FDA Requires Boxed Warning for All Botulinum Toxin Products

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Title: FDA Requires Boxed Warning for All Botulinum Toxin Products

FDA Requires Boxed Warning for All Botulinum Toxin Products
Wed, 29 Apr 2009 23:00:00 -0500

Prompted by reports of serious adverse events, the U.S. Food and Drug Administration today announced that safety label changes, including a boxed warning, and a Risk Evaluation and Mitigation Strategy (REMS), are necessary for all botulinum toxin products.


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