Although the recall was announced on September 30, 2004, problems with
the drug were evidence years before this announcement. Numerous clinical studies have
led medical researchers to conclude that Vioxx presents a significant and unnecessary
risk to patients.
In conjunction with Kaiser Permanente, the FDA conducted a study to
evaluate the risks of Vioxx. The study, which analyzed data from more than 1.4 million
people, found that Vioxx patients were at a three times greater risk of suffering a heart
attack.
The delay in responding to important safety studies compromised the health
of millions of people throughout Canada and worldwide. Merck & Co. could have acted
proactively to warn consumers and doctors of the danger, but instead continued to aggressively
market the dangerous drug.
If you have been injured by Vioxx, you may be entitled to compensation. |