Exploring the FDA adverse event reporting system to generate hypotheses for monitoring of disease characteristics

Clinical Pharmacology and Therapeutics

Volumn 95, Issue 5, 2014, Pages 496-498

  Fang, H ^a   Su, Z ^a   Wang, Y ^a   Miller, A ^b   Liu, Z ^a   Howard, P C ^a   Tong, W ^a   Lin, S M ^b  

^a NATIONAL CENTER FOR TOXICOLOGICAL RESEARCH   (United States)

^b MARSHFIELD CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADVERSE EVENT REPORTING SYSTEM; ARTICLE; DATA BASE; DRUG LABELING; DRUG SAFETY; DRUG SURVEILLANCE PROGRAM; FOOD AND DRUG ADMINISTRATION; HUMAN; HYPOTHESIS; POSTMARKETING SURVEILLANCE; PRIORITY JOURNAL; SEX DIFFERENCE; SIGNAL DETECTION; UNITED STATES;

ADVERSE DRUG REACTION REPORTING SYSTEMS; DATA MINING; DATABASES, FACTUAL; DRUG LABELING; DRUG-RELATED SIDE EFFECTS AND ADVERSE REACTIONS; HUMANS; PRODUCT SURVEILLANCE, POSTMARKETING; UNITED STATES; UNITED STATES FOOD AND DRUG ADMINISTRATION;

EID: 84899431562     PISSN: 00099236     EISSN: 15326535     Source Type: Journal    
DOI: 10.1038/clpt.2014.17     Document Type: Article

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