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Bextra is a prescription pain drug manufactured by Pfizer and prescribed for the treatment of osteoarthritis and adult rheumatoid arthritis. In October 2004, manufacturers warned that Bextra - one of two U.S. approved Vioxx sister drugs - may cause rare skin and heart side effects. The warning came in connection with Merck's voluntary withdrawal of Vioxx in September 2004, which was determined to increase patients' risk of heart attack and stroke. Because Bextra is a COX-2 inhibitor and has the same mechanism of action as Vioxx, more attention is being paid to whether it too increases heart risk.
In December 2004, the FDA announced that Bextra will come with a new warning about possible heart and blood clotting problems when the drug is used by patients who have just had heart bypass surgery. In addition, the new Bextra label will also include a "black box" warning about the possibility of serious skin reactions. Bextra has also been linked to Stevens Johnson Syndrome - a rare, potentially fatal skin disease.
The attorneys of James F. Humphreys & Associates have a thorough understanding of COX-2 inhibitors and the adverse effects this class of drugs often have on patients. If you have taken Bextra and suffered side effects, you may have a case. The attorneys of James F. Humphreys & Associates will not allow you or a loved one to suffer due to the negligence of a pharmaceutical company or drug manufacturer.
If you think you may be suffering from side effects caused by Bextra, contact an attorney of James F. Humphreys & Associates. Fill out a free case evaluator now.