AERS (Adverse Event Reporting System)

The Adverse Event Reporting System (AERS) is a database used by the U.S. Food and Drug Administration (FDA) to collect and analyze reports of potential side effects and health problems caused by medications, medical devices, and other healthcare products. It helps identify patterns or new risks associated with these products, ensuring their safety. Healthcare providers, manufacturers, and even consumers can report adverse events, which the FDA reviews to make informed decisions about public health. Overall, AERS is a crucial tool for monitoring the safety of medical products and protecting patient well-being.