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論文・技術情報

• • Safety assessment of basiliximab using real-world adverse event data from the FDA Adverse Event Reporting System Database: A retrospective observational study.
    タグ:

    • FAERS
    2024/9/10
  • Toxicity profiles of immune checkpoint inhibitors in nervous system cancer: a comprehensive disproportionality analysis using FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/9/9
  • A national analysis of systemic adverse events of beta-blockers used for glaucoma therapy.
    タグ:

    • FAERS
    2024/9/12
  • A real-world pharmacovigilance study of KRAS G12C mutation inhibitors based on the food and drug administration adverse event reporting system.
    タグ:

    • FAERS
    2024/9/12
  • Cyclosporine-induced alopecia:a case report, FDA adverse event reporting system analysis and literature assessment.
    タグ:

    • FAERS
    2024/9/12
  • Toxicity profiles associated with EGFR-TKIs combined with angiogenesis inhibitors in non-small cell lung cancer: an epidemiological surveillance analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/9/12
  • ORENITRAM’s decadal journey: unveiling safety profiles and adverse event through a real-world pharmacovigilance study of FAERS events.
    タグ:

    • FAERS
    2024/9/11
  • Pharmacovigilance study of the association between peripheral neuropathy and antibody-drug conjugates using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/9/14
  • Safety analysis of fluoroquinolone drugs in elderly patients over 65 based on FAERS.
    タグ:

    • FAERS
    2024/9/13
  • Safety analysis of quinolones use in minors-based on the FAERS database.
    タグ:

    • FAERS
    2024/9/13

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