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FDA Begins Real-Time Reporting of Adverse Event Data
Aug 24, 2025, 12:35

FDA Begins Real-Time Reporting of Adverse Event Data

FDA shared a post on LinkedIn:

“Today, the FDA began daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS). This represents a significant step forward in modernizing the agency’s safety monitoring infrastructure and demonstrates our commitment to real-time protection of public health.

Read further.”

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