FDA Adverse Event Reporting System (FAERS) public dashboard

Summary

FAERS is the U.S. Food and Drug Administration (FDA) primary database for collecting and analysing adverse event reports, serious medication errors, and product quality complaints for prescription drugs and therapeutic biologics, containing reports submitted by healthcare professionals, consumers, and manufacturers.

The FDA has begun daily publication of adverse event data from FAERS. This represents a significant step forward in modernising the agency’s safety monitoring infrastructure and demonstrates its commitment to radical transparency and real-time protection of public health.