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論文・技術情報

• • 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
  • Hyperacusis-inducing drug candidates.
    タグ:

    • FAERS
    2026/5/18
  • Comparative adverse event reporting patterns of desogestrel versus norethisterone in third-generation combined oral contraceptives: A disproportionality analysis of the FAERS satabase.
    タグ:

    • FAERS
    2026/5/23
  • Pharmacovigilance Analysis of Vonoprazan: A Disproportionality Analysis Based on the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2026/5/18
  • A retrospective analysis of gastrointestinal adverse events associated with nicorandil using the FDA Adverse Event Reporting System (FAERS) following STROBE guidelines.
    タグ:

    • FAERS
    2026/5/23
  • Comprehensive safety analysis of the clinical spectrum of adverse events associated with immune checkpoint inhibitors based on FAERS.
    タグ:

    • FAERS
    2026/5/18

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