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論文・技術情報

• • Potential Eye Disorders in People With and Without Type 2 Diabetes Mellitus Exposed to GLP-1 Receptor Agonists: An Examination of the FAERS (FDA Adverse Event Reporting System) Database.
    タグ:

    • FAERS
    2025/12/23
  • Comprehensive safety assessment of donepezil: pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/26
  • Adverse Events Reported Following RSV Prefusion F Protein Vaccines Administration Among Approved Populations: A Cross-Sectional Study.
    タグ:

    • VAERS
    • FAERS
    2025/12/26
  • Machine learning prediction of pediatric adverse drug reactions using consensus-derived scarce data.
    タグ:

    • FAERS
    2025/12/26
  • Neurological drugs induced congenital anomalies: A pharmacovigilance analysis of neonatal reports in the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/12/26
  • Isotretinoin-related adverse sexual and reproductive outcomes: a real-world pharmacovigilance study of the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/25
  • Toxicity profiles of cyclin-dependent kinase 4/6 inhibitors: safety analysis from clinical trials and the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/29
  • A real-world disproportionality analysis of roflumilast using the US food and drug administration adverse event reporting system data.
    タグ:

    • FAERS
    2025/12/29
  • Vismodegib and Sonidegib Are Associated With an Elevated Reporting Odds of Squamous Cell Carcinoma; a Comparative Pharmacovigilance Study of the FDA Adverse Events Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/27
  • A real-world pharmacovigilance study of modafinil events in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/27

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