Opioids and Frequency Counts in the U.S. Food and Drug Administration Adverse Event Reporting System (FAERS) Database
Background: The FDA’s Adverse Event Reporting System, or FAERS, provides data on adverse events and medication error reports sent to the agency through the MedWatch programme. A high percentage of adverse events reported in the FAERS database have been connected to opioid use. The goal of this study was...
Read More