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Legal News

: Lawyers and Settlements

Do Raptiva's Risks outweigh Benefits?

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Washington, DC: On February 19 the US Food and Drug Administration (FDA) issued a public health advisory concerning three confirmed, and one possible report of progressive multifocal leukoencephalopathy (PML), a rare brain infection, in patients using the psoriasis drug Raptiva. However, the FDA knew of Raptiva's potentially lethal side effects back in October 2008. Critics-and legal experts--say Raptiva was put on the market too early, and consumers have suffered the consequences.

Full post as published by Lawyers and Settlements on March 16, 2009 (boomark / email).

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