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論文・技術情報

• • Immune checkpoint inhibitor-induced nephrotic syndrome: a pharmacovigilance analysis of 404 FAERS cases and literature case series.
    タグ:

    • FAERS
    2025/10/15
  • Assessment of Adverse Events of Teplizumab: A Real-world Pharmacovigilance Study Based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/10/15
  • Real-world pharmacovigilance study on neonatal congenital anomalies associated with maternal drug exposure using the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/10/14
  • A study on adverse drug events of PD-1/PD-L1 inhibitors in lung cancer treatment: a decade-long data mining.
    タグ:

    • FAERS
    2025/10/14
  • Sex Differences in Cardiotoxicity of Anaplastic Lymphoma Kinase Inhibitors: An Analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/10/13
  • Immune checkpoint inhibitor-related gastrointestinal adverse events: a disproportionality analysis based on the FAERS database.
    タグ:

    • FAERS
    2025/10/13
  • Gastrointestinal adverse events associated with Hedgehog pathway inhibitors: a disproportionality analysis.
    タグ:

    • FAERS
    2025/10/13
  • Profiles and influencing factors of pulmonary fibrosis associated with biologic and conventional disease-modifying antirheumatic drugs for autoimmune diseases: a disproportionality study based on FAERS and VigiAccess.
    タグ:

    • FAERS
    2025/10/13
  • FDA-Approved Biologics for CRSwNP: A Five-Year Analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/10/13
  • Venous thromboembolism events associated with tofacitinib in rheumatoid arthritis patients: a real-world study from FAERS database.
    タグ:

    • FAERS
    2025/10/11

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