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論文・技術情報

• • Post-market safety profile of cefiderocol: a real-world pharmacovigilance exploratory analysis based on U.S. FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/3/12
  • Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis.
    タグ:

    • VAERS
    • FAERS
    2025/3/12
  • The real-world safety profile of sertraline: Pharmacovigilance analysis of the FAERS database.
    タグ:

    • FAERS
    2025/3/12
  • Comprehensive evaluation of flumazenil adverse reactions: Insights from FAERS data and signal detection algorithms.
    タグ:

    • FAERS
    2025/3/12
  • Changes in the blood cyclosporine level after switching from voriconazole to isavuconazole in a patient with aplastic anemia: insights from physiologically based pharmacokinetic model simulation and the Adverse Event Reporting System database study.
    タグ:

    • FAERS
    2025/3/11
  • Post-marketing safety surveillance of vortioxetine hydrobromide: a pharmacovigilance study leveraging FAERS database.
    タグ:

    • FAERS
    2025/3/11
  • Drug-Related Hypertension: A Disproportionality Analysis Leveraging the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/3/11
  • Eosinophil-induced adverse events induced by treatment with programmed cell death 1/ligand 1 inhibitors: A comprehensive disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/3/11
  • Comparative safety signals of dopamine agonists: psychiatric and cardiovascular risks derived from FDA adverse event reporting system (FAERS) data.
    タグ:

    • FAERS
    2025/3/11
  • Alopecia Associated With the Use of Immune Checkpoint Inhibitors: A Disproportionality Analysis Using the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/3/11

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