In September 2004, Merck announced
it would be withdrawing Vioxx worldwide after a company study
discovered a link between Vioxx and serious cardiovascular
problems, including heart attacks and strokes. A number of
other clinical trials and research studies also had established
a link.
Medical researchers immediately
were suspicious that other pharmaceuticals in the same family
of drugs also exhibited the same problems. In November 2004,
a study reported in the New York Times found that Bextra users
were three times more likely to suffer a heart attack or stroke
than those people taking a placebo.
As the evidence continued to
mount, it became clear that health agencies worldwide would
be forced to respond to the risk presented by Bextra. On April
7, 2005, Health Canada and the FDA forced Pfizer to issue
a Bextra recall. The agencies were concerned that any benefits
of the drug were outweighed by the serious health consequences.
Not only was Bextra associated with cardiovascular problems,
but it previously has been linked to a serious—and even
fatal—skin condition known as Stevens-Johnson Syndrome.
Our law firm is representing
people injured by Bextra. We encourage you to contact us for
more information about your legal rights to file a Bextra
lawsuit.
For free answers to your questions about filing a Bextra lawsuit,
please complete our online contact form. |