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論文・技術情報

• • Deep exploration of sotorasib-related hepatobiliary AEs: Based on FDA Adverse Event reporting system.
    タグ:

    • FAERS
    2026/2/12
  • Disproportionality analysis of fondaparinux associated adverse events based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/2/11
  • Root cause analysis of advers events in a public hospital: a mixed-method study on reporting culture and contributing factors.
    タグ:

    • FAERS
    2026/2/11
  • Age and Gender Heterogeneity in Adverse Drug Reactions Associated with Hemp Use: Evidence from the FDA Pharmacovigilance Data in the Last Two Decades.
    タグ:

    • FAERS
    2026/2/11
  • Exploring the risk of depression and suicide/self-injury in patients receiving GLP-1RAs combined with metformin versus GLP-1RA monotherapy: a real-word analysis of the FAERS database.
    タグ:

    • FAERS
    2026/2/11
  • Analysis of ASMs and male infertility using the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2026/2/11
  • Assessing the real-world safety of sparsentan for immunoglobulin A nephropathy: insights from a comprehensive analysis of FAERS database.
    タグ:

    • FAERS
    2026/2/11
  • Atrial fibrillation associated with tyrosine kinase inhibitors: A case-control study of real-world pharmacovigilance data.
    タグ:

    • FAERS
    2026/2/10
  • Thrombotic and Hemorrhagic Adverse Events of Direct Oral Anticoagulants: An Analysis of Sex-Related Differences Using Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/2/10
  • Male sexual dysfunction associated with selective serotonin reuptake inhibitors (SSRIs): A pharmacovigilance disproportionality analysis of FAERS data.
    タグ:

    • FAERS
    2026/2/10

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