FDA Adverse Event Reporting System (FAERS) is offered by S&P Global Market Intelligence from the U.S. Food and Drug Administration (FDA). The FAERS database contains records of adverse event reports, medication error reports and product quality complaints resulting in adverse events that were submitted to the FDA.

This dataset provides details for related events including:

• Demographics
• Drugs
• Indications
• Outcomes
• Reactions
• Sources
• Therapies