Bextra - Valdecoxib

Bextra, also known as valdecoxib, is indicated for the treatment of pain, tenderness and swelling caused by osteoarthritis and adult rheumatoid arthritis. Belonging to a class of nonsteroidal anti-inflammatory medications (NSAIDs) called COX-2 inhibitors, Bextra blocks the action of the COX-2 enzyme, which causes arthritis pain and inflammation. Bextra was approved by the U.S. Food and Drug Administration (FDA) in 2001 and is made by Pharmacia/Pfizer.

Side effects of Bextra use include, but may not be limited to, stomach pain, diarrhea, heartburn, back pain, headache, nausea and upper respiratory infection.

In November 2002, FDA and Pharmacia/Pfizer strengthened the CONTRAINDICATIONS, WARNINGS, and ADVERSE REACTIONS sections of the prescribing information for Bextra. In postmarketing experience, rare reports of hypersensitivity reactions (i.e., anaphylactic reactions and angioedema) and skin reactions, including cases of Stevens-Johnson syndrome, toxic epidermal necrolysis, exfoliative dermatitis, and erythema multiforme, have been received. These cases, some of which were serious and life threatening, have occurred in patients with and without a history of allergic reactions to sulfonamides.

See your doctor if you have concerns about the safety of Bextra or if you have experienced serious side effects associated with the drug. In addition, it may be important to contact an attorney who can help you protect your legal rights. Please keep in mind that there may be time limits time limits within which you must commence suit.

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