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

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

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 (USFDA) has suspended the biologics license of Ixchiq (Chikungunya Vaccine, Live), ...

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

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

New studies found that Americans with type 2 diabetes who are taking GLP-1 drugs like Ozempic and Mounjaro could face an ...

Preventable adverse drug events associated with inpatient injectable medications affect approximately 1.2 million hospitalizations annually and result in $600,000 in extra costs per hospital annually.

Zoetis told us 27 million doses of the drug have been given to cats and dogs and adverse events are rare saying, “We remain confident in the safety and effectiveness of Librela and Solensia.” ...

Ninety-three percent of the emerging economy generic drugs in the study were made in India; 81% of the advanced economy generic drugs in the study were made in the United States. Results showed that ...

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 ...