What types of adverse events should be reported to MedWatch?

Adverse events that should be reported to MedWatch include serious and unexpected side effects, medication errors, product quality problems, therapeutic failures, and use during pregnancy. Any adverse event that causes significant harm or poses a serious risk to the patient or public health needs to be reported. This can include severe allergic reactions, hospitalizations due to medication issues, deaths, and new safety information. Additionally, any unexpected changes in drug effectiveness, such as sudden ineffectiveness or decreased effectiveness, should be reported. Adverse events related to medical devices, including malfunctions, serious injuries, or deaths caused by their use should also be reported. It is crucial to promptly report these events to MedWatch to identify potential safety issues and protect public health.