NOTE: April 7, 2005, Pfizer agreed to suspend sales and marketing of Bextra in the U.S., pending further discussions with the with the FDA. For more information, please read the
FDA press release.
Medications and Drugs
GENERIC NAME: VALDECOXIB 10MG - ORAL (val-deh-COX-ib)
BRAND NAME(S): Bextra
Warning | Medication Uses | Other Uses | How To Use | Side Effects | Precautions | Drug Interactions | Overdose | Notes | Missed Dose | Storage
WARNING: Rarely, serious (possibly fatal) allergic reactions have occurred with valdecoxib, including skin reactions. Seek immediate medical attention if an allergic reaction occurs. Symptoms of an allergic reaction may include: rash, mouth sores, itching, swelling, dizziness, trouble breathing.
USES: Valdecoxib is a nonsteroidal anti-inflammatory drug (NSAID) used to relieve pain and swelling (inflammation). It is used to treat arthritis (osteoarthritis or rheumatoid arthritis). This drug should not be used for relieving pain after surgery, especially heart bypass surgery (CABG). There is an increased risk of blood clots forming, resulting in heart attacks and strokes, in heart bypass patients (see also Precautions section). This drug works by blocking the enzyme in your body that makes prostaglandins. Decreasing prostaglandins helps to reduce pain and swelling.
OTHER USES: This medication may also be used to relieve menstrual pain (dysmenorrhea) and to reduce fever.
HOW TO USE: Take this medication by mouth usually once or twice daily either with or without food or take as directed by your doctor. Take this medication with a full glass of water (8 oz or 240 ml) unless your doctor directs you otherwise. Do not lie down for 30 minutes after taking this medication. The dosage is based on your medical condition and response to therapy. The lowest effective dosage should always be used (see also Precautions section).
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.

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