FDA Adverse Event Reporting System

The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses FAERS to monitor for new adverse events and medication errors that might occur with these products.

Source: Wikipedia — FDA Adverse Event Reporting System (CC BY-SA 4.0)

FDA Adverse Event Reporting System

The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses FAERS to monitor for new adverse events and medication errors that might occur with these products.

Source: Wikipedia "FDA Adverse Event Reporting System" · CC BY-SA 4.0

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