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• • A comprehensive study on drug-related Raynaud’s phenomenon based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/9/2
  • Triptorelin associated adverse events evaluated using FAERS pharmacovigilance data.
    タグ:

    • FAERS
    2025/9/2
  • Adverse events of pexidartinib for the treatment of TGCT: a real-world disproportionality analysis using FDA Adverse Event Reporting System database.
    タグ:

    • FAERS
    2025/9/3
  • One Man’s Meat Is Another Man’s Poison: High Incidence of Severe Cutaneous Drug Reactions Induced by Enfortumab Vedotin.
    タグ:

    • FAERS
    2025/9/2
  • Post marketing safety assessment of the novel postpartum depression drug, Zuranolone: evidence from real-world pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/9/2
  • Seasonality and Trends in Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Before and During the COVID-19 Pandemic: A Pharmacovigilance Study.
    タグ:

    • FAERS
    2025/9/2
  • Aioli: Standardising Drugs in the FDA Adverse Event Reporting System (FAERS) to RxNorm and Anatomical Therapeutic Chemical (ATC) Codes.
    タグ:

    • FAERS
    2025/9/5
  • Pharmacovigilance study of ramucirumab: A safety analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/9/4
  • Characterizing the Real-World Risks of Kidney Injuries Associated with Chimeric Antigen Receptor T Cell Therapies-Evidence and Safety.
    タグ:

    • FAERS
    2025/9/4
  • Association of Anti-VEGF Therapy with Reported Ocular Adverse Events: A Global Pharmacovigilance Analysis.
    タグ:

    • FAERS
    2025/9/4

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