News

The primary path to full approval from conditional approval is the pivotal efficacy study—a tightly controlled, high-quality ...
A newly published study in Psychological Medicine raises questions about a widely cited 2024 meta-analysis that downplayed ...
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 has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...
The FDA announced it has commenced daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS ...
The FDA now provides daily updates on adverse event reports for drugs and biologics via FAERS. Read more here.
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 has started "real-time reporting of adverse event data," according to an annoucement ...
A new commission will investigate the prevalence of SSRI antidepressants as adverse event reports document hundreds of cases ...
The FDA says to throw away certain Great Value frozen shrimp sold at Walmart in Louisiana and 12 other states. Here’s what ...
(NYSE: BMY) today announced the presentation of new clinical and real-world data from its cardiovascular portfolio at the European Society of Cardiology (ESC) Congress, taking place August 29 – ...