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Title MedWatch [electronic resource] : the FDA Safety Information and Adverse Event Reporting Program / Food and Drug Administration
Publ info Rockville, MD : U.S. Food and Drug Administration, 2001-

  E-RESOURCE 
LocationWorld Wide Web 

LOCATION CALL NO. STATUS
 World Wide Web  E-RESOURCE  ON THE WEB
Call # E-RESOURCE
Note Title from title screen
Articles in PDF and Html format
Summary Presents MedWatch, the FDA Safety Information and Adverse Events Reporting Program, serves both healthcare prefessionals and the medical product-using public. Provides clinical information about safety issues involving medical products, including drugs, biologics, medical and radiation-emitting devices, and special nutritional products. Allows healthcare professionals and consumers to report adverse events and problems to the FDA and/or manufacturer
Note System requirements: Html browser, JPeg compatible browser or image viewer, Adobe acrobat reader
Mode of access: Internet
Subject Pharmaceutical Preparations -- adverse effects
Product Surveillance, Postmarketing
Adverse Drug Reaction Reporting Systems
Biological Products -- adverse effects
Dietary Supplements -- adverse effects
Equipment and Supplies -- adverse effects
Health Food -- adverse effects
Infant Food -- adverse effects
Alt author United States. Food and Drug Administration
OCLC # 50872897
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