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論文・技術情報

• • Oseltamivir-induced hepatotoxicity: A retrospective analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/2/25
  • Assessing hemorrhagic risks in combination therapy: implications of angiogenesis inhibitors and immune checkpoint inhibitors.
    タグ:

    • FAERS
    2025/2/25
  • Second-Generation Antipsychotic-Associated Serious Adverse Events in Women: An Analysis of a National Pharmacoepidemiologic Database.
    タグ:

    • FAERS
    2025/2/27
  • Severe Acute Respiratory Failure Associated With Trimethoprim/Sulfamethoxazole Among Adolescent and Young Adults: An Active Comparator-Restricted Disproportionality Analysis From the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/2/27
  • Fosfomycin-associated adverse events: A disproportionality analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/2/27
  • Disproportionality analysis of upadacitinib-related adverse events in inflammatory bowel disease using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/2/26
  • Diabetic Ketoacidosis and the Use of New Hypoglycemic Groups: Real-World Evidence Utilizing the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/2/26
  • Mining and analysis of dizziness adverse event signals in postoperative analgesia patients based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/2/28
  • Real-world pharmacovigilance investigation of imipenem/cilastatin: signal detection using the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/2/28
  • Disproportionality analysis of vibegron-associated adverse events using the FDA adverse event reporting system (FAERS): a real-world pharmacovigilance study.
    タグ:

    • FAERS
    2025/2/28

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