According to a survey, a prescription drug for rheumatoid arthritis has been connected to dozens of serious liver injuries and 12 deaths which should be banned.// Arava began selling in 1998 as a competitor to the gold-standard treatment for rheumatoid arthritis, called methotrexate. When the Food and Drug Administration approved Arava, the agency noted Arava worked no better than the older drug, but said patients needed some different options.
According to Dr. Sidney Wolfe, FDA received many reports of severe liver toxicity linked to Arava use, including 50 hospitalizations and 10 deaths. Two of the deaths were people in their 20s. Since Arava and methotrexate work equally well, and methotrexate also bears a warning about possible liver damage, Wolfe compared the two. The FDA has six times more reports of liver damage among Arava users than methotrexate users - even though thousands more people use methotrexate.
Citing similar reactions abroad, the European Union last year warned patients and doctors about Arava's toxicity, Wolfe said. He wants the FDA to go further and ban Arava's sales. The FDA said it would carefully consider Wolfe's petition.
A spokeswoman for Arava manufacturer Aventis Pharma said she had not seen the petition and declined comment about liver damage. Lise Geduldig said Arava was ``an important therapeutic option'' taken by 200,000 people. The American College of Rheumatology last summer warned doctors to take special care in prescribing Arava, by repeatedly testing patients' livers for signs of harm.
Unlike other drugs that can clear the body shortly after patients swallow a dose, Arava can takes months to dissipate. According to him, there is not much doctors can do if a patient shows signs of trouble. Yet some insurance companies pay only for Arava, not more expensive newer therapies that do not come with the same risks.
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