**Overview** The FDA Adverse Event Reporting System (FAERS) data package contains information on medication errors, quality complaints and drug related adverse events that were submitted to FDA in 20
This FAIRsharing record describes: The Adverse Event Reporting Ontology (AERO) is an ontology aimed at supporting clinicians at the time of data entry, increasing quality and accuracy of reported adv
The FEARS datasets include adverse drug events for mulitpe periods. The FDA released the datasets publicly. More information can be seen in the website of FDA:https://open.fda.gov/data/faers/