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論文・技術情報

• • Hepatobiliary Adverse Events Linked to Immune Checkpoint Inhibitors: A Real-World Pharmacovigilance Analysis Using FAERS Data.
    タグ:

    • FAERS
    2025/11/17
  • Post-marketing safety profile of cladribine in multiple sclerosis: a disproportionality analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/11/15
  • The real-world safety of lacosamide and perampanel in children: a disproportionality analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/11/17
  • Real-world safety of Symdeko: insights from the food and drug administration adverse event reporting system.
    タグ:

    • FAERS
    2025/11/17
  • A Real-World Disproportionality Analysis of Avacopan in Anti-Neutrophil Cytoplasmic Antibodies Associated Vasculitis: Insights From FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/11/17
  • Identifying high-risk drugs and demographic patterns in drug-induced liver injury from FAERS and CVARD analyses.
    タグ:

    • CVAR
    • FAERS
    2025/11/19
  • A pharmacovigilance study of daptomycin use in infants under 1 year old based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/11/19
  • Disproportionality Analysis of Nemolizumab in Patients with Atopic Dermatitis: A Real-World Pharmacovigilance Study.
    タグ:

    • FAERS
    2025/11/19
  • Drug-induced liver injury: a real-world pharmacovigilance study using the FDA Adverse Event Reporting System database (2004-2024).
    タグ:

    • FAERS
    2025/11/18
  • Comparative safety evaluation of pentavalent (DTaP-IPV-Hib) and hexavalent (DTaP-IPV-Hib-HepB) vaccines in infants: a real-world analysis based on VAERS.
    タグ:

    • VAERS
    • FAERS
    2025/11/17

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