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: Lawyers and SettlementsThe Real Impact of FDA Raptiva Removal
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Washington, DC: The recent decision to suspend Raptiva by its manufacturer due to concerns over Raptiva and PML (progressive multifocal leukoencephalopathy) represents a bit of good news for critics who had reservations that Raptiva's risks outweighed the benefits. The US Food and Drug Administration (FDA) has been closely monitoring Raptiva for a while now. However the precursor to Raptiva FDA removal from the US market is Health Canada, which ordered the suspension of Raptiva in that country in February.Full post as published by Lawyers and Settlements on April 27, 2009 (boomark / email).
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