Adverse Event Reporting Systems

Adverse Event Reporting Systems are organized methods used by healthcare providers, researchers, and regulators to collect and monitor reports of negative or unexpected reactions related to medications, vaccines, or medical devices. These systems help identify potential safety issues by gathering information about side effects or problems experienced by patients. The goal is to ensure public health by detecting risks early and taking appropriate actions to improve safety. They rely on healthcare professionals, patients, and manufacturers to submit detailed reports, facilitating continuous evaluation and regulation of medical products.