Are healthcare professionals required to report adverse events to MedWatch?

Yes, healthcare professionals are required to report adverse events to MedWatch. Adverse events refer to any unexpected or harmful effects that occur after the use of a medical product or device. Reporting these events to MedWatch is critical for the monitoring and surveillance of drug safety. It helps identify potential risks, assess the benefits and risks of medical products, and ultimately improve patient safety. Healthcare professionals play a vital role in detecting and reporting adverse events as they possess valuable clinical experience and expertise. Reporting can be done through various means, such as online forms, fax, mail, or phone. Timely and accurate reporting ensures the continuous evaluation and improvement of medical products to safeguard public health.