FDA Launches Daily Adverse Event Dashboard Updates
The FDA daily adverse event dashboard updates are designed to provide faster access to safety information for drugs and biologics. By offering FDA daily adverse event dashboard updates, the agency aims to reduce delays and improve the transparency of reported data.
Background on the FAERS System
The FDA Adverse Event Reporting System (FAERS) serves as the foundation for post-market safety monitoring of drugs and therapeutic biologics. It compiles reports from healthcare professionals, consumers, and manufacturers, and the information is accessible through the FAERS Public Dashboard (https://www.fda.gov/drugs/fdas-adverse-event-reporting-system-faers/fda-adverse-event-reporting-system-faers-public-dashboard). In the past, the dashboard was refreshed only on a quarterly basis.
What Has Changed
In August 2025, the FDA began releasing daily updates to the adverse event data available through the FAERS dashboard. This transition is part of a broader plan to streamline reporting systems and modernize how data is made available. (https://www.fda.gov/news-events/press-announcements/fda-begins-real-time-reporting-of-adverse-event-data)
Purpose and Benefits
The introduction of daily updates is intended to improve timeliness and accessibility. Healthcare providers, researchers, and industry observers can now monitor potential safety signals with greater immediacy (https://www.techtarget.com/pharmalifesciences/news/366629940/FDA-begins-publishing-daily-adverse-drug-reports-for-drugs-biologics). According to FDA Commissioner Marty Makary, the goal is to eliminate lengthy delays in public access to adverse event data.
What Is Next
The FDA has indicated that further streamlining of reporting systems is planned. Upcoming improvements may expand frequent updates to other product categories and enhance integration with legacy reporting tools.
Further Reading:
- https://seekingalpha.com/news/4488462-fda-starts-daily-publication-of-adverse-event-data
- https://www.statnews.com/2025/08/22/fda-faers-drugs-adverse-events/
- https://www.fiercepharma.com/pharma/fda-rolls-out-daily-updates-adverse-event-dashboard-plans-further-streamline-system
- https://www.europeanpharmaceuticalreview.com/news/264977/fda-daily-adverse-event-data-publication-faers/
Subscribe to DailyClout so you never miss an update!
