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

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Bibliographic Details
Online Access: Online Access
Online Access
Online Access
Corporate Author: United States. Food and Drug Administration
Other title:MedWatch (United States. Food and Drug Administration)
Med Watch.
Subtitle, <1997->: FDA medical products reporting program.
Subtitle, <2002>-: FDA safety information and adverse event reporting program.
Format: Government Document Electronic Website
Language:English
Published: Rockville, Md. : U.S. Food and Drug Administration.
Subjects:
Drugs > Side effects.
Drugs > Side effects > Information services.
Drugs > Side effects > Reporting > United States.
Medical supplies > Health aspects > Reporting > United States.
Health products > Health aspects > Reporting > United States.
Biological products > Health aspects > Reporting > United States.
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.
Description
Published:Began in 1997?
Physical Description:1 online resource.
Publication Frequency:Updated irregularly.
Format:Mode of access: Internet at the FDA website. Previously availabe as of 5/25/2007: http://www.fda.gov/medwatch/
Source of Description, Etc. Note:Contents viewed Jan. 15, 2021; title from web page.

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