MedWatch : the FDA safety information and adverse event reporting program

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

Other author/creator	United States. Food and Drug Administration.
Format	Electronic and Book
Publication Info	Rockville, Md. : U.S. Food and Drug Administration
Description	1 online resource
Supplemental Content	https://purl.fdlp.gov/GPO/LPS81698
Subject(s)	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

Uniform title	MedWatch (United States. Food and Drug Administration)
Variant title	Med Watch
Variant title	Subtitle, <1997->: FDA medical products reporting program
Variant title	Subtitle, <2002>-: FDA safety information and adverse event reporting program
Frequency	Updated irregularly
General note	GPO Cataloging Record Distribution Program (CRDP).
Technical details	Mode of access: Internet at the FDA website. Previously availabe as of 5/25/2007: http://www.fda.gov/medwatch/.
Source of description	Contents viewed Jan. 15, 2021; title from web page.
GPO item number	0475-A-02 (online)
Govt. docs number	HE 20.4058:

Library	Location	Call Number	Status	Item Actions
Joyner	Electronic Resources	Access Content Online	✔ Available