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• • Adverse events after tetanus toxoid, reduced diphtheria toxoid and acellular pertussis (Tdap) vaccine administered to adults 65 years of age and older reported to the Vaccine Adverse Event Reporting System (VAERS), 2005-2010.
    タグ:

    • VAERS
    2011/09/17
  • Adverse event profiles of platinum agents: data mining of the public version of the FDA adverse event reporting system, AERS, and reproducibility of clinical observations.
    タグ:

    • FAERS
    2011/9/8
  • Network analysis of possible anaphylaxis cases reported to the US vaccine adverse event reporting system after H1N1 influenza vaccine.
    タグ:

    • VAERS
    2011/09/07
  • Causality assessment of serious neurologic adverse events following 2009 H1N1 vaccination.
    タグ:

    • VAERS
    2011/9/7
  • Fluoroquinolone-associated myasthenia gravis exacerbation: evaluation of postmarketing reports from the US FDA adverse event reporting system and a literature review.
    タグ:

    • FAERS
    2011/9/2
  • Adverse events following administration to pregnant women of influenza A (H1N1) 2009 monovalent vaccine reported to the Vaccine Adverse Event Reporting System.
    タグ:

    • VAERS
    2011/08/25
  • Association between leukotriene-modifying agents and suicide: what is the evidence?
    タグ:

    • FAERS
    2011/6/15
  • Detecting drug interactions from adverse-event reports: interaction between paroxetine and pravastatin increases blood glucose levels.
    タグ:

    • FAERS
    2011/5/27
  • Platinum agent-induced hypersensitivity reactions: data mining of the public version of the FDA adverse event reporting system, AERS.
    タグ:

    • FAERS
    2011/5/26
  • Status and problems of adverse event reporting systems in korean hospitals.
    タグ:

    • KAERS
    2011/8/6

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