The FDA is making more safety-related information available to consumers and physicians about recently approved drugs and biologics. The Food and Drug Administration Amendments Act of 2007 requires the agency to prepare safety summaries within 18 months after it approves a product or after a product has been used by 10,000 patients, whichever is later. Such summaries now will be posted online.
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FDA to Report on Safety Monitoring of Recently Approved Drugs, Biologics
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