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論文・技術情報

• • Fedratinib in chronic kidney disease: antifibrotic potential and renal safety signals from integrated network toxicology and pharmacovigilance.
    タグ:

    • FAERS
    2025/12/19
  • Real-world safety of Tepotinib: Insights from the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/12/18
  • Real-world data of verteporfin-related ocular adverse events: A disproportionality analysis.
    タグ:

    • FAERS
    2025/12/20
  • Adverse event reporting of mirtazapine: A disproportionality analysis of FDA adverse event reporting system (FAERS) database from 2004-2024.
    タグ:

    • FAERS
    2025/12/19
  • Calcitonin gene-related peptide antagonists in Raynaud’s phenomenon: a disproportionality study based on real data and drug-gene network analysis.
    タグ:

    • FAERS
    2025/12/19
  • Post-Marketing Safety of Tazemetostat in Antitumor Therapy: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/12/19
  • Gastrointestinal risk profile of tigecycline, omadacycline and eravacycline: Evidence from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/19
  • A real-world pharmacovigilance study of adverse events associated with esketamine: disproportionality analysis and detection of potential drug-drug interaction signals.
    タグ:

    • FAERS
    2025/12/22
  • Itraconazole-associated adverse events in fungal infections: a study of a large real-world sample based on the FAERS database (2019-2024).
    タグ:

    • FAERS
    2025/12/22
  • Differential risk of adverse drug reactions with baricitinib across age groups: integrating real-world pharmacovigilance and genetic causal inference.
    タグ:

    • FAERS
    2025/12/22

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