FDA Daily Adverse Event Reporting
News Context
At a glance
- The Food and Drug Administration (FDA) is significantly increasing clarity and accelerating public health protections by transitioning to daily publication of data from the FDA adverse Event Reporting...
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FDA Moves to Real-Time Adverse Event Reporting for enhanced Public Safety
Published August 23,2025
Faster Access to Critical Safety Data
The Food and Drug Administration (FDA) is significantly increasing clarity and accelerating public health protections by transitioning to daily publication of data from the FDA adverse Event Reporting System (FAERS). previously, these reports were released on a quarterly basis, creating a substantial lag in the availability of crucial safety information.