255: "Guides Concerning the Use of Endorsements and Testimonials."

All of the content appearing on our website is produced, selected, and reviewed by talented and experienced health writers and editors. We focus on providing promoting valuable health information and savings on health-related products and solutions for better managing your health. We have one mission, and one mission only: to help you live a healthier, longer life.

Disclaimer: © 2016 All Rights Reserved. The information provided on this site is intended for your general knowledge only and is not a substitute for professional medical advice or treatment for specific medical conditions. You should not use this information to diagnose or treat* a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Your use of this website indicates your agreement to this websites published terms of use and all site policies. All trademarks, registered trademarks and service-marks mentioned on this site are the property of their respective owners.

Copyright ©2016 DailyHealthAnswers. com. All Rights Reserved.

Dovonex Ointment - Fda Prescribing Information, Side Effects And Uses, Doxonex

Dovonex Ointment

FOR TOPICAL DERMATOLOGIC USE ONLY.

Not for Ophthalmic, Oral or Intravaginal Use.

Dovonex Ointment Description

Dovonex ® (calcipotriene ointment), 0.005% contains the compound calcipotriene, a synthetic vitamin D 3 derivative, for topical dermatological use.

Chemically, calcipotriene is (5Z,7E,22E,24S)-24-cyclopropyl-9,10-secochola-5,7,10(19), 22-tetraene-1α,3β,24-triol-, with the empirical formula C 27 H 40 O 3. a molecular weight of 412.6, and the following structural formula:

Calcipotriene is a white or off-white crystalline substance. Dovonex ® ointment contains calcipotriene 50 μg/g in an ointment base of dibasic sodium phosphate, edetate disodium, mineral oil, petrolatum, propylene glycol, tocopherol, steareth-2 and water.

Dovonex Ointment - Clinical Pharmacology

In humans, the natural supply of vitamin D depends mainly on exposure to the ultraviolet rays of the sun for conversion of 7-dehydrocholesterol to vitamin D 3 (cholecalciferol) in the skin. Calcipotriene is a synthetic analog of vitamin D 3 .

Clinical studies with radiolabelled calcipotriene ointment indicate that approximately 6% (± 3%, SD) of the applied dose of calcipotriene is absorbed systemically when the ointment is applied topically to psoriasis plaques or 5% (± 2.6%, SD) when applied to normal skin, and much of the absorbed active is converted to inactive metabolites within 24 hours of application.

Vitamin D and its metabolites are transported in the blood, bound to specific plasma proteins. The active form of the vitamin, 1,25-dihydroxy vitamin D 3 (calcitriol), is known to be recycled via the liver and excreted in the bile. Calcipotriene metabolism following systemic uptake is rapid, and occurs via a similar pathway to the natural hormone. The primary metabolites are much less potent than the parent compound.

There is evidence that maternal 1,25-dihydroxy vitamin D 3 (calcitriol) may enter the fetal circulation, but it is not known whether it is excreted in human milk. The systemic disposition of calcipotriene is expected to be similar to that of the naturally occurring vitamin.

Clinical Studies

Adequate and well-controlled trials of patients treated with Dovonex ® ointment have demonstrated improvement usually beginning after two weeks of therapy. This improvement continued in patients using Dovonex ® once daily and twice daily. After 8 weeks of once daily Dovonex ®. 56.7% of patients showed at least marked improvements (6.4% showed complete clearing). After 8 weeks of twice daily Dovonex ®. 70.0% of patients showed at least marked improvement (11.3% showed complete clearing).

Subtracting percentages of patients using placebo (vehicle only) from percentages of patients using Dovonex ® who had at least marked improvements after 8 weeks yields 39.9% for once daily and 49.6% for twice daily. This adjustment for placebo effect indicates that what might appear to be differences between once daily and twice daily use may reflect differences in the studies independent from the frequency of dosing. Although there was a numerical difference in comparison across studies, twice daily dosing has not been shown to be superior in efficacy to once daily dosing.

Over 400 patients have been treated in open label clinical studies of Dovonex ® for periods of up to one year. In half of these studies, patients who previously had not responded well to Dovonex ® were excluded. The adverse events in these extended studies included skin irritation in approximately 25% of patients and worsening of psoriasis in approximately 10% of patients. In one of these open label studies, half of the patients no longer required Dovonex ® by 16 weeks of treatment, because of satisfactory therapeutic results.

Indications and Usage for Dovonex Ointment

Dovonex ® (calcipotriene ointment), 0.005%, is indicated for the treatment of plaque psoriasis in adults. The safety and effectiveness of topical calcipotriene in dermatoses other than psoriasis have not been established.

Contraindications

Dovonex ® is contraindicated in those patients with a history of hypersensitivity to any of the components of the preparation. It should not be used by patients with demonstrated hypercalcemia or evidence of vitamin D toxicity. Dovonex ® should not be used on the face.

Precautions

General

Use of Dovonex ® may cause irritation of lesions and surrounding uninvolved skin. If irritation develops, Dovonex ® should be discontinued.

For external use only. Keep out of the reach of children. Always wash hands thoroughly after use.

Transient, rapidly reversible elevation of serum calcium has occurred with use of Dovonex ®. If elevation in serum calcium outside the normal range should occur, discontinue treatment until normal calcium levels are restored.

Information for Patients

Patients using Dovonex ® should receive the following information and instructions:

This medication is to be used as directed by the physician. It is for external use only. Avoid contact with the face or eyes. As with any topical medication, patients should wash hands after application.

This medication should not be used for any disorder other than that for which it was prescribed.

Patients should report to their physician any signs of local adverse reactions.

Patients that apply Dovonex ® to exposed portions of the body should avoid excessive exposure to either natural or artificial sunlight (including tanning booths, sun lamps, etc.).

Carcinogenesis, Mutagenesis, Impairment of Fertility

When calcipotriene was applied topically to mice for up to 24 months at dosages of 3, 10 and 30 µg/kg/day (corresponding to 9, 30 and 90 µg/m 2 /day), no significant changes in tumor incidence were observed when compared to control. In a study in which albino hairless mice were exposed to both UVR and topically applied calcipotriene, a reduction in the time required for UVR to induce the formation of skin tumors was observed (statistically significant in males only), suggesting that calcipotriene may enhance the effect of UVR to induce skin tumors. Patients that apply Dovonex ® to exposed portions of the body should avoid excessive exposure to either natural or artificial sunlight (including tanning booths, sun lamps, etc.). Physicians may wish to avoid use of phototherapy in patients that use Dovonex ® .

Calcipotriene did not elicit any mutagenic effects in an Ames mutagenicity assay, a mouse lymphoma TK locus assay, a human lymphocyte chromosome aberration assay, or in a micronucleus assay conducted in mice.

Studies in rats at doses up to 54 μg/kg/day (324 μg/m 2 /day) of calcipotriene indicated no impairment of fertility or general reproductive performance.

Pregnancy

Teratogenic effects: Pregnancy Category C

Studies of teratogenicity were done by the oral route where bioavailability is expected to be approximately 40-60% of the administered dose. In rabbits, increased maternal and fetal toxicity were noted at a dosage of 12 μg/kg/day (132 μg/m 2 /day); a dosage of 36 μg/kg/day (396 μg/m 2 /day) resulted in a significant increase in the incidence of incomplete ossification of the pubic bones and forelimb phalanges of fetuses. In a rat study, a dosage of 54 μg/kg/day (318 μg/m 2 /day) resulted in a significantly increased incidence of skeletal abnormalities (enlarged fontanelles and extra ribs). The enlarged fontanelles are most likely due to calcipotriene's effect upon calcium metabolism. The estimated maternal and fetal no-effect exposure levels in the rat (43.2 μg/m 2 /day) and rabbit (17.6 μg/m 2 /day) studies are approximately equal to the expected human systemic exposure level (18.5 μg/m 2 /day) from dermal application. There are no adequate and well-controlled studies in pregnant women. Therefore, Dovonex ® ointment should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.

Nursing Mothers

It is not known whether calcipotriene is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when Dovonex ® (calcipotriene ointment), 0.005% is administered to a nursing woman.

Pediatric Use

Safety and effectiveness of Dovonex ® in pediatric patients have not been established. Because of a higher ratio of skin surface area to body mass, pediatric patients are at greater risk than adults of systemic adverse effects when they are treated with topical medication.

Geriatric Use

Of the total number of patients in clinical studies of calcipotriene ointment, approximately 12% were 65 or older, while approximately 4% were 75 and over. The results of an analysis of severity of skin-related adverse events showed a statistically significant difference for subjects over 65 years (more severe) compared to those under 65 years (less severe).

Adverse Reactions

In controlled clinical trials, the most frequent adverse reactions reported for Dovonex ® were burning, itching and skin irritation, which occurred in approximately 10-15% of patients. Erythema, dry skin, peeling, rash, dermatitis, worsening of psoriasis including development of facial/scalp psoriasis were reported in 1 to 10% of patients. Other experiences reported in less than 1% of patients included skin atrophy, hyperpigmentation, hypercalcemia, and folliculitis. Once daily dosing has not been shown to be superior in safety to twice daily dosing.

Overdosage

Topically applied Dovonex ® can be absorbed in sufficient amounts to produce systemic effects. Elevated serum calcium has been observed with excessive use of Dovonex ® ointment.

Dovonex Ointment Dosage and Administration

Apply a thin layer of Dovonex ® ointment once or twice daily and rub in gently and completely.

How is Dovonex Ointment Supplied

Dovonex ® (calcipotriene ointment), 0.005% is available in:

60 gram aluminum tubes N 0430-3010-15 120 gram aluminum tubes N 0430-3010-17

STORAGE

Store at controlled room temperature 15° C - 25° C (59° F - 77° F). Do not freeze.

Manufactured by LEO Laboratories Ltd. Dublin, Ireland

Warner Chilcott (US), Inc. Rockaway, NJ 07866 USA 1-800-521-8813

3010G061 Revised November 2007

CARTON IMAGE - Dovonex 0.005% 60g

(calcipotriene ointment), 0.005%

WARNING: Keep Out of Reach of Children.

For Topical Dermatologic Use Only.

Not for Ophthalmic, Oral or Intravaginal Use.

Usual Dosage: Apply twice daily, or as directed by physician. See insert for complete information.

Read all Panels.

Each gram contains 0.05mg of calcipotriene in an ointment base of dibasic sodium phosphate, edetate disodium, mineral oil, petrolatum, propylene glycol, tocopherol, steareth-2 and water.

Store at controlled room temperature 15 o C - 15 o C (59 o F - 77 o F).

Lot no. and expiration date on carton end and crimp of tube.

CARTON IMAGE - Dovonex 0.005% 120g

(calcipotriene ointment), 0.005%

WARNING: Keep Out of Reach of Children.

For Topical Dermatologic Use Only.

Not for Ophthalmic, Oral or Intravaginal Use.

Usual Dosage: Apply twice daily, or as directed by physician. See insert for complete information.

Read all Panels.

Each gram contains 0.05mg of calcipotriene in an ointment base of dibasic sodium phosphate, edetate disodium, mineral oil, petrolatum, propylene glycol, tocopherol, steareth-2 and water.

Store at controlled room temperature 15 o C - 15 o C (59 o F - 77 o F).

Lot no. and expiration date on carton end and crimp of tube.

Apoprin - ?Tu Colega Siempre En Linea, Apoprin

APOPRIN

APOPRIN TABLETAS Antiulceroso APOTEX (PROTEIN, S. A. de C. V.) .

- FORMA FARMACEUTICA Y FORMULACION - INDICACIONES TERAPEUTICAS - FARMACOCINETICA Y FARMACODINAMIA EN HUMANOS - CONTRAINDICACIONES - PRECAUCIONES O RESTRICCIONES DE USO DURANTE EL EMBARAZO O LA LACTANCIA - REACCIONES SECUNDARIAS Y ADVERSAS - INTERACCIONES MEDICAMENTOSAS Y DE OTRO GENERO - ALTERACIONES DE PRUEBAS DE LABORATORIO - PRECAUCIONES Y RELACION CON EFECTOS DE CARCINOGENESIS, MUTAGENESIS, TERATOGENESIS Y SOBRE LA FERTILIDAD - DOSIS Y VIA DE ADMINISTRACION - SOBREDOSIFICACION O INGESTA ACCIDENTAL: MANIFESTACIONES Y MANEJO (ANTIDOTOS) - PRESENTACIONES - RECOMENDACIONES PARA ALMACENAMIENTO - LEYENDAS DE PROTECCION - NOMBRE DEL LABORATORIO Y DIRECCION - NUMERO DE REGISTRO DEL MEDICAMENTO

FORMA FARMACEUTICA Y FORMULACION: Cada tableta contiene:

Clorhidrato de ranitiaina equivalente a. 150 mg de ranitidina base Clorhidrato de ranitidina equivalente a. 300 mg de ranitidina base Excipiente c. b.p. 1 tableta

INDICACIONES TERAPEUTICAS: Tratamiento de la ulcera duodenal activa y en la prevencion de la ulcera duodenal recurrente. En el tratamiento de la ulcera gastrica activa benigna. En el tratamiento de la hipersecrecion gastrica. En el tratamiento del sindrome de Zollinger-Ellison.

En el tratamiento de la hipersecrecion gastrica asociada a la neoplasia endocrina multiple tipo-1. En el tratamiento de la enfermedad por reflujo gastroesofagico. Se ha usado en el tratamiento del sangrado del tubo digestivo alto (secundario a ulcera gastrica, ulcera duodenal o gastritis hemorragica).

En la profilaxis y tratamiento del sangrado del tubo digestivo alto inducido por estres, especialmente en pacientes graves con cuidados intensivos.

En la profilaxis de la neumonitis posaspiracion (sindrome de Mendelson) en la anestesia.

FARMACOCINETICA Y FARMACODINAMIA EN HUMANOS: APOPRIN es rapidamente absorbido despues de su administracion oral por lo que su biodisponibilidad es rapida, de 39 a 87%. La presencia de alimento no afecta su absorcion. Su union a proteinas es baja (15%). Su biotransformacion es a traves del higado. Su vida media de eliminacion por via oral es de 2.5 horas y parenteral de 2 a 2.5 horas. En insuficiencia renal con depuracion de creatinina entre 20 a 30 ml/min es de 8 a 9 horas por via oral y con depuracion de creatinina entre 25 a 35 ml/min es de 4.8 horas por via parenteral.

Su concentracion serica promedio para inhibir la secrecion gastrica al 50% posestimulacion con pentagastrina es de 100 mg/ml. El pico maximo de concentracion despues de una dosis oral es de 2 a 3 horas. Por via oral el tiempo necesario para su efecto maximo es de 1 a 3 horas. La duracion de su accion despues de una dosis nocturna es de 13 horas. Su eliminacion renal sin cambios despues de una dosis oral es de 30% y parenteral es de 70%.

Su mecanismo de accion es a traves de ser un antagonista de los receptores H2 con lo que inhibe la secrecion gastrica basal y nocturna por inhibir por competencia la accion de la histamina en los receptores H2 de las celulas parietales. APOPRIN tambien inhibe la secrecion gastrica estimulada por alimentos, betazol, pentagastrina, cafeina, insulina y el reflejo fisiologico vagal. La ranitidina es un leve inhibidor del sistema de la enzima citocromo P450 y por lo tanto produce pequenas y transitorias elevaciones de la prolactina serica que clinicamente son insignificantes.

Todos los antagonistas de los receptores H2 pasan a la leche materna.

CONTRAINDICACIONES: APOPRIN esta contraindicado en la cirrosis hepatica con encefalopatia secundaria. Tambien en la insuficiencia hepatica y renal. En estos casos la ranitidina aumenta sus concentraciones en plasma y asi, el riesgo de efectos colaterales, especialmente sobre el SNC, por lo que debe reducirse su posologia en dichas entidades clinicas.

APOPRIN esta contraindicado cuando hay antecedentes de hipersensibilidad a otros antagonistas de los receptores H2.

En su administracion prolongada, deben hacerse determinaciones periodicas de cianocobalamina (vitamina B12) por la posibilidad de inhibir la secrecion del factor intrinseco sobre todo en casos de gastritis de fundus gastrico para prevenir la mala absorcion de cianocobalamina.

PRECAUCIONES O RESTRICCIONES DE USO DURANTE EL EMBARAZO O LA LACTANCIA: Estudios en ratas y conejos con dosis mayores a 160 veces la dosis recomendada en humanos no han reportado reacciones adversas en el feto.

En humanos no se han reportado problemas en la lactancia; sin embargo, la ranitidina es excretada en la leche materna, por lo que existe la posibilidad de inhibir la acidez gastrica, inhibir el metabolismo de ciertos farmacos y estimulaciones del SNC en el nino lactando.

REACCIONES SECUNDARIAS Y ADVERSAS: Su administracion intramuscular puede causar dolor en el sitio de la aplicacion. La administracion intravenosa puede causar sensacion de quemadura y ardor. En ensayos clinicos se han reportado los siguientes efectos colaterales, sin embargo, su relacion con ranitidina no esta bien establecida.

SNC: Son raros; malestar general, mareo, somnolencia, insomnio y vertigo; confusion mental, agitacion, depresion y alucinaciones principalmente en ancianos. Vision borrosa sugestiva de cambios en la acomodacion.

Cardiovascular: Como con otros antagonistas de los receptores H2, se han reportado taquicardia, bradicardia, asistolia, bloqueo auriculoventricular y extrasistoles.

Gastrointestinal: Estrenimiento, diarrea, nauseas, vomito, malestar abdominal, dolor abdominal y reportes excepcionales de pancreatitis.

Hepaticos: En voluntarios normales, elevacion de la TGPS en 6 de 12 sujetos que recibieron 100 mg cada 6 horas por via intravenosa por 7 dias y en 4 de 24 sujetos que recibieron 50 mg c/6 horas por via intravenosa por 5 dias. Reportes ocasionales de hepatitis con dano hepatocelular o hepatocanalicular o mixta, con o sin ictericia. En estos casos la ranitidina debe ser suspendida inmediatamente.

Esto es reversible, pero hay reportes de muerte.

Musculoesqueletico: Casos raros de artralgias.

Hematologicos: En algunos pacientes se han presentado leucopenia, agranulocitosis y trombocitopenia. Tambien casos raros de agranulocitosis con pancitopenia e hipoplasia de medula osea.

Endocrino: En estudios controlados en animales y en el hombre no se ha demostrado estimulacion de hormonas hipofisiarias, ni accion antiandrogenica, ni ginecomastia, ni impotencia. Sin embargo, se han reportado casos raros de pacientes con ginecomastia, impotencia y perdida de la libido; pero su incidencia no difiere de la encontrada en la poblacion general.

Tegumentos: Eritema, incluyendo eritema multiforme y rara vez alopecia.

Otros: Hipersensibilidad (broncospasmo, fiebre, urticaria, eosinofilia), anafilaxia, edema angioneurotico y elevaciones pequenas de creatinina.

INTERACCIONES MEDICAMENTOSAS Y DE OTRO GENERO: Los antiacidos usados concomitantemente pueden ser utiles para disminuir el dolor de la ulcera peptica, sin embargo, su abuso puede disminuir la absorcion de los antagonistas de los receptores H2.

El uso simultaneo con ketoconazol puede alterar su absorcion y reducirse por el aumento del pH gastrico.

La alteracion potencial del sistema enzimatico del citocromo P450, puede alterar el metabolismo hepatico de ciertos farmacos y retardar su eliminacion y por lo tanto aumentar sus niveles sanguineos; glipicida, gliburonide, metoprolol, midazolam, nifedipina, fenilhidantoina, teofilina o warfarinicos. La procainamida aumenta sus niveles sanguineos al disminuir su eliminacion tubular renal activa por competencia.

ALTERACIONES DE PRUEBAS DE LABORATORIO: Antagoniza las pruebas de pentagastrina e histamina para evaluar la funcion secretora gastrica. Puede inhibir la respuesta cutanea a pruebas de alergenos. Hay una reaccion falsa-positiva en las reacciones urinarias para presencia de proteinas. Pueden aparecer incrementadas las pruebas para creatinina, glutamil-transpeptidasa y transaminasas en suero.

PRECAUCIONES Y RELACION CON EFECTOS DE CARCINOGENESIS, MUTAGENESIS, TERATOGENESIS Y SOBRE LA FERTILIDAD: Estudios a largo plazo en ratones y ratas con dosis hasta de 2 g/kg de peso no han demostrado carcinogenesis. No hay reportes de que los antagonistas de los receptores H2 sean mutagenicos en humanos.

Estudios en ratas y conejos con dosis hasta 160 veces mayores que la dosis recomendada en humanos no han alterado la fertilidad.

DOSIS Y VIA DE ADMINISTRACION:

o Ulcera duodenal: 150 mg cada 12 horas o 300 mg al acostarse.

o Profilaxis de la ulcera duodenal recurrente: 150 mg @t acoVtarse.

o Ulcera gastrica benigna activa: 150 mg c/12 horas.

La dosis debe ajustarse si hay necesidad y mantenerse mientras esta indicada.

Pueden usarse dosis hasta de 6 g/dia en casos graves. En pacientes con dano renal 150 mg/24 horas. Se debe reducir la dosis si hay evidencia previa de alteracion de la funcion hepatica.

o En ninos: 2 a 4 mg/kg de peso corporal cada 12 horas hasta una dosis maxima de 300 mg al dia.

o En ancianos: La dosis usual para adulto.

Via de administracion: Oral.

SOBREDOSIFICACION O INGESTA ACCIDENTAL: MANIFESTACIONES Y MANEJO (ANTIDOTOS): No hay experiencia hasta la fecha, en la ingestion excesiva voluntaria. Se debe emplear monitoreo clinico y tratamiento de apoyo al paciente. Estudios en perros que han recibido dosis de ranitidina mayores de 225 mg/kg/dia han demostrado temblor, vomito y polipnea. Dosis unicas de 1,000 mg/kg en ratones y ratas no fueron letales. La dosis letal media (DL50) en ratones y ratas, ha sido de 77 a 83 mg/kg respectivamente.

Caja con 10 tabletas de 300 mg.

Caja con 20 tabletas de 150 mg.

Frasco con 100 tabletas de 150 y 300 mg.

RECOMENDACIONES PARA ALMACENAMIENTO: Conservese entre 15 y 30°C, en un frasco bien cerrado y protegido de la luz.

LEYENDAS DE PROTECCION: Literatura exclusiva para medicos. No se deje al alcance de los ninos. Su venta requiere receta medica. El empleo de este medicamento durante el embarazo y la lactancia queda bajo responsabilidad del medico.

NOMBRE DEL LABORATORIO Y DIRECCION: PROTEIN, S. A. de C. V. Anil No. 865 Colonia Granjas Mexico 08400 Mexico, D. F.

NUMERO DE REGISTRO DEL MEDICAMENTO: Reg. Num. 070M92, S. S. A. IEAR-25924/96/IPPA

Luften, Luften

Luften

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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I luften finns det massor med gasmolekyler som flyger runt. Mest finns det av en gas som heter kväve. Nästan fyra femtedelar, 78 %, av luften består av kväve. Kväve varken smakar eller luktar. Den kemiska beteckningen är N, men kvävemolekylerna brukar sitta ihop två och två. De gillar inte att flyga ensamma, så oftast skriver man N2. Om man har kväve där det är riktigt kallt, ungefär -200 grader, så blir kvävet flytande. Men så kallt blir det ju aldrig ute som tur är.

Den allra viktigaste gasen i luften är syre. Den behöver alla däggdjur och drakar för att överleva. 21 %, ca en femtedel, av luften är syre. Den kemiska beteckningen för syre är O, men syreatomerna sitter också ihop två och två, så vanligen skriver man O2.

Sen finns det lite ädelgaser i luften också. Argon heter en och den gillar att flyga ensam. Ca 1 % av luften består av argon. Den kemiska beteckningen för argon är Ar.

Sen finns det massor med skräp i luften också, som bilar sprutar ut. Den luften är inte riktigt lika bra. Men bilarna är bra på att rena sina avgaser numera och bättre blir det.

PS. % betyder procent och är en hundradel, 1 % = 1/100

Delaware Tax-Free Pa Fund (Delix), Delix

Delaware Tax-Free PA Fund

About DELIX

The investment seeks as high a level of current income exempt from federal income tax and from Pennsylvania state personal income tax as is consistent with preservation of capital. Under normal circumstances, the fund will invest at least 80% of its net assets, plus the amount of any borrowings for investment purposes, in securities that provide income that is exempt from federal income tax, including the federal alternative minimum tax, and the personal income taxes of the Commonwealth of Pennsylvania. It will invest its assets in securities with maturities of various lengths, depending on market conditions.

Rankings

U. S. News evaluated 77 Muni Pennsylvania Funds. Our list highlights the top-rated funds for long-term investors based on the ratings of leading fund industry researchers.

DELIX is listed as:

Scorecard

Trailing Total Returns Monthly

Barclays Municipal TR USD

Performance

The fund has returned 7.43 percent over the past year, 5.89 percent over the past three years, 5.56 percent over the past five years, and 4.96 percent over the past decade.

Fees

Fees are Below Average compared to funds in the same category. Delaware Tax-Free PA Fund has an expense ratio of 0.89 percent.

Net Expense Ratio

Category average: 0.98

Category average: 0.47

Risk

Risk is Above Average compared to funds in the same category according to Morningstar.

Volatility Measurements

Volitility measures reflect the uncertainty or risk of change in a security's value.

Standard Deviation. 3.068

Dimitone Generic Name Dapsone Online, Dimitone

Dimitone General Information

Dimitone - Pharmacology:

Dimitone acts against bacteria and protozoa in the same way as sulphonamides, that is by inhibiting the synthesis of dihydrofolic acid through competition with para-amino-benzoate for the active site of dihydropteroate synthetase. The anti-inflammatory action of the drug is unrelated to its antibacterial action and is still not fully understood.

Dimitone for patients

1. Patients should use ACZONE ® Gel, 5%, as directed by the physician. ACZONE ® Gel, 5%, is for external topical use only. ACZONE ® Gel, 5%, is not for oral, ophthalmic or intravaginal use.

2. Patients should not use this medication for any disorder other than that for which it was prescribed.

3. Patients should tell their physician if they have any history of anemia or an enzyme deficiency (such as G6PD deficiency).

4. Patients should be informed as to the need for laboratory evaluation prior to starting ACZONE ® Gel, 5%.

5. Patients should report any signs of adverse reactions to their physician.

6. Protect ACZONE ® Gel, 5%, from freezing and light. Return to the original carton after application to protect from light.

PATIENT INSERT

ACZONE ® (dapsone) Gel 5%

Read this important information before you start using ACZONE ® (AK-zon) Gel and each time you refill your prescription. There may be new information that you need to know. This summary is not meant to take the place of your doctoris advice. If you have any questions or want more information about ACZONE ® Gel, ask your doctor or pharmacist.

What is ACZONE ® Gel?

ACZONE ® Gel is a prescription skin use (topical) medicine used to help treat acne in people 12 years and older.

ACZONE ® Gel has not been studied in children under 12 years of age.

Who should not use ACZONE ® Gel?

Do not use ACZONE ® Gel if you are allergic any of the ingredients in ACZONE ® Gel. Ask your doctor or pharmacist for a list of these ingredients. The active ingredient is dapsone. See the end of this leaflet for a complete list of ingredients in ACZONE ® Gel.

What should I tell my doctor before using ACZONE ® Gel?

Tell your doctor about all of your medical conditions, including if you:

· are pregnant or planning to become pregnant. It is not known if ACZONE Gel may harm your unborn baby.

· are breastfeeding. ACZONE ® Gel passes into your milk and may harm your baby. You should choose either to use ACZONE ® Gel, or breastfeed, but not both. Talk to you doctor about the best way to feed your baby while using ACZONE ® Gel.

· have a history of anemia or have been diagnosed with glucose-6-phosphate dehydrogenase deficiency

Tell your doctor about all the medicines you are taking including prescription and nonprescription medicines, vitamins and herbal supplements. Especially, tell your doctor if you are using any other medicines applied to the skin.

How do I use ACZONE ® Gel?

· Use ACZONE ® Gel exactly as prescribed by your doctor. ACZONE ® Gel is usually used on your affected skin twice a day, once in the morning and once in the evening.

· Wash the areas of your skin where you will apply ACZONE ® Gel. Gently pat your skin dry with a clean towel.

· Apply a thin layer of ACZONE ® Gel to the areas of your skin that have acne. A pea - sized amount of ACZONE ® Gel will usually be enough.

· Rub the medicine in gently and completely

· Make sure to put the cap back on the ACZONE ® Gel tube. Close it tightly and put the tube back in its original box.

· Wash your hands after applying ACZONE ® Gel.

· Keep ACZONE ® Gel away from your mouth and eyes. Do not swallow ACZONE ® Gel. If you swallow ACZONE ® Gel, call your doctor or poison control center right away.

· If your acne does not get better after using ACZONE ® for 12 weeks, talk to your doctor about other treatments for acne.

What are the possible side effects of ACZONE ® Gel?

Like all medicines, ACZONE ® Gel can cause some side effects. These side effects are usually mild. The most common side effects of ACZONE ® Gel are dryness, redness, oiliness and peeling of the skin being treated.

Call your doctor if you have excessive tiredness or any side effects that do not go away or bother you. This is not a complete list of all the side effects. If you have any questions, ask your doctor or pharmacist.

How should I store ACZONE ® Gel?

Store ACZONE ® Gel at room temperature 68 to 76 ?F. Do not freeze ACZONE ® Gel. Protect ACZONE ® Gel tube from light. Store in original box after using it.

Keep ACZONE ® Gel out of the reach of children less than 12 years of age.

Where can I find more information about ACZONE ® Gel?

If you have any questions or want more information about ACZONE ® Gel, ask your doctor or pharmacist. Your doctor or pharmacist can also give you a copy of the ACZONE ® Gel Package Insert written for health professionals. Ask them to explain anything you do not understand.

You may call 1-800-727-7003 to obtain more information about ACZONE ® Gel.

This description is suitable for active ingredient Dapsone

Dimitone Interactions

A drug-drug interaction study evaluated the effect of the use of ACZONE Gel, 5%, in combination with double strength (160 mg/800 mg) trimethoprim/sulfamethoxazole (TMP/SMX). During co-administration, systemic levels of TMP and SMX were essentially unchanged. However, levels of dapsone and its metabolites increased in the presence of TMP/SMX. Systemic exposure (AUC 0-12 ) of dapsone and N-acetyl-dapsone (NAD) were increased by about 40% and 20% respectively in presence of TMP/SMX. Notably, systemic exposure (AUC 0-12 ) of dapsone hydroxylamine (DHA) was more than doubled in the presence of TMP/SMX. Exposure from the proposed topical dose is about 1% of that from the 100 mg oral dose, even when co-administered with TMP/SMX.

Certain concomitant medications (such as rifampin, anticonvulsants, St. Johnis wort) may increase the formation of dapsone hydroxylamine, a metabolite of dapsone associated with hemolysis. With oral dapsone treatment, folic acid antagonists such as pyrimethamine have been noted to possibly increase the likelihood of hematologic reactions.

Dimitone Contraindications

Levant, Levant

Levant

Levant , (from the French lever, “to rise,” as in sunrise, meaning the east), historically the countries along the eastern Mediterranean shores. Common use of the term is associated with Venetian and other trading ventures and the establishment of commerce with cities such as Tyre and Sidon as a result of the Crusades. It was applied to the coastlands of Asia Minor and Syria. sometimes extending from Greece to Egypt. It was also used for Anatolia and as a synonym for the Middle or Near East. In the 16th and 17th centuries, the term High Levant referred to the Far East. The name Levant States was given to the French mandate of Syria and Lebanon after World War I, and the term is sometimes still used for those two countries, which became independent in 1946.

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Buy Generic Lansoprazole Online, Lansazol

Lansoprazole

Lansoprazole Product Description

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Feel free to contact our Customer Care Specialists by: Calling Us Toll-Free: 1-866-293-3904 Faxing Us Toll-Free: 1-866-732-0306 Emailing Us: info@pharmapassport. com

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Colsancetine - Situs Nama Obat, Colsancetine

Colsancetine Kapsul 250 mg . Informasi obat kali ini akan menjelaskan jenis obat antibiotik batuk rejan, brusellosis, rickettsiosis Chloramphenicol / Kloramfenikol, yang diantaranya menjelaskan dosis obat, komposisi atau kandungan obat, manfaat atau kegunaan dan khasiat atau dalam bahasa medis indikasi, aturan pakai Colsancetine, cara minum/makan atau cara menggunakannya, juga akan menerangkan efek samping atau kerugian, pantangan atau kontra indikasi serta bahayanya, over dosis atau keracunan, dan farmakologi serta meknisme kerja dan harga dari obat Colsancetine, dan inilah penjelasannya:

COLSANCETINE GOLONGAN K Merah

KANDUNGAN Chloramphenicol / Kloramfenikol.

INDIKASI Demam tifoid, batuk rejan, brusellosis, rickettsiosis, pneumonia, bronkhopneumonia, infeksi saluran kemih, infeksi yang sensitif terhadap Kloramfenikol.

KONTRA INDIKASI Hipersensitifitas. Anemia. Trimester ke-3 masa hamil, dan menyusui.

PERHATIAN Pengobatan jangka panjang. Bayi. Kekurangan G6PD. Kerusakan ginjal atau hati. Harus sudah dilakukan pemeriksaan darah.

Interaksi obat : Parasetamol bisa mempengaruhi kadar Kloramfenikol dalam serum. Mempotensiasi efek antikoagulan oral, hipoglikemik oral, Siklofosfamida, Fenitoin.

EFEK SAMPING Depresi sumsum tulang, anemia aplastik, Gray syndrome pada anak-anak, gangguan lambung-usus, neuritis optik dan perifer (radang saraf mata dan saraf tepi).

INDEKS KEAMANAN PADA WANITA HAMIL Penelitian pada hewan menunjukkan efek samping pada janin ( teratogenik atau embriosidal atau lainnya) dan belum ada penelitian yang terkendali pada wanita atau penelitian pada wanita dan hewan belum tersedia. Obat seharusnya diberikan bila hanya keuntungan potensial memberikan alasan terhadap bahaya potensial pada janin.

KEMASAN Kapsul 250 mg x 10 x 10 biji.

DOSIS Dewasa. 3-4 kali sehari 1-2 kapsul.

PENYAJIAN Dikonsumsi pada perut kosong (1 atau 2 jam sebelum/sesudah makan)

HARGA : Rp. 54.395/kemasan

Nemozole Tablet - Uses, Side-Effects, Reviews, Composition, Interactions, Precautions, Substitutes,

Nemozole Tablet

Nemozole Tablet - Uses, Composition, Side Effects and Reviews

Nemozole Tablet is indicated for the treatment of infections caused by roundworm, infections caused by tapeworm, infections caused by pinworm and other conditions. Nemozole Tablet contains the following active ingredients: Albendazole. It is available in tablet form. Ipca Labs manufactures Nemozole Tablet. Detailed information related to Nemozole Tablet's uses, composition, dosage, side effects and reviews is listed below:

Nemozole Tablet Uses

Nemozole Tablet is used in the treatment, control, prevention, & improvement of the following diseases, conditions and symptoms:

Learn more: Uses (in more detail)

Nemozole Tablet Working, Mechanism of Action and Pharmacology

Nemozole Tablet improves the patient's condition by performing the following functions:

Nemozole Tablet Composition and Active Ingredients

Nemozole Tablet is composed of the following active ingredients (salts)

Please note that this medicine may be available in various strengths for each active ingredient listed above.

Nemozole Tablet Side-effects

The following is a list of possible side effects that may occur from all constituting ingredients of Nemozole Tablet. This is not a comprehensive list. These side effects are possible, but do not always occur. Some of the side effects may be rare but serious. Consult your doctor if you observe any of the following side effects, especially if they do not go away.

If you notice other side effects not listed above, contact your doctor for medical advice. You may also report side effects to your local food and drug administration authority.

Learn more: Side-effects (in more detail)

Nemozole Tablet Precautions & How to Use

Before using this drug, inform your doctor about your current list of medications, over the counter products (e. g. vitamins, herbal supplements, etc.), allergies, pre-existing diseases, and current health conditions (e. g. pregnancy, upcoming surgery, etc.). Some health conditions may make you more susceptible to the side effects of the drug. Take as directed by your doctor or follow the direction printed on the product insert. Dosage is based on your condition. Tell your doctor if your condition persists or worsens. Important counseling points are listed below.

Consult your doctor in case of renal impairment

Liver disease

Take fluid and fiber rich diet

Take medicine with meals or snacks

Take non hormonal contraceptive measures during and after therapy

Learn more: Precautions & How to Use (in more detail)

Nemozole Tablet Frequently asked Questions

Can Nemozole Tablet be used for Infections caused by roundworm and Infections caused by tapeworm?

Yes, infections caused by roundworm and infections caused by tapeworm are among the most common reported uses for Nemozole Tablet. Please do not use Nemozole Tablet for infections caused by roundworm and infections caused by tapeworm without consulting first with your doctor. Click here to find out what other patients report as common uses for Nemozole Tablet.

Is it safe to drive or operate heavy machinery when consuming?

If you experience drowsiness, dizziness, hypotension or headache as side-effects when eating Nemozole Tablet medicine then it maybe not be safe to drive a vehicle or operate heavy machinery. One should not drive a vehicle if eating the medicine makes you drowsy, dizzy or lowers your blood-pressure extensively. Pharmacists also advise patients not to drink alcohol with medicines as alcohol intensifies drowsiness side-effects. Please check for these effects on your body when using Nemozole Tablet. Always consult with your doctor for recommendations specific to your body and health conditions.

Is this medicine or product addictive or habit forming?

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Can it be stopped immediately or do I have to slowly ween off consumption?

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Is Nemozole Tablet safe to consume or apply when pregnant?

Please consult with your doctor for case-specific recommendations.

Is Nemozole Tablet safe while breastfeeding?

Please discuss the risks and benefits with your doctor.

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The following are the results of on-going survey on TabletWise. com for Nemozole Tablet. These results only indicate the perceptions of the website users. Please base your medical decisions only on the advice of a doctor or a registered medical professional.

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Buy Cartisorb - Fda Approved Prescription Drug At, Cartisorb

FAQ. How to buy Cartisorb without Prescription Drugs? Q. Where is your drugstore situated? A. We have branches all over the world: in the south of the Pacific ocean, Europe and Middle East. All will depend on Cartisorb which you have ordered, manufacturer and from the wholesale seller who delivers Cartisorb.

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Q. Do I need a Cartisorb prescription to order a medicine? A. No, you do not. The recipe on Cartisorb is not necessary for you. We work under the laws of those countries from which we make dispatches.

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Dinopen, Dinopen

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

Use Diclofenac as directed by your doctor.

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

Drug Class and Mechanism

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

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

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

Do not use Diclofenac if:

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

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

Possible Side Effects

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

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

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

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

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Azomid Marketing Information

Azomid Description

Azomid is a sulfa drug.

Azomid is used for glaucoma treatment (excessive pressure in the eyes), epilepsy treatment (for both brief and unlocalized seizures), fluid retention due to congestive heart failure or drugs.

Azomid works by controlling fluid secretion.

Generic name of Azomid is Acetazolamide.

Brand name of Azomid is Azomid.

Azomid Dosage

Azomid is available in:

250mg Standard Dosage

Azomid is available in tablets and injectable forms.

The dosage depends on the disease and its prescribed treatmen.

250 mg to 1 gram per 24 hours in 2 or more smaller doses.

In secondary glaucoma and before surgery in acute congestive (closed-angle) glaucoma, the usual dosage is 250 mg every 4 hours or, in some cases, 250 mg twice a day.

The daily dosage is 8 to 30 mg per 2.2 pounds of body weight in 2 or more doses. Typical dosage may range from 375 to 1,000 mg per day.

Congestive Heart Failure treatment:

The usual dosage is 250 mg to 375 mg per day or 5 mg per 2.2 pounds of body weight, taken in the morning.

Azomid can be used by children.

If you want to achieve most effective results do not stop taking Azomid suddenly.

Azomid Missing of dose

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

Azomid Overdose

If you overdose Azomid and you don't feel good you should visit your doctor or health care provider immediately.

Azomid Side effects

Azomid has its side effects. The most common are:

change in tastediarrheaincrease in amount or frequency of urinationloss of appetitenausearinging in the earstingling or pins and needles in hands or feetvomiting

Less common but more serious side effects during taking Azomid: allergy reactions (urticaria, breathing difficulties, rash, and eruption).

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

Azomid Contra-indications

Do not take Azomid if you are allergic to Azomid components.

Be careful with Azomid if you're pregnant or you plan to have a baby, or you are a nursing mother.

Do not take Azomid if your sodium or potassium levels are low.

Do not take Azomid if you have kidney or liver disease, including cirrhosis.

Be careful with Azomid if you suffer from or have a history of emphysema or other breathing disorders.

Be careful with Azomid if you take high doses of aspirin.

Be careful with Azomid if you are taking Amitriptyline, Cyclosporine, Lithium, Methenamine, oral diabetes drugs such as Glyburide, Quinidine.

Do not use potassium supplements or salt substitutes.

If you want to achieve most effective results without any side effects it is better to avoid alcohol.

Do not stop taking Azomid suddenly.

Azomid Frequently asked questions

Q: What is Azomid?

A: Azomid is a sulfa drug, helping to control fluid secretion.

Q: What Azomid is used for?

A: Azomid is used for glaucoma treatment (excessive pressure in the eyes); epilepsy treatment (for both brief and unlocalized seizures); fluid retention due to congestive heart failure or drugs.

Q: How does Azomid work?

A: Azomid works by controlling fluid secretion.

Q: Does the generic available?

A: Yes, the generic is available. Generic name is Acetazolamide.

Q: What should I do if I missed the dose?

A: In case of dose missing you should take your tablet as soon as possible. Do not take double dosage. And if it is right time for the next dosage you should continue your regular schedule of Azomid taking.

Q: Are there any side effects of Azomid taking?

A: Common side effects of Azomid are change in taste, diarrhea, increase in amount or frequency of urination, loss of appetite, nausea, ringing in the ears, tingling or pins and needles in hands or feet, vomiting, allergy reactions (urticaria, breathing difficulties, rash, and eruption).

Betnesol V, Betnesol-V

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Ingredient matches for Betnesol V

Betamethasone is reported as an ingredient of Betnesol V in the following countries:

Betamethasone 17?-valerate (a derivative of Betamethasone) is reported as an ingredient of Betnesol V in the following countries:

Costa Rica

Dominican Republic

El Salvador

Germany

Guatemala

Honduras

Panama

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.

Clotil Walcott - National Workers Union, Clotil

Clotil Walcott (7th September 1925 to 15th November 2007) was born on Wellington Street, St. Joseph, Trinidad and Tobago but six years later her parents moved to Arima in search of employment. She attended the St. Joseph Roman Catholic school and then the Arima Roman Catholic School.

Early experiences

Her first working experience was in a dry goods store and later began work at the Ministry of Agriculture's Central Experimental Station at Centeno but, a few years later, was among a group of workers at the Station who were ‘laid off’ on grounds of redundancy.

In February 1964, she began employment at the Cannings Poultry Processing Plant in Arima. This was a branch of the larger Cannings Group of Companies which included, among its many subsidiaries, a chain of supermarkets, stationery stores, meat wholesalers, a soft drink and ice cream factory and many others. According to Walcott, it was her bitter experiences with both the union and the employer while working with this company for fifteen years which, helped to develop her interest in the oppression and exploitation of working women.

Trade Union activist

In 1965 Clotil Walcott began her activities in the Labour Movement by joining the Union of Commercial and Industrial Workers (UCIW). This union was eventually replaced as the representative union for the Cannings workers by the National Union of Government and Federated Workers (NUGFW) and in 1967 she joined that union. In her own words …

“I became particularly concern about the problems of the working women being oppressed and exploited, to do this effectively I discovered I had also to be conversant with the problems of male workers.”

From about 1966, Walcott began to participate actively in politics. Initially this comprised mainly activities involved in electoral campaigns in support of people seeking political office. During the period 1969-1972, she became a member of NJAC - The National Joint Action Committee - and participated in the Black Power and Black consciousness movement which swept the country.

It was in 1974 that she was approached by domestic workers for assistance with their plight of non-recognition or protection by the existing labour laws in Trinidad and Tobago which did not recognise domestics as “workers” under Industrial Relations Act 1972. In response, along with James Lynch, Salisha Ali and others, the National Union of Domestic Employees (NUDE) was established as a section of the Union of Ship Builders, Ship Repairers and Allied Workers Union (USSR).

The bulletin announcing its formation stated: “Calling all persons serving in the capacity of cooks, kitchen helpers, maids, butlers, seamstresses, laundresses, barmen, babysitters, chauffeurs, messengers, yardmen and household assistants” heralding the union’s concern with low income workers more generally in addition to domestic workers.

Politics

During the 1976 election campaign of 1976, she supported the Democratic Action Congress (DAC) a centre party, because in her own words:

“I felt it my duty to find a platform through which I could influence a programme and promote the women’s role in our society… I had the opportunity of encouraging one of the leading platform speaker Mrs. Jennifer Johnson of the DAC to give prominence to both the international and local aspect of women Progressive Programme …”

Later she would shift her allegiance, as many trade unionists would, to the United Labour Front. In addition, she was also a member of the Trinidad and Tobago Peace Council, a branch of the World Peace Council, under the leadership of Dr. James Millette and sold copies of the newspaper Moko through the streets of Port of Spain.

Written works

Driven by the failure to get her views aired in the press, Walcott did her own publishing. She taught herself to type with two fingers, and bought a typewriter. Using this she prepared stencils which were printed on Gestetner machines by friends and associates. On completion these pamphlets were sold by Clotil herself at fifty cents each, around the town, at political meetings and at the parliament building. Four of these early publications dealt with her struggle at the Cannings Poultry Processing Plant and were entitled:

The Exploitation of Working-Class Women – v - Cannings Ltd. Guilty? Part I.

A Woman’s Fight – An example of Exploitation of The Working-Class Woman. Part II.

Women’s Aim Now is to end Exploitation. Part III.

On May Day 1979, at a Trade Union Rally, she delivered a paper entitled:-

Working-Class Woman Speaks Out.

These four essays were published in a booklet entitled "Fight Back Says a Woman" . by the Institute of Social Studies, The Hague in the 1980s.

International work

In 1980, Walcott was invited to attend an international conference on Women’s Struggles and Research at the Institute of Social Studies in The Hague in The Netherlands. That was an important turning point in her development. It was at this meeting that she met Selma James and Wilmette Brown of the International Wages for Housework Campaign. Immediately the connection between the rights of domestic workers and the struggle for the recognition of women’s unwaged domestic labour became clear and from henceforth a relationship would develop which would continue for close to thirty years.

She would subsequently speak at conferences in Vienna, Austria; Turin, Italy; Nairobi, Kenya; Beijing, China and London in The United Kingdom as well as Kingston, Jamaica. NUDE became the local representative of the International Wages for Housework Campaign.

Successes

Amongst the successes attributed to Clotil Walcott and her campaigns through the NUDE were:

The passing of the '''Minimum Wages and Terms and Conditions of Service for Household Assistants Order''' under the Minimum Wages Act Chapter 88:04:18- 17, November 1982; This included - minimum wages, a 44 hour work week; overtime rates for public holidays, maternity leave, vacation leave etc.;

The passing of the '''Unremunerated Work Act, 1995''' which allows for the counting of unwaged work in national statistics. This made Trinidad and Tobago one of the first countries in the world to pass such legislation and the Trinidad and Tobago language being used as the model for the Beijing Declaration on Women.

Honours

Over the years, Clotil Walcott's were recognised by many organisation including:

9th June, 1984 - Bank and General Workers Union, Grand Certificate of Honour for service and dedication in the trade union movement.

1985 - The Star Citizen Award - Peoples Popular Movement.

1991 - Servant and Hero of Labour Award - Council of Progressive Trade Unions (CPTU).

1991 - Network of NGO’s for the Advancement of Women for Outstanding Contribution to the Women’s Movement.

8th March 1998 - Guardian Women of Trinidad and Tobago Award - for her sterling contributions to the social life of Trinidad and Tobago.

1995 - The Partners of The Americas - In Recognition of your 30 years of dedicated service which achieved recognition of the value of women’s work.

31st August 1998 - The Humming Bird Medal (silver) - for Loyal and Devoted service to the Republic of Trinidad and Tobago in the sphere of Trade Unionism.

24th January 1999, Women of the Year - Women Working for Social Progress,

2000 - The Mayor, members of Council and the Burgesses of Arima award for Community Service in Recognition of her Contribution towards the Development of Arima.

8th March 2003 - Network of NGO’s for the Advancement of Women - International Women’s Day 2003 as a Pioneering Women.

8th March 2006 - Ministry of Community Development, Culture and Gender Affairs, in recognition of her contribution to the creation of legislation for the counting of unwaged work.

Note

Most of the information for this article, and much of the text, has been reproduced from a tribute written by Dr. Rhona Reddock following Clotil Walcott's death on 20th November 2007.

For further information see:

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Consult your Health Provider about the dosage appropriate for you.

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

Do not take hyaluronic acid unless administered by a healthcare professional if:

You are pregnant or breast-feeding.

Hyaluronic Acid is not known to have any side effects if taken as per the prescribed dosage.

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Setamol News - Updates, Setamol

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Posted 17 Aug 2016 by Drugs. com

WEDNESDAY, Aug. 17, 2016 – Acetaminophen does not worsen asthma symptoms in young children, a new study finds. Acetaminophen (Tylenol, Panadol) and ibuprofen (Advil, Motrin) are often used to treat pain and fever. Some previous research has suggested that frequent use of acetaminophen may worsen asthma in kids with the respiratory condition. To investigate, researchers studied 300 children between the ages of 1 and 5 with mild, persistent asthma, which is defined as having symptoms more than two days a week, but not daily. All of the children used daily inhaled treatments to manage their asthma. During the study, they received either acetaminophen or ibuprofen to treat pain or fever. The small percentage of kids whose asthma symptoms worsened was about the same with both medications, according to the study published in the Aug. 18 issue of the New England Journal of Medicine. The. Read more

Posted 15 Aug 2016 by Drugs. com

MONDAY, Aug. 15, 2016 – Pregnant women who take acetaminophen – best known as Tylenol – might raise the risk that their child will develop behavioral problems such as attention-deficit/hyperactivity disorder (ADHD), a new study suggests. Acetaminophen is generally considered safe in pregnancy – so safe, in fact, that at least two-thirds of women turn to it while expecting, according to the American Academy of Family Physicians. But when pregnant women in Britain used the pain reliever, it appeared to increase the risk of behavior problems cropping up in their children by the time they turned 7, said lead researcher Evie Stergiakouli, a lecturer in genetic epidemiology at the University of Bristol. Still, the study couldn't prove cause-and-effect, and Stergiakouli believes that women should still take the drug if needed. In the study, taking acetaminophen between 18 and 32 weeks in. Read more

Posted 29 Jul 2016 by Drugs. com

FRIDAY, July 29, 2016 – More people are surviving cancer, but many are left with persistent pain after treatment. New guidelines from the American Society of Clinical Oncology (ASCO) recommend that doctors routinely screen for such pain. The guidelines also advise doctors to consider the use of non-traditional treatments for pain. These include hypnosis, meditation and medical marijuana where it's legal. ASCO also cautioned doctors to assess patients' risk for overuse of opioid painkillers. "Many oncologists and primary care physicians are not trained to recognize or treat long-term pain associated with cancer," guideline panel co-chair Judith Paice said in an ASCO news release. "This guideline will help clinicians identify pain early and develop comprehensive treatment plans, using a broad range of approaches," she said. Advances in cancer diagnosis and treatment have led to a record. Read more

Posted 22 Jul 2016 by Drugs. com

FRIDAY, July 22, 2016 – The more pain they have, the more likely people are to become addicted to powerful prescription opioid painkillers, a new study suggests. "In light of the national opioid abuse epidemic, these new results underscore the importance of developing effective. approaches to managing common painful medical conditions," said senior author Dr. Mark Olfson. He is a professor of psychiatry at Columbia University Medical Center in New York City. The study included results from a survey on alcohol and drug use. More than 34,000 Americans completed the survey. The researchers found that people with moderate to severe pain had a 41 percent higher risk of opioid addiction than those with no pain. That increased risk was independent of other factors such as age, gender, anxiety and mood disorders, and family history of drug, alcohol, and behavioral problems, the study. Read more

Posted 23 May 2016 by Drugs. com

MONDAY, May 23, 2016 – Legions of arthritis sufferers try physical therapy and anti-inflammatory drugs to no avail. Now, a new study looks East for relief – to the martial art tai chi. Researchers concluded that tai chi offers an alternative to physical therapy for common knee osteoarthritis – and it might also boost well-being. This ancient Chinese exercise may particularly benefit overweight older adults, the researchers said. Heavier people are more likely to develop osteoarthritis than people with a healthy weight, according to the U. S. Centers for Disease Control and Prevention. "This research strengthened the evidence that the effectiveness and durability of both tai chi and physical therapy extend to obese older adults with knee osteoarthritis," said Dr. Chenchen Wang. "Such people typically face limited options due to ineffectiveness of osteoarthritis treatments," Wang said. Read more

Posted 3 May 2016 by Drugs. com

TUESDAY, May 3, 2016 – While doing your spring cleaning, don't just toss out expired or unused prescription medications. Unwanted drugs need to be properly disposed of to reduce the risk of abuse or accidental use, the U. S. Food and Drug Administration says. Follow disposal instructions on the drug label or patient information that came with the medicine. Don't put medicines down the sink or flush them down the toilet unless this information specifically says to do so. Call local law enforcement agencies to find out if your community has a medication take-back program or event. Or, ask your local trash or recycling services about medication disposal services and guidelines, the FDA suggests. Another option is to deliver unused medicines to collectors registered with the U. S. Drug Enforcement Administration (DEA). These authorized sites may be retail, clinic or hospital pharmacies, and. Read more

Posted 18 Mar 2016 by Drugs. com

THURSDAY, March 17, 2016 – Acetaminophen – commonly known as Tylenol in the United States – isn't an effective choice for relieving osteoarthritis pain in the hip or knee, or for improving joint function, a new study finds. Although the drug rated slightly better than placebo in studies, nonsteroidal anti-inflammatory drugs (NSAIDs) such as ibuprofen (Advil, Motrin) or diclofenac are better choices for short-term pain relief, the researchers said. "Regardless of dose, the prescription drug diclofenac is the most effective drug among painkillers in terms of improving pain and function in osteoarthritis," said lead researcher Dr. Sven Trelle. He's co-director of clinical trials at the University of Bern in Switzerland. However, even diclofenac comes with side effects. "If you are thinking of using a painkiller for osteoarthritis, you should consider diclofenac," Trelle said, but also. Read more

Posted 15 Mar 2016 by Drugs. com

-- While fever is part of the body's defense against illness, it doesn't mean having one is a comfortable experience. To help deal with the symptoms of fever, the University of Portland suggests: Take ibuprofen or acetaminophen. Never give a child aspirin. Soak in a warm or tepid bath to help bring down a fever. Don't take a cool or cold bath. Drink plenty of fluids. Get immediate treatment for complications of fever, such as seizure, difficulty breathing, delirium, severe headache with stiff neck, or fever of 104 degrees or higher. Read more

Posted 10 Feb 2016 by Drugs. com

WEDNESDAY, Feb. 10, 2016 – Pregnant women who take the painkiller acetaminophen – best known under the brand name Tylenol – may be more likely to have a child with asthma, new research suggests. Although the study wasn't designed to prove cause-and-effect, researchers found that prenatal exposure to the over-the-counter medicine was associated with an increased risk for asthma in children. However, the study authors and a U. S. expert agreed that the effect seen in the study doesn't yet warrant any change in guidelines regarding pain relief during pregnancy. In the study, Norwegian researchers tracked data from a large database – the Norwegian Mother and Child Cohort Study. The investigators focused on conditions during pregnancy for which some expectant mothers took acetaminophen, and compared that data against rates of asthma among 114,500 children as they reached the ages of 3 and. Read more

Posted 26 Jan 2016 by Drugs. com

MONDAY, Jan. 25, 2016 – Many people with chronic pain ignore dosing instructions on over-the-counter pain medicines and put themselves at risk for an overdose, a new survey suggests. An overdose of these medicines can result in serious side effects, such as stomach bleeding, ulcers, liver damage and even death, according to the American Gastroenterological Association (AGA). The AGA-commissioned poll of more than 1,000 U. S. adults aged 30 and older and 251 gastroenterologists found that 43 percent of chronic pain sufferers said they knowingly have taken more than the recommended dose of an over-the-counter (OTC) pain medicine at some point. Common types of OTC pain medicines include acetaminophen (Tylenol) and nonsteroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen (Advil, Motrin), naproxen (Aleve) and aspirin. "Pain is incredibly personal, but taking more than the recommended. Read more

Posted 13 Jan 2016 by Drugs. com

WEDNESDAY, Jan. 13, 2016 – Infants are just as susceptible to accidental poisonings as older children are, especially when it comes to medication errors, new research reports. A decade of poison control center calls in the United States showed that acetaminophen (such as Tylenol) was the most common medication mistake for infants. This was followed by H2-blockers (for acid reflux), gastrointestinal medications, combination cough/cold products, antibiotics and ibuprofen (such as Motrin or Advil). The most common non-medication exposures were diaper care and rash products, plants and creams, lotions and make-up, the investigators found. "I was surprised with the large number of exposures even in this young age group," said lead author Dr. A. Min Kang, a medical toxicology fellow at Banner-University Medical Center Phoenix in Arizona. "Pediatricians typically do not begin poison. Read more

Posted 18 Dec 2015 by Drugs. com

FRIDAY, Dec. 18 – Heavy luggage may be more than a hassle for holiday travels – those overloaded bags can sometimes cause health problems, the American Academy of Orthopaedic Surgeons (AAOS) warns. "Individuals are at high risk for back, neck and shoulder strains when carelessly handling heavy luggage," Dr. Nitin Khanna, an orthopedic surgeon and AAOS spokesperson, said in an academy news release. "Always be cognizant of the way you are lifting heavy luggage to avoid painful injuries," Khanna advised. In 2014, Americans suffered almost 73,000 luggage-related injuries, according to the U. S. Consumer Product Safety Commission. When you shop for new luggage, look for a sturdy, light piece with wheels and a handle, the AAOS said. Pack lightly. If possible, put items in a few smaller bags rather than one large piece of luggage. Never twist your body when carrying or lifting luggage. Read more

Posted 14 Dec 2015 by Drugs. com

SUNDAY, Dec. 13, 2015 – Snow removal is a major cause of winter-related injuries, but there are several ways to reduce your risk, an expert says. "Individuals tend to haste through snow shoveling to avoid being outside in the cold for long periods of time," orthopedic surgeon Dr. Joseph Abboud, spokesman for the American Academy of Orthopaedic Surgeons (AAOS), said in an academy news release. "Unfortunately, rushing through this task can lead to injuries. It should always be done at a slow and steady pace because of the energy and focus that's required. Always check with your doctor before shoveling snow and consider hiring someone to do it for you if you're unable to," he advised. In 2014, more than 203,000 Americans required treatment for injuries suffered while manually clearing snow, and nearly 27,000 were injured using snow blowers or throwers, according to the U. S. Consumer. Read more

Posted 10 Dec 2015 by Drugs. com

THURSDAY, Dec. 10, 2015 – X-rays don't detect hip arthritis in many patients, resulting in delayed diagnosis and treatment, researchers report. The researchers looked at information from almost 4,500 Americans taking part in two arthritis studies. In one study, only 16 percent of patients with hip pain had X-ray evidence of osteoarthritis in the hip and only 21 percent of those with X-ray evidence of arthritis had hip pain. In the other study, the rates were 9 percent and 24 percent, respectively, according to the findings reported recently in the journal BMJ. "The majority of older subjects with high suspicion for clinical hip osteoarthritis did not have radiographic hip osteoarthritis, suggesting that many older persons with hip osteoarthritis might be missed if diagnosticians relied on hip radiographs to determine if hip pain was due to osteoarthritis," said study corresponding. Read more

Posted 4 Dec 2015 by Drugs. com

FRIDAY, Dec. 4, 2015 – Electrical nerve stimulation may offer some relief for older adults with chronic back pain, a new study suggests. While wearing and activating the "transcutaneous electrical nerve stimulation" (TENS) device, people had significant improvement in pain when resting, according to the researchers. The study participants also had a reduction in pain while moving, along with improvement in physical functioning, the researchers said. "TENS is not a new treatment. It's been around 50 years or more," said lead researcher Corey Simon, a postdoctoral researcher, in the University of Florida's Pain Research and Intervention Center in Gainesville. The TENS unit is a small battery-powered machine that delivers low-volt electrical current through electrodes placed on the skin. TENS can be used to treat acute pain, including pain with childbirth, or chronic pain, such as. Read more

Novecin, Novecin

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Novecin - General Information

A synthetic fluoroquinolone (fluoroquinolones) antibacterial agent that inhibits the supercoiling activity of bacterial DNA gyrase, halting DNA replication. [PubChem]

Pharmacology of Novecin

Novecin is a quinolone/fluoroquinolone antibiotic. Novecin is bactericidal and its mode of action depends on blocking of bacterial DNA replication by binding itself to an enzyme called DNA gyrase, which allows the untwisting required to replicate one DNA double helix into two. Notably the drug has 100 times higher affinity for bacterial DNA gyrase than for mammalian. Novecin is a broad-spectrum antibiotic that is active against both Gram-positive and Gram-negative bacteria.

Novecin for patients

PATIENT INFORMATION Patients should be advised:

- to drink fluids liberally;

- that mineral supplements, vitamins with iron or minerals, calcium-, aluminum-, or magnesium-based antacids, sucralfate or Videx?, (Didanosine), chewable/buffered tablets or the pediatric powder for oral solution should not be taken within the two-hour period before or within the two-hour period after taking ofloxacin (See Drug Interactions);

- that ofloxacin can be taken without regard to meals;

- that ofloxacin may cause neurologic adverse effects (e. g. dizziness. lightheadedness) and that patients should know how they react to ofloxacin before they operate an automobile or machinery or engage in activities requiring mental alertness and coordination

- to discontinue treatment and inform their physician if they experience pain, inflammation, or rupture of a tendon, and to rest and refrain from exercise until the diagnosis of tendinitis or tendon rupture has been confidently excluded;

- that ofloxacin may be associated with hypersensitivity reactions, even following the first dose, to discontinue the drug at the first sign of a skin rash, hives or other skin reactions, a rapid heartbeat, difficulty in swallowing or breathing, any swelling suggesting angioedema (e. g. swelling of the lips, tongue, face; tightness of the throat, hoarseness), or any other symptom of an allergic reaction

- to avoid excessive sunlight or artificial ultraviolet light while receiving ofloxacin and to discontinue therapy if phototoxicity (e. g. skin eruption) occurs;

- that if they are diabetic and are being treated with insulin or an oral hypoglycemic drug, to discontinue ofloxacin immediately if a hypoglycemic reaction occurs and consult a physician

- that convulsions have been reported in patients taking quinolones, including ofloxacin, and to notify their physician before taking this drug if there is a history of this condition.

Novecin Interactions

Antacids, Sucralfate, Metal Cations, Multivitamins: Quinolones form chelates with alkaline earth and transition metal cations. Administration of quinolones with antacids containing calcium, magnesium, or aluminum, with sucralfate, with divalent or trivalent cations such as iron, or with multivitamins containing zinc or with Videx®, (Didanosine), chewable/buffered tablets or the pediatric powder for oral solution may substantially interfere with the absorption of quinolones resulting in systemic levels considerably lower than desired. These agents should not be taken within the two-hour period before or within the two-hour period after ofloxacin administration. Caffeine: Interactions between ofloxacin and caffeine have not been detected.

Cimetidine: Cimetidine has demonstrated interference with the elimination of some quinolones. This interference has resulted in significant increases in half-life and AUC of some quinolones. The potential for interaction between ofloxacin and cimetidine has not been studied.

Cyclosporine: Elevated serum levels of cyclosporine have been reported with concomitant use of cyclosporine with some other quinolones. The potential for interaction between ofloxacin and cyclosporine has not been studied.

Drugs metabolized by Cytochrome P450 enzymes: Most quinolone antimicrobial drugs inhibit cytochrome P450 enzyme activity. This may result in a prolonged half-life for some drugs that are also metabolized by this system (e. g. cyclosporine, theophylline/methylxanthines, warfarin) when co-administered with quinolones. The extent of this inhibition varies among different quinolones.

Non-steroidal anti-inflammatory drugs: The concomitant administration of a non-steroidal anti-inflammatory drug with a quinolone, including ofloxacin, may increase the risk of CNS stimulation and convulsive seizures.

Probenecid: The concomitant use of probenecid with certain other quinolones has been reported to affect renal tubular secretion. The effect of probenecid on the elimination of ofloxacin has not been studied.

Theophylline: Steady-state theophylline levels may increase when ofloxacin and theophylline are administered concurrently. As with other quinolones, concomitant administration of ofloxacin may prolong the half-life of theophylline, elevate serum theophylline levels, and increase the risk of theophylline-related adverse reactions. Theophylline levels should be closely monitored and theophylline dosage adjustments made, if appropriate, when ofloxacin is co-administered. Adverse reactions (including seizures) may occur with or without an elevation in the serum theophylline level.

Warfarin: Some quinolones have been reported to enhance the effects of the oral anticoagulant warfarin orits derivatives. Therefore, if a quinolone antimicrobial is administered concomitantly with warfarin or its derivatives, the prothrombin time or other suitable coagulation test should be closely monitored.

Antidiabetic agents (e. g. insulin, glyburide/glibenclamide): Since disturbances of blood glucose, including hyperglycemia and hypoglycemia, have been reported in patients treated concurrently with quinolones and an antidiabetic agent, careful monitoring of blood glucose is recommended when these agents are used concomitantly.

Novecin Contraindications

FLOXIN (ofloxacin) is contraindicated in persons with a history of hypersensitivity associated with the use of ofloxacin or any member of the quinolone group of antimicrobial agents.

Additional information about Novecin

Novecin Indication: For the treatment of infections (respiratory tract, kidney, skin, soft tissue, UTI), urethral and cervical gonorrhoea. Mechanism Of Action: Novecin acts on DNA gyrase, an enzyme which, like human topoisomerase, prevents the excessive supercoiling of DNA during replication or transcription. Drug Interactions: Aluminium Formation of non-absorbable complexes Bismuth Formation of non-absorbable complexes Calcium Formation of non-absorbable complexes Iron Formation of non-absorbable complexes Magnesium oxide Formation of non-absorbable complexes Magnesium Formation of non-absorbable complexes Sucralfate Formation of non-absorbable complexes Zinc Formation of non-absorbable complexes Warfarin The quinolone increases the anticoagulant effect Acenocoumarol The quinolone increases the anticoagulant effect Dicumarol The quinolone increases the anticoagulant effect Anisindione The quinolone increases the anticoagulant effect Dihydroquinidine barbiturate Increased risk of cardiotoxicity and arrhythmias Quinidine Increased risk of cardiotoxicity and arrhythmias Quinidine barbiturate Increased risk of cardiotoxicity and arrhythmias Foscarnet Increased risk of convulsions Procainamide The quinolone increases the effect of procainamide Food Interactions: Not Available Generic Name: Ofloxacin Synonyms: Not Available Drug Category: Anti-Bacterial Agents; Anti-Infectives; Quinolones Drug Type: Small Molecule; Approved Other Brand Names containing Ofloxacin: Akilen; Baccidal; Bactocin; Danoflox; Effexin; Exocin; Exocine; Flobacin; Flodemex; Flotavid; Flovid; Floxal; Floxil; Floxstat; Fugacin; Inoflox; Kinflocin; Kinoxacin; Liflox; Loxinter; Marfloxacin; Medofloxine; Mergexin; Novecin; Nufafloqo; O-Flox; Obide; Occidal; Ofcin; Oflin; Oflocee; Oflocet; Oflocin; Oflodal; Oflodex; Oflodura; Oflox; Ofloxin; Ofus; Onexacin; Operan; Orocin; Otonil; Pharflox; Praxin; Puiritol; Qinolon; Qipro; Quinolon; Quotavil; Rilox; Sinflo; Tabrin; Taravid; Tariflox; Tarivid; Telbit; Tructum; Uro Tarivid; Viotisone; Zanocin; Floxin; Absorption: Bioavailability of ofloxacin in the tablet formulation is approximately 98% Toxicity (Overdose): LD 50 =5450 mg/kg (orally in mice) Protein Binding: 32% Biotransformation: Hepatic Half Life: 9 hours Dosage Forms of Novecin: Tablet Oral Solution Ophthalmic Liquid Ophthalmic Chemical IUPAC Name: (+/-)-9-fluoro-2, 3-dihydro-3-methyl-10-(4-methyl-1-piperazinyl)-7-oxo-7H-pyrido[1, 2, 3-de]-1, 4-benzoxazine-6-carboxylic acid Chemical Formula: C18H20FN3O4 Ofloxacin on Wikipedia: http://en. wikipedia. org/wiki/Ofloxacin Organisms Affected: Enteric bacteria and other eubacteria

Buy Clinda-Ipp Clindamycin Online Without Prescriptions, Clinda-Ipp

Cleocin is used for treating serious infections caused by certain bacteria. Cleocin is a lincomycin antibiotic. Cleocin kills sensitive bacteria by stopping the production of essential proteins needed by the bacteria to survive.

Use Cleocin as directed by your doctor.

Take Cleocin by mouth with or without food.

Take Cleocin with a full glass of water (8 oz/240 mL).

Cleocin works best if it is taken at the same time each day.

To clear up your infection completely, take Cleocin for the full course of treatment. Keep taking it even if you feel better in a few days.

If you miss a dose of Cleocin, 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 Cleocin.

Store Cleocin at room temperature, between 68 to 77 degrees F (20 to 25 degrees C) in a tightly-closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Cleocin out of the reach of children and away from pets.

Active Ingredient: Clindamycin hydrochloride.

Do NOT use Cleocin if:

you are allergic to any ingredient in Cleocin or to lincomycin

you have certain intestinal problems (eg, antibiotic-associated colitis, Crohn disease, ulcerative colitis) or meningitis.

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

Some medical conditions may interact with Cleocin. 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 diarrhea, or a history of liver problems or stomach or bowel problems (eg, colitis)

if you are allergic to tartrazine.

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

Nondepolarizing muscle relaxants (eg, vecuronium) or succinylcholine because the risk of their side effects may be increased by Cleocin.

Erythromycin because it may decrease Cleocin's effectiveness.

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

Cleocin only works against bacteria; it does not treat viral infections (eg, the common cold).

Be sure to use Cleocin for the full course of treatment. If you do not, the medicine may not clear up your infection completely. The bacteria could also become less sensitive to this or other medicines. This could make the infection harder to treat in the future.

Long-term or repeated use of Cleocin may cause a second infection. Tell your doctor if signs of a second infection occur. Your medicine may need to be changed to treat this.

This product may contain tartrazine dye. This may cause an allergic reaction in some patients. If you have ever had an allergic reaction to tartrazine, ask your pharmacist if your product has tartrazine in it.

Mild diarrhea is common with antibiotic use. However, a more serious form of diarrhea (pseudomembranous colitis) may rarely occur. This may develop while you use the antibiotic or within several months after you stop using it. Contact your doctor right away if stomach pain or cramps, severe diarrhea, or bloody stools occur. Do not treat diarrhea without first checking with your doctor.

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

Use Cleocin with caution in the elderly; they may be more sensitive to its effects, especially diarrhea.

Use Cleocin with extreme caution in children younger 10 years who have diarrhea or an infection of the stomach or bowel.

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

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

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

Mild diarrhea; nausea; 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); bloody or tarry stools; decreased urination; joint pain or swelling; red, swollen, blistered, or peeling skin; severe or persistent diarrhea; severe stomach cramps or pain; unusual vaginal discharge, itching, or odor; 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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Ketron® Peek, Ketron

Ketron® PEEK

Excellent chemical resistance

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Unaffected by continuous exposure to hot water or steam

Ketron® PEEK grades offer chemical and hydrolysis resistance similar to PPS, but can operate at higher temperatures. PEEK 1000 offers steam and wear resistance, while carbon-reinforced PEEK provides excellent wear capabilities. Our latest grade, PEEK HPV, offers outstanding bearing performance. PEEK can be used continuously to 480°F (250°C) and in hot water or steam without permanent loss in physical properties. For hostile environments, PEEK is a high strength alternative to fluoropolymers. PEEK carries a V-O flammability rating and exhibits very low smoke and toxic gas emission when exposed to flame.

Ketron® PEEK 1000

This general purpose grade is unreinforced and offers the highest elongation and toughness of all PEEK grades. The newly available black PEEK 1000 is ideal for instrument components where aesthetics are important, as well as for seal components where ductility and inertness are important.

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Bushings, Bearings, Seals, Back Up Rings

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The addition of glass fibers significantly reduces the expansion rate and increases the flexural modulus of PEEK. This grade is ideal for structural applications that require improved strength, stiffness or stability, especially at temperatures above 300°F (150°C).

Ketron® PEEK CA30 (30% Carbon Fiber-Reinforced)

The addition of carbon fibers enhances the compressive strength and stiffness of PEEK, and dramatically lowers its expansion rate. It offers designers optimum wear resistance and load carrying capability in a PEEK-based product. This grade provides more thermal conductivity than unreinforced PEEK -- increasing heat dissipation from bearing surfaces improving bearing life and capability.

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Ketron® PEEK CA30 improves centrifugal pump efficiency by permitting closer running tolerances and eliminating corrosion, galling and wear problems. (Prior material: Bronze)

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Injection Molded Ketron® PEEK advanced polymers shapes are ideal for machined back-up rings and v-seals. Ketron® PEEK offers excellent chemical and wear resistance across a broad range of operating temperatures. In addition to the widely used Ketron 1000 PEEK grade, several specific grades are available that incorporate glass or carbon fibers, or wear resistant additives that increase the wear life of machined parts.

Unfilled Ketron 1000 PEEK performs to 320F (160C)

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Carbon fiber reinforced with graphite and PTFE lubricants, our newest grade of PEEK offers the lowest coefficient of friction and the best machinability for all PEEK grades. An excellent combination of low friction, low wear, high LPV, low mating part wear and easy machining, make it ideal for aggressive service bearings.

Ciproquinol Generic Name Ciprofloxacin Online, Ciproquinol

Ciproquinol General Information

The bactericidal action of ciprofloxacin results from inhibition of the enzymes topoisomerase II (DNA gyrase) and topoisomerase IV, which are required for bacterial DNA replication, transcription, repair, and recombination.

Ciproquinol for patients

Patients should be advised:

· that antibacterial drugs, including Proquin XR, should only be used to treat bacterial infections. They do not treat viral infections (e. g. the common cold). When Proquin XR is prescribed to treat a bacterial infection, patients should be told that although it is common to feel better early in the course of therapy, the medication should be taken exactly as directed. Skipping doses or not completing the full course of therapy may (1) decrease the effectiveness of the immediate treatment and (2) increase the likelihood that bacteria will develop resistance and will not be treatable by Proquin XR or other antibacterial drugs in the future.

· that Proquin XR should only be used to treat uncomplicated urinary tract infections (also known as bladder infections). The safety and efficacy of Proquin XR to treat other urinary tract or non-urinary tract infections have not been studied.

· that Proquin XR should be taken with a main meal of the day, preferably the evening meal. The patient should not take more than one Proquin XR tablet per day, even if the patient misses a dose.

· that Proquin XR tablets should be taken whole and never split, crushed, or chewed.

· that concomitant administration of Proquin XR with aluminum or magnesium-containing antacids, sucralfate, VIDEX (didanosine) chewable buffered tablets or pediatric powder, metal cations such as iron and calcium, and multivitamin preparations containing zinc should be avoided. Proquin XR should be administered at least 4 hours before or 2 hours after these products.

· that Proquin XR should not be taken with dairy products (like milk or yogurt) or calcium-fortified juices alone, since the absorption of ciprofloxacin may be significantly reduced. However, Proquin XR may be taken with a meal that contains these products.

· that ciprofloxacin may be associated with hypersensitivity reactions, even following a single dose, and to discontinue Proquin XR at the first sign of a skin rash or other allergic reaction and contact their physician.

· to avoid excessive sunlight or artificial ultraviolet (UV) light while receiving Proquin XR and to discontinue therapy if phototoxicity occurs.

· that peripheral neuropathies have been associated with ciprofloxacin use. If symptoms of peripheral neuropathy including pain, burning, tingling, numbness and/or weakness develop, patients should discontinue treatment and contact their physician.

· that if they experience pain, inflammation, or rupture of a tendon to discontinue treatment, to inform their physician, and to rest and refrain from exercise.

· to contact their doctor if they do not feel better of if they develop fever and back pain while or after taking Proquin XR.

· that Proquin XR may cause dizziness and lightheadedness; therefore, patients should know how they react to this drug before they operate an automobile or machinery or engage in activities requiring mental alertness or coordination.

· that Proquin XR may increase the effects of theophylline and caffeine. There is a possibility of caffeine accumulation when products containing caffeine are consumed while taking quinolones.

· that convulsions have been reported in patients receiving quinolones, including ciprofloxacin, and to notify their physician before taking this drug if there is a history of this condition.

PROQUIN XR (ciprofloxacin hydrochloride) Extended-Release Tablets

Extended-Release Tablets, 500 mg

This leaflet contains important information about Proquin XR (ciprofloxacin hydrochloride) extended-release tablets and should be read before you begin treatment. This leaflet does not replace talking with your doctor about your medical condition or your treatment. This leaflet does not list all benefits and risks of Proquin XR. Proquin XR can be prescribed only by a doctor. If you have any questions about Proquin XR, talk to your doctor. Only your doctor can tell you if Proquin XR is right for you.

What is Proquin XR?

Proquin XR is an antibiotic in the class known as "quinolones" that is used to treat adults with simple (uncomplicated) urinary tract infections (also known as "bladder infections") caused by bacteria. It is not known if Proquin XR will treat infections other than bladder infections. Proquin XR, like all other antibiotics, does not kill viruses.

You should contact your doctor if you do not feel better or if you develop fever and back pain while or after taking Proquin XR.

Proquin XR tablets are blue and contain 500 mg of active drug.

How should I take Proquin XR?

· Proquin XR should be taken once a day for 3 days shortly after a main meal of the day, preferably the evening meal. Proquin XR does not work as well if you take it without a meal. You should try to take Proquin XR at about the same time each day.

· Take Proquin XR for all 3 days, even if you are feeling better. If you stop taking Proquin XR before all 3 doses, Proquin XR may not cure your bladder infection.

· Do not split, crush, or chew Proquin XR tablets. Proquin XR tablets must be swallowed whole. Tell your doctor if you cannot swallow tablets whole. Your doctor will prescribe a different medicine for you.

· Do not take more than one Proquin XR tablet a day, even if you miss a dose.

· Do not take Proquin XR at the same time that you drink milk or juices with added calcium, unless you drink them with a main meal.

· Many antacids and multivitamins may interfere with the absorption of Proquin XR if taken at the same time. Take Proquin XR at least 4 hours before or 2 hours after antacids that contain magnesium or aluminum. Proquin XR should also be taken at least 4 hours before or 2 hours after sucralfate, VIDEX ® (didanosine) chewable buffered tablets or pediatric powder, iron, calcium, and vitamins that contain zinc.

Who should not take Proquin XR?

Do not take Proquin XR if you are allergic to or have ever had a severe reaction to ciprofloxacin or to any other "quinolone" antibiotics.

Proquin XR is not recommended for use during pregnancy or nursing, as the effects on the unborn child or nursing infant are unknown. If you are pregnant or planning to become pregnant while taking Proquin XR, talk to your doctor before taking this medication.

Proquin XR is not recommended for children.

What should I tell my doctor before taking Proquin XR?

Tell you doctor about all of your medical conditions, including if you have or ever had seizures (epilepsy), asthma, or liver or kidney problems.

Tell your doctor about all the medicines you take, including prescription and nonprescription medicines, vitamins and herbal supplements. Proquin XR and certain other medicines can affect each other. You may have to adjust the times you take certain other medicines, vitamins, and herbal supplements. Especially, tell your doctor if you take: theophylline, VIDEX ® (didanosine) chewable buffered tablets or pediatric powder; warfarin (Coumadin ® ); glyburide (Glucovance ®. Micronase ®. DiaBeta ® ); phenytoin (Dilantin ® ); sucralfate (Carafate ® ); or antacids or vitamins that contain magnesium, calcium, aluminum, iron, or zinc.

Know the medicines you take. Keep a list of them to show your doctor and pharmacist.

What are the possible side effects of Proquin XR?

Proquin XR is generally well tolerated. The most common side effects with Proquin XR include vaginal yeast infection and headache. Less common side effects include nausea, diarrhea, dizziness, and abdominal pain.

You should be careful about driving or operating machinery until you are sure the Proquin XR is not causing dizziness or lightheadedness.

Rare cases of allergic reactions have been reported in patients receiving quinolones, including ciprofloxacin, even after just one dose. Stop taking Proquin XR and call your doctor or get emergency medical attention right away if you develop a rash, hives, swelling of your face or throat, or have trouble breathing.

Some patients taking quinolone antibiotics may become more sensitive to sunlight or ultraviolet light such as that used in tanning salons. You should avoid excessive exposure to sunlight or ultraviolet light while taking Proquin XR.

Ciproquinol has rarely been associated with inflammation of the tendons. Stop taking Proquin XR and call your doctor if you experience pain, swelling, or rupture of a tendon.

Convulsions have been reported in patients receiving quinolone antibiotics including ciprofloxacin. Tell your doctor if you have experienced convulsions in the past. Quinolones, including ciprofloxacin, have been rarely associated with other central nervous system events including confusion, tremors, hallucinations, and depression. Stop taking Proquin XR and call your doctor right away if you get any of these symptoms.

These are not all the side effects with Proquin XR. For more information, ask your doctor or pharmacist.

How should I store Proquin XR?

· Store Proquin XR at room temperature, 59° to 86° F (15° to 30° C).

· Keep Proquin XR and all medicines out of the reach of children.

General information about Proquin XR

Medicines are sometimes prescribed for conditions that are not mentioned in patient information leaflets. Do not use Proquin XR for a condition for which it was not prescribed. Do not give Proquin XR to other people, even if they have the same symptoms you have. It may harm them.

Keep this medication out of the reach of children.

This leaflet summarizes the most important information about Proquin XR. If you would like more information, talk with your doctor. You can ask your pharmacist or doctor for information about Proquin XR that is written for health care professionals. Further information is also provided at:

1-800-206-2945 and www. Proquin. com

What are the ingredients in Proquin XR?

Active Ingredient: ciprofloxacin hydrochloride

Inactive Ingredients: film coating, magnesium stearate, polyethylene oxide, and povidone

This description is suitable for active ingredient Ciprofloxacin

Ciproquinol Interactions

Some quinolones, including ciprofloxacin, have also been shown to interfere with the metabolism of caffeine. This may lead to reduced clearance of caffeine and a prolongation of its serum half-life.

Some quinolones, including ciprofloxacin, have been associated with transient elevations in serum creatinine in patients receiving cyclosporine concomitantly.

The concomitant administration of ciprofloxacin with the sulfonylurea glyburide has, on rare occasions, resulted in severe hypoglycemia.

Histamine H2-receptor antagonists

Histamine H 2 - receptor antagonists appear to have no significant effect on the bioavailability of ciprofloxacin.

Renal tubular transport of methotrexate may be inhibited by concomitant administration of ciprofloxacin, potentially leading to increased plasma levels of methotrexate. This might increase the risk of methotrexate toxic reactions. Therefore, patients under methotrexate therapy should be carefully monitored when concomitant ciprofloxacin therapy is indicated.

Multivalent Cation-Containing Products

Concurrent administration of a quinolone, including ciprofloxacin, with multivalent cation-containing products such as magnesium or aluminum antacids, sucralfate, VIDEX chewable/buffered tablets or pediatric powder, or products containing calcium, iron, or zinc may substantially decrease the absorption of ciprofloxacin, resulting in serum and urine levels considerably lower than desired. Proquin XR should be administered at least 4 hours before or 2 hours after these products. This time window is different than for other oral formulations of ciprofloxacin, which are usually administered 2 hours before or 6 hours after antacids.

Non-steroidal anti-inflammatory drugs (but not aspirin)

These drugs in combination with very high doses of quinolones have been shown to provoke convulsions in pre-clinical studies.

The rate and extent of absorption of ciprofloxacin was bioequivalent when Proquin XR was given alone or when Proquin XR was given 2 hours after omeprazole at the dose that maximally suppresses gastric acid secretion. Omeprazole should be taken as directed and Proquin XR should be taken with a main meal of the day, preferably the evening meal..

Altered serum levels of phenytoin (increased and decreased) have been reported in patients receiving concomitant ciprofloxacin.

Probenecid interferes with renal tubular secretion of ciprofloxacin and produces an increase in the level of ciprofloxacin in serum.

As with some other quinolones, concurrent administration of ciprofloxacin with theophylline may lead to elevated serum concentrations of theophylline and prolongation of its elimination half-life. This may result in increased risk of theophylline-related adverse reactions. If concomitant use cannot be avoided, serum levels of theophylline should be monitored and dosage adjustments made as appropriate.

Quinolones have been reported to enhance the effects of the oral anticoagulant warfarin or its derivatives. When these products are administered concomitantly, prothrombin time or other suitable coagulation tests should be monitored.

Ciproquinol Contraindications

Proquin XR is contraindicated in persons with a history of hypersensitivity to ciprofloxacin or any member of the quinolone class of antimicrobial agents, or any of the product components.

This description is suitable for active ingredient Ciprofloxacin

Ciproquinol tags categories:

Baxo, Baxo

Artist Statement

Impressionism, Pointillism, Expressionism, Cubism, Surrealism are just a few examples of popular art styles. Canvases, paper and wood have been common surfaces on which to create a masterpiece. However, the world evolves and new technologies and methods are presented in all aspects of life. I felt the need to explore and experiment with different materials and methods that are outside the realm of traditional paintings. After years of experimenting I have come up a style that I call Aluminism.

The difference is in the elements. I utilize the 4 elements to create the artwork: fire, wind, earth and water.

The foundation of my art is aluminium. I grind and carve designs right into the aluminium then I use my specialized process which invokes the four elements. The end result is a mesmerizing effect that is unparallel to what can be achieved on canvas. Lighting brings out stunning movement, colours and texture. As you move and observe the art from various vantage points you will see it change before your very eyes. My artwork is topped with a high-gloss finish. This allows the light to penetrate through the layers of colour and refract off the grinds in the aluminium to achieve a stunning illusion.

Whether the subject matter is serene sunset landscapes, nebulas portraying the very depths of space, or even abstract pieces that test the imagination of its viewers, my Aluminism style never fails to captivate.

Artist CV

Exhibitions

2016. Welland Rose Festival Art Exhibition - Welland, Ontario

2016. Thunder Art Gallery Grand Opening Exhibition - Niagara Falls, Ontario

2016. Millpond Art Show & Sale - St. Catharines, Ontario

2016. Pelham Art Festival - Fonthill, Ontario

2016. Late Winter/Early Spring Group Show - TAG Art Gallery - St. Catharines, Ontario

2016. Art Lovers Show & Soiree - St. Catharines, Ontario

2015. Welland Rose Festival Art Exhibition - Welland, Ontario

2015. Brampton Wellness Cantre - Brampton, Ontario

2015. Millpond Art Show & Sale - St. Catharine's, Ontario

2014. Baxo Fine Art Gallery Grand Opening - Fonthill, Ontario

2014. In The Soil Arts Festival - St. Catharines, Ontario

2014. Welland Rose Festival Juried Art Show - Welland, Ontario

2014. Millpond Art Show & Sale - St. Catharines, Ontario

2014. Small Start Art Show - Welland, Ontario

2014. Wall Of Art - Welland Civic Centre - Welland, Ontario

2013. CGV Art Gallery Group Show - Niagara-On-The-Lake, Ontario

2013. Welland Rose Festival Juried Art Show - Welland, Ontario

Awards

2014. Welland Rose Festival Juried Art Show - People's Choice

2014. Welland Rose Festival Juried Art Show - Honourable Mention

Art Donations

2015. Hungarian Hunting & Fishing Gala - Welland

2015. Millpond Art Show Raffle - St. Catharines

2014. Niagara Land Trust Silent Auction - St. Catharines

2014. Mayor's Gala Silent Auction - Welland

2013. Friends Of We Care Silent Auction - Toronto

Gallery Curator

2014-2015 - Baxo Fine Art Gallery - Fonthill, Ontario

Current Gallery Representation

Thunder Art Gallery, Niagara Falls, Ontario

TAG Art Galery, St. Catharines, Ontario

News & Events

Come meet Baxo at the following events:

Art Lovers Show & Soiree - February 12th-15th 2016

Azithromycin 200mg, Binozyt

2. Qualitative and quantitative composition

Each 5 ml prepared suspension contain 204.8 mg azithromycin monohydrate equivalent to 200 mg azithromycin.

Each 1 ml prepared suspension contains 40.96 mg azithromycin monohydrate equivalent to 40 mg azithromycin.

Excipients with known effect:

• Sucrose 3.70 g/ 5 ml

• Aspartame (E951) 0.030 g/ 5 ml

For the full list of excipients, see section 6.1.

3. Pharmaceutical form

Powder for oral suspension.

White or off-white crystalline powder.

4. Clinical particulars

4.1 Therapeutic indications

Azithromycin powder for oral suspension is indicated for the treatment of the following infections, when caused by microorganisms sensitive to azithromycin (see section 4.4 and 5.1):

− acute bacterial sinusitis (adequately diagnosed)

− acute bacterial otitis media (adequately diagnosed)

− pharyngitis, tonsillitis

− acute exacerbation of chronic bronchitis (adequately diagnosed)

− mild to moderately severe community acquired pneumonia

- skin and soft tissue infections

- uncomplicated Chlamydia trachomatis urethritis and cervicitis

Considerations should be given to official guidance on the appropriate use of antibacterial agents.

4.2 Posology and method of administration

In uncomplicated Chlamydia trachomatis urethritis and cervicitis , the dosage is 1,000 mg in one single oral dose.

For all other indications the dosage is 1,500 mg, to be administered as 500 mg per day for three consecutive days. Alternatively the same total dosage (1,500 mg) can also be given over a period of 5 days with 500 mg on the first day and then 250 mg on days 2 to 5.

To treat these patients other pharmaceutical forms are also available.

The same dosage as in adult patients is used in the older people. Since older patients can be patients with ongoing proarrhythmic conditions a particular caution is recommended due to the risk of developing cardiac arrhythmia and torsades de pointes (see section 4.4).

Children and adolescents (< 18 years)

The total dosage in children aged 1 year and older is 30 mg/kg administered as 10 mg/kg once daily for three days, or over a period of five days starting with a single dose of 10 mg/kg on the first day, followed by doses of 5 mg/kg per day for the following 4 days, according to the tables shown below. There are limited data on use in children younger than 1 year.

The dosage for the treatment of pharyngitis caused by Streptococcus pyogenes is an exception: in the treatment of pharyngitis caused by Streptococcus pyogenes Azithromycin has proved to be effective when it is administered to children as a single dose of 10 mg/kg or 20 mg/kg for 3 days with a maximum daily dosage of 500 mg. At these two dosages a comparable clinical effect was observed, even if the eradication of the bacteria was more significant at a daily dosage of 20 mg/kg.

Penicillin is however the drug of first choice in the treatment of pharyngitis caused by Streptococcus pyogenes and the prevention of subsequent rheumatic fever.

Patients with renal impairment:

No dose adjustment is necessary in patients with mild to moderate renal impairment (GFR 10-80 ml/min) (see section 4.4).

Patients with hepatic impairment:

A dose adjustment is not necessary for patients with mild to moderately impaired liver function (see section 4.4).

Method of administration

Before use the powder should be reconstituted with water into a white to off white, homogenous suspension, see section 6.6. After reconstitution the drug can be administered using a PE/PP syringe for oral use.

After taking the suspension a bitter after-taste can be avoided by drinking fruit juice directly after swallowing. Azithromycin powder for oral suspension should be given in a single daily dosage. The suspension may be taken together with food.

The use of this product is contraindicated in patients with hypersensitivity to azithromycin, erythromycin, any macrolide or ketolide antibiotic, or to any of the excipients listed in section 6.1 (see also section 4.4).

4.4 Special warnings and precautions for use

As with erythromycin and other macrolides, rare serious allergic reactions, including angioedema and anaphylaxis (rarely fatal), have been reported. Some of these reactions with azithromycin have resulted in recurrent symptoms and required a longer period of observation and treatment.

Since liver is the principal route of elimination for azithromycin, the use of azithromycin should be undertaken with caution in patients with significant hepatic disease. Cases of fulminant hepatitis potentially leading to life-threatening liver failure have been reported with azithromycin (see section 4.8). Some patients may have had pre-existing hepatic disease or may have been taking other hepatotoxic medicinal products.

In case of signs and symptoms of liver dysfunction, such as rapid developing asthenia associated with jaundice, dark urine, bleeding tendency or hepatic encephalopathy, liver function tests / investigations should be performed immediately. Azithromycin administration should be stopped if liver dysfunction has emerged.

In patients receiving ergot derivatives, ergotism has been precipitated by co-administration of some macrolide antibiotics. There are no data concerning the possibility of an interaction between ergot and azithromycin. However, because of the theoretical possibility of ergotism, azithromycin and ergot derivatives should not be coadministered.

As with any antibiotic preparation, observation for signs of superinfection with non - susceptible organisms, including fungi is recommended.

Clostridium difficile associated diarrhoea (CDAD) has been reported with the use of nearly all antibacterial agents, including azithromycin, and may range in severity from mild diarrhoea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile .

C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhoea following antibiotic use. Careful medical history is necessary since CDAD has been reported to occur over two months after the administration of antibacterial agents.

In patients with severe renal impairment (GFR <10 ml/min) a 33% increase in systemic exposure to azithromycin was observed (see Section 5.2).

Prolonged cardiac repolarisation and QT interval, imparting a risk of developing cardiac arrhythmia and torsades de pointes, have been seen in treatment with macrolides including azithromycin (see section 4.8). Therefore as the following situations may lead to an increased risk for ventricular arrhythmias (including torsade de pointes) which can lead to cardiac arrest, azithromycin should be used with caution in patients with ongoing proarrhythmic conditions (especially women and elderly patients) such as patients:

• With congenital or documented QT prolongation

• Currently receiving treatment with other active substances known to prolong QT interval such as antiarrhythmics of class IA (quinidine and procainamide ) and class III (dofetilide, amiodarone and sotalol), cisapride and terfenadine; antipsychotic agents such as pimozide; antidepressants such as citalopram; and fluoroquinolones such as moxifloxacin and levofloxacin

• With electrolyte disturbance, particularly in cases of hypokalaemia and hypomagnesemia

• With clinically relevant bradycardia, cardiac arrhythmia or severe cardiac insufficiency

Exacerbations of the symptoms of myasthenia gravis and new onset of myasthenia syndrome have been reported in patients receiving azithromycin therapy (see section 4.8).

Safety and efficacy for the prevention or treatment of ( Mycobacterium avium complex) in children have not been established.

The following should be considered before prescribing azithromycin:

Azithromycin powder for oral solution is not suitable for treatment of severe infections where a high concentration of the antibiotic in the blood is rapidly needed.

Azithromycin is not the first choice for the empiric treatment of infections in areas where the prevalence of resistant isolates is 10% or more (see section 5.1).

In areas with a high incidence of erythromycin A resistance, it is especially important to take into consideration the evolution of the pattern of susceptibility to azithromycin and other antibiotics.

As for other macrolides, high resistance rates of Streptococcus pneumoniae (> 30 %) have been reported for azithromycin in some European countries (see section 5.1). This should be taken into account when treating infections caused by Streptococcus pneumoniae .

Azithromycin is not the substance of first choice for the treatment of pharyngitis and tonsillitis caused by Streptococcus pyogenes . For this and for the prophylaxis of acute rheumatic fever penicillin is the treatment of first choice.

Often, azithromycin is not the substance of first choice for the treatment of sinusitis.

Acute otitis media

Often, azithromycin is not the substance of first choice for the treatment of acute otitis media.

Skin and soft tissue infections

The main causative agent of soft tissue infections, Staphylococcus aureus . is frequently resistant to azithromycin. Therefore, susceptibility testing is considered a precondition for treatment of soft tissue infections with azithromycin.

Infected burn wounds

Azithromycin is not indicated for the treatment of infected burn wounds.

Sexually transmitted disease

In case of sexually transmitted diseases a concomitant infection by T. palladium should be excluded.

Neurological or psychiatric diseases

Azithromycin should be used with caution in patients with neurological or psychiatric disorders.

Caution in diabetic patients: 5 ml of reconstituted suspension contain 3.70 g of sucrose.

Patients with rare hereditary problems of fructose intolerance, glucose-galactose malabsorption or sucrase-isomaltase insufficiency should not take this medicine since it contains sucrose.

Azithromycin 200mg/5 ml c ontain aspartame which is a source of phenylalanine. It may be harmful for people with phenylketonuria.

4.5 Interaction with other medicinal products and other forms of interaction

In a pharmacokinetic study investigating the effects of simultaneous administration of antacid with azithromycin, no effect on overall bioavailability was seen although peak serum concentrations were reduced by approximately 25%. In patients receiving both azithromycin and antacids, the drugs should not be taken simultaneously.

In healthy volunteers, coadministration of a 5-day regimen of azithromycin with cetirizine 20 mg at steady-state resulted in no pharmacokinetic interaction and no significant changes in the QT interval.

Coadministration of 1200 mg/day azithromycin with 400 mg/day didanosine in 6 HIV-positive subjects did not appear to affect the steady-state pharmacokinetics of didanosine as compared with placebo.

Digoxin (P-gp substrates)

Concomitant administration of macrolide antibiotics, including azithromycin, with P-glycoprotein substrates such as digoxin, has been reported to result in increased serum levels of the P-glycoprotein substrate. Therefore, if azithromycin and P-gp substrates such as digoxin are administered concomitantly, the possibility of elevated serum concentrations of the substrate should be considered.

Single 1000 mg doses and multiple 1200 mg or 600 mg doses of azithromycin had little effect on the plasma pharmacokinetics or urinary excretion of zidovudine or its glucuronide metabolite. However, administration of azithromycin increased the concentrations of phosphorylated zidovudine, the clinically active metabolite, in peripheral blood mononuclear cells. The clinical significance of this finding is unclear, but it may be of benefit to patients.

Azithromycin does not interact significantly with the hepatic cytochrome P450 system. It is not believed to undergo the pharmacokinetic drug interactions as seen with erythromycin and other macrolides. Hepatic cytochrome P450 induction or inactivation via cytochrome-metabolite complex does not occur with azithromycin.

Due to the theoretical possibility of ergotism, the concurrent use of azithromycin with ergot derivatives is not recommended (see Section 4.4).

Pharmacokinetic studies have been conducted between azithromycin and the following drugs known to undergo significant cytochrome P450 mediated metabolism.

Ergotamine derivatives . Due to the theoretical possibility of ergotism, the concurrent use of azithromycin with ergot derivatives is not recommended (see section 4.4). Astemizole, alfentanil

There are no known data on interactions with astemizole or alfentanil. Caution is advised in the co-administration of these medicines with Azithromycin because of the known enhancing effect of these medicines when used concurrently with the macrolid antibiotic erythromycin.

Coadministration of atorvastatin (10 mg daily) and azithromycin (500 mg daily) did not alter the plasma concentrations of atorvastatin (based on a HMG CoA-reductase inhibition assay). However, post-marketing cases of rhabdomyolysis in patients receiving azithromycin with statins have been reported.

In a pharmacokinetic interaction study in healthy volunteers, no significant effect was observed on the plasma levels of carbamazepine or its active metabolite in patients receiving concomitant azithromycin.

Cisapride is metabolized in the liver by the enzyme CYP 3A4. Because macrolides inhibit this enzyme, concomitant administration of cisapride may cause the increase of QT interval prolongation, ventricular arrhythmias and torsades de pointes.

In a pharmacokinetic study investigating the effects of a single dose of cimetidine, given 2 hours before azithromycin, on the pharmacokinetics of azithromycin, no alteration of azithromycin pharmacokinetics was seen.

Coumarin-Type Oral Anticoagulants

In a pharmacokinetic interaction study, azithromycin did not alter the anticoagulant effect of a single 15 mg dose of warfarin administered to healthy volunteers. There have been reports received in the post-marketing period of potentiated anticoagulation subsequent to coadministration of azithromycin and coumarin-type oral anticoagulants. Although a causal relationship has not been established, consideration should be given to the frequency of monitoring prothrombin time when azithromycin is used in patients receiving coumarin-type oral anticoagulants.

In a pharmacokinetic study with healthy volunteers that were administered a 500 mg/day oral dose of azithromycin for 3 days and were then administered a single 10 mg/kg oral dose of cyclosporin, the resulting cyclosporin C max and AUC 0-5 were found to be significantly elevated. Consequently, caution should be exercised before considering concurrent administration of these drugs. If coadministration of these drugs is necessary, cyclosporin levels should be monitored and the dose adjusted accordingly.

Coadministration of a 600 mg single dose of azithromycin and 400 mg efavirenz daily for 7 days did not result in any clinically significant pharmacokinetic interactions.

Coadministration of a single dose of 1200 mg azithromycin did not alter the pharmacokinetics of a single dose of 800 mg fluconazole. Total exposure and half-life of azithromycin were unchanged by the coadministration of fluconazole, however, a clinically insignificant decrease in C max (18%) of azithromycin was observed.

Coadministration of a single dose of 1200 mg azithromycin had no statistically significant effect on the pharmacokinetics of indinavir administered as 800 mg three times daily for 5 days.

In a pharmacokinetic interaction study in healthy volunteers, azithromycin had no significant effect on the pharmacokinetics of methylprednisolone.

In healthy volunteers, coadministration of azithromycin 500 mg/day for 3 did not cause clinically significant changes in the pharmacokinetics and pharmacodynamics of a single 15 mg dose of midazolam.

Coadministration of azithromycin (1200 mg) and nelfinavir at steady state (750 mg three times daily) resulted in increased azithromycin concentrations. No clinically significant adverse effects were observed and no dose adjustment is required.

Coadministration of azithromycin and rifabutin did not affect the serum concentrations of either drug.

Neutropenia was observed in subjects receiving concomitant treatment of azithromycin and rifabutin. Although neutropenia has been associated with the use of rifabutin, a causal relationship to combination with azithromycin has not been established (see Section 4.8).

In normal healthy male volunteers, there was no evidence of an effect of azithromycin (500 mg daily for 3 days) on the AUC and C max of sildenafil or its major circulating metabolite.

Pharmacokinetic studies have reported no evidence of an interaction between azithromycin and terfenadine. There have been rare cases reported where the possibility of such an interaction could not be entirely excluded; however there was no specific evidence that such an interaction had occurred.

There is no evidence of a clinically significant pharmacokinetic interaction when azithromycin and theophylline are co-administered to healthy volunteers.

In 14 healthy volunteers, coadministration of azithromycin 500 mg on Day 1 and 250 mg on Day 2 with 0.125 mg triazolam on Day 2 had no significant effect on any of the pharmacokinetic variables for triazolam compared to triazolam and placebo.

Coadministration of trimethoprim/sulfamethoxazole (160 mg/800 mg) for 7 days with azithromycin 1200 mg on Day 7 had no significant effect on peak concentrations, total exposure or urinary excretion of either trimethoprim or sulfamethoxazole. Azithromycin serum concentrations were similar to those seen in other studies.

Substances that prolong the QT interval

Azithromycin should not be used concurrently with other active substances that prolong the QT interval (see section 4.4).

4.6 Fertility, pregnancy and lactation

There are no adequate data from the use of Azithromycin in pregnant women. In reproduction toxicity studies in animals azithromycin was shown to pass the placenta, but no teratogenic effects were observed. The safety of azithromycin has not been confirmed with regard to the use of the active substance during pregnancy. Therefore Azithromycin should only be used during pregnancy if the benefit outweighs the risk.

Azithromycin has been reported to be secreted into human breast milk, but there are no adequate and well-controlled clinical studies in nursing women that have characterized the pharmacokinetics of azithromycin excretion into human breast milk.

In fertility studies conducted in rat, reduced pregnancy rates were noted following administration of azithromycin. The relevance of this finding to humans is unknown.

4.7 Effects on ability to drive and use machines

There is no evidence to suggest that azithromycin may have an effect on a patient's ability to drive or operate machinery.

4.8 Undesirable effects

The table below lists the adverse reactions identified through clinical trial experience and post-marketing surveillance by system organ class and frequency.

The frequency grouping is defined using the following convention: Very common (≥ 1/10); common (≥ 1/100 to < 1/10); uncommon (≥ 1/1,000 to < 1/100); rare (≥ 1/10,000 to < 1/1,000); very rare (< 1/10,000); and not known (cannot be estimated from the available data).

Within each frequency grouping, undesirable effects are presented in order of decreasing seriousness.

Adverse reactions possibly or probably related to azithromycin based on clinical trial experience and post-marketing surveillance:

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme: www. mhra. gov. uk/yellowcard .

Adverse events experienced in higher than recommended doses were similar to those seen at normal doses. In the event of overdosage, general symptomatic and supportive measures are indicated as required

5. Pharmacological properties

5.1 Pharmacodynamic properties

Pharmacotherapeutic group: antibacterials for systemic use; macrolides; azithromycin, ATC code: J01FA10

Azithromycin is an azalide, a sub-class of the macrolide antibiotics. By binding to the 50S-ribosomal sub-unit, azithromycin avoids the translocation of peptide chains from one side of the ribosome to the other. As a consequence of this, RNA-dependent protein synthesis in sensitive organisms is prevented.

For azithromycin the AUC/MIC is the major PK/PD parameter correlating best with the efficacy of azithromycin.

Mechanism of resistance

Resistance to azithromycin may be inherent or acquired. There are three main mechanisms of resistance in bacteria: target site alteration, alteration in antibiotic transport and modification of the antibiotic.

Complete cross resistance exists among Streptococcus pneumoniae . betahaemolytic streptococcus of group A, Enterococcus faecalis and Staphylococcus aureus . including methicillin resistant S. aureus (MRSA) to erythromycin, azithromycin, other macrolides and lincosamides.

EUCAST (European Committee on Antimicrobial Susceptibility Testing)

The prevalence of acquired resistance may vary geographically and with time for selected species and local information on resistance is desirable, particularly when treating severe infections. As necessary, expert advice should be sought when the local prevalence of resistance is such that the utility of the agent in at least some types of infections is questionable.

Pathogens for which resistance may be a problem: prevalence of resistance is equal to or greater than 10% in at least one country in the European Union.

Table of susceptibility

Commonly susceptible species

Aerobic Gram-negative microorganisms

Species for which acquired resistance may be a problem

Aerobic Gram-positive microorganisms

Inherently resistant organisms

Aerobic Gram-positive microorganisms

Staphylococcus aureus – methicillin resistant and erythromycin resistant strains

Streptococcus pneumoniae – penicillin resistant strains

Aerobic Gram-negative microorganisms

Anaerobic Gram-negative microorganisms

* Clinical effectiveness is demonstrated by sensitive isolated organisms for approved clinical indications.

5.2 Pharmacokinetic properties

The biological availability of azithromycin after oral administration is approximately 37%. Peak plasma levels are achieved 2-3 hours after taking the medicinal product.

After oral administration, azithromycin is distributed throughout the entire body. Pharmacokinetic studies have shown clearly higher azithromycin levels in the tissues than in the plasma (up to 50 times the maximum observed concentration in plasma). This indicates that the substance is bound in the tissues in considerable quantities.

Concentrations in the infected tissues, such as lungs, tonsil and prostate are higher than the MRC90 of the most frequently occurring pathogens after a single dose of 500 mg.

The protein binding of azithromycin in serum is variable and varies, depending on the serum concentration, from 52% at 0.05 mg/l to 12% at 0.5 mg/l. The steady state distribution volume is 31.1 l/kg.

The terminal plasma-elimination half-life closely follows the tissue depletion half-life from 2 to 4 days.

Approximately 12% of an intravenously administered dose of azithromycin is, over a period of 3 days, excreted unchanged in the urine. High concentrations of unchanged azithromycin were found in human bile. In this, ten metabolites were also detected (formed by N - and O - desmethylation, by hydroxylation of the desosamin and aglycon rings and by splitting the cladinose conjugate). A comparison of fluid chromatography and microbiological assessment methods shows that the metabolites are microbiologically inactive.

In animal models high concentrations of azithromycin were found in phagocytes. Also it has been shown that during active phagocytosis higher concentrations of azithromycin are released than during inactive phagocytosis. In animal models this process was shown to contribute to the accumulation of azithromycin in infectious tissue.

Pharmacokinetics in special populations

Following a single oral dose of azithromycin 1 g, mean C max and AUC 0-120 increased by 5.1% and 4.2% respectively, in subjects with mild to moderate renal impairment (glomerular filtration rate of 10-80 ml/min) compared with normal renal function (GFR > 80 ml/min). In subjects with severe renal impairment, the mean C max and AUC 0-120 increased 61% and 33% respectively compared to normal.

In patients with mild to moderate hepatic impairment, there is no evidence of a marked change in serum pharmacokinetics of azithromycin compared to normal hepatic function. In these patients, urinary recovery of azithromycin appears to increase perhaps to compensate for reduced hepatic clearance.

The pharmacokinetics of azithromycin in elderly men was similar to that of young adults; however, in elderly women, although higher peak concentrations (increased by 30-50%) were observed, no significant accumulation occurred.

Infants, toddlers, children and adolescents

Pharmacokinetics have been studied in children aged 4 months – 15 years taking capsules, granules or suspension. At 10 mg/kg on day 1 followed by 5 mg/kg on days 2-5, the C max achieved is slightly lower than adults with 224 ug/l in children aged 0.6-5 years and after 3 days dosing and 383 ug/l in those aged 6-15 years. The t 1/2 of 36 h in the older children was within the expected range for adults.

5.3 Preclinical safety data

In animal tests in which the dosages used amounted to 40 times the clinical therapeutic dosages, azithromycin was found to have caused reversible phospholipidosis, but as a rule no true toxicological consequences were observed which were associated with this. The relevance of this finding to humans receiving azithromycin in accordance with the recommendations is unknown.

Electrophysiological investigations have shown that azithromycin prolongs the QT interval.

There was no evidence of a potential for genetic and chromosome mutations in in-vivo and in-vitro test models.

In embryotoxicity studies in mice and rats no teratogenic effects were observed. In rats, azithromycin dosages of 100 and 200 mg/kg bodyweight/day led to slight retardations in fetal ossification and in maternal weight gain. In peri-/postnatal studies in rats, slight retardations in physical development and delay in reflex development were observed following treatment with 50 mg/kg/day azithromycin and above.

6. Pharmaceutical particulars

6.1 List of excipients

Clavuxil Para Que Sirve, Clavuxil

Clavuxil

Acceso rapido al contenido

Especial antencion con menores de 12 anos

Tenga especial cuidado durante el embarazo .

No usar Clavuxil con lactantes.

Revise siempre que no sea alergico a ninguno de los componentes de Clavuxil . 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

FORMULA

CLAVUXIL® 500 mg-125 mg, cada CAPLET contiene: Amoxicilina trihidrato equivalente a: Amoxicilina 500 mg Clavulanato de potasio equivalente a: Acido clavulanico 125 mg

CLAVUXIL

® 250 mg - 62.50 mg SUSPENSION PEDIATRICA, cada 5 ml contienen: Amoxicilina trihidrato equivalente a: Amoxicilina 250 mg Clavulanato de potasio equivalente a: Acido clavulanico 62.5 mg Biclavuxil® 400 mg-57 mg, SUSPENSION PEDIATRICA, cada 5 ml contienen: Amoxicilina trihidrato equivalente a: Amoxicilina 400 mg Clavulanato de potasio equivalente a: Acido clavulanico 57 mg

INDICACIONES

Es bactericida contra un amplio rango de bacterias que incluyen: Bacterias grampositivas: Aerobios: S. aureus, S. sapro­phyticus, S. faecalis, S. pneumoniae, S. pyogenes, S. viridans. Anaerobios: especies de Clos­tridium, especies de Peptococcus, especies de Peptos­treptococcus. Bacterias gramnegativas: Aerobios: H. influen­zae, M. catarrhalis, E. coli, especies de Klebsiella, Proteus mirabilis, Proteus vulgaris, Neisseria gonorrhoeae, especies de Legionella. Anaerobios: Especies de bacteroides, incluyendo B. fragilis.

CLAVUXIL

® esta indicado en el tratamiento de las infecciones bacterianas en las condiciones siguientes: sinusitis, otitis media, bronquitis aguda y cronica, neumonia, bronco­neu­monia, cistitis, tonsilitis, uretritis, pielonefritis, infecciones de la piel y los tejidos blandos, vaginitis en ninas, abscesos periodontales.

PRECAUCIONES

Durante el embarazo y lactancia: Categoria B.

CONTRAINDICACIONES

Hipersensibilidad a la penicilina. Antecedentes de disfuncion hepatica e ictericia colestacica asociada a la combinacion.

EFECTOS COLATERALES

Los efectos colaterales son de naturaleza transitoria. Se han reportado nauseas, indigestion, vomitos, diarrea y can­didiasis. Las nauseas se asocian con dosis altas, pudiendo disminuirse tales efectos ingiriendo el medicamento antes de las comidas. Los problemas de urticaria ocurren con menos frecuencia. DOSIS: Adultos: 250 mg. Cada 8 horas o 500 mg cada 12 horas. Neonatos o infantes menores de 12 semanas 30 mg/kg/dia cada 8 horas. Pacientes mayores a 12 semanas 40 mg/kg/dia, cada 8 horas. Ninos con peso mayor de 40 kg de acuerdo a recomendaciones de adulto. Biclavuxil® 20-40 mg/kg/dia, cada 12 horas.

PRESENTACIONES

CLAVUXIL

® 250-62.50 mg granulos para suspension oral: Frasco con 60 ml.

CLAVUXIL

® 500-125 mg caplet: Caja con 12 y 30 capletas en blister pack. Biclavuxil® 400 mg-57 mg/5 ml granulos para suspension oral: frasco con 50 ml.

ICTERICIA . Es la pigmentacion amarilla del blanco de los ojos o de la piel, provocada por un exceso de bilirrubina en la sangre que acaba depositandose en los tejidos.

URTICARIA . Existen multiples causas de la urticaria, pero la erupcion se caracteriza siempre por ronchas rojas pruriginosas.

Opiniones

Crotamitex - Drug Review Dosage, Side Effects, Action, Buy Crotamitex, Crotamitex

Crotamitex

Crotamitex is a scabicidal, a medication specifically for the intervention of scabies. It comes in a cream and lotion that is applied to the skin to get rid of parasites that cause itching.

CROTAMITEX ACTION

Crotamitex is usable under the brand names Eurax. Euraxil. Veteusan. and Crotan. It is commended for adults and children with pruritis or skin itching resulting from scabies and even sunburn. Crotamitex produces counter-irritation by cooling the infected area after it evaporates from the skin.

CROTAMITEX DOSAGE

Dosage of this medication varies based on the condition of the scabies. It is common that physicians prescribe Crotamitex twice a week - once in one day, and again the following day. Dosage can be increased for more severe cases. Children may have a lesser dosage as prescribed by their physician.

For affected roles with itching skin, apply Crotamitex on the affected area until the medication is completely absorbed.

For affected roles with scabies, apply enough Crotamitex on the affected area. Rub the medication in well, specifically in folds and creases, hands, the area between the toes and fingers, and areas that are usually moist such as the groin and underarms.

Leave the treated area to dry. The second coat of Crotamitex should come a day after the first coat. The following day, place a freshly washed cloth on the affected area then allow the area to dry. Change the beddings to avoid re-infection. Two days after the second coating, take a bath to get rid of the medication.

Crotamitex should not be applied to the mucous membranes including the eye and internal portion of the nose since it can cause irritation. In case the cream or lotion is accidentally applied to these areas, users should thoroughly flush the area with running water.

This medication should always be kept away from children and should not be exposed directly to heat or light.

CROTAMITEX SIDE EFFECTS

While Crotamitex can effectively cure itching caused by scabies it can also result in side effects. The chances may be low, but users may still suffer from unwanted effects. Side effects may require medical help in case they persist or worsen.

Some of the side effects of Crotamitex are skin irritation and rashes that were not present prior to the use of the medication.

CROTAMITEX PRECAUTIONS

For those with scabies, good hygiene is required to prevent the chances of re-infection or infecting other people. Always machine wash underwear, sheets, towels, pajamas, and clothes in hot water.

Those who are using Crotamitex for the first time should tell their doctors of their medical history, particularly any possible atopy to Crotamitex. An atopy to other substances like dyes should also be revealed.

Users should avoid sexual contact while Crotamitex has not yet cured the infection. They should also avoid using combs, clothing, and hair accessories since these can easily transmit the infections.

The use of this medication can also worsen certain skin conditions such as inflamed skin. Always make sure to get the approval of a doctor before using Crotamitex.

Crotamitex has the following structural formula:

Molecular formula of crotamitex is C13H17NO Chemical IUPAC Name is N-ethyl-N-(2-methylphenyl)-but-2-enamide Molecular weight is 203.28 g/mol Crotamitex available. 10% cream 60gm Tube, 10% lotion, 10% lotion 60ml bottle

Generic name: Crotamiton

Filters - Housings, Salomax

Filters play an important role in any industrial society. Filtration is the separation of particles from a fluid by passage of that fluid through a permeable medium.

We offer the following different kinds of filters for the application of mechanical filtration in domestic households, industries and institutions:

Polypropylene (PP) fiber type sediment cartridges

These sediment cartridges made of polypropylene fibers. They provide excellent filtration of sand, silt, rust and suspended solids from portable water. They are individually shrink wrapped for purity. Micron ratings: 1, 5, 10, 20 and 50 Height/ Length: 10, 20, 30 and 40 Inch Filter Diameter: 2.5 and 4.5 Inch

Polypropylene string type sediment cartridges

These sediment cartridges are made of polypropylene US FDA approved strings. They provide excellent filtration of sand, silt, rust and suspended solids from portable water. The cartridges should not be used for microbiological contaminated water. Micron ratings: 1, 5,10, 20 and 50 Height/ Length: 10 and 20 Inch Filter diameter: 2.5 and 4.5 Inch

Pleated cartridges

100% cellulose free synthetic media for increased dirt holding capacity, longer life and reduced filter costs. No additives or binders • Increased surface area and longer life • Washable and reusable: Filter is cleanable, 5 micron and up, to lower cartridge replacement cost

Micron ratings . 0.2, 0.45, 0.5, 1, 5, 10, 20 and 50 Height/ Length: 10, 20, 30 and 40 Inch Filter diameter: 2.5 and 4.5 Inch

Activated carbon block filter cartridges

5 micron nominal, extruded coconut shell carbon block cartridge ideal for the removal of chlorine, taste, color and odor. Height/ Length: 10 and 20 Inch Filter diameter: 2.5 and 4.25 Inch

10 inch reusable ceramic filter cartridge

• Fits industry 10 inch housings • Filtration efficiency of more than 99.9 % at 0.5 micron • Highly efficient bacteriological filtration • Ideal for post filtration • Complimentary to UV systems

Filter Bags

Popular applications; • Waste vegetable oil filtration • Bio – Diesel filtration • Aquarium filtration • Juice clarification • Fermented beer clarification

In-Line Filter Housings and Portable Domestic Water Purifiers

We supply filter housings for filters, filter bags, other purpose filters and reverse osmosis components.

We also supply dosmetic water purifiers;

Cetriwal Tab Price, Side-Effects, Uses Generic-Alternatives & Dosage Of Cetriwal Tab In India, Cetri

LIPAGLYN 4 mg. Pack of 10 Tablets

Side Effects of Incid-L Tab:

Somnolence, insomnia, malaise, headache, dizziness; GI discomfort, dry mouth, abdominal pain, diarrhoea, nausea, vomiting; occasional hypersensitivity; epistaxis, pharyngitis, bronchospasm.

Drug Interactions of Incid-L Tab:

Risk of increased INR and epistaxis when taken together with warfarin. Potentially Fatal: CNS depressants and anticholinergics may potentiate CNS depression of cetirizine.

Contraindications of Incid-L Tab:

Mechanism of Action of Incid-L Tab:

Cetirizine is a potent and highly selective antagonist of the peripheral histamine H1-receptor on effector cells in the GI tract, blood vessels and respiratory tract. Absorption: Absorbed rapidly from the GI tract (oral); peak plasma concentrations after 1 hr. Rate, but not extent, of absorption altered by food. Distribution: Enters breast milk; crosses the blood-brain barrier (insignificant amounts). Protein-binding: Highly bound. Excretion: Via the urine (as unchanged); 10 hr (elimination half-life).

Special Precautions for Incid-L Tab:

Hepatic or renal impairment; elderly; tasks requiring mental alertness eg, driving or operating heavy machinery; pregnancy.

Categories

Decordex, Decordex

Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas).

Availability: In Stock (34 packs)

Other names of Decadron:

Product Description Common use Decadron is used to treat conditions such as arthritis, blood/hormone/immune system disorders, allergic reactions, certain skin and eye conditions, breathing problems, certain bowel disorders. Also it is used in the treatment of cancers of the white blood cells (leukemias), and lymph gland cancers (lymphomas). Finally, Decadron is used as replacement therapy in patients whose adrenal glands are unable to produce sufficient amounts of corticosteroids.

Dosage and direction Take this medication by mouth as directed by your doctor. The initial oral dose is 0.75 to 9 mg daily depending on the disease. The initial dose should be adjusted according to the response to therapy. Take with food or milk to prevent stomach upset. Take this medication by mouth with food or a full glass of water or milk unless your doctor directs you otherwise. If you take this medication once daily, take it in the morning before 9 AM. Use this medication regularly in order to get the most benefit from it. Take it at the same time(s) each day. It is important to continue taking this medication even if you feel well. Follow the dosing schedule carefully, and take this medication exactly as prescribed. Do not stop taking this medication without consulting your doctor. Inform your doctor if your condition does not improve or worsens.

Precautions Do not get immunizations, vaccinations, or skin tests unless specifically directed by your doctor. Before taking Decadron, tell your doctor or pharmacist if you have any allergies, your medical history: active fungal infections, kidney or liver disease, mental/mood conditions, low blood minerals, thyroid disease, stomach/intestinal problems, high blood pressure, heart problems, diabetes, eye diseases, brittle bones, history of blood clots. If you have been taking this medication for a long time, your body may not make enough natural hormones while you are under physical stress. Your dose may need to be adjusted. If you have stopped taking this drug within the past 12 months, you may need to start taking it again if your body is under physical stress. Before having surgery, tell your doctor or dentist that you are using this medication or have taken it within the last 12 months. If you have a history of ulcers or take large doses of aspirin or other arthritis medication. Limit alcoholic beverages while taking this medication to decrease the risk of stomach/intestinal bleeding. If you have diabetes, this drug may make it harder to control your blood sugar levels. Monitor your blood sugar levels regularly and inform your doctor of the results. During pregnancy, this medication should be used only when clearly needed. Discuss the risks and benefits with your doctor. This drug may pass into breast milk and could have undesirable effects on a nursing infant. Therefore, breast-feeding is not recommended while using this medication. Avoid contact with people who have recently received oral polio vaccine or flu vaccine inhaled through the nose, chickenpox or measles unless you have previously had these diseases (in childhood). If you are exposed to one of these infections and you have not previously had it, seek immediate medical attention.

Contraindications Do NOT use Decadron if you are allergic to any ingredient in Decadron, you have a systemic fungal infection, you are taking mifepristone. Contact your doctor or health care provider immediately if any of these apply to you.

Possible side effects

Side effects of Decadron depend on the dose, the duration and the frequency of administration. Short courses of dexamethasone usually are well tolerated with few and mild side effects. Long term, high dose dexamethasone usually will produce predictable and potentially serious side effects. Whenever possible, the lowest effective dose of dexamethasone should be used for the shortest possible length of time to minimize side effects. Alternate day dosing also can help reduce side effects. Side effects include fluid retention, weight gain, high blood pressure, loss of potassium, headache, muscle weakness, puffiness, and hair growth on the face, thinning and easy bruising of skin, glaucoma, cataracts, peptic ulceration, worsening of diabetes, irregular menses, growth retardation in children, convulsions, stomach upset, headache, dizziness, menstrual changes, trouble sleeping, increased appetite, or weight gain may occur, depression, euphoria, insomnia, mood swings, personality changes, and even psychotic behavior. A very serious allergic reaction to this drug is rare. If any of these effects persist or worsen, notify your doctor or pharmacist promptly.

Drug interactions Drugs such as phenobarbital, ephedrine, phenytoin (Dilantin), and rifampin (Rifadin, Rimactane) may increase the breakdown of corticosteroids by the liver. As a result it may be lower blood levels and reduced effects. Therefore, the dose of corticosteroid may need to be increased if treatment with any of these agents is begun.

Missed dose If you are taking this medication daily and on a regular schedule, and you miss a dose, take it as soon as you remember. If it is near the time of the next dose, skip the missed dose and resume your usual dosing schedule. Do not double the dose to catch up.

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

Storage Decadron should be stored at 68-77 F (20-25 C) and not frozen

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.

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Buy Otoflox Online - Self Healing Centre, Otoflox

Otoflox

Medication guide about Otoflox (Ofloxacin)

Brand name: Otoflox Generic name: Ofloxacin

What is the most important information I should know about Otoflox? Take this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Otoflox will not treat a viral infection such as the common cold or flu. Take Otoflox with a full glass of water (8 ounces). Drink several extra glasses of fluid each day to prevent crystals from forming in the urine. Take Otoflox on an empty stomach 1 hour before or 2 hours after meals. Otoflox 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. Do not give this medicine to a child younger than 18 years old. Otoflox may interfere with bone development in a child. There are certain medicines you should not take within the 2 hours before or after you take Otoflox. This includes antacids that contain magnesium or aluminum (Tums or Rolaids), the ulcer medicine sucralfate (Carafate), didanosine (Videx), and vitamin or mineral supplements that contain iron or zinc. Taking these other medicines too close to your dose of Otoflox can make the antibiotic much less effective.

What is Otoflox? Otoflox is in a group of antibiotics called fluoroquinolones (flor-o-KWIN-o-lones). Otoflox fights bacteria in the body. Otoflox is used to treat bacterial infections that cause bronchitis, pneumonia, chlamydia, gonorrhea, skin infections, urinary tract infections, and infections of the prostate. Otoflox may also be used for purposes other than those listed in this medication guide.

What should I discuss with my healthcare provider before taking Otoflox? Before taking Otoflox, tell your doctor if you have: kidney disease; seizures or epilepsy; or a history of head injury or brain tumor. If you have any of these conditions, you may not be able to use Otoflox, or you may need a dosage adjustment or special tests during treatment. FDA pregnancy category C. This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. Otoflox 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. Do not give this medicine to a child younger than 18 years old. Otoflox may interfere with bone development in a child.

How should I take Otoflox? Take this medication exactly as it was prescribed for you. Do not take the medication in larger amounts, or take it for longer than recommended by your doctor. Take Otoflox with a full glass of water (8 ounces). Drink several extra glasses of fluid each day to prevent crystals from forming in the urine. Take Otoflox on an empty stomach 1 hour before or 2 hours after meals. Take Otoflox at evenly spaced intervals. Follow your doctor’s instructions. Take this medication for the entire length of time prescribed by your doctor. Your symptoms may get better before the infection is completely treated. Otoflox will not treat a viral infection such as the common cold or flu. To be sure this medication is not causing harmful effects, your blood will need to be tested on a regular basis. Your kidney or liver function may also need to be tested. It is important that you not miss any scheduled visits to your doctor. This medication can cause you to have unusual results with certain medical tests. Tell any doctor who treats you that you are using Otoflox. Store this medication at room temperature away from moisture and heat. 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. If you are more than 2 hours late in taking your medicine, 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 taken too much of this medicine. Symptoms of an Otoflox overdose may include drowsiness, nausea, hot or cold feeling, confusion, and slurred speech.

What should I avoid while taking Otoflox? There are certain medicines you should not take within the 2 hours before or after you take Otoflox. This includes antacids that contain magnesium or aluminum (Tums or Rolaids), the ulcer medicine sucralfate (Carafate), didanosine (Videx), and vitamin or mineral supplements that contain iron or zinc. Taking these other medicines too close to your dose of Otoflox can make the antibiotic much less effective. Avoid exposure to sunlight or artificial UV rays (sunlamps or tanning beds). Otoflox can make your skin more sensitive to sunlight and sunburn may result. Use a sunscreen (minimum SPF 15) and wear protective clothing if you must be out in the sun. Antibiotic medicines can cause diarrhea, which may be a sign of a new infection. If you have diarrhea that is watery or has blood in it, call your doctor. Do not use any medicine to stop the diarrhea unless your doctor has told you to. Otoflox 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.

What are the possible side effects of Otoflox? 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 Otoflox and call your doctor at once if you have any of these serious side effects: seizure (convulsions); confusion, hallucinations (seeing things that are not there); a red, blistering, peeling skin rash; urinating less than usual or not at all; tremors or shaking; easy bruising or bleeding, unusual weakness; unusual thoughts or behavior; nausea, stomach pain, low fever, loss of appetite, dark urine, clay-colored stools, jaundice (yellowing of the skin or eyes); sudden pain or swelling near your joints (especially in your arm or ankle); numbness, burning, pain, or tingly feeling; or diarrhea that is watery or bloody. Continue using Otoflox and talk with your doctor if you have any of these less serious side effects: feeling restless, nervous, or agitated; nausea, vomiting, diarrhea; headache, drowsiness; vaginal itching or discharge; ringing in the ears; or sleep problems (insomnia). 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 Otoflox? Before taking Otoflox, tell your doctor if you are taking any of the following drugs: theophylline (Theo-Dur, Theolair, Slo-Phyllin, Slo-Bid, Elixophyllin); probenecid (Benemid); a blood thinner such as warfarin (Coumadin); cimetidine (Tagamet, Tagamet HB); cyclosporine (Neoral, Sandimmune, Gengraf); insulin or an oral diabetes medication such as glipizide (Glucotrol), glyburide (Micronase, Diabeta, Glynase), and others; or aspirin or other NSAIDs (non-steroidal anti-inflammatory drugs) such as ibuprofen (Motrin, Advil), diclofenac (Voltaren), indomethacin, naproxen (Aleve, Naprosyn), piroxicam (Feldene), nabumetone (Relafen), etodolac (Lodine), and others. If you are using any of these drugs, you may not be able to use Otoflox, or you may need dosage adjustments or special tests during treatment. There may be other drugs not listed that can affect Otoflox. 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.

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Taiproton, Taiproton

Prevacid decreases the amount of acid produced in the stomach. It is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.

Availability: In Stock (34 packs)

Other names of Prevacid:

What is this medicine?

LANSOPRAZOLE prevents the production of acid in the stomach. It is used to treat gastroesophageal reflux disease (GERD), ulcers, certain bacteria in the stomach, inflammation of the esophagus, and Zollinger-Ellison Syndrome. It can also be used to prevent and treat ulcers in patients taking medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions: liver disease an unusual or allergic reaction to lansoprazole, other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth. Swallow the capsules whole with a drink of water. Do not crush or chew. This medicine works best if taken on an empty stomach 30 to 60 minutes before food. Take your medicine at regular intervals. Do not take more often than directed.

If you have difficulty swallowing the capsules, you may open the capsule and sprinkle the contents on a tablespoon of any of the following foods: applesauce, Ensure brand pudding, cottage cheese, yoghurt, or strained pears. Do not crush the contents of the capsule into the food. Swallow the dose immediately after preparing it. Do not chew. Follow with a drink of water.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine, contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with the following: atazanavir

This medicine may also interact with the following medications: ampicillin delavirdine digoxin iron salts itraconazole, ketoconazole, voriconazole, or other prescription medicines for fungus or yeast infections sucralfate theophylline warfarin

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

It can take several days before your stomach pain gets better. Check with your doctor or health care professional if your condition does not start to get better or if it gets worse.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible. dark yellow or brown urine fever or sore throat unusual skin rash, blistering, or peeling unusual bleeding or bruising yellowing of the eyes or skin vomiting

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): diarrhea or constipation headache nausea stomach pain or gas

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Protect from moisture. Throw away any unused medicine after the expiration date.

Prevacid decreases the amount of acid produced in the stomach. It is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.

Availability: In Stock (34 packs)

Other names of Prevacid:

What is this medicine?

LANSOPRAZOLE prevents the production of acid in the stomach. It is used to treat gastroesophageal reflux disease (GERD), ulcers, certain bacteria in the stomach, inflammation of the esophagus, and Zollinger-Ellison Syndrome. It can also be used to prevent and treat ulcers in patients taking medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions: liver disease an unusual or allergic reaction to lansoprazole, other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth. Swallow the capsules whole with a drink of water. Do not crush or chew. This medicine works best if taken on an empty stomach 30 to 60 minutes before food. Take your medicine at regular intervals. Do not take more often than directed.

If you have difficulty swallowing the capsules, you may open the capsule and sprinkle the contents on a tablespoon of any of the following foods: applesauce, Ensure brand pudding, cottage cheese, yoghurt, or strained pears. Do not crush the contents of the capsule into the food. Swallow the dose immediately after preparing it. Do not chew. Follow with a drink of water.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine, contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with the following: atazanavir

This medicine may also interact with the following medications: ampicillin delavirdine digoxin iron salts itraconazole, ketoconazole, voriconazole, or other prescription medicines for fungus or yeast infections sucralfate theophylline warfarin

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

It can take several days before your stomach pain gets better. Check with your doctor or health care professional if your condition does not start to get better or if it gets worse.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible. dark yellow or brown urine fever or sore throat unusual skin rash, blistering, or peeling unusual bleeding or bruising yellowing of the eyes or skin vomiting

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): diarrhea or constipation headache nausea stomach pain or gas

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Protect from moisture. Throw away any unused medicine after the expiration date.

Prevacid decreases the amount of acid produced in the stomach. It is used to treat and prevent stomach and intestinal ulcers, erosive esophagitis (damage to the esophagus from stomach acid) and other conditions involving excessive stomach acid such as Zollinger-Ellison syndrome.

Availability: In Stock (34 packs)

Other names of Prevacid:

What is this medicine?

LANSOPRAZOLE prevents the production of acid in the stomach. It is used to treat gastroesophageal reflux disease (GERD), ulcers, certain bacteria in the stomach, inflammation of the esophagus, and Zollinger-Ellison Syndrome. It can also be used to prevent and treat ulcers in patients taking medicines called non-steroidal anti-inflammatory drugs (NSAIDs).

What should I tell my health care provider before I take this medicine?

They need to know if you have any of these conditions: liver disease an unusual or allergic reaction to lansoprazole, other medicines, foods, dyes, or preservatives pregnant or trying to get pregnant breast-feeding

How should I take this medicine?

Take this medicine by mouth. Swallow the capsules whole with a drink of water. Do not crush or chew. This medicine works best if taken on an empty stomach 30 to 60 minutes before food. Take your medicine at regular intervals. Do not take more often than directed.

If you have difficulty swallowing the capsules, you may open the capsule and sprinkle the contents on a tablespoon of any of the following foods: applesauce, Ensure brand pudding, cottage cheese, yoghurt, or strained pears. Do not crush the contents of the capsule into the food. Swallow the dose immediately after preparing it. Do not chew. Follow with a drink of water.

Talk to your pediatrician regarding the use of this medicine in children. Special care may be needed.

If you think you have taken too much of this medicine, contact a poison control center or emergency room at once.

NOTE: This medicine is only for you. Do not share this medicine with others.

What if I miss a dose?

If you miss a dose, take it as soon as you can. If it is almost time for your next dose, take only that dose. Do not take double or extra doses.

What may interact with this medicine?

Do not take this medicine with the following: atazanavir

This medicine may also interact with the following medications: ampicillin delavirdine digoxin iron salts itraconazole, ketoconazole, voriconazole, or other prescription medicines for fungus or yeast infections sucralfate theophylline warfarin

Tell your prescriber or health care professional about all other medicines you are taking, including non-prescription medicines, nutritional supplements, or herbal products. Also tell your prescriber or health care professional if you are a frequent user of drinks with caffeine or alcohol, if you smoke, or if you use illegal drugs. These may affect the way your medicine works. Check with your health care professional before stopping or starting any of your medicines.

What should I watch for while taking this medicine?

It can take several days before your stomach pain gets better. Check with your doctor or health care professional if your condition does not start to get better or if it gets worse.

What side effects may I notice from this medicine?

Side effects that you should report to your prescriber or health care professional as soon as possible. dark yellow or brown urine fever or sore throat unusual skin rash, blistering, or peeling unusual bleeding or bruising yellowing of the eyes or skin vomiting

Side effects that usually do not require medical attention (report to your prescriber or health care professional if they continue or are bothersome): diarrhea or constipation headache nausea stomach pain or gas

This list may not describe all possible side effects.

Where can I keep my medicine?

Keep out of the reach of children.

Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F). Protect from moisture. Throw away any unused medicine after the expiration date.

Citalopram (Celexa, Cipramil, Seropram) For Depression, Seropram

Information About Citalopram, Sold As Celexa, Cipramil or Seropram

Type of Medication: SSRI

Citalopram is a Selective Serotonin Reuptake Inhibitor with a chemical structure unrelated to that of other SSRIs (except its chemical relative Escitalopram) or of tricyclic, tetracyclic, or other available antidepressant medications.

Benefits of Citalopram (Celexa) for Depression

Citalopram is widely prescribed to help treat depression. It is highly selective in its action on the neurotransmitter serotonin and shows minimal effects on norepinephrine and dopamine neuronal reuptake.

Side Effects of Citalopram (Celexa)

Please note that the following side effects include only some of the most common and somewhat less common but do not include rarer side effects; the list is not exhaustive. Many people taking Citalopram (Celexa, Cipramil, Seropram) experience none of these side effects. Please consult a physician about any unusual symptoms.

Common

Some of the more common side effects of Citalopram (Celexa, Cipramil, Seropram) include:

sexual problems in males

Less Common

Some of the less common side effects of Citalopram (Celexa, Cipramil, Seropram) include:

nausea

dry mouth

sleepiness

increase in sweating

Citalopram (Celexa) and Alcohol

Although Citalopram (Celexa, Cipramil, Seropram) has not been shown to potentiate the cognitive or motor effects of alcohol, the manufacturer recommends against the use of alcohol with the medication.

Stopping Citalopram (Celexa): Discontinuation Effects or Withdrawal Symptoms

It is best to consult a physician before discontinuing SSRIs. Specific information on the effects of stopping taking Citalopram (Celexa, Cipramil, Seropram) was not available from the sources consulted at the time of writing, but the discontinuation effects of stopping other SSRIs include:

dizziness

vertigo/light-headedness

nausea

fatigue

headache

insomnia

abdominal cramps

chills

increased dreaming

agitation

anxiety

Should You Buy Citalopram (Celexa) Online?

Particularly in the United States, many individuals choose to purchase medications online, either for reasons of cost savings, privacy, or both. Both brand-name Celexa and so-called ‘generic Celexa’ (i. e. Citalopram without the Celexa brand name) can sometimes be purchased at deep discounts (and sometimes without a prescription) in this way. Before undertaking any purchase of medications online, however — and certainly if you are contemplating doing so without a prior prescription — please consider the integrity of the supplier and the national and/or local laws which may apply where you live.

For more on the political and safety controversies about buying drugs online (including VIPPS, price-gouging, and more) see our separate site MedsDebate. com .

Information Sources and Disclaimer

The information provided here has been summarized in good faith purely for educational purposes. It is not intended in any way to replace the advice of a qualified medical professional. Please do not take any action on the basis of information contained here without consulting a physician. Unless otherwise specified, information is intended to apply only to adult use of the medication. Drug interaction precautions have not been included; please consult another source for this information .

All registered trademarks are the property of their respective owners.

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Normelox, Normelox

Ruduo skaiciuoja dar tik pirmasias dienas, taciau peršalimo ligos pradeda savo plitimo sezona. Permainingas rudeninis oras bei nepakankamas rupinimasis savo ir šeimos nariu sveikata daznai nulemia viena nemaloniausiu bei sunkiausiai prognozuojamu sveikatos sutrikimu – gerkles skausma. „Dazniausiai gerkles skausmo sukelejai yra virusai, kurie pazeidzia gerkles gleivine. Uzklupus virusiniam gerkles uzdegimui peršti, skauda gerkle, juntamas burnos sausumas, kosejama ar ciaudejama, vargina sloga, neretai uzkimstama, šiek tiek pakyla temperatura.

Buvo manoma, kad gyvunams tapus socialesniais, jie tuo paciu pradejo keistis ir ivairiomis infekcijomis, todel išaugo stiprios imunines sistemos poreikis. Mokslininkai iš Virdzinijos universiteto pirma karta irode, kad imunine sistema tiesiogiai reguliuoja smegenu dali, atsakinga uz socialini elgesi. Tai reiškia, kad iš tiesu gyvunu evoliucijos procese viskas vyko atvirkšciai, nei manyta. Zurnale „Nature“ aprašytas tyrimas su grauzikais. Mokslininkai pastebejo, kad peles, kurios neturejo imunines molekules – interferono gama (IFN-γ), buvo maziau socialios ir net turejo polinki i autizma.

Lietuva pradeda bendradarbiavima su Japonijos medicinos tyrimu agentura AMED. Tai buvo sutarta susitikimo Sveikatos apsaugos ministerijoje metu, kuomet sveikatos apsaugos viceministras Valentinas Gavrilovas susitiko su Japonijos delegacija, vadovaujama dr. Makoto Suematsu.

Vyrai kile iš Marso, moterys – iš Veneros. Vieniems šis posakis gali pasirodyti visiškai neteisingas, tuo tarpu kiti mano – „tiesiai i dešimtuka“. Visgi šis posakis tikrai turi pagrindo, ypac kalbant apie svorio metima. Moterims kur kas sunkiau nei vyrams numesti nepageidaujama svori del ivairiu priezasciu. Kartais tai rodosi visiškai neteisinga. Atrodo, jog moterims uztenka zvilgtelti i skanu deserta, ir šlaunys bei klubai savaime paplateja. Tuo tarpu vyrai, tik nezymiai sumazine maisto porciju dydi, pasiekia puikiu rezultatu. Priezastis, kodel moterims sunkiau numesti svorio nei vyrams, ivardija tinklarašcio apie mityba, sveika gyvensena ir sporta ikurejas ir autorius Arnas Slenys.

Ankstyvas senejimas yra viena didziausiu moteru baimiu. Saules spinduliai ir aplinkos tarša daro itaka musu odai, del to atsiranda pigmentines demes, raukšles ir kiti ankstyvo senejimo pozymiai. Puoseledamos grozi, visuomet labiau rupinames veido oda, o pamirštame kakla ir rankas. Tuo tarpu kaklas ir rankos yra tos vietos, kurios labiausiai atspindi musu amziu. Todel ju prieziurai reiketu skirti zymiai daugiau demesio. Tinklapis Econet pateikia efektyvias naturalias priemones, kurias galite pasigaminti pacios.

Ar esate sau uzdave klausima, koks jusu gyvenimo tikslas? Kokia apskritai gyvenimo ir Visatos prasme? Kas jus padaro laimingais? Meikas Wikingas, zinomas Danijos laimes guru ir knygu apie laime autorius, Laimes tyrinejimu instituto Danijoje direktorius, atskleidzia, ka iš tikruju reiškia buti laimingiems. „Hygge“ – štai kuo vadovaujasi danai. Taip vadinamas konceptas, kuris šiems zmonems padeda iškesti ilga ir tamsia ziema. O visa tai, kas slypi tame, suteikia ir itin daug dziaugsmo.

Ieskomiausiu TOP 5

Skaitos kompiuteriu servisas UAB Farmaciniu informaciniu sistemu skyrius K. Petrausko 19A, Kaunas tel: (8

Atsakomybes apribojimas Copyright © 2013 Skaitos kompiuteriu servisas UAB. Visos teises saugomos.

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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.

Was this page helpful?

Caltrans District 1 - Willits Bypass - Reports And Presentations, Cozep

Willits Bypass - Reports and Presentations

Sherwood Road Intersection Improvement (Geometric Upgrades) Project

Ryan Creek Fish Passage Mitigation Project

Final Mitigation and Monitoring Proposal (MMP) approved by the California Department of Fish and Wildlife and the North Coast Regional Water Quality Control Board - June 2014

Mitigation and Monitoring Proposal (MMP) submitted to the U. S Army Corps of Engineers - January 2012

Mitigation and Monitoring Proposal (MMP) submitted to the U. S Army Corps of Engineers - October 2011

Public Open House Held August 22, 2007 The materials presented at the open house:

Final Environmental Impact Statement/Environmental Impact Report (FEIS/EIR) October 2006

Tegretol - Pain Relief, Folkalepsin

Tegretol (carbamazepine) is an anticonvulsant. It works by decreasing nerve impulses that cause seizures and pain. Tegretol is used to treat seizures and nerve pain such as trigeminal neuralgia and diabetic neuropathy. Carbamazepine is also used to treat bipolar disorder. Tegretol may also be used for purposes not listed in this medication guide.

Take Tegretol 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. Your doctor may occasionally change your dose to make sure you get the best results.

Do not crush, chew, or break an extended-release Tegretol tablet. Swallow the pill whole. Breaking the pill would cause too much of the drug to be released at one time.

Shake the Tegretol oral suspension (liquid) well just before you measure a dose. Measure the liquid with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

It may take up to 4 weeks before your symptoms improve. Keep using the medication as directed and call your doctor promptly if this medicine seems to stop working as well in preventing your seizures. Tegretol can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill.

To be sure Tegretol is not causing harmful effects, your blood cells and kidney function may need to be tested often. Do not miss any follow up visits to your doctor for blood or urine tests. Your doctor may also recommend having your eyes checked regularly while you are taking this medicine.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using this medicine suddenly. Wear a medical alert tag or carry an ID card stating that you take Tegretol. Any medical care provider who treats you should know that you take seizure medication.

Store this medicine at room temperature away from moisture, heat, and light.

Active Ingredient: Carbamazepine

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction. Seek emergency medical attention if you have a fever, sore throat, headache and skin pain, followed by a red or purple skin rash that spreads and causes blistering and peeling.

You should not take Tegretol if you have a history of bone marrow suppression, if you are also taking nefazodone, or if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Tegretol may cause harm to an unborn baby, but having a seizure during pregnancy could harm both the mother and the baby. Tell your doctor right away if you become pregnant while taking Tegretol for seizures. Do not start or stop taking Tegretol during pregnancy without your doctor's advice.

Before you take Tegretol, tell your doctor if you have heart disease, high blood pressure, high cholesterol, liver or kidney disease, glaucoma, a thyroid disorder, lupus, porphyria, or a history of mental illness or psychosis.

You may have thoughts about suicide while taking Tegretol. Your doctor will need to check you at regular visits. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

There are many other drugs that can interact with Tegretol. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Keep a list of all your medicines and show it to any healthcare provider who treats you.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using Tegretol suddenly.

Do not use Tegretol if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. You should not take Tegretol if you are allergic to carbamazepine, or if you have:

a history of bone marrow suppression

if you are also taking nefazodone; or

if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Important safety information:

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

To make sure you can safely take Tegretol, tell your doctor if you have any of these other conditions:

heart disease, high blood pressure, high cholesterol or triglycerides;

liver or kidney disease;

a thyroid disorder;

a history of mental illness or psychosis.

Patients of Asian ancestry may have a higher risk of developing a rare but serious skin reaction to Tegretol. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

You may have thoughts about suicide while taking Tegretol. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed. Seizure control is very important during pregnancy. The benefit of preventing seizures may outweigh any risks posed by taking Tegretol. Follow your doctor's instructions about taking Tegretol while you are pregnant.

FDA pregnancy category D. Tegretol may cause harm to an unborn baby. Do not start taking this medcine without telling your doctor if you are pregnant or planning to become pregnant. Use effective birth control while you are taking this medicine. Although Tegretol may harm an unborn baby, having a seizure during pregnancy could harm both mother and baby. If you become pregnant while taking Tegretol, do not stop taking the medicine without your doctor's advice.

Carbamazepine can pass into breast milk and may harm a nursing baby. You should not breast-feed while you are using Tegretol. Carbamazepine can make birth control pills less effective. Ask your doctor about using a non-hormone method of birth control (such as a condom, diaphragm, spermicide) to prevent pregnancy while taking Tegretol.

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Avoid drinking alcohol. It can increase some of the side effects of Tegretol, and can also increase your risk of seizures.

Avoid exposure to sunlight or tanning beds. Tegretol can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

Grapefruit and grapefruit juice may interact with Tegretol and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor.

Get emergency medical help if you have any of these signs of an allergic reaction to Tegretol: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Call your doctor at once if you have a serious side effect such as:

pale skin, feeling light-headed, rapid heart rate, trouble concentrating;

fever, chills, sore throat, mouth and throat ulcers;

easy bruising or bleeding, severe tingling, numbness, pain, muscle weakness;

confusion, agitation, vision problems, hallucinations;

feeling short of breath, swelling of your ankles or feet;

urinating less than usual;

jaundice (yellowing of the skin or eyes); or

severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Less serious Tegretol side effects may include:

feeling dizzy, drowsy, or unsteady;

nausea, vomiting, diarrhea, constipation, stomach pain;

headache, ringing in your ears;

dry mouth, swollen tongue; or

joint or muscle pain, leg cramps.

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

Tegretol (carbamazepine) is an anticonvulsant. It works by decreasing nerve impulses that cause seizures and pain. Tegretol is used to treat seizures and nerve pain such as trigeminal neuralgia and diabetic neuropathy. Carbamazepine is also used to treat bipolar disorder. Tegretol may also be used for purposes not listed in this medication guide.

Take Tegretol 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. Your doctor may occasionally change your dose to make sure you get the best results.

Do not crush, chew, or break an extended-release Tegretol tablet. Swallow the pill whole. Breaking the pill would cause too much of the drug to be released at one time.

Shake the Tegretol oral suspension (liquid) well just before you measure a dose. Measure the liquid with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

It may take up to 4 weeks before your symptoms improve. Keep using the medication as directed and call your doctor promptly if this medicine seems to stop working as well in preventing your seizures. Tegretol can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill.

To be sure Tegretol is not causing harmful effects, your blood cells and kidney function may need to be tested often. Do not miss any follow up visits to your doctor for blood or urine tests. Your doctor may also recommend having your eyes checked regularly while you are taking this medicine.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using this medicine suddenly. Wear a medical alert tag or carry an ID card stating that you take Tegretol. Any medical care provider who treats you should know that you take seizure medication.

Store this medicine at room temperature away from moisture, heat, and light.

Active Ingredient: Carbamazepine

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction. Seek emergency medical attention if you have a fever, sore throat, headache and skin pain, followed by a red or purple skin rash that spreads and causes blistering and peeling.

You should not take Tegretol if you have a history of bone marrow suppression, if you are also taking nefazodone, or if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Tegretol may cause harm to an unborn baby, but having a seizure during pregnancy could harm both the mother and the baby. Tell your doctor right away if you become pregnant while taking Tegretol for seizures. Do not start or stop taking Tegretol during pregnancy without your doctor's advice.

Before you take Tegretol, tell your doctor if you have heart disease, high blood pressure, high cholesterol, liver or kidney disease, glaucoma, a thyroid disorder, lupus, porphyria, or a history of mental illness or psychosis.

You may have thoughts about suicide while taking Tegretol. Your doctor will need to check you at regular visits. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

There are many other drugs that can interact with Tegretol. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Keep a list of all your medicines and show it to any healthcare provider who treats you.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using Tegretol suddenly.

Do not use Tegretol if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. You should not take Tegretol if you are allergic to carbamazepine, or if you have:

a history of bone marrow suppression

if you are also taking nefazodone; or

if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Important safety information:

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

To make sure you can safely take Tegretol, tell your doctor if you have any of these other conditions:

heart disease, high blood pressure, high cholesterol or triglycerides;

liver or kidney disease;

a thyroid disorder;

a history of mental illness or psychosis.

Patients of Asian ancestry may have a higher risk of developing a rare but serious skin reaction to Tegretol. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

You may have thoughts about suicide while taking Tegretol. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed. Seizure control is very important during pregnancy. The benefit of preventing seizures may outweigh any risks posed by taking Tegretol. Follow your doctor's instructions about taking Tegretol while you are pregnant.

FDA pregnancy category D. Tegretol may cause harm to an unborn baby. Do not start taking this medcine without telling your doctor if you are pregnant or planning to become pregnant. Use effective birth control while you are taking this medicine. Although Tegretol may harm an unborn baby, having a seizure during pregnancy could harm both mother and baby. If you become pregnant while taking Tegretol, do not stop taking the medicine without your doctor's advice.

Carbamazepine can pass into breast milk and may harm a nursing baby. You should not breast-feed while you are using Tegretol. Carbamazepine can make birth control pills less effective. Ask your doctor about using a non-hormone method of birth control (such as a condom, diaphragm, spermicide) to prevent pregnancy while taking Tegretol.

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Avoid drinking alcohol. It can increase some of the side effects of Tegretol, and can also increase your risk of seizures.

Avoid exposure to sunlight or tanning beds. Tegretol can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

Grapefruit and grapefruit juice may interact with Tegretol and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor.

Get emergency medical help if you have any of these signs of an allergic reaction to Tegretol: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Call your doctor at once if you have a serious side effect such as:

pale skin, feeling light-headed, rapid heart rate, trouble concentrating;

fever, chills, sore throat, mouth and throat ulcers;

easy bruising or bleeding, severe tingling, numbness, pain, muscle weakness;

confusion, agitation, vision problems, hallucinations;

feeling short of breath, swelling of your ankles or feet;

urinating less than usual;

jaundice (yellowing of the skin or eyes); or

severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Less serious Tegretol side effects may include:

feeling dizzy, drowsy, or unsteady;

nausea, vomiting, diarrhea, constipation, stomach pain;

headache, ringing in your ears;

dry mouth, swollen tongue; or

joint or muscle pain, leg cramps.

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

Tegretol (carbamazepine) is an anticonvulsant. It works by decreasing nerve impulses that cause seizures and pain. Tegretol is used to treat seizures and nerve pain such as trigeminal neuralgia and diabetic neuropathy. Carbamazepine is also used to treat bipolar disorder. Tegretol may also be used for purposes not listed in this medication guide.

Take Tegretol 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. Your doctor may occasionally change your dose to make sure you get the best results.

Do not crush, chew, or break an extended-release Tegretol tablet. Swallow the pill whole. Breaking the pill would cause too much of the drug to be released at one time.

Shake the Tegretol oral suspension (liquid) well just before you measure a dose. Measure the liquid with a special dose-measuring spoon or medicine cup, not with a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.

It may take up to 4 weeks before your symptoms improve. Keep using the medication as directed and call your doctor promptly if this medicine seems to stop working as well in preventing your seizures. Tegretol can lower blood cells that help your body fight infections. This can make it easier for you to bleed from an injury or get sick from being around others who are ill.

To be sure Tegretol is not causing harmful effects, your blood cells and kidney function may need to be tested often. Do not miss any follow up visits to your doctor for blood or urine tests. Your doctor may also recommend having your eyes checked regularly while you are taking this medicine.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using this medicine suddenly. Wear a medical alert tag or carry an ID card stating that you take Tegretol. Any medical care provider who treats you should know that you take seizure medication.

Store this medicine at room temperature away from moisture, heat, and light.

Active Ingredient: Carbamazepine

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction. Seek emergency medical attention if you have a fever, sore throat, headache and skin pain, followed by a red or purple skin rash that spreads and causes blistering and peeling.

You should not take Tegretol if you have a history of bone marrow suppression, if you are also taking nefazodone, or if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Tegretol may cause harm to an unborn baby, but having a seizure during pregnancy could harm both the mother and the baby. Tell your doctor right away if you become pregnant while taking Tegretol for seizures. Do not start or stop taking Tegretol during pregnancy without your doctor's advice.

Before you take Tegretol, tell your doctor if you have heart disease, high blood pressure, high cholesterol, liver or kidney disease, glaucoma, a thyroid disorder, lupus, porphyria, or a history of mental illness or psychosis.

You may have thoughts about suicide while taking Tegretol. Your doctor will need to check you at regular visits. Call your doctor at once if you have any new or worsening symptoms such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

There are many other drugs that can interact with Tegretol. Tell your doctor about all medications you use. This includes prescription, over-the-counter, vitamin, and herbal products. Do not start a new medication without telling your doctor. Keep a list of all your medicines and show it to any healthcare provider who treats you.

Do not stop using Tegretol without first talking to your doctor, even if you feel fine. You may have increased seizures or unpleasant withdrawal symptoms if you stop using Tegretol suddenly.

Do not use Tegretol if you have used an MAO inhibitor such as furazolidone (Furoxone), isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam, Zelapar), or tranylcypromine (Parnate) in the last 14 days. You should not take Tegretol if you are allergic to carbamazepine, or if you have:

a history of bone marrow suppression

if you are also taking nefazodone; or

if you are allergic to an antidepressant such as amitriptyline (Elavil, Vanatrip, Limbitrol), desipramine (Norpramin), imipramine (Tofranil), or nortriptyline (Pamelor).

Important safety information:

Tegretol may cause severe or life-threatening skin rash, especially in people of Asian ancestry. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

To make sure you can safely take Tegretol, tell your doctor if you have any of these other conditions:

heart disease, high blood pressure, high cholesterol or triglycerides;

liver or kidney disease;

a thyroid disorder;

a history of mental illness or psychosis.

Patients of Asian ancestry may have a higher risk of developing a rare but serious skin reaction to Tegretol. Your doctor may recommend a blood test before you start the medication to determine your risk of this skin reaction.

Your family or other caregivers should also be alert to changes in your mood or symptoms. Your doctor will need to check you at regular visits. Do not miss any scheduled appointments.

You may have thoughts about suicide while taking Tegretol. Tell your doctor if you have new or worsening depression or suicidal thoughts during the first several months of treatment, or whenever your dose is changed. Seizure control is very important during pregnancy. The benefit of preventing seizures may outweigh any risks posed by taking Tegretol. Follow your doctor's instructions about taking Tegretol while you are pregnant.

FDA pregnancy category D. Tegretol may cause harm to an unborn baby. Do not start taking this medcine without telling your doctor if you are pregnant or planning to become pregnant. Use effective birth control while you are taking this medicine. Although Tegretol may harm an unborn baby, having a seizure during pregnancy could harm both mother and baby. If you become pregnant while taking Tegretol, do not stop taking the medicine without your doctor's advice.

Carbamazepine can pass into breast milk and may harm a nursing baby. You should not breast-feed while you are using Tegretol. Carbamazepine can make birth control pills less effective. Ask your doctor about using a non-hormone method of birth control (such as a condom, diaphragm, spermicide) to prevent pregnancy while taking Tegretol.

This medication may impair your thinking or reactions. Be careful if you drive or do anything that requires you to be alert. Avoid drinking alcohol. It can increase some of the side effects of Tegretol, and can also increase your risk of seizures.

Avoid exposure to sunlight or tanning beds. Tegretol can make you sunburn more easily. Wear protective clothing and use sunscreen (SPF 30 or higher) when you are outdoors.

Grapefruit and grapefruit juice may interact with Tegretol and lead to potentially dangerous effects. Discuss the use of grapefruit products with your doctor.

Get emergency medical help if you have any of these signs of an allergic reaction to Tegretol: hives; difficulty breathing; swelling of your face, lips, tongue, or throat. Report any new or worsening symptoms to your doctor, such as: mood or behavior changes, depression, anxiety, or if you feel agitated, hostile, restless, hyperactive (mentally or physically), or have thoughts about suicide or hurting yourself.

Call your doctor at once if you have a serious side effect such as:

pale skin, feeling light-headed, rapid heart rate, trouble concentrating;

fever, chills, sore throat, mouth and throat ulcers;

easy bruising or bleeding, severe tingling, numbness, pain, muscle weakness;

confusion, agitation, vision problems, hallucinations;

feeling short of breath, swelling of your ankles or feet;

urinating less than usual;

jaundice (yellowing of the skin or eyes); or

severe skin reaction -- fever, sore throat, swelling in your face or tongue, burning in your eyes, skin pain, followed by a red or purple skin rash that spreads (especially in the face or upper body) and causes blistering and peeling.

Less serious Tegretol side effects may include:

feeling dizzy, drowsy, or unsteady;

nausea, vomiting, diarrhea, constipation, stomach pain;

headache, ringing in your ears;

dry mouth, swollen tongue; or

joint or muscle pain, leg cramps.

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

Nitrocard, Nitrocard

Nitroglycerin

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.

Was this page helpful?

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Voltaren Tablets - Paris Forum, Voltarenactigo

Voltaren Tablets - Paris Forum

Voltaren Tablets

I'm hoping someone can help me with a question on a pharmacy medication.

I am taking Voltaren Tablets for inflammation (Diclofenac), I have seen on another thread that the Voltaren gel is available in France. Do they sell the tablets as well?

I don't want to leave with an enormous supply from home & I was wondering if these are available OTC in France. Last time I was in Paris I was taking Nurofen Plus (Ibuprofen & Codeine), these were not available only Ibuprofen on it's own.

My Dr has now put me on Voltaren tablets & they seem to be much better for the inflammation. They are OTC here, but if I need a script, I could have one written by my Dr here, before I leave.

Thank you for any help!

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#1,149 of 1,811 hotels in Paris

Hong D June 21, 2016

1. Re: Voltaren Tablets

May 15, 2012, 8:44 AM

Always, always travel with a copy of your prescription. It will make your life far easier should something happen to the ones you packed. (someone here dropped a pill bottle down the loo. so it doesn't have to be loss or theft!)

Bring the tablets you need for your comfort and well-being. Don't count on buying something you *need*.

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Thanks for all the replies, and thank you Pvoyageuse. That's what I wanted to know. Voltaren are OTC here, so I'll bring extra.

It is only a pain reliever, not a life saving medication. I would be fine on Ibuprofen, if I had to. I just wanted to know if it was OTC in France.

This is why I like to have a hotel with a bath (thank goodness they are common in France) - a nice soak after a long day sightseeing usually does wonders as well!

Thank you again, every time I get on this forum, I thank goodness I'm not travelling 30 years ago, before the internet. LOL !

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Polarized Lens Technology & Supreme Sunglass Frame Construction, Sportflex

LENS TECHNOLOGY

LENS TECHNOLOGY

NATIVE EYEWEAR'S PREMIUM LENS

The most innovative and advanced polarized lens on the market. N3 ™ lenses block up to 4X more infrared light than regular polarized lenses, pass Z87.1 testing, provide UV protection up to 400nm, and by significantly reducing blue light and selectively filtering UV, they deliver high contrast, crisp definition, and peak visual acuity.

STATE-OF-THE-ART PERFORMANCE

INFRARED HEAT PROTECTION

CONTRAST ENHANCEMENT

SUPERIOR IMPACT RESISTANCE

P. C.C. POLARIZED LENS

POLY CRYSTAL CARBONATE

Optical-quality, impact-resistant lenses block 100 percent of the harmful UV light and eliminate glare for sharp, clear vision with increased contrast and depth perception. P. C.C. lenses provide outstanding vision and protection in any lighting condition. Polarized Reflex ™ lenses provide superior glare reduction and enhanced styling.

BENEFITS OF POLARIZATION

CUT THROUGH GLARE AND REDUCE EYE FATIGUE

POLARIZATION

Whether you're hiking, fishing, or just walking down the street, the sun's waves are being reflected off everything from pavement to snow, which creates glare in your vision. Native's polarized sunglasses work as a filter, only letting in the natural light needed to experience the world with clarity.

WHAT IS GLARE?

Glare is reflected light that travels on a horizontal plane. Virtually any surface can be a source of glare, including water, sand, pavement, ice, and snow. All of Native's N3 ™ and P. C.C. ® lenses incorporate a polarized filter that absorbs the horizontal light, thus eliminating glare. You're left with sharp, crisp, glare-free vision, with increased contrast and depth perception.

LENS COLORS

LENS COLORS

FRAME TECHNOLOGY

FRAME TECHNOLOGY

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