FDA Adverse Event Reporting System (FAERS)

The FDA Adverse Event Reporting System (FAERS) is a database that collects reports of side effects, problems, or reactions experienced by patients or healthcare providers after using medications or medical products. Its purpose is to monitor the safety of these products, identify potential risks, and support regulatory actions if needed. Reporting is voluntary for healthcare professionals and consumers, but the data helps the FDA detect patterns that might indicate safety concerns, ultimately protecting public health by ensuring medications are used safely and effectively.