Adverse Event Reporting System

The Adverse Event Reporting System is a structured process used by healthcare providers and patients to report any negative or unexpected side effects or issues related to medical treatments, medications, or vaccines. Its purpose is to monitor safety, identify potential risks, and improve health product safety by collecting and analyzing data on adverse events. This system helps regulatory agencies, like the FDA, detect patterns or concerns early, ensuring appropriate actions are taken to protect public health. Overall, it is a critical tool for maintaining safe medical practices and informing updates to product usage guidelines.