The FDA Adverse Event Reporting System, which Commissioner Marty Makary called “clunky,” previously published updates on a ...

The FDA announced it has commenced daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS ...

A new commission will investigate the prevalence of SSRI antidepressants as adverse event reports document hundreds of cases ...

As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and ...

The U.S. Food and Drug Administration said that it has begun the daily publication of adverse event reports related to drugs ...

The FDA will now publish adverse event data from FAERS on a daily basis, marking a major step toward greater transparency in drug development.

By providing these search capabilities--and enabling users to visualize the output--the team members think they can improve the utility of data in FDA’s Adverse Event Reporting System.

The US Food and Drug Administration on Friday revealed it has begun daily publication of adverse event data from the FDA ...

The FDA has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...

The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...