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

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

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

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

President Trump’s FDA Begins Real-Time Reporting of Adverse Event Data Including for Product Quality Complaints for ...

Genetic testing prior to starting standard chemotherapy for gastrointestinal cancer could substantially reduce toxicities for ...

The agency shared information from reports by users of compounded semaglutide and tirzepatide who have experienced health issues.

More than 20 Republican attorneys general are demanding that the Trump administration reinstate safety protocols for the ...

Severe, life-threatening, disabling, and death adverse events have been reported, and are far more likely to be avoided if a surgical abortion is used instead of chemical abortion drugs.

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 ...