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FDA Advises of Adverse Effects from New Cholesterol Drugs
The Wall Street Journal (online registration required): The U.S. Food and Drug Administration has become aware of cognitive adverse events related to a closely watched group of experimental cholesterol drugs being developed by large drug firms, Sanofi SA said in a regulatory filing Friday.
The FDA has asked Sanofi and Regeneron Pharmaceuticals Inc., which are co-developing one of the drugs, known as PCSK9 inhibitors, to assess the potential for their drug to cause neurocognitive adverse...
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