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• • A real-world pharmacovigilance study of lorazepam based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/6/25
  • Safety evaluation of irinotecan: a real-world disproportionality analysis using FAERS and JADER databases during the time period 2004-2024.
    タグ:

    • JADER
    • FAERS
    2025/6/24
  • An integrated approach based on FDA adverse event reporting system, network pharmacology, molecular docking, and molecular dynamics simulation analysis to study the cardiac adverse reactions and mechanism of action of osimertinib.
    タグ:

    • FAERS
    2025/6/24
  • Postmarketing safety analysis of remimazolam: Identifying unlabelled serious events.
    タグ:

    • JADER
    • FAERS
    2025/6/24
  • Adverse events associated with gepants: a pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/6/24
  • Association Between Melatonin Receptor Agonists and Cardiac Arrhythmia; Disproportionality Analysis Studies Using Pharmacovigilance Databases.
    タグ:

    • FAERS
    2025/6/24
  • Beyond pain relief: the thrombosis threat of celecoxib.
    タグ:

    • CVAR
    • JADER
    • FAERS
    2025/6/24
  • Comprehensive Analysis of Proteinuria and Nephrotic Syndrome Using the Japanese Adverse Drug Event Reporting Database.
    タグ:

    • JADER
    2025/6/28
  • Risk Factors Associated With Thrombocytopenia Induced by Intravenous Immunoglobulin Formulations: An Analysis Using the JADER database.
    タグ:

    • JADER
    2025/6/28
  • JADER Database-based Analysis of the Association Between Tranexamic Acid and Thromboembolism and Related Risk Factors.
    タグ:

    • JADER
    2025/6/28

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