Tuesday 23 June 2009

Cetrimide




In some countries, this medicine may only be approved for veterinary use.

Scheme

Rec.INN

ATC (Anatomical Therapeutic Chemical Classification)

D08AJ04,D11AC01

CAS registry number (Chemical Abstracts Service)

0008044-71-1

Therapeutic Categories

Antiseptic

Disinfectant

Chemical Name

Mixture of chiefly tetradecyltrimethylammonium bromide with smaller amounts of dodecyltrimethylammonium bromide and hexadecyltrimethylammonium bromide

Foreign Names

  • Cetrimidum (Latin)
  • Cetrimid (German)
  • Cétrimide (French)
  • Cetrimida (Spanish)

Generic Names

  • Cetrimide (OS: JAN, BAN)
  • Cétrimide (OS: DCF)
  • Zetrimid (IS)
  • Cetrimid (PH: Ph. Eur. 6)
  • Cetrimide (PH: BP 2010, Ph. Int. 4, USP 30, Ph. Eur. 6)
  • Cétrimide (PH: Ph. Eur. 6)
  • Cetrimidum (PH: Ph. Int. 4, Ph. Eur. 6)
  • Strong Cetrimide Solution (PH: BP 2010)

Brand Names

  • Acnederm Foam Wash (Cetrimide and Chlorhexindine)
    Ego, New Zealand


  • Antiseptic Udder Cream (Cetrimide and Chlorhexidine (veterinary use))
    DeLaval, Australia


  • Aseptol (Cetrimide and Chlorhexidine (veterinary use))
    Apex Laboratories, Australia


  • Baxidin (Cetrimide and Chlorhexidine)
    Sanitas, Italy


  • Benzomid (Cetrimide and Benzocaine)
    Surya Dermato Medica, Indonesia


  • Biodicaine (Cetrimide and Lidocaine)
    Biodica, France


  • Boucren
    Bouzen, Argentina


  • Burnol
    Boots, Singapore


  • Cet A Creme (veterinary use)
    AgVantage Animal Health Products, Australia


  • Cetavlex
    AstraZeneca, United Arab Emirates; AstraZeneca, Bahrain; AstraZeneca, Egypt; AstraZeneca, Iraq; AstraZeneca, Jordan; AstraZeneca, Kuwait; AstraZeneca, Lebanon; AstraZeneca, Libya; AstraZeneca, Qatar; AstraZeneca, Saudi Arabia; AstraZeneca, Syria; AstraZeneca, Yemen; Bioglan, Iceland; Centrapharm, United Kingdom; CS, Portugal; Tramedico, Luxembourg


  • Cetavlon
    Cana, Greece; Pierre Fabre, Burkina Faso; Pierre Fabre, Benin; Pierre Fabre, Central African Republic; Pierre Fabre, Congo; Pierre Fabre, Cote D'ivoire; Pierre Fabre, Cameroon; Pierre Fabre, Gabon; Pierre Fabre, Guinea; Pierre Fabre, Madagascar; Pierre Fabre, Mali; Pierre Fabre, Mauritania; Pierre Fabre, Niger; Pierre Fabre, Senegal; Pierre Fabre, Chad; Pierre Fabre, Togo; Pierre Fabre, Vietnam; Pierre Fabre, Zaire; Pierre Fabre Médicament, France


  • Cetream (veterinary use)
    Pettifer, United Kingdom


  • Cetrexidin (Cetrimide and Chlorhexidine)
    Gaba Vebas, Italy


  • Cetriad (veterinary use)
    Fort Dodge, United Kingdom


  • Cetridine (Cetrimide and Chlorhexidine (veterinary use))
    Mavlab, Australia


  • Cetrifarm (Cetrimide and Chlorhexidine)
    Nuova Farmec, Italy


  • Cetrimide Shampoo
    Orion, New Zealand


  • Cetrimide
    Orion, New Zealand; Pharco, Bahrain; PSM, New Zealand; Vitamed, Israel


  • Cevlodil
    Saidal, Algeria


  • Chemilon Antiseptic Solution (Cetrimide and Chlorhexidine)
    Multichem, New Zealand


  • Chlorhexidine & Cetrimide Irrigation (Cetrimide and Chlorhexidine)
    Baxter, New Zealand; Pfizer, New Zealand


  • Corneregel (Cetrimide and Dexpanthenol)
    Riel, Austria


  • Dicagel (Cetrimide and Lidocaine)
    Biodica, France


  • Drapolene (Cetrimide and Benzalkonium chloride)
    Chefaro, United Kingdom


  • Eczema (Cetrimide andAminobenzoic Acid (veterinary use))
    Bomac, New Zealand


  • Equis Fre Itch (veterinary use)
    Mavlab, Australia


  • Farvicett (Cetrimide and Chlorhexidine)
    Nuova Farmec, Italy


  • Fido's Mycodex (veterinary use)
    Mavlab, Australia


  • Foot Rot Aerosol (veterinary use)
    Battle, United Kingdom


  • Hibicet (Cetrimide and Chlorhexidine)
    Cana, Greece; Regent Medical, Netherlands


  • Karicare Barrier Cream (Cetrimide and Dimeticone)
    Nutricia, New Zealand


  • Lanacane C (Cetrimide and Benzocaie)
    Wilson, New Zealand


  • Lidocaina Ogna (Cetrimide and Lidocaine)
    Ogna, Italy


  • Lignosol (Cetrimide and Lidocaine)
    Arab Center, Oman; Arab Centre, Bahrain


  • Lysocalmspray (Cetrimide and Lidocaine)
    Pierre Fabre Médicament, France


  • Morhonine For Dental Use (Cetrimide and Edetic Acid)
    Showa Yakuhin Kako, Japan


  • Neo Resiguard (Cetrimide and Chlorhexidine)
    Nicholas, Indonesia


  • Savlon (Cetrimide and Chlorhexidine)
    AstraZeneca, Oman; Reckitt Benckiser, New Zealand


  • Siopel (Cetrimide and Dimeticone)
    Centrapharm, United Kingdom


  • SOOV Bite (Cetrimide and Lidocaine)
    Ego, New Zealand


  • Sorbicet
    Bouzen, Argentina


  • Stérilène
    Gifrer Barbezat, France


  • Tecsep (Cetrimide and Chlorhexidine (veterinary use))
    Virbac, New Zealand


  • Tisept (Cetrimide and Chlorhexidine)
    Mölnlycke, United Kingdom


  • Travasept (Cetrimide and Chlorhexidine)
    Baxter, United Kingdom


  • Trochain (Cetrimide and Benzocaine)
    Adcock Ingram Pharmaceuticals, South Africa


  • Vanodine Udder Salve (veterinary use)
    Evans Vanodine, United Kingdom


  • Vesagex
    Rybar, Ireland


  • Veterinary Wound Powder (veterinary use)
    Battle, United Kingdom


  • Vetzyme Veterinary Skin Cream (veterinary use)
    Seven Seas, United Kingdom


  • Vidisic
    Angelini, Portugal; Mann, Ireland; Riel, Austria


  • Woundcare Powder (veterinary use)
    Animalcare, United Kingdom


  • Xylonor (Cetrimide and Lidocaine)
    Septodont, Austria; Wild, Switzerland; Prats, Spain; Sanolabor, Slovenia

International Drug Name Search

Glossary

BANBritish Approved Name
DCFDénomination Commune Française
ISInofficial Synonym
JANJapanese Accepted Name
OSOfficial Synonym
PHPharmacopoeia Name
Rec.INNRecommended International Nonproprietary Name (World Health Organization)

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

Sunday 21 June 2009

Berbesolone F




Berbesolone F may be available in the countries listed below.


Ingredient matches for Berbesolone F



Betamethasone

Betamethasone 21-(disodium phosphate) (a derivative of Betamethasone) is reported as an ingredient of Berbesolone F in the following countries:


  • Japan

Neomycin

Neomycin sulfate (a derivative of Neomycin) is reported as an ingredient of Berbesolone F in the following countries:


  • Japan

International Drug Name Search

Fortonol




Fortonol may be available in the countries listed below.


Ingredient matches for Fortonol



Acenocoumarol

Acenocoumarol is reported as an ingredient of Fortonol in the following countries:


  • Argentina

International Drug Name Search

Saturday 20 June 2009

Totalon




In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Totalon



Levamisole

Levamisole is reported as an ingredient of Totalon in the following countries:


  • United States

International Drug Name Search

Friday 19 June 2009

Acido Ascorbico




Acido Ascorbico may be available in the countries listed below.


Ingredient matches for Acido Ascorbico



Ascorbic Acid

Acido Ascorbico (DCIT) is known as Ascorbic Acid in the US.

International Drug Name Search

Glossary

DCITDenominazione Comune Italiana

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

DextroStat




In the US, DextroStat (dextroamphetamine systemic) is a member of the drug class CNS stimulants and is used to treat ADHD, Hypersomnia, Narcolepsy and Sexual Dysfunction - SSRI Induced.

US matches:

  • Dextrostat

Ingredient matches for DextroStat



Dexamfetamine

Dexamfetamine is reported as an ingredient of DextroStat in the following countries:


  • United States

Dexamfetamine sulfate (a derivative of Dexamfetamine) is reported as an ingredient of DextroStat in the following countries:


  • United States

International Drug Name Search

Thursday 18 June 2009

Tafil




Tafil may be available in the countries listed below.


Ingredient matches for Tafil



Alprazolam

Alprazolam is reported as an ingredient of Tafil in the following countries:


  • Costa Rica

  • Denmark

  • El Salvador

  • Germany

  • Guatemala

  • Honduras

  • Iceland

  • Mexico

  • Nicaragua

  • Panama

  • Venezuela

International Drug Name Search

Wednesday 17 June 2009

Respa-AR Sustained-Release Tablets


Pronunciation: bell-a-DON-a AL-ka-loids/klor-fen-EER-a-meen/sue-do-eh-FED-rin
Generic Name: Belladonna Alkaloids/Chlorpheniramine/Pseudoephedrine
Brand Name: Examples include Respa-AR and Ru-Tuss


Respa-AR Sustained-Release Tablets are used for:

Relieving congestion, sneezing, runny nose, and itchy, watery eyes due to colds, flu, or hay fever. It may also be used for other conditions as determined by your doctor.


Respa-AR Sustained-Release Tablets are an antihistamine, decongestant, and anticholinergic combination. It works by blocking histamine, a substance in the body that causes sneezing, runny nose, and watery eyes. It also relieves nasal congestion by shrinking the nasal mucous membranes, which promotes nasal drainage, and dries the chest by decreasing lung secretions.


Do NOT use Respa-AR Sustained-Release Tablets if:


  • you are allergic to any ingredient in Respa-AR Sustained-Release Tablets

  • you are pregnant or breast-feeding

  • you take sodium oxybate (GHB) or you have taken furazolidone or a monoamine oxidase (MAO) inhibitor (eg, phenelzine) within the last 14 days

  • you have severe heart blood vessel disease, severe high blood pressure, narrow-angle glaucoma, severe bleeding, severe irritation of the esophagus or other serious problems with the esophagus (eg, esophageal achalasia), peptic ulcer, a blockage of your stomach or bowel, bowel motility problems, severe bowel inflammation (eg, ulcerative colitis), certain muscle problems (eg, myasthenia gravis), or uncontrolled bleeding

  • you are unable to urinate or are having an asthma attack

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



Before using Respa-AR Sustained-Release Tablets:


Some medical conditions may interact with Respa-AR Sustained-Release Tablets. Tell your doctor or pharmacist if you have any medical conditions, especially if any of the following apply to you:


  • if you are planning to become pregnant

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

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

  • if you have a history of diabetes, an enlarged prostate, bladder or kidney problems, high blood pressure, diarrhea, asthma, nerve problems, heart problems, blood clots, a hiatal hernia, an adrenal gland tumor, glaucoma, breathing problems during sleep, seizures, myasthenia gravis (muscle weakness), or an overactive thyroid

Some MEDICINES MAY INTERACT with Respa-AR Sustained-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Alpha-blockers (eg, prazosin, guanethidine, methyldopa), beta-blockers (eg, atenolol), diuretics (eg, furosemide, hydrochlorothiazide), furazolidone, MAO inhibitors (eg, phenelzine), or tricyclic antidepressants (eg, amitriptyline)

  • Alkalizers (eg, calcium or magnesium antacids), anticholinergics (eg, atropine, benztropine, dicyclomine), carbonic anhydrase inhibitors (eg, acetazolamide), ergotamine, or sodium bicarbonate because the side effects of Respa-AR Sustained-Release Tablets may be increased

  • Bromocriptine, catechol-O-methyltransferase (COMT) inhibitors (eg, entacapone), certain stimulants (eg, doxapram, pseudoephedrine), cocaine, digoxin, droxidopa, potassium chloride, or sodium oxybate (GHB) because side effects may be increased by Respa-AR Sustained-Release Tablets

  • Guanadrel, guanethidine, mecamylamine, methyldopa, or reserpine because effectiveness may be decreased by Respa-AR Sustained-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Respa-AR Sustained-Release Tablets 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 Respa-AR Sustained-Release Tablets:


Use Respa-AR Sustained-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Respa-AR Sustained-Release Tablets may be taken with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • Do not take Respa-AR Sustained-Release Tablets at the same time as an antacid, certain medicines for diarrhea (eg, kaolin, pectin, attapulgite, bismuth), or ketoconazole. Take these medicines 2 or 3 hours before or after taking Respa-AR Sustained-Release Tablets.

  • Swallow whole. Do not crush or chew before swallowing. Some brands of Respa-AR Sustained-Release Tablets may be broken in half before they are taken. If you have difficulty swallowing the whole tablet, ask your pharmacist if your brand may be broken in half.

  • If you miss a dose of Respa-AR Sustained-Release Tablets and you are taking it regularly, 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 Respa-AR Sustained-Release Tablets.



Important safety information:


  • Respa-AR Sustained-Release Tablets may cause drowsiness, dizziness, or blurred vision. Do not drive, operate machinery, or do anything else that could be dangerous until you know how you react to Respa-AR Sustained-Release Tablets. Using Respa-AR Sustained-Release Tablets alone, with certain other medicines, or with alcohol may lessen your ability to drive or perform other potentially dangerous tasks.

  • If your symptoms do not improve within 7 days or if you develop a high fever or persistent headache, check with your doctor.

  • Respa-AR Sustained-Release Tablets may cause dry mouth. To relieve dry mouth, suck on sugarless hard candy or ice chips, chew sugarless gum, drink water, or use a saliva substitute.

  • Respa-AR Sustained-Release Tablets may cause your eyes to become sensitive to sunlight. Wearing sunglasses may help.

  • Respa-AR Sustained-Release Tablets may reduce sweating. Do not become overheated in hot weather or during exercise or other activities; heatstroke may occur.

  • Do not take diet or appetite control medicines while you are taking Respa-AR Sustained-Release Tablets without checking with your doctor.

  • Respa-AR Sustained-Release Tablets contains pseudoephedrine. Before you begin taking any new prescription or nonprescription medicine, read the ingredients to see if it also contains pseudoephedrine. If it does or if you are uncertain, contact your doctor or pharmacist.

  • If you have trouble sleeping, ask your doctor or pharmacist about the best time of the day to take Respa-AR Sustained-Release Tablets.

  • Respa-AR Sustained-Release Tablets may interfere with certain lab test results. Be sure your doctors and lab personnel know that you are taking Respa-AR Sustained-Release Tablets.

  • Before you have any medical or dental treatments, emergency care, or surgery, tell the doctor or dentist that you are using Respa-AR Sustained-Release Tablets.

  • Diabetes patients - Respa-AR Sustained-Release Tablets may affect your blood sugar. Check blood sugar levels closely and ask your doctor before adjusting the dose of your diabetes medicine.

  • Caution is advised when using Respa-AR Sustained-Release Tablets the ELDERLY because they may be more sensitive to its effects.

  • Caution is advised when using Respa-AR Sustained-Release Tablets in CHILDREN because they may be more sensitive to its effects.

  • PREGNANCY and BREAST-FEEDING: It is unknown if Respa-AR Sustained-Release Tablets can cause harm to the fetus. If you become pregnant while taking Respa-AR Sustained-Release Tablets, discuss with your doctor the benefits and risks of using Respa-AR Sustained-Release Tablets during pregnancy. Respa-AR Sustained-Release Tablets are excreted in breast milk. Do not breast-feed while taking Respa-AR Sustained-Release Tablets.


Possible side effects of Respa-AR Sustained-Release Tablets:


All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome:



Constipation; diarrhea; dizziness; drowsiness; dry mouth, nose, or throat; excitability; headache; loss of appetite; nausea; nervousness or anxiety; trouble sleeping; upset stomach; vomiting; weakness.



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

Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); difficulty urinating or inability to urinate; fast or irregular heartbeat; hallucinations; mental or mood changes; seizures; severe dizziness, lightheadedness, or headache; tremor; 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.


See also: Respa-AR side effects (in more detail)


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 deep sleep or loss of consciousness; hot or cool skin; irregular heartbeat; irritability, anxiety, or panic; large pupils; numbness or tingling in the arms or legs; seizures; slowed or shallow breathing.


Proper storage of Respa-AR Sustained-Release Tablets:

Store Respa-AR Sustained-Release Tablets at room temperature, between 59 and 86 degrees F (15 and 30 degrees C), in a tightly closed container. Store away from heat, moisture, and light. Do not store in the bathroom. Keep Respa-AR Sustained-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Respa-AR Sustained-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Respa-AR Sustained-Release Tablets are 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 is a summary only. It does not contain all information about Respa-AR Sustained-Release Tablets. If you have questions about the medicine you are taking or would like more information, check with your doctor, pharmacist, or other health care provider.



Issue Date: February 1, 2012

Database Edition 12.1.1.002

Copyright © 2012 Wolters Kluwer Health, Inc.

More Respa-AR resources


  • Respa-AR Side Effects (in more detail)
  • Respa-AR Use in Pregnancy & Breastfeeding
  • Respa-AR Drug Interactions
  • Respa-AR Support Group
  • 6 Reviews for Respa-AR - Add your own review/rating


Compare Respa-AR with other medications


  • Sinus Symptoms

Bertocil




Bertocil may be available in the countries listed below.


Ingredient matches for Bertocil



Betaxolol

Betaxolol hydrochloride (a derivative of Betaxolol) is reported as an ingredient of Bertocil in the following countries:


  • Portugal

International Drug Name Search

Tuesday 16 June 2009

Corsamycin




Corsamycin may be available in the countries listed below.


Ingredient matches for Corsamycin



Oxytetracycline

Oxytetracycline hydrochloride (a derivative of Oxytetracycline) is reported as an ingredient of Corsamycin in the following countries:


  • Indonesia

International Drug Name Search

Saturday 13 June 2009

Minocycline Disphar




Minocycline Disphar may be available in the countries listed below.


Ingredient matches for Minocycline Disphar



Minocycline

Minocycline hydrochloride (a derivative of Minocycline) is reported as an ingredient of Minocycline Disphar in the following countries:


  • Netherlands

International Drug Name Search

Friday 12 June 2009

Insulin Novo Nordisk




Insulin Novo Nordisk may be available in the countries listed below.


Ingredient matches for Insulin Novo Nordisk



Insulin Injection, Soluble

Insulin Injection, Soluble human (a derivative of Insulin Injection, Soluble) is reported as an ingredient of Insulin Novo Nordisk in the following countries:


  • Ethiopia

International Drug Name Search

Sunday 7 June 2009

Coumadin


Coumadin is a brand name of warfarin, approved by the FDA in the following formulation(s):


COUMADIN (warfarin sodium - injectable; injection)



  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: February 7, 1995

    Strength(s): 5MG/VIAL [RLD]

COUMADIN (warfarin sodium - tablet; oral)



  • Manufacturer: BRISTOL MYERS SQUIBB

    Approved Prior to Jan 1, 1982

    Strength(s): 10MG [RLD][AB], 2.5MG [AB], 2MG [AB], 5MG [AB], 7.5MG [AB]


  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: March 1, 1990

    Strength(s): 1MG [AB]


  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: August 24, 1993

    Strength(s): 4MG [AB]


  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: November 18, 1996

    Strength(s): 3MG [AB], 6MG [AB]

Has a generic version of Coumadin been approved?


Yes. The following products are equivalent to Coumadin:


JANTOVEN (warfarin sodium tablet; oral)



  • Manufacturer: USL PHARMA

    Approval date: October 2, 2003

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]

warfarin sodium tablet; oral



  • Manufacturer: BARR

    Approval date: March 26, 1997

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 4MG [AB], 5MG [AB], 7.5MG [AB]


  • Manufacturer: BARR

    Approval date: November 5, 1998

    Strength(s): 3MG [AB], 6MG [AB]


  • Manufacturer: INVAGEN PHARMS

    Approval date: May 25, 2011

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]


  • Manufacturer: MYLAN

    Approval date: September 27, 2004

    Strength(s): 10MG [AB], 1MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]


  • Manufacturer: MYLAN

    Approval date: September 29, 2004

    Strength(s): 2.5MG [AB]


  • Manufacturer: PLIVA

    Approval date: July 5, 2006

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]


  • Manufacturer: TARO

    Approval date: July 15, 1999

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]


  • Manufacturer: ZYDUS PHARMS USA

    Approval date: May 30, 2006

    Strength(s): 10MG [AB], 1MG [AB], 2.5MG [AB], 2MG [AB], 3MG [AB], 4MG [AB], 5MG [AB], 6MG [AB], 7.5MG [AB]

Note: No generic formulation of the following product is available.


  • warfarin sodium - injectable; injection

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Coumadin. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Coumadin.

See also...

  • Coumadin Consumer Information (Drugs.com)
  • Coumadin Consumer Information (Wolters Kluwer)
  • Coumadin Tablets Consumer Information (Wolters Kluwer)
  • Coumadin Consumer Information (Cerner Multum)
  • Coumadin Advanced Consumer Information (Micromedex)
  • Coumadin Intravenous Advanced Consumer Information (Micromedex)
  • Coumadin AHFS DI Monographs (ASHP)
  • Warfarin Consumer Information (Drugs.com)
  • Warfarin Consumer Information (Wolters Kluwer)
  • Warfarin Tablets Consumer Information (Wolters Kluwer)
  • Warfarin Consumer Information (Cerner Multum)
  • Warfarin Advanced Consumer Information (Micromedex)
  • Warfarin Intravenous Advanced Consumer Information (Micromedex)
  • Warfarin Sodium AHFS DI Monographs (ASHP)

Formulatus




Formulatus may be available in the countries listed below.


Ingredient matches for Formulatus



Dextromethorphan

Dextromethorphan hydrobromide (a derivative of Dextromethorphan) is reported as an ingredient of Formulatus in the following countries:


  • Spain

International Drug Name Search

Saturday 6 June 2009

Perphenazin-neuraxpharm




Perphenazin-neuraxpharm may be available in the countries listed below.


Ingredient matches for Perphenazin-neuraxpharm



Perphenazine

Perphenazine is reported as an ingredient of Perphenazin-neuraxpharm in the following countries:


  • Germany

International Drug Name Search

Wednesday 3 June 2009

Tectonik




Tectonik may be available in the countries listed below.


In some countries, this medicine may only be approved for veterinary use.

Ingredient matches for Tectonik



Permethrin

Permethrin is reported as an ingredient of Tectonik in the following countries:


  • Belgium

International Drug Name Search