News

The FDA Adverse Event Reporting System, which Commissioner Marty Makary called “clunky,” previously published updates on a ...
As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and ...
The FDA announced it has commenced daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS ...
The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...
The U.S. Food and Drug Administration said that it has begun the daily publication of adverse event reports related to drugs ...
A new commission will investigate the prevalence of SSRI antidepressants as adverse event reports document hundreds of cases ...
A recent study sheds light on issues surrounding the system's functionality, transparency, and responsiveness. The Vaccine Adverse Event Reporting System (VAERS), comanaged by the CDC and FDA, may ...
Experts say that the Singulair incident highlights a flawed system — both in the U.S. and globally — for monitoring adverse reactions after a drug is on the market.
The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...
The FDA has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...