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

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 four-page form includes sections detailing accreditation, the nature of the adverse events, quality improvement efforts, sedation/anesthesia and medication administration. Download the adverse ...

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 said that it has begun the daily publication of adverse event reports related to drugs ...

Adverse Event: Any untoward or unfavorable medical occurrence in a human subject, including any abnormal sign (for example, abnormal physical exam or laboratory findings), symptom, or disease, ...

2. The new reporting requirements will require centers to transfer the patient to a hospital or emergency center for medical treatment following an adverse event. 3. The board also eliminated several ...

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 ...