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 ...

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