FDA Adverse Event Reporting System(English)

• a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products. Formerly known as AER[S]
• FDA, AE, MedDRA, AER, AERS
• Quality and outcomes, Organizations (documentation), Pharmacology / pharmaceutics, Surveillance
• https://open.fda.gov/data/faers/