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

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 ...

The Vaccine Adverse Event Reporting System was established in 1990 to keep an accounting of such events and is jointly managed by the CDC and the FDA. Physicians and drug manufacturers are ...

Reforming the current Vaccine Adverse Event Reporting System has long been part of Kennedy’s agenda to raise questions about the safety of immunizations that are currently in use.