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論文・技術情報

• • Evaluating the Evolving Real-World Adverse Events of GLP-1RAs Using FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2026/3/9
  • Evaluation of Anticancer Therapy-Related Tumor Flare Reaction: Insights From Food and Drug Administration’s Adverse Event Reporting System Dataset.
    タグ:

    • FAERS
    2026/3/10
  • Leukotriene receptor antagonists and eosinophilic granulomatosis with polyangiitis: a disproportionality analysis from FAERS, JADER, CVAR databases integrated with network pharmacology.
    タグ:

    • JADER
    • FAERS
    2026/3/9
  • Ischemic optic neuropathy with semaglutide: global observational analysis of sex- and formulation-specific risk.
    タグ:

    • FAERS
    2026/3/11
  • Prioritization of adverse events related to integrase inhibitors and NNRTIs: a disproportionality analysis using data from the FAERS database.
    タグ:

    • FAERS
    2026/3/11
  • Adverse events associated with use of immunoglobulin in pediatric patients reported to the US Food and Drug Administration Adverse Event Reporting System, 2001-2023.
    タグ:

    • FAERS
    2026/3/11
  • Investigating tralokinumab-related adverse events in treating atopic dermatitis: insights from the FAERS database.
    タグ:

    • FAERS
    2026/3/11
  • Risk assessment of drug-associated miscarriage using XGBoost and SHAP explainability: a real-world pharmacovigilance analysis based on the FAERS database.
    タグ:

    • FAERS
    2026/3/11
  • Drug-associated insomnia and sex-specific disproportionality in the FDA adverse event reporting system (2019-Q1 2025).
    タグ:

    • FAERS
    2026/3/11
  • Post-marketing safety profile of lumacaftor/ivacaftor in cystic fibrosis treatment: a pharmacovigilance analysis based on FAERS.
    タグ:

    • FAERS
    2026/3/11

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