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論文・技術情報

• • Interstitial lung disease associated with antiandrogen agents: a pharmacovigilance study based on FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/5/19
  • Medication-related nephrotic syndrome: a real-world study from 2004 to 2024 based on the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/5/19
  • Antibiotic use and immune-related adverse events in patients treated with immune checkpoint inhibitors: analysis of the FAERS database.
    タグ:

    • FAERS
    2026/5/21
  • Characterization of Safety Signals for Spinal Muscular Atrophy Treatments in Children Aged 0 to 3 Years Potential Safety Patterns for Further Investigation.
    タグ:

    • FAERS
    2026/5/21
  • Sex-specific risk profiles of drug-associated joint stiffness and deformity: a FAERS-based pharmacovigilance study with Canadian Vigilance Adverse Reaction Database validation.
    タグ:

    • FAERS
    2026/5/19
  • The safety profile of lenalidomide, dexamethasone, daratumumab, and bortezomib combinations in multiple myeloma: a retrospective analysis of the FAERS database.
    タグ:

    • FAERS
    2026/5/22
  • Hypotensive Events Associated With PDE-5 Inhibitors in Pulmonary Arterial Hypertension: Assessment of the USFDA Adverse Event Reporting System Using Disproportionality and Interaction Analysis.
    タグ:

    • FAERS
    2026/5/22
  • Drug-Induced Noninfectious Myocarditis/Pericarditis: A Real-World Pharmacovigilance Study Using the FAERS Database.
    タグ:

    • FAERS
    2026/5/22
  • Biomedical Large Language Models and Prompt Engineering for Causality Assessment of Individual Case Safety Reports in Pharmacovigilance.
    タグ:

    • VAERS
    • FAERS
    2026/5/23
  • Exploratory research on drugs after lung surgery based on real-world data from the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2026/5/22

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