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program for reporting adverse drug and device events

MedWatch is the FDA's safety information and adverse event reporting program. It allows healthcare professionals and consumers to report serious problems they suspect are associated with the drugs and medical devices they prescribe, dispense, or use. This helps the FDA monitor product safety and take necessary actions to protect public health.

Related Terms

• Pharmacovigilance
• FDA Adverse Event Reporting System
• FDA approval
• Patient-Reported Outcome Measures
• Everolimus
• Preventive Care
• Food and Drug Administration
• Regulatory Approval