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

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

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 ...

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

The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...

From Oct. 7, 2022, to Oct. 6, 2023, these facilities reported 610 adverse health events, including 222 that resulted in serious injury and 16 that resulted in a patient's death.

According to the vaccine's maker, Valneva, the FDA based its decision to suspend the shot on four new serious adverse events ...

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

Vascular toxicity associated with cancer therapies is a leading cause of cardiovascular adverse events in patients with ...

Shares of French drugmaker Valneva slumped more than 20% on Monday after the U.S. Food and Drug Administration suspended the ...

In patients with active lupus nephritis, iscalimab shows efficacy in reducing proteinuria and is generally well tolerated.