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論文・技術情報

• • Real-world safety of apremilast: A pharmacovigilance analysis using the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/9/18
  • Analyzing real-world adverse events of spironolactone with the FAERS database.
    タグ:

    • FAERS
    2025/9/17
  • Evaluating the toxicity profile of combination immune checkpoint inhibitors: a disproportionality analysis of real-world adverse events from the FDA Adverse Event Reporting System for tremelimumab, durvalumab, ipilimumab, and nivolumab.
    タグ:

    • FAERS
    2025/9/17
  • Disproportionality analysis of ixekizumab-associated adverse events in the FAERS database: A real-world pharmacovigilance study.
    タグ:

    • FAERS
    2025/9/17
  • Immune checkpoint inhibitor-induced vitiligo: A large-scale real world pharmacovigilance study.
    タグ:

    • FAERS
    2025/9/18
  • An analysis of the association between atypical antipsychotic drugs and glaucoma risk: a disproportionality assessment based on the FAERS database.
    タグ:

    • FAERS
    2025/9/18
  • Adverse Events Associated With Dabrafenib, Trametinib, and Their Combination Therapy: A Disproportionality Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/9/18
  • Pharmacovigilance-based 12-year post-marketing safety analysis of quadrivalent influenza vaccines in children: a VAERS surveillance study.
    タグ:

    • VAERS
    • FAERS
    2025/9/18
  • Real-world safety comparison between cenobamate and lacosamide: a pharmacovigilance study based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/9/18
  • Medications as precipitating factors for potential eating disorders: A disproportionality analysis using FDA adverse event reports.
    タグ:

    • FAERS
    2025/9/20

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