Adverse Event Reports

What Is An Adverse Event Report?

The FDA Adverse Event Reporting System (FAERS) is a database that contains adverse event reports, medication error reports and product quality complaints resulting in adverse events that were submitted to FDA. The database is designed to support the FDA’s post-marketing safety surveillance program for drug and therapeutic biologic products.

https://www.fda.gov/Drugs/

What is drugadverseeventreports.com?

The company behind this company, Walnut St. Labs, is a data services company that seeks to make important datasets accessible to more people. The openFDA data is a rich source of insight into pharmaceutical drugs. This site aims to simplify access to the data.