What is MedWatch?

MedWatch is a vital program created by the U.S. Food and Drug Administration (FDA) to ensure the safety of medicines and medical devices. It serves as a comprehensive healthcare surveillance system that collects and analyzes information about adverse events, medication errors, and product problems related to FDA-regulated products. MedWatch acts as a bridge between healthcare professionals and consumers, allowing them to report any concerns or issues they experience with medications or devices. These reports help the FDA to identify potential safety concerns, enhance product labeling, and take necessary actions to protect public health. MedWatch encourages individuals, including patients, healthcare providers, and manufacturers, to submit voluntary reports through its user-friendly online reporting tools or by phone, fax, or mail, facilitating early detection and prevention of potential risks associated with FDA-regulated products.