Add Yahoo as a preferred source to see more of our stories on Google. The FDA announced it will now update its Adverse Event Reporting System every day, instead of once per quarter. Photo courtesy FDA ...

The FDA Adverse Event Reporting System (FAERS) contains reports from health care professionals, consumers, and manufacturers on adverse events, serious medication errors, and product quality ...

Please provide your email address to receive an email when new articles are posted on . Only 11.5% of adults given simultaneous administration of RZV and aIIV4 had one or more severe reactions. Severe ...

The FDA has launched a new adverse event reporting system that will consolidate several systems it has for reporting different types of adverse events, the agency announced Wednesday. The new system, ...

The US Food and Drug Administration (FDA) announced it is unifying its various adverse reporting systems into a single system called the Adverse Event Monitoring System (AEMS). The agency said the ...