Sunday, 26 December 2010

Digoxin



Pronunciation: di-JOX-in
Generic Name: Digoxin
Brand Name: Lanoxin


Digoxin is used for:

Treating heart failure or slowing the heart rate in patients with chronic atrial fibrillation, a type of abnormal heart rhythm. It may also be used for other conditions as determined by your doctor.


Digoxin is a digitalis glycoside. It works by increasing the force of contraction of the heart and slowing heart rate.


Do NOT use Digoxin if:


  • you are allergic to any ingredient in Digoxin or other digitalis medicines

  • you have certain types of heart rhythm problems, such as ventricular fibrillation

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



Before using Digoxin:


Some medical conditions may interact with Digoxin. 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 severe heart failure or other heart problems (eg, inflammation, heart block, cor pulmonale, cardiomyopathy, amyloid heart disease ), extra heart beats (premature ventricular contractions [PVCs]), other types of abnormal heart rhythm, heart problems due to low thiamine (eg, beriberi heart disease), Wolff-Parkinson-White syndrome, heart blood vessel problems, or fainting due to a heart problem

  • if you have severe kidney, liver, or lung problems, or a thyroid problem

  • if you have low blood levels of calcium, magnesium, or potassium, or high blood levels of potassium or calcium

  • if you have had a recent heart attack

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


  • Alprazolam, amiodarone, amphotericin B, anticholinergics (eg, propantheline), beta-blockers (eg, propranolol, carvedilol), bupivacaine, calcium, cyclosporine, diltiazem, diphenoxylate, diuretics (eg, hydrochlorothiazide, furosemide), indomethacin, itraconazole, macrolides (eg, erythromycin), propafenone, quinidine, quinine, spironolactone, stimulants (eg, amphetamine), succinylcholine, sympathomimetics (eg, albuterol, pseudoephedrine), tetracyclines (eg, doxycycline), thioamines (eg, methimazole), or verapamil because they may increase the risk of Digoxin's side effects, especially on the heart

  • Acarbose, penicillamine, rifampin, or thyroid hormones (eg, levothyroxine) because they may decrease Digoxin's effectiveness

  • Oral aminoglycosides (eg, neomycin) because the actions and side effects of Digoxin may be increased or decreased

  • Spironolactone because it may interfere with certain lab tests for digoxin blood levels and give false readings

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


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


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

  • Do not use Digoxin if it contains particles, is cloudy or discolored, or if the vial is cracked or damaged.

  • 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 Digoxin, 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 Digoxin.



Important safety information:


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

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

  • Digoxin may interfere with certain lab tests, including an electrocardiogram (ECG). Be sure your doctor and lab personnel know you are using Digoxin.

  • Lab tests, including ECG, electrolytes, kidney function, and blood digoxin levels, may be performed while you use Digoxin. These tests may be used to monitor your condition or check for side effects. Be sure to keep all doctor and lab appointments.

  • Use Digoxin with caution in the ELDERLY; they may be more sensitive to its effects.

  • Use Digoxin with extreme caution in NEWBORN INFANTS, especially those who are premature or immature; they may be more sensitive to its effects.

  • Poisoning may occur in children who accidently swallow Digoxin or receive too much medicine. In case of an overdose, call a doctor or poison control center right away.

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


Possible side effects of Digoxin:


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:



Diarrhea; nausea.



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 vision, yellow vision, or other vision changes; confusion; fast, slow, or irregular heartbeat; hallucinations; mood or mental changes (eg, depression); severe or persistent nausea, vomiting, or stomach pain; unusual bruising or bleeding; unusual tiredness or weakness.



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 very fast, very slow, or irregular heartbeat.


Proper storage of Digoxin:

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


General information:


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

  • Digoxin 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 is a summary only. It does not contain all information about Digoxin. 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 Digoxin resources


  • Digoxin Use in Pregnancy & Breastfeeding
  • Drug Images
  • Digoxin Drug Interactions
  • Digoxin Support Group
  • 6 Reviews for Digoxin - Add your own review/rating


  • Digoxin Professional Patient Advice (Wolters Kluwer)

  • Digoxin Monograph (AHFS DI)

  • digoxin Advanced Consumer (Micromedex) - Includes Dosage Information

  • Lanoxicaps Prescribing Information (FDA)

  • Lanoxin Prescribing Information (FDA)

  • Lanoxin Consumer Overview



Compare Digoxin with other medications


  • Atrial Fibrillation
  • Heart Failure

Losartan AL




Losartan AL may be available in the countries listed below.


Ingredient matches for Losartan AL



Losartan

Losartan potassium salt (a derivative of Losartan) is reported as an ingredient of Losartan AL in the following countries:


  • Germany

International Drug Name Search

Saturday, 25 December 2010

Carvedilol Merck




Carvedilol Merck may be available in the countries listed below.


Ingredient matches for Carvedilol Merck



Carvedilol

Carvedilol is reported as an ingredient of Carvedilol Merck in the following countries:


  • Netherlands

  • Portugal

International Drug Name Search

GERD (Gastroesophageal Reflux Disease) Medications


Definition of GERD: Gastroesophageal reflux disease (GERD) is when food or liquid travels from the stomach back up into the esophagus (the tube from the mouth to the stomach). This partially digested material is usually acidic and can irritate the esophagus, often causing heartburn and other symptoms.

Drugs associated with GERD

The following drugs and medications are in some way related to, or used in the treatment of GERD. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.

See sub-topics

Topics under GERD

  • Barrett's Esophagus (12 drugs)

Learn more about GERD (Gastroesophageal Reflux Disease)





Drug List:

Friday, 24 December 2010

Apokinon




Apokinon may be available in the countries listed below.


Ingredient matches for Apokinon



Apomorphine

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


  • Argentina

  • France

International Drug Name Search

Trimiron




Trimiron may be available in the countries listed below.


Ingredient matches for Trimiron



Desogestrel

Desogestrel is reported as an ingredient of Trimiron in the following countries:


  • Estonia

  • Lithuania

  • Sweden

Ethinylestradiol

Ethinylestradiol is reported as an ingredient of Trimiron in the following countries:


  • Estonia

  • Lithuania

  • Sweden

International Drug Name Search

Thursday, 23 December 2010

Adrénaline




Adrénaline may be available in the countries listed below.


Ingredient matches for Adrénaline



Epinephrine

Adrénaline (DCF) is known as Epinephrine in the US.

International Drug Name Search

Glossary

DCFDénomination Commune Française

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

Tuesday, 21 December 2010

Azomax




Azomax may be available in the countries listed below.


Ingredient matches for Azomax



Azithromycin

Azithromycin is reported as an ingredient of Azomax in the following countries:


  • Oman

  • Turkey

Azithromycin dihydrate (a derivative of Azithromycin) is reported as an ingredient of Azomax in the following countries:


  • Mexico

International Drug Name Search

Monday, 20 December 2010

Indatens




Indatens may be available in the countries listed below.


Ingredient matches for Indatens



Indapamide

Indapamide is reported as an ingredient of Indatens in the following countries:


  • Latvia

International Drug Name Search

Thursday, 16 December 2010

Trausan




Trausan may be available in the countries listed below.


Ingredient matches for Trausan



Citicoline

Citicoline is reported as an ingredient of Trausan in the following countries:


  • Portugal

International Drug Name Search

Monday, 13 December 2010

Betahistin-Mepha




Betahistin-Mepha may be available in the countries listed below.


Ingredient matches for Betahistin-Mepha



Betahistine

Betahistine dihydrochloride (a derivative of Betahistine) is reported as an ingredient of Betahistin-Mepha in the following countries:


  • Switzerland

International Drug Name Search

Sunday, 12 December 2010

Faston




Faston may be available in the countries listed below.


Ingredient matches for Faston



Dydrogesterone

Dydrogesterone is reported as an ingredient of Faston in the following countries:


  • Bangladesh

International Drug Name Search

Thursday, 9 December 2010

Progut




Progut may be available in the countries listed below.


Ingredient matches for Progut



Esomeprazole

Esomeprazole is reported as an ingredient of Progut in the following countries:


  • Bangladesh

Flavoxate

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


  • Japan

International Drug Name Search

Wednesday, 1 December 2010

Pentazocina




Pentazocina may be available in the countries listed below.


Ingredient matches for Pentazocina



Pentazocine

Pentazocina (DCIT) is known as Pentazocine in the US.

International Drug Name Search

Glossary

DCITDenominazione Comune Italiana

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

Thursday, 25 November 2010

Vitamin D3-Doms Adrian




Vitamin D3-Doms Adrian may be available in the countries listed below.


Ingredient matches for Vitamin D3-Doms Adrian



Colecalciferol

Colecalciferol is reported as an ingredient of Vitamin D3-Doms Adrian in the following countries:


  • Luxembourg

International Drug Name Search

Saturday, 20 November 2010

Postanesthetic Shivering Medications


Drugs associated with Postanesthetic Shivering

The following drugs and medications are in some way related to, or used in the treatment of Postanesthetic Shivering. This service should be used as a supplement to, and NOT a substitute for, the expertise, skill, knowledge and judgment of healthcare practitioners.





Drug List:

Litijum karbonat




Litijum karbonat may be available in the countries listed below.


Ingredient matches for Litijum karbonat



Lithium

Lithium carbonate (a derivative of Lithium) is reported as an ingredient of Litijum karbonat in the following countries:


  • Serbia

International Drug Name Search

Thursday, 18 November 2010

Dialens




Dialens may be available in the countries listed below.


Ingredient matches for Dialens



Dextran

Dextran average molecular weight about 70000 (a derivative of Dextran) is reported as an ingredient of Dialens in the following countries:


  • Switzerland

International Drug Name Search

Tuesday, 16 November 2010

Chlortetracycline Pneumonia




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

Ingredient matches for Chlortetracycline Pneumonia



Chlortetracycline

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


  • United States

International Drug Name Search

Monday, 15 November 2010

Lazanda


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


LAZANDA (fentanyl citrate - spray, metered; nasal)



  • Manufacturer: ARCHIMEDES

    Approval date: June 30, 2011

    Strength(s): EQ 0.1MG BASE, EQ 0.4MG BASE [RLD]

Has a generic version of Lazanda been approved?


No. There is currently no therapeutically equivalent version of Lazanda available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Lazanda. 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


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Pectin compositions and methods of use for improved delivery of drugs to mucosal surfaces
    Patent 6,432,440
    Issued: August 13, 2002
    Inventor(s): Peter James; Watts & Lisbeth; Illum
    Assignee(s): West Pharmaceutical Services Drug Delivery & Clinical Research Centre Limited
    Liquid pharmaceutical compositions for administration to a mucosal surface, comprising a therapeutic agent and a pectin with a low degree of esterification are described. Such compositions gel, or can be adapted to gel, at the site of application in the absence of an extraneous source of divalent metal ions.
    Patent expiration dates:

    • April 20, 2018
      ✓ 
      Patent use: MANAGEMENT OF BREAKTHROUGH PAIN IN CANCER PATIENTS 18 YEARS OF AGE AND OLDER WHO ARE RECEIVING AND TOLERANT TO OPIOID THERAPY FOR THEIR UNDERLYING PERSISTENT CANCER PAIN
      ✓ 
      Drug product



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • June 30, 2014 - NEW DOSAGE FORM

See also...

  • Lazanda Consumer Information (Drugs.com)
  • Lazanda Spray Consumer Information (Wolters Kluwer)
  • Lazanda nasal Consumer Information (Cerner Multum)
  • Fentanyl Consumer Information (Drugs.com)
  • Fentanyl Consumer Information (Wolters Kluwer)
  • Fentanyl Lozenge Consumer Information (Wolters Kluwer)
  • Fentanyl Patch Consumer Information (Wolters Kluwer)
  • Fentanyl Soluble Film Consumer Information (Wolters Kluwer)
  • Fentanyl Spray Consumer Information (Wolters Kluwer)
  • Fentanyl Tablet Consumer Information (Wolters Kluwer)
  • Fentanyl buccal Consumer Information (Cerner Multum)
  • Fentanyl citrate oral transmucosal Consumer Information (Cerner Multum)
  • Fentanyl nasal Consumer Information (Cerner Multum)
  • Fentanyl sublingual Consumer Information (Cerner Multum)
  • Fentanyl transdermal device Consumer Information (Cerner Multum)
  • Fentanyl transdermal skin patch Consumer Information (Cerner Multum)
  • Fentanyl Buccal mucosa, Oromucosal Advanced Consumer Information (Micromedex)
  • Fentanyl Nasal Advanced Consumer Information (Micromedex)
  • Fentanyl Transdermal Advanced Consumer Information (Micromedex)
  • Fentanyl Citrate AHFS DI Monographs (ASHP)

Friday, 12 November 2010

Selectol




Selectol may be available in the countries listed below.


Ingredient matches for Selectol



Celiprolol

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


  • Austria

  • Belgium

  • Chile

  • Finland

  • Germany

  • Greece

  • Hong Kong

  • Ireland

  • Japan

  • Luxembourg

  • Switzerland

International Drug Name Search

Sunday, 31 October 2010

Midazolam Torrex




Midazolam Torrex may be available in the countries listed below.


Ingredient matches for Midazolam Torrex



Midazolam

Midazolam is reported as an ingredient of Midazolam Torrex in the following countries:


  • Hungary

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


  • Austria

  • Croatia (Hrvatska)

  • Czech Republic

  • Poland

  • Romania

  • Serbia

  • Slovakia

  • Slovenia

International Drug Name Search

Saturday, 23 October 2010

Coxalin TS




Coxalin TS may be available in the countries listed below.


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

Ingredient matches for Coxalin TS



Cloxacillin

Cloxacillin benzathine (a derivative of Cloxacillin) is reported as an ingredient of Coxalin TS in the following countries:


  • Austria

International Drug Name Search

Tuesday, 19 October 2010

Pamoato de Pirantel Genfar




Pamoato de Pirantel Genfar may be available in the countries listed below.


Ingredient matches for Pamoato de Pirantel Genfar



Pyrantel

Pyrantel embonate (a derivative of Pyrantel) is reported as an ingredient of Pamoato de Pirantel Genfar in the following countries:


  • Colombia

  • Ecuador

International Drug Name Search

Tuesday, 12 October 2010

Gonadotropine sérique




Gonadotropine sérique may be available in the countries listed below.


Ingredient matches for Gonadotropine sérique



Gonadotrophin, Serum

Gonadotropine sérique (DCF) is also known as Gonadotrophin, Serum (Ph. Eur.)

International Drug Name Search

Glossary

DCFDénomination Commune Française
Ph. Eur.European Pharmacopoeia

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

Monday, 11 October 2010

Austrapen




Austrapen may be available in the countries listed below.


Ingredient matches for Austrapen



Ampicillin

Ampicillin sodium salt (a derivative of Ampicillin) is reported as an ingredient of Austrapen in the following countries:


  • Australia

International Drug Name Search

Friday, 8 October 2010

Lox




Lox may be available in the countries listed below.


Ingredient matches for Lox



Ciprofloxacin

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


  • Bangladesh

International Drug Name Search

Hidrocortisona Fabra




Hidrocortisona Fabra may be available in the countries listed below.


Ingredient matches for Hidrocortisona Fabra



Hydrocortisone

Hydrocortisone 21-(sodium succinate) (a derivative of Hydrocortisone) is reported as an ingredient of Hidrocortisona Fabra in the following countries:


  • Argentina

International Drug Name Search

Thursday, 7 October 2010

Bayer Low Adult Strength Controlled-Release Tablets


Pronunciation: AS-pir-in
Generic Name: Aspirin
Brand Name: Examples include Bayer Low Adult Strength and ZORprin


Bayer Low Adult Strength Controlled-Release Tablets are used for:

Relieving arthritis symptoms. It may also be used for other conditions as determined by your doctor.


Bayer Low Adult Strength Controlled-Release Tablets are a salicylate. It works by inhibiting several different chemical processes within the body that cause pain, inflammation, and fever. It also reduces the tendency for blood to clot.


Do NOT use Bayer Low Adult Strength Controlled-Release Tablets if:


  • you are allergic to any ingredient in Bayer Low Adult Strength Controlled-Release Tablets

  • you are a child or teenager with influenza (flu) or chicken pox

  • you have bleeding problems such as hemophilia, von Willebrand disease, or low blood platelets

  • you have had a severe allergic reaction (eg, severe rash, hives, breathing difficulties, dizziness), to aspirin, tartrazine, or an NSAID (eg, ibuprofen, naproxen, celecoxib)

  • you are taking anticoagulants (eg, heparin, warfarin) or methotrexate

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



Before using Bayer Low Adult Strength Controlled-Release Tablets:


Some medical conditions may interact with Bayer Low Adult Strength Controlled-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 pregnant, plan 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 or other substances

  • if you have alcoholism or if you consume 3 or more alcohol-containing drinks every day

  • if you have asthma, bleeding or clotting problems, growths in the nose (nasal polyps), kidney or liver problems, stomach or peptic ulcers (bleeding ulcers), heartburn, upset stomach, stomach pain, influenza (flu) or chicken pox, or vitamin K deficiency

  • if you are a child with a stroke, a weakened blood vessel (cerebral aneurysm) or bleeding in the brain, or Kawasaki syndrome (a rare inflammation causing heart problems in children)

Some MEDICINES MAY INTERACT with Bayer Low Adult Strength Controlled-Release Tablets. Tell your health care provider if you are taking any other medicines, especially any of the following:


  • Carbonic anhydrase inhibitors (eg, acetazolamide) because they may decrease Bayer Low Adult Strength Controlled-Release Tablets's effectiveness

  • Anticoagulants (eg, heparin, warfarin) or nonsteroidal anti-inflammatory drugs (NSAIDs) (eg, ibuprofen, celecoxib) because the risk of their side effects, including risk of bleeding, may be increased by Bayer Low Adult Strength Controlled-Release Tablets

  • Insulin and oral antidiabetics (eg, glyburide, nateglinide) because the risk of their side effects, including low blood sugar (eg, hunger, shakiness or weakness, dizziness, headache, sweating), may be increased by Bayer Low Adult Strength Controlled-Release Tablets

  • Methotrexate or valproic acid because the risk of their actions and side effects may be increased by Bayer Low Adult Strength Controlled-Release Tablets

  • Angiotensin-converting enzyme inhibitors (eg, enalapril), probenecid, or sulfinpyrazone because their effectiveness may be decreased by Bayer Low Adult Strength Controlled-Release Tablets

This may not be a complete list of all interactions that may occur. Ask your health care provider if Bayer Low Adult Strength Controlled-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 Bayer Low Adult Strength Controlled-Release Tablets:


Use Bayer Low Adult Strength Controlled-Release Tablets as directed by your doctor. Check the label on the medicine for exact dosing instructions.


  • Take Bayer Low Adult Strength Controlled-Release Tablets by mouth with or without food. If stomach upset occurs, take with food to reduce stomach irritation.

  • Swallow Bayer Low Adult Strength Controlled-Release Tablets whole. Do not break, crush, or chew before swallowing unless directed by your health care provider.

  • Take Bayer Low Adult Strength Controlled-Release Tablets with a full glass of water (8 oz/240 mL).

  • Use Bayer Low Adult Strength Controlled-Release Tablets exactly as directed on the package, unless instructed differently by your doctor. If you are taking Bayer Low Adult Strength Controlled-Release Tablets without a prescription, follow any warnings and precautions on the label.

  • If you miss a dose of Bayer Low Adult Strength Controlled-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 Bayer Low Adult Strength Controlled-Release Tablets.



Important safety information:


  • Bayer Low Adult Strength Controlled-Release Tablets has aspirin in it. Before you start any new medicine, check the label to see if it has aspirin in it too. If it does or if you are not sure, check with your doctor or pharmacist.

  • Talk to your doctor before you take Bayer Low Adult Strength Controlled-Release Tablets or other pain relievers/fever reducers if you drink more than 3 drinks with alcohol per day. Serious stomach ulcers or bleeding can occur with the use of Bayer Low Adult Strength Controlled-Release Tablets. Taking it in high doses or for a long time, smoking, or drinking alcohol increases the risk of these side effects. Taking Bayer Low Adult Strength Controlled-Release Tablets with food will NOT reduce the risk of these effects. Contact your doctor or emergency room at once if you develop severe stomach or back pain; black, tarry stools; vomit that looks like blood or coffee grounds; or unusual weight gain or swelling.

  • Bayer Low Adult Strength Controlled-Release Tablets may reduce the number of clot-forming cells (platelets) in your blood. Avoid activities that may cause bruising or injury. Tell your doctor if you have unusual bruising or bleeding. Tell your doctor if you have dark, tarry, or bloody stools.

  • Aspirin has been linked to a serious illness called Reye syndrome. Do not give Bayer Low Adult Strength Controlled-Release Tablets to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

  • If Bayer Low Adult Strength Controlled-Release Tablets has a strong vinegar-like smell upon opening, do not use. It means the medicine is breaking down. Throw the bottle away safely and out of the reach of children; contact your pharmacist and replace.

  • Tell your doctor or dentist that you take Bayer Low Adult Strength Controlled-Release Tablets before you receive any medical or dental care, emergency care, or surgery.

  • Do not take Bayer Low Adult Strength Controlled-Release Tablets for at least 7 days after any surgery unless directed by your health care provider.

  • Do not take Bayer Low Adult Strength Controlled-Release Tablets for more than 10 days for pain or for more than 3 days for fever unless directed to do so by your health care provider.

  • Diabetes patients-Bayer Low Adult Strength Controlled-Release Tablets may affect your blood sugar. Check blood sugar levels closely. Ask your doctor before you change the dose of your diabetes medicine.

  • Use Bayer Low Adult Strength Controlled-Release Tablets with caution in the ELDERLY; they may be more sensitive to its effects, especially those with a blood coagulation disorder.

  • Different brands of Bayer Low Adult Strength Controlled-Release Tablets may have different dosing instructions for CHILDREN. Follow the dosing instructions on the package labeling. If your doctor has given you instructions, follow those. If you are unsure of the dose to give a child, check with your doctor or pharmacist.

  • PREGNANCY and BREAST-FEEDING: If you become pregnant, contact your doctor. You will need to discuss the benefits and risks of using Bayer Low Adult Strength Controlled-Release Tablets while you are pregnant. Bayer Low Adult Strength Controlled-Release Tablets are not recommended during the last 3 months (third trimester) of pregnancy because it may cause harm to the fetus. Bayer Low Adult Strength Controlled-Release Tablets are found in breast milk. If you are or will be breast-feeding while you use Bayer Low Adult Strength Controlled-Release Tablets, check with your doctor. Discuss any possible risks to your baby.


Possible side effects of Bayer Low Adult Strength Controlled-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:



Heartburn; nausea; upset stomach.



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

Severe allergic reactions (rash; hives; itching; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); black or bloody stools; confusion; diarrhea; dizziness; drowsiness; hearing loss; ringing in the ears; severe stomach pain; vomiting.



This is not a complete list of all side effects that may occur. If you have questions about side effects, contact your health care provider. Call your doctor for medical advice about side effects. To report side effects to the appropriate agency, please read the Guide to Reporting Problems to FDA.


See also: Bayer Low Adult Strength 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 agitation; fever; hearing loss; lethargy; lightheadedness, especially upon standing; nausea; rapid breathing; rapid or irregular heartbeat; ringing in the ears; seizures; shortness of breath; stomach pain; vomiting.


Proper storage of Bayer Low Adult Strength Controlled-Release Tablets:

Store Bayer Low Adult Strength Controlled-Release Tablets at room temperature, between 68 and 77 degrees F (20 and 25 degrees C). Store away from heat, moisture, and light. Do not store in the bathroom. Keep Bayer Low Adult Strength Controlled-Release Tablets out of the reach of children and away from pets.


General information:


  • If you have any questions about Bayer Low Adult Strength Controlled-Release Tablets, please talk with your doctor, pharmacist, or other health care provider.

  • Bayer Low Adult Strength Controlled-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 Bayer Low Adult Strength Controlled-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 Bayer Low Adult Strength resources


  • Bayer Low Adult Strength Side Effects (in more detail)
  • Bayer Low Adult Strength Use in Pregnancy & Breastfeeding
  • Bayer Low Adult Strength Drug Interactions
  • Bayer Low Adult Strength Support Group
  • 0 Reviews for Bayer Low Adult Strength - Add your own review/rating


Compare Bayer Low Adult Strength with other medications


  • Angina
  • Angina Pectoris Prophylaxis
  • Heart Attack
  • Ischemic Stroke
  • Ischemic Stroke, Prophylaxis
  • Myocardial Infarction, Prophylaxis
  • Niacin Flush
  • Prosthetic Heart Valves
  • Prosthetic Heart Valves, Mechanical Valves
  • Revascularization Procedures, Prophylaxis
  • Thromboembolic Stroke Prophylaxis
  • Transient Ischemic Attack

Tuesday, 5 October 2010

Azulene Sodium Sulfonate




Azulene Sodium Sulfonate may be available in the countries listed below.


Ingredient matches for Azulene Sodium Sulfonate



Sodium Gualenate

Sodium Gualenate is reported as an ingredient of Azulene Sodium Sulfonate in the following countries:


  • Japan

International Drug Name Search

Sunday, 26 September 2010

Didrex


Pronunciation: benz-FET-ah-meen
Generic Name: Benzphetamine
Brand Name: Didrex


Didrex is used for:

Short-term (few weeks) management of obesity, as part of a weight-loss plan including a reduced-calorie diet. It may also be used for other conditions as determined by your doctor.


Didrex is an anorectic. Exactly how it works is not known. It may work in part by acting on the appetite center in the brain to cause a temporary reduction in hunger or craving for food.


Do NOT use Didrex if:


  • you are allergic to any ingredient in Didrex

  • you have had a bad reaction to a sympathomimetic amine (eg, pseudoephedrine)

  • you are in an agitated state

  • you are pregnant or may become pregnant

  • you have glaucoma, an overactive thyroid, moderate to severe or uncontrolled high blood pressure, severe heart blood vessel problems, irregular heartbeat, or certain other heart problems (eg, murmur, heart valve problems)

  • you are taking furazolidone, guanadrel, or guanethidine, or you have taken a monoamine oxidase inhibitor (MAOI) (eg, phenelzine) in the past 14 days

  • you take other anorectic medicines (eg, amphetamine) or have taken anorectic medicines within the past year

  • you have a history of alcohol or other substance abuse

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



Before using Didrex:


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


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

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

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

  • if you have a history of heart problems, blood vessel problems, lung or breathing problems, high blood pressure, diabetes, thyroid problems, or mental or mood problems

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


  • Furazolidone or MAOIs (eg, phenelzine) because side effects, such as headache, elevated body temperature, or severe high blood pressure, may occur

  • Selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because the risk of side effects, such as mental or mood changes, may be increased

  • Urinary acidifiers (eg, ascorbic acid) because they may decrease Didrex's effectiveness

  • Stimulants (eg, amphetamine) or urinary alkalinizers (eg, sodium bicarbonate) because they may increase the risk of Didrex's side effects

  • Tricyclic antidepressants (eg, amitriptyline) because actions and side effects may be increased by Didrex

  • Guanadrel, guanethidine, or other medicines for high blood pressure because their effectiveness may be decreased by Didrex

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


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


  • Didrex may be taken with or without food.

  • If you miss a dose of Didrex, 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 Didrex.



Important safety information:


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

  • Do not take more than the recommended dose of Didrex or take for longer than prescribed without checking with your doctor. Doing so may cause serious side effects, including severe heart or lung problems.

  • Do not suddenly stop taking Didrex without first talking with your doctor.

  • Do not take other prescription medicines, over-the-counter medicines, or herbal supplements to treat obesity without first talking with your doctor.

  • Do not use Didrex for any reason or condition other than the one for which it was prescribed.

  • Didrex may cause sleeplessness. If you have trouble sleeping, you may need to take Didrex earlier in the day. Talk to your doctor before adjusting your dose of Didrex.

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

  • Didrex should not be used in CHILDREN younger than 12 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Do not use Didrex if you are pregnant. If you think you may be pregnant, contact your doctor right away. Didrex is found in breast milk. Do not breast-feed while taking Didrex.

When used for long periods of time or at high doses, some people develop a need to continue taking Didrex. This is known as DEPENDENCE or addiction. When used for long periods of time or at high doses, Didrex may not work as well and may require higher doses to obtain the same effect as when originally taken. This is known as TOLERANCE. Talk with your doctor if Didrex stops working well. Do not take more than prescribed.


If you suddenly stop taking Didrex, you may experience WITHDRAWAL symptoms, such as extreme fatigue, mental depression, or sleep changes.



Possible side effects of Didrex:


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:



Changes in sex drive; diarrhea; dizziness; dry mouth; headache; nausea; restlessness; sleeplessness; tremor; unpleasant taste.



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 vision; chest pain; fainting; fast or irregular heartbeat; mental or mood changes; new or unusual shortness of breath; pounding in the chest; severe excitability; severe or persistent dizziness or headache; swelling of the feet or legs.



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: Didrex 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 confusion; depression; high fever; irregular heartbeat; loss of consciousness; panic; rapid breathing; restlessness; seizures; severe nausea or diarrhea; severe tiredness; stomach cramps; tremor; vomiting.


Proper storage of Didrex:

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


General information:


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

  • Didrex 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 is a summary only. It does not contain all information about Didrex. 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 Didrex resources


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


  • Didrex Prescribing Information (FDA)

  • Didrex Advanced Consumer (Micromedex) - Includes Dosage Information

  • Didrex Consumer Overview

  • Benzphetamine Prescribing Information (FDA)



Compare Didrex with other medications


  • Obesity

Tuesday, 21 September 2010

Hydralazine Hydrochloride




Ingredient matches for Hydralazine Hydrochloride



Hydralazine

Hydralazine Hydrochloride (BANM) is known as Hydralazine in the US.

International Drug Name Search

Glossary

BANMBritish Approved Name (Modified)

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

Friday, 17 September 2010

Ampicilina Drawer




Ampicilina Drawer may be available in the countries listed below.


Ingredient matches for Ampicilina Drawer



Ampicillin

Ampicillin sodium salt (a derivative of Ampicillin) is reported as an ingredient of Ampicilina Drawer in the following countries:


  • Argentina

International Drug Name Search

Monday, 13 September 2010

Neripros




Neripros may be available in the countries listed below.


Ingredient matches for Neripros



Risperidone

Risperidone is reported as an ingredient of Neripros in the following countries:


  • Indonesia

International Drug Name Search

Monday, 6 September 2010

Cetamine




Cetamine may be available in the countries listed below.


Ingredient matches for Cetamine



Ascorbic Acid

Ascorbic Acid is reported as an ingredient of Cetamine in the following countries:


  • Belgium

  • Luxembourg

International Drug Name Search

Wednesday, 1 September 2010

Dinaxcinco




Dinaxcinco may be available in the countries listed below.


Ingredient matches for Dinaxcinco



Minoxidil

Minoxidil is reported as an ingredient of Dinaxcinco in the following countries:


  • Spain

International Drug Name Search

Friday, 20 August 2010

Zolpidem Tartrate




UK matches:

  • Zolpidem Tartrate 10 mg Tablets (SPC)
  • Zolpidem Tartrate 10mg Tablets (Sandoz Limited) (SPC)
  • Zolpidem Tartrate 5 mg Tablets. (SPC)

Ingredient matches for Zolpidem Tartrate



Zolpidem

Zolpidem Tartrate (BANM, USAN) is known as Zolpidem in the US.

International Drug Name Search

Glossary

BANMBritish Approved Name (Modified)
SPC Summary of Product Characteristics (UK)
USANUnited States Adopted Name

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

Tuesday, 17 August 2010

Acebutolol A




Acebutolol A may be available in the countries listed below.


Ingredient matches for Acebutolol A



Acebutolol

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


  • Netherlands

International Drug Name Search

Sunday, 15 August 2010

Selokeen




Selokeen may be available in the countries listed below.


Ingredient matches for Selokeen



Metoprolol

Metoprolol tartrate (a derivative of Metoprolol) is reported as an ingredient of Selokeen in the following countries:


  • Netherlands

International Drug Name Search

Saturday, 14 August 2010

Paranausine




Paranausine may be available in the countries listed below.


Ingredient matches for Paranausine



Dimenhydrinate

Dimenhydrinate is reported as an ingredient of Paranausine in the following countries:


  • Belgium

International Drug Name Search

Sunday, 8 August 2010

Sporiline




Sporiline may be available in the countries listed below.


Ingredient matches for Sporiline



Tolnaftate

Tolnaftate is reported as an ingredient of Sporiline in the following countries:


  • France

International Drug Name Search

Saturday, 7 August 2010

Dolobid


Pronunciation: dye-FLOO-ni-sal
Generic Name: Diflunisal
Brand Name: Dolobid

Dolobid is a nonsteroidal anti-inflammatory drug (NSAID). It may cause an increased risk of serious and sometimes fatal heart and blood vessel problems (eg, heart attack, stroke). The risk may be greater if you already have heart problems or if you take Dolobid for a long time. Do not use Dolobid right before or after bypass heart surgery.


Dolobid may cause an increased risk of serious and sometimes fatal stomach ulcers and bleeding. Elderly patients may be at greater risk. This may occur without warning signs.





Dolobid is used for:

Treating rheumatoid arthritis, osteoarthritis, or mild to moderate pain. It may also be used for other conditions as determined by your doctor.


Dolobid is an NSAID. Exactly how it works is not known. It may block certain substances in the body that are linked to inflammation. NSAIDs treat the symptoms of pain and inflammation. They do not treat the disease that causes those symptoms.


Do NOT use Dolobid if:


  • you are allergic to any ingredient in Dolobid

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

  • you have recently had or will be having bypass heart surgery

  • you are also taking another NSAID (eg, ibuprofen)

  • you are in the last 3 months of pregnancy

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



Before using Dolobid:


Some medical conditions may interact with Dolobid. 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 product, or dietary supplement

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

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

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

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

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

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


  • Anticoagulants (eg, warfarin), aspirin, corticosteroids (eg, prednisone), heparin, or selective serotonin reuptake inhibitors (SSRIs) (eg, fluoxetine) because risk of stomach bleeding may be increased

  • Antacids, other NSAIDs (eg, ibuprofen), or probenecid because they may increase the risk of Dolobid's side effects

  • Acetaminophen, cyclosporine, lithium, methotrexate, quinolones (eg, ciprofloxacin), or sulfonylureas (eg, glipizide) because the risk of their side effects may be increased by Dolobid

  • Angiotensin-converting enzyme (ACE) inhibitors (eg, enalapril), angiotensin receptor blockers (eg, losartan), or diuretics (eg, furosemide, hydrochlorothiazide) because their effectiveness may be decreased by Dolobid

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


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


  • Dolobid comes with an extra patient information sheet called a Medication Guide. Read it carefully. Read it again each time you get Dolobid refilled.

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

  • Swallow Dolobid whole. Do not break, crush, or chew before swallowing.

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

  • If you miss a dose of Dolobid 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. 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 the proper use of Dolobid.



Important safety information:


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

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

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

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

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

  • Dolobid may interfere with certain lab tests. Be sure your doctor and lab personnel know that you take Dolobid.

  • Aspirin has been linked to a serious illness called Reye Syndrome. Do not give Dolobid to a child or teenager who has the flu, chickenpox, or a viral infection. Contact your doctor with any questions or concerns.

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

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

  • Dolobid should not be used in CHILDREN younger than 12 years old; safety and effectiveness in these children have not been confirmed.

  • PREGNANCY and BREAST-FEEDING: Dolobid may cause harm to the fetus. Do not use it during the last 3 months of pregnancy. If you think you may be pregnant, contact your doctor. You will need to discuss the benefits and risks of using Dolobid while you are pregnant. Dolobid is found in breast milk. Do not breast-feed while taking Dolobid.


Possible side effects of Dolobid:


All medicines can 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; gas; headache; heartburn; nausea; stomach upset.



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

Severe allergic reactions (rash; hives; itching; trouble breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); bloody or black, tarry stools; change in the amount of urine produced; chest pain; confusion; dark urine; depression; fainting; fast or irregular heartbeat; fever, chills, or persistent sore throat; mental or mood changes; numbness of an arm or leg; one-sided weakness; red, swollen, blistered, or peeling skin; ringing in the ears; seizures; severe headache or dizziness; severe or persistent stomach pain or nausea; severe vomiting; shortness of breath; sudden or unexplained weight gain; swelling of hands, legs, or feet; unusual bruising or bleeding; unusual joint or muscle pain; unusual tiredness or weakness; vision or speech changes; vomit that looks like coffee grounds; 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. 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: Dolobid 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 confusion; decreased urination; increased sweating; loss of consciousness; ringing in the ears; seizures; severe dizziness or drowsiness; severe nausea or stomach pain; slow, fast, or troubled breathing; unusual bleeding or bruising; vomit that looks like coffee grounds.


Proper storage of Dolobid:

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


General information:


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

  • Dolobid 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 is a summary only. It does not contain all information about Dolobid. 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 Dolobid resources


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


  • Dolobid Advanced Consumer (Micromedex) - Includes Dosage Information

  • Dolobid Concise Consumer Information (Cerner Multum)

  • Dolobid Monograph (AHFS DI)

  • Diflunisal Prescribing Information (FDA)

  • Diflunisal Professional Patient Advice (Wolters Kluwer)



Compare Dolobid with other medications


  • Osteoarthritis
  • Pain
  • Rheumatoid Arthritis

Thursday, 5 August 2010

Trimébutine Winthrop




Trimébutine Winthrop may be available in the countries listed below.


Ingredient matches for Trimébutine Winthrop



Trimebutine

Trimebutine maleate (a derivative of Trimebutine) is reported as an ingredient of Trimébutine Winthrop in the following countries:


  • France

International Drug Name Search

Saturday, 31 July 2010

Octanine




Octanine may be available in the countries listed below.


Ingredient matches for Octanine



Coagulation Factor IX, Human

Coagulation Factor IX, Human is reported as an ingredient of Octanine in the following countries:


  • Austria

  • Belgium

  • Bosnia & Herzegowina

  • Czech Republic

  • Germany

  • Luxembourg

  • Oman

  • Poland

  • Serbia

  • Slovakia

  • Slovenia

  • Switzerland

International Drug Name Search

Monday, 26 July 2010

Robitussin CoughGels


Generic Name: dextromethorphan (dex troe meth OR fan)

Brand Names: Babee Cof, Benylin DM Pediatric, Buckley's Mixture Cough Suppressant, Buckleys Mixture, Creo-Terpin, Creomulsion, Delsym, Delsym 12 Hour Cough Relief, Delsym 12 Hour Cough Relief for Children & Adults, DexAlone, Elixsure Cough, Hold DM, Pediacare, Robitussin CoughGels, Robitussin Honey Cough, Robitussin Maximum Strength, Robitussin Pediatric Cough Suppressant, Scot-Tussin Diabetic, Scot-Tussin DM Cough Chasers, Silphen DM, St. Joseph Cough Suppressant, Sucrets DM Cough, Theraflu Thin Strips Cough, Triaminic Long Acting Cough, Triaminic Softchew, Vicks 44 Cough Relief


What is Robitussin CoughGels (dextromethorphan)?

Dextromethorphan is a cough suppressant. It affects the signals in the brain that trigger cough reflex.


Dextromethorphan is used to treat a cough.


Dextromethorphan will not treat a cough that is caused by smoking, asthma, or emphysema.

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


What is the most important information I should know about Robitussin CoughGels (dextromethorphan)?


Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving a cough or cold medicine to a child. Death can occur from the misuse of cough and cold medicines in very young children. Do not use dextromethorphan if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take dextromethorphan before the MAO inhibitor has cleared from your body. Do not use any other over-the-counter cough, cold, or allergy medication without first asking your doctor or pharmacist. If you take certain products together you may accidentally take too much of one or more types of medicine. Read the label of any other medicine you are using to see if it contains dextromethorphan. Dextromethorphan will not treat a cough that is caused by smoking, asthma, or emphysema.

What should I discuss with my healthcare provider before taking Robitussin CoughGels (dextromethorphan)?


Do not use dextromethorphan if you have used an MAO inhibitor such as isocarboxazid (Marplan), phenelzine (Nardil), rasagiline (Azilect), selegiline (Eldepryl, Emsam), or tranylcypromine (Parnate) within the past 14 days. Serious, life-threatening side effects can occur if you take dextromethorphan before the MAO inhibitor has cleared from your body.

Ask a doctor or pharmacist about using this medicine if you have emphysema or chronic bronchitis.


This medication may be harmful to an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant during treatment. This medication may pass into breast milk and could harm a nursing baby. Do not use this medication without telling your doctor if you are breast-feeding a baby.

Artificially-sweetened liquid forms of cough medicine may contain phenylalanine. This would be important to know if you have phenylketonuria (PKU). Check the ingredients and warnings on the medication label if you are concerned about phenylalanine.


How should I take Robitussin CoughGels (dextromethorphan)?


Use this medication exactly as directed on the label, or as it has been prescribed by your doctor. Do not use the medication in larger amounts, or use it for longer than recommended. Cough medicine is usually taken only for a short time until your symptoms clear up.


Do not give this medication to a child younger than 4 years old. Always ask a doctor before giving cough or cold medicine to a child. Death can occur from the misuse of cough or cold medicine in very young children.

Measure the liquid form of this medicine with a special dose-measuring spoon or cup, not a regular table spoon. If you do not have a dose-measuring device, ask your pharmacist for one.


Allow the dextromethorphan lozenge or disintegrating strip to dissolve in your mouth.


Drink extra fluids to help loosen the congestion and lubricate your throat while you are taking this medication. Talk with your doctor if your symptoms do not improve after 7 days of treatment, or if you have a fever with a headache, cough, or skin rash.

If you need to have any type of surgery, tell the surgeon ahead of time if you have taken a cough medicine within the past few days.


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

What happens if I miss a dose?


Since cough medicine is usually taken only as needed, you may not be on a dosing schedule. If you are taking the medication regularly, take the missed dose as soon as you remember. If it is almost time for your next dose, skip the missed dose and take the medicine at your next regularly scheduled time. Do not take extra medicine to make up the missed dose.


What happens if I overdose?


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

Overdose symptoms may include feeling restless or nervous.


What should I avoid while taking Robitussin CoughGels (dextromethorphan)?


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

Avoid taking diet pills, caffeine pills, or other stimulants (such as ADHD medications) without your doctor's advice. Taking a stimulant together with cough medicine can increase your risk of unpleasant side effects.


Do not use any other over-the-counter cough, cold, or allergy medication without first asking your doctor or pharmacist. Dextromethorphan is contained in many combination medicines available over the counter. If you take certain products together you may accidentally take too much of this medicine. Read the label of any other medicine you are using to see if it contains dextromethorphan.

Robitussin CoughGels (dextromethorphan) side effects


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

  • severe dizziness, anxiety, restless feeling, or nervousness;




  • confusion, hallucinations; or




  • slow, shallow breathing.



Less serious side effects are more likely, such as stomach upset.


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


What other drugs will affect Robitussin CoughGels (dextromethorphan)?


Before taking dextromethorphan, tell your doctor if you are using any of the following drugs:



  • celecoxib (Celebrex);




  • cinacalcet (Sensipar);




  • darifenacin (Enablex);




  • imatinib (Gleevec);




  • quinidine (Quinaglute, Quinidex);




  • ranolazine (Ranexa)




  • ritonavir (Norvir);




  • sibutramine (Meridia);




  • terbinafine (Lamisil);




  • medicines to treat high blood pressure; or




  • antidepressant medications such as amitriptyline (Elavil, Etrafon), bupropion (Wellbutrin, Zyban), fluoxetine (Prozac, Sarafem), fluvoxamine (Luvox), imipramine (Janimine, Tofranil), paroxetine (Paxil), sertraline (Zoloft), and others.



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



More Robitussin CoughGels resources


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Compare Robitussin CoughGels with other medications


  • Cough


Where can I get more information?


  • Your pharmacist can provide more information about dextromethorphan.

See also: Robitussin CoughGels side effects (in more detail)