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論文・技術情報

• • Alpelisib-related adverse events: The FDA Adverse Event Reporting System Database (FAERS) pharmacovigilance study.
    タグ:

    • FAERS
    2024/3/21
  • Guillain-Barre syndrome and checkpoint inhibitor therapy: insights from pharmacovigilance data.
    タグ:

    • FAERS
    2024/3/19
  • A real-world disproportionality analysis of FDA adverse event reporting system (FAERS) events for alpelisib.
    タグ:

    • FAERS
    2024/3/18
  • The association of hypophysitis with immune checkpoint inhibitors use: Gaining insight through the FDA pharmacovigilance database.
    タグ:

    • FAERS
    2024/3/29
  • Reports of COVID-19 Vaccine Adverse Events in Predominantly Republican vs Democratic States.
    タグ:

    • VAERS
    • FAERS
    2024/3/29
  • Post-marketing safety evaluation of lurbinectedin: a pharmacovigilance analysis based on the FAERS database.
    タグ:

    • FAERS
    2024/3/29
  • Gastrointestinal infections and gastrointestinal haemorrhage are underestimated but serious adverse events in chimeric antigen receptor T-cell recipients: A real-world study.
    タグ:

    • FAERS
    2024/3/29
  • Real-World Safety Data of the Orphan Drug Onasemnogene Abeparvovec (Zolgensma((R))) for the SMA Rare Disease: A Pharmacovigilance Study Based on the EMA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/3/28
  • The Association between Molecular Initiating Events and Drug-Induced Hiccups.
    タグ:

    • FAERS
    2024/3/28
  • Serious Safety Signals and Prediction Features Following COVID-19 mRNA Vaccines Using the Vaccine Adverse Event Reporting System.
    タグ:

    • KAERS
    • VAERS
    • FAERS
    2024/3/28

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