Valneva must immediately cease U.S. shipments and sales of Ixchiq, a vaccine for chikungunya virus. The FDA recently lifted 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 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 FDA has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...

The study analyzed the bloodwork of 232 horses, 34 percent of which were receiving firocoxib for more than two months.

Twenty-seven years of research has raised our awareness about ACEs and their harmful consequences. Recent trends, however, ...

Beyond clear examples of an adverse employment action, like being fired, suspended, or having your pay cut, it gets murky about what other actions rise to this level. Indeed, federal courts around ...

Adverse drug-related events, defined as injuries due to drugs, occur frequently among inpatients. 1–4 In one study, 6.5 percent of hospitalized patients had an adverse drug event, and 28 percent ...

We conducted an in-depth review of 140 reports of adverse events involving dietary supplements containing ephedra alkaloids that were submitted to the FDA between June 1, 1997, and March 31, 1999 ...