MEDWATCH ADVERSE EVENT REPORTING PROGRAM | UNITED STATES DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION
10903 New Hampshire Avenue, Silver Spring, MD 20993
Eligibility
Hours
Voice
Application process
Fill out the MedWatch Online Voluntary Reporting Form and submit here: https://www.accessdata.fda.gov/scripts/medwatch/index.cfm
Fees
No fee for services.
Service area
United States
Description
* Receives reports from the public for FDA-regulated products such as: Prescription and over-the-counter medicines Biologics such as blood components, blood/plasma derivatives and gene therapies Medical devices such as hearing aids breast pumps, and pacemakers Combination products such as pre-filled drug syringe, metered-dose inhalers and nasal spray Special nutritional products such as dietary supplements, medical foods and infant formulas Cosmetics such as moisturizers, makeup, shampoos, hair dyes and tattoos Food such as beverages and ingredients added to foods
Data provided by
211 Life Line Finger Lakes
What's Here
Providing organization
UNITED STATES DEPARTMENT OF HEALTH AND HUMAN SERVICES FOOD AND DRUG ADMINISTRATION
The United States Department of Health and Human Services Food and Drug Administration (FDA) is responsible for protecting public health by assuring the safety, efficacy, and security of human and veterinary drugs, biological products, medical devices, our nation's food supply, cosmetics, and products that emit radiation.