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

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 ...

For example, in 2017, the FDA launched a new dashboard that improves access to data on adverse events associated with drug and biologic products in its database called FAERS (FDA's Adverse Event ...

In February 2012, two health IT startups aimed to help patients sift through the reams of adverse event data collected by the U.S. Food and Drug Administration, according to a report in the Wall ...

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 ...