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論文・技術情報

• • Mining and analysis of drug-induced shock adverse reactions: A comprehensive pharmacovigilance study based on the US FAERS database.
    タグ:

    • FAERS
    2025/11/13
  • Comparative Renal Safety of Tirzepatide and Semaglutide: An FDA Adverse Event Reporting System (FAERS)-Disproportionality Study.
    タグ:

    • FAERS
    2025/11/13
  • Dysphagia after COVID-19 Vaccination: A Report of Two Cases.
    タグ:

    • VAERS
    • FAERS
    2025/11/13
  • Signal mining and analysis of influencing factors for adverse events of Nivolumab and Cetuximab in the treatment of head and neck cancer based on the US FAERS database.
    タグ:

    • FAERS
    2025/11/14
  • Evaluation of the post-marketing safety of eculizumab from 2007 to 2025: A real-world pharmacovigilance study and signal analysis based on the FAERS database.
    タグ:

    • FAERS
    2025/11/9
  • Adverse events associated with third-generation cephalosporins: Analysis of the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/11/8
  • Gaps in the detection of drug-drug interactions between antipsychotic and cardiometabolic medications: a multisource analysis.
    タグ:

    • CVAR
    • FAERS
    2025/11/8
  • A Real-World Pharmacovigilance Study of Fruquintinib Based on the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/11/7
  • Drug-related adverse events in people with dementia – Statistical data from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/11/7
  • Nivolumab in gastric cancer with liver metastasis complicated by immune-mediated hepatitis: a case report and FAERS database analysis.
    タグ:

    • FAERS
    2025/11/7

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