Bextra withdrawal may be too late for Thousands of Victims

posted on:
April 15, 2005

author:
Staff

Montgomery, ALA – Already preparing for the first Vioxx trial against Merck in May, Beasley Allen law firm in Montgomery, Alabama believes that Pfizer’s Bextra, another COX-2 inhibitor, posed a dual danger to thousands of consumers before its withdrawal last week.

“Bextra not only has shown an increased risk for serious cardiovascular events in patients, it has also been linked to Stevens Johnson Syndrome (SJS), a skin disease that produces deadly, widespread lesions,” according to attorney Paul Sizemore who is handling 1000 potential Bextra cases for the firm.

“Problems with Bextra have been recognized for some time in the medical community,” says Sizemore.

He cites the Journal of Thoracic and Cardiovascular Surgery that in 2003 reported: “Statistically significant increase in thromboembolic events (myocardial infarction, ischemia, cerebrovascular accident, deep vein thrombosis, pulmonary embolism) found in the group treated with Bextra (paracoxib/valdecoxib) post-op as compared to the placebo group, the relative risk for a thromboembolic event was 351 percent.”

Sizemore reveals that a second similar study was conducted by Pfizer, with results released in October 2004. This study again showed a statistically significant rise in the incidence of thromboembolic events where the relative risk was 288 percent.

Dr. Garrett Fitzgerald, a cardiologist and pharmacologist at the University of Pennsylvania, said in a New York Times interview on November 10, 2004: “The magnitude of the safety signal with Bextra is even higher than what we saw in Vioxx… this is a time bomb waiting to go off.”

Dr. Curt Furberg, Department of Public Health Sciences, Wake Forest University School of Medicine, was quoted in the same article as saying: “Bextra is no different than Vioxx and Pfizer is trying to suppress that information.”

“Pfizer has long ignored the safety signals associated with Bextra, ignored the warnings from leading scientists about its hazards, and ignored the results of multiple clinical studies evidencing a clear safety risk associated with this drug,” says Sizemore.

“Were it not for the renewed safety focus within the FDA, no doubt triggered by the Vioxx debacle, Pfizer would have continued to market and profit from a drug whose risks were not only well known, but also well proven,” adds Sizemore.

Beasley Allen has 36 pending lawsuits against Pfizer regarding Bextra, and another 1,000 case to be filed.

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