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Case series of liver failure associated with rosiglitazone and pioglitazone.
タグ:
FAERS
2009/07/23
An evaluation of three signal-detection algorithms using a highly inclusive reference event database.
タグ:
FAERS
2009/5/23
Finding, evaluating, and managing drug-related risks: approaches taken by the US Food and Drug Administration (FDA).
タグ:
FAERS
2009/05/21
Postmarketing surveillance of serious adverse events associated with the use of rofecoxib from 1999-2002.
タグ:
FAERS
2009/5/21
Systematic investigation of time windows for adverse event data mining for recently approved drugs.
タグ:
FAERS
2009/05/20
Identification of structure-activity relationships for adverse effects of pharmaceuticals in humans. Part A: use of FDA post-market reports to create a database of hepatobiliary and urinary tract toxicities.
タグ:
FAERS
2009/5/8
Healthcare safety committee in Japan: mandatory accountability reporting system and punishment.
タグ:
FAERS
2009/04/25
Safety of green tea extracts : a systematic review by the US Pharmacopeia.
タグ:
FAERS
2008/5/20
Syncope after vaccination–United States, January 2005-July 2007.
タグ:
VAERS
2008/05/03
Safety of varicella vaccine after licensure in the United States: experience from reports to the vaccine adverse event reporting system, 1995-2005.
タグ:
VAERS
2008/5/3
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