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MedWatch.
US Food and Drug Administration.

MedWatch, the Food and Drug Administration (FDA) Safety Information and Adverse Event Reporting Program, serves both health care professionals and consumers of health care products. The site shares safety information about medications and medical products that are regulated by the FDA.
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Related Resources
PRESS RELEASE/ANNOUNCEMENT
FDA preliminary public health notification: update of information about Ralstonia spp. associated with Vapotherm Respiratory Gas Administration device.
Schultz DG. Rockville, MD: Center for Devices and Radiological Health, Food and Drug Administration; December 20, 2005.
BOOK/REPORT
Consumer Guide to Adverse Health Events.
St. Paul, MN: Minnesota Department of Health; January 2009.
PRESS RELEASE/ANNOUNCEMENT
Potential signals of serious risks/new safety information identified by the Adverse Event Reporting System (AERS).
Center for Drug Evaluation and Research, US Food and Drug Administration.
PRESS RELEASE/ANNOUNCEMENT
Public Health Notification from FDA: Vail Products Enclosed Bed Systems.
Schultz DG. Rockville, MD: Center for Devices and Radiological Health, US Food and Drug Administration. December 4, 2007.
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