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MedWatch : the FDA safety information and adverse event reporting program / U.S. Food and Drug Administration.

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Format:
Government document
Website/Database
Contributor:
United States. Food and Drug Administration
Standardized Title:
MedWatch (United States. Food and Drug Administration)
Language:
English
Subjects (All):
Drugs--Side effects.
Drugs.
Drugs--Side effects--Information services.
Drugs--Side effects--Reporting--United States.
Medical supplies--Health aspects--Reporting--United States.
Medical supplies.
Health products--Health aspects--Reporting--United States.
Health products.
Biological products--Health aspects--Reporting--United States.
Biological products.
Drug-Related Side Effects and Adverse Reactions.
Product Surveillance, Postmarketing.
Adverse Drug Reaction Reporting Systems.
Biological Factors--adverse effects.
Dietary Supplements--adverse effects.
Equipment and Supplies--adverse effects.
Food, Organic--adverse effects.
Infant Food--adverse effects.
Technology, Radiologic--instrumentation.
Drugs--Side effects--Reporting.
United States.
Medical Subjects:
Drug-Related Side Effects and Adverse Reactions.
Product Surveillance, Postmarketing.
Adverse Drug Reaction Reporting Systems.
Biological Factors--adverse effects.
Dietary Supplements--adverse effects.
Equipment and Supplies--adverse effects.
Food, Organic--adverse effects.
Infant Food--adverse effects.
Technology, Radiologic--instrumentation.
Physical Description:
1 online resource
Updated irregularly
Began in 1997?
Other Title:
Med Watch
Subtitle, <1997->: FDA medical products reporting program
Subtitle, <2002>-: FDA safety information and adverse event reporting program
Former Title:
MedWatch : the FDA medical products reporting program <1997->
Place of Publication:
Rockville, Md. : U.S. Food and Drug Administration
Summary:
"MedWatch, The FDA Safety Information and Adverse Event Reporting Program, serves both healthcare professionals and the medical product-using public. We provide important and timely clinical information about safety issues involving medical products, including prescription and over-the-counter drugs, biologics, medical and radiation-emitting devices, and special nutritional products (e.g., medical foods, dietary supplements and infant formulas). Medical product safety alerts, recalls, withdrawals, and important labeling changes that may affect the health of all Americans are quickly disseminated to the medical community and the general public via this web site and the MedWatch E-list. Select Safety Information to see reports, safety notifications, and labeling changes posted to the website since 1996. MedWatch allows healthcare professionals and consumers to report serious problems that they suspect are associated with the drugs and medical devices they prescribe, dispense, or use. Reporting can be done on line, by phone, or by submitting the MedWatch 3500 form by mail or fax. Select How to Report for more details."
Notes:
Contents viewed Jan. 15, 2021; title from web page.
OCLC:
39982375

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