Healio

Transparency or ‘unnecessary alarm’? Explaining FDA’s reporting tool for cosmetic harms

Please provide your email address to receive an email when new articles are posted on . The FDA launched a new online dashboard for reporting adverse events related to cosmetic products. This ...
The Scientist

The FDA's New Adverse Event Dashboard: More Data Doesn't Mean a Better Understanding

On March 11, the FDA launched the Adverse Event Monitoring System (AEMS), consolidating several fragmented reporting databases into a single real-time public dashboard with artificial intelligence ...
Healio

FDA begins daily reporting of adverse event data

Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...
RAPS

FDA consolidates adverse events reporting systems

The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS). The agency said the ...
Becker's Hospital Review

FDA launches single adverse event platform

The FDA has launched a single public platform for adverse event reports related to drugs, biologics, vaccines, cosmetics and animal food. The Adverse Event Monitoring System will publish reports in ...