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論文・技術情報

• • Safety analysis of compounded GLP-1 receptor agonists: a pharmacovigilance study using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/4/26
  • Nephrotoxicity risks of colistin-combination therapy: a USFDA adverse event reporting system analysis using disproportionality and interaction assessment.
    タグ:

    • FAERS
    2025/4/26
  • Expanded Spectrum and Increased Incidence of Adverse Events Linked to COVID-19 Genetic Vaccines: New Concepts on Prophylactic Immuno-Gene Therapy, Iatrogenic Orphan Disease, and Platform-Inherent Challenges.
    タグ:

    • KAERS
    • VAERS
    • FAERS
    2025/4/26
  • Mechanistic Insights into Drug-Induced Guillain-Barre Syndrome: A Large-Cohort Analysis of the FAERS Database.
    タグ:

    • FAERS
    2025/4/26
  • The real-world safety profile of pemetrexed and platinum with or without pembrolizumab: insights from a comparative analysis of FAERS database.
    タグ:

    • FAERS
    2025/4/25
  • Safety of lifitegrast: A real-world pharmacovigilance study based on FAERS.
    タグ:

    • FAERS
    2025/4/24
  • Adverse events associated with lecanemab: A disproportionality analysis of data from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/4/23
  • The safety analysis of lurasidone based on the real-world data of FAERS database.
    タグ:

    • FAERS
    2025/4/23
  • Pancreatitis associated with BRAF inhibitors: a disproportionality analysis based on the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/4/23
  • Adverse drug reaction assessment of pembrolizumab in cervical cancer treatment: a real-world pharmacovigilance study using the FAERS database.
    タグ:

    • FAERS
    2025/4/23

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