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Bextra is a NSAID (Non-Steroidal Anti-Inflammatory Drug) It is prescribed for the relief of symptoms of osteoarthritis, management of acute pain in adults, treatment of menstrual symptoms and relief of rheumatoid arthritis symptoms. On April 7, 2005, the FDA and European regulators formally asked Pfizer to suspend sales of Bextra in the United States and Europe, with which Pfizer immediately complied. The FDA stated that the risks posed by Bextra outweigh its benefits. These risks include a high rate of heart attacks, strokes, other cardiovascular injuries and Stevens Johnson Syndrome. If you or a loved one has been affected by Bextra, our experienced pharmaceutical litigation attorneys can help.

Doctor Pleads Guilty After Being Accused Of Health Care Fraud
February 23, 2010

Chief of acute pain at the Bay Shore Hospital has pleaded guilty of health care fraud involving post-surgical benefits of drugs.

FDA Rejects Pfizer Pain Drug
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Regulators reject Pfizer Inc. to market an injectable drug.

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