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Tylenol recalls investigated by FDA

Posted on May 25th, 2010 No Comments

The Food and Drug Administration continues to investigate the drug manufacturer McNeil (a division of Johnson & Johnson) after reports of 775 serious side effects were reported by consumers. McNeil has initiated four recalls in the past seven months and recently shut down operations at a Fort Washington, Pennsylvania location. The FDA typically considers adverse [...]

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Raptiva Recalled Due to Risk of Neurological Disease

Posted on April 9th, 2009 No Comments

Raptiva (efalizumab) a psoriasis drug manufactured and marketed by Genentech, Inc., was recently recalled by the company in response to concerns about the drug's association with progressive multifocal leukoencephalopathy (PML), a rare and deadly brain disease. In October 2008, the FDA changed Raptiva's label to warn about the increased risk of PML. By early 2009, [...]

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