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Safety monitoring of drugs receiving pediatric marketing exclusivity.
タグ:
FAERS
2008/9/3
Hepatic effects of duloxetine-III: analysis of hepatic events using external data sources.
タグ:
FAERS
2008/8/12
Effects of stratification on data mining in the US Vaccine Adverse Event Reporting System (VAERS).
タグ:
VAERS
2008/7/19
The safety of niacin in the US Food and Drug Administration adverse event reporting database.
タグ:
FAERS
2008/06/14
Postlicensure monitoring of intussusception after RotaTeq vaccination in the United States, February 1, 2006, to September 25, 2007.
タグ:
VAERS
2008/06/04
Bleeding complications with warfarin use: a prevalent adverse effect resulting in regulatory action.
タグ:
FAERS
2007/7/11
Guillain-Barre syndrome after vaccination in United States a report from the CDC/FDA Vaccine Adverse Event Reporting System.
タグ:
VAERS
2007/06/15
[Iatrogenic angioedema: the role of angiotensin converting enzyme inhibitor and angiotensin II receptor blockers].
タグ:
FAERS
2007/06/02
Atazanavir-associated nephrolithiasis: cases from the US Food and Drug Administration’s Adverse Event Reporting System.
タグ:
FAERS
2007/05/16
Serious adverse events with infliximab: analysis of spontaneously reported adverse events.
タグ:
FAERS
2007/05/08
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