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American Association of Oral and Maxillofacial Surgeons

MedWatch Adverse Event Reporting Program

In order to keep effective drugs and devices available on the market for use by you and your patients, the FDA relies on the voluntary reporting of all adverse events. FDA uses the data to maintain its safety surveillance of all FDA-regulated products. Your report may be the critical action that prompts a modification in use or design of the product, improves the safety profile of the drug or device and leads to increased patient safety.

FDA Alerts & Reporting