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論文・技術情報

• • 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
  • Elective termination of pregnancy after vaccination reported to the Vaccine Adverse Event Reporting System (VAERS): 1990-2006.
    タグ:

    • VAERS
    2008/04/15
  • Mixed-effects Poisson regression analysis of adverse event reports: the relationship between antidepressants and suicide.
    タグ:

    • FAERS
    2008/4/12

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