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論文・技術情報

• • Ocular Adverse Events Associated with Pegcetacoplan and Avacincaptad Pegol for Geographic Atrophy: A Population-Based Pharmacovigilance Study.
    タグ:

    • FAERS
    2025/4/28
  • Postmarketing safety analysis of upadacitinib in atopic dermatitis: A Food and Drug Administration adverse reporting system review of boxed warning-related adverse events.
    タグ:

    • FAERS
    2025/4/28
  • Association of antibiotics with Stevens-Johnson syndrome and toxic epidermal necrolysis: A real-world pharmacovigilance study.
    タグ:

    • FAERS
    2025/4/28
  • Selective Serotonin Reuptake Inhibitors and Risk of Serotonin Syndrome as Consequence of Drug-Drug Interactions: Analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/4/28
  • Tacrolimus-Related Fanconi Syndrome: A Real World Pharmacovigilance Study based on FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/4/27
  • A Real-World Pharmacovigilance Analysis of Lorlatinib-Associated Metabolic Effects Using the FDA Adverse Events Reporting System (FAERS) Database From 2013 to 2024.
    タグ:

    • FAERS
    2025/4/27
  • Post-marketing safety of pralsetinib: a real-world disproportionality analysis based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/4/26
  • 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

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