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Some patients have developed Stevens Johnson syndrome (SJS) as a result of an allergic reaction in response to Bextra, a popular prescription painkiller. Stevens Johnson syndrome is a severe inflammatory condition that attacks the skin and mucous membranes and is akin to burning from the inside out. Development of the condition causes the skin and other tissues to erupt and can lead to a number of serious complications.
Bextra (valdecoxib) is manufactured by Pfizer and was approved for use in the United States in November 2001. The FDA approved Bextra as a prescription drug treatment to manage chronic pain associated with:
Bextra is also used in the treatment of menstrual cramps.
In response to mounting reports of Stevens Johnson syndrome among Bextra users, the U.S. Food and Drug Administration (FDA) asked that the makers of the drug upgrade its warning on Bextra’s label. The agency approved an updated label in 2004 that strengthened the warning of Stevens Johnson Syndrome and toxic epidermal necrolysis (TEN). A new warning was added at the same time to warn consumers of the potential risk of heart and blood clotting problems.
Bextra Stevens Johnson syndrome must be detected early and properly treated to mitigate the risk of more serious complications such as extensive skin damage, lung problems, joint problems, serious eye conditions, blindness, and even death. It is estimated that between three and fifteen percent of Bextra Stevens Johnson syndrome victims will die as a result of this devastating drug reaction.
If you or a loved one is taking Bextra and you are concerned about Stevens Johnson syndrome, you may wish to speak to your doctor in greater detail. If you have suffered SJS while taking the medication, you may wish to explore your legal rights and options by contacting a qualified and experienced Stevens Johnson Syndrome attorney in your area.
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