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論文・技術情報

• • Colitis following the use of immune checkpoint inhibitors: A real-world analysis of spontaneous reports submitted to the FDA adverse event reporting system.
    タグ:

    • FAERS
    2020/5/19
  • Hematological toxicities in immune checkpoint inhibitors: A pharmacovigilance study from 2014 to 2019.
    タグ:

    • FAERS
    2020/5/10
  • Association of eszopiclone, zaleplon, or zolpidem with complex sleep behaviors resulting in serious injuries, including death.
    タグ:

    • FAERS
    2020/4/24
  • Adverse events with sacubitril/valsartan in the real world: emerging signals to target preventive strategies from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2020/4/22
  • US Food and Drug Administration Safety Advisories and Reporting to the Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2020/3/18
  • Safety Profile of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Disproportionality Analysis of FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2020/3/18
  • Systematic review: hepatosplenic T-cell lymphoma on biologic therapy for inflammatory bowel disease, including data from the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2020/1/29
  • Analysis of Pharmacovigilance Databases for Dolutegravir Safety in Pregnancy.
    タグ:

    • EudraVigilance
    • FAERS
    2019/10/9
  • Adverse Events Associated With the Use of Sipuleucel-T Reported to the US Food and Drug Administration’s Adverse Event Reporting System, 2010-2017.
    タグ:

    • FAERS
    2019/8/15
  • Postpartum Bleeding in Pregnant Women Receiving SSRIs/SNRIs: New Insights From a Descriptive Observational Study and an Analysis of Data from the FAERS Database.
    タグ:

    • FAERS
    2019/8/3

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