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U.S. Food and Drug Administration



  • Adverse Event Reporting System ( Database )

    "Also available is the FDA's Adverse Event Reporting System (AERS) database, which is a publically available resource that supports the FDA's post-marketing surveillance program. This database contains information on consumer, provider and manufacturer reported adverse events, potentially related pharmaceuticals, and outcomes when known."

Last updated: 2014-08-18T11:20:16.106-04:00

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