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論文・技術情報

• • Drug reaction with eosinophilia and systemic symptoms syndrome in association with novel antineoplastic pharmacotherapy: Characterizing reported clinical patterns and outcomes utilizing the Food and Drug Administration Adverse Event Reporting System database.
    タグ:

    • FAERS
    2025/9/18
  • Exploring the top 30 drugs associated with drug-induced thrombotic microangiopathy based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/10/6
  • Temporal trends in treatment-related cardiopulmonary disease-specific mortality in NSCLC based on pathological subtypes: a retrospective population-based cohort study.
    タグ:

    • FAERS
    2025/10/6
  • Real-World Safety of Anti-EGFR Antibodies: 20-Year Pharmacovigilance of Cetuximab and Panitumumab.
    タグ:

    • FAERS
    2025/10/6
  • Investigation of the causal effects of hypertension, candesartan, lisinopril, and ramipril on gout.
    タグ:

    • FAERS
    2025/10/4
  • Real-world Hepatobiliary Toxicity After Bispecific T-Cell Engager Therapy: A 10-Year Disproportionality Analysis of the Food and Drug Administration Adverse Event Reporting System and the World Health Organization’s Global Individual Case Safety Report Database.
    タグ:

    • VigiBase
    • FAERS
    2025/10/8
  • Exploration of the potential association between new oral anticoagulants and anxiety symptoms adverse events: Evidence from a real-world analysis.
    タグ:

    • FAERS
    2025/10/8
  • Comprehensive analysis of metformin-associated lactic acidosis: Insights from the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/10/7
  • What does data on adverse reactions reveal about benzodiazepines and suicide-related risk?: A disproportionality analysis using FDA FAERS pharmacovigilance data.
    タグ:

    • FAERS
    2025/10/7
  • A retrospective pharmacovigilance study of ocrelizumab in multiple sclerosis: Analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/10/7

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