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論文・技術情報

• • A Drug Safety Rating System Based on Postmarketing Costs Associated with Adverse Events and Patient Outcomes.
    タグ:

    • FAERS
    2015/12/19
  • Cardiotoxicity in targeted therapy for breast cancer: A study of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2015/12/15
  • FDA Adverse Event Reporting System: Recruiting Doctors to Make Surveillance a Little Less Passive.
    タグ:

    • VAERS
    • FAERS
    2015/12/04
  • Injection-Site Nodules Associated With the Use of Exenatide Extended-Release Reported to the U.S. Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2015/11/26
  • Natalizumab-induced hepatic injury: A case report and review of literature.
    タグ:

    • FAERS
    2015/11/23
  • Evaluation of the risk of venous thromboembolism after quadrivalent human papillomavirus vaccination among US females.
    タグ:

    • FAERS
    • VAERS
    2015/11/10
  • Disproportionality Measures Used in Signal Detection: An Assessment on Pharmacovigilance Adverse Event Reporting System Data.
    タグ:

    • FAERS
    2015/11/05
  • Overall conceptual framework for studying the genetics of autoimmune diseases following vaccination: a regulatory perspective.
    タグ:

    • VAERS
    2015/11/04
  • Association between Selective Serotonin Reuptake Inhibitor Therapy and Suicidality: Analysis of U.S. Food and Drug Administration Adverse Event Reporting System Data.
    タグ:

    • FAERS
    2015/11/3
  • Surveillance of adverse events after the first trivalent inactivated influenza vaccine produced in mammalian cell culture (Flucelvax((R))) reported to the Vaccine Adverse Event Reporting System (VAERS), United States, 2013-2015.
    タグ:

    • VAERS
    • FAERS
    2015/11/1

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