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LEADER 03290cai 2200673 a 4500

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003 OCoLC;

005 20210115152533.0;

006 m o d ;

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016 7 a| 98123472| DNLM;

019 a| 1098381777;

043 a| n-us---;

049 a| ERE#;

060 10 a| QZ 42;

074 a| 0475-A-02 (online);

086 0 a| HE 20.4058:;

130 0 a| MedWatch (United States. Food and Drug Administration)?| UNAUTHORIZED;

245 10 a| MedWatch :b| the FDA safety information and adverse event reporting program /c| U.S. Food and Drug Administration.;

246 3 a| Med Watch;

246 1 i| Subtitle, <1997->:a| FDA medical products reporting program;

246 1 i| Subtitle, <2002>-:a| FDA safety information and adverse event reporting program;

260 a| Rockville, Md. :b| U.S. Food and Drug Administration;

300 a| 1 online resource;

310 a| Updated irregularly;

336 a| textb| txt2| rdacontent;

337 a| computerb| c2| rdamedia;

338 a| online resourceb| cr2| rdacarrier;

362 1 a| Began in 1997?;

538 a| Mode of access: Internet at the FDA website. Previously availabe as of 5/25/2007: http://www.fda.gov/medwatch/.;

588 a| Contents viewed Jan. 15, 2021; title from web page.;

500 a| GPO Cataloging Record Distribution Program (CRDP).;

650 0 a| Drugsx| Side effects.=| ^A1404;

650 0 a| Drugsx| Side effectsx| Information services.=| ^A1404;

650 12 a| Drug-Related Side Effects and Adverse Reactions0| (DNLM)D064420=| ^A1173664;

650 12 a| Product Surveillance, Postmarketing0| (DNLM)D011358=| ^A928242;

650 22 a| Adverse Drug Reaction Reporting Systems0| (DNLM)D016907=| ^A933200;

650 22 a| Biological Factorsx| adverse effects0| (DNLM)D001685Q000009=| ^A1362061;

650 22 a| Dietary Supplementsx| adverse effects.0| (DNLM)D019587Q000009=| ^A936861;

650 22 a| Equipment and Suppliesx| adverse effects.0| (DNLM)D004864Q000009=| ^A1196034;

650 22 a| Food, Organicx| adverse effects.0| (DNLM)D058870Q000009?| UNAUTHORIZED;

650 22 a| Infant Foodx| adverse effects0| (DNLM)D007225Q000009=| ^A1196038;

650 22 a| Technology, Radiologicx| instrumentation0| (DNLM)D013679Q000295=| ^A1196042;

650 7 a| Drugsx| Side effects.2| fast0| (OCoLC)fst00898912;

651 7 a| United States.2| fast0| (OCoLC)fst01204155?| UNAUTHORIZED;

710 1 a| United States.b| Food and Drug Administration.=| ^A1253;

856 40 u| https://purl.fdlp.gov/GPO/LPS81698;

922 a| CONSERCHANGEDb| 20210115;

949 a| Click on web addressw| asish| joyner94;

596 a| 1;

998 a| 1087305;

999 a| CLICK ON WEB ADDRESSw| ASISc| 1i| MQ1914714d| 8/7/2007l| JNETm| JOYNERr| Ys| Yt| JNE1DOu| 7/12/2007x| EDOCUMENTz| JERESOURCEo| .STAFF. 0;

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

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

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:

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

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