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論文・技術情報

• • Melanosis Secondary to Drugs: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/26
  • The guanylate cyclase stimulator vericiguat: Insights and adverse events from a FAERS-based pharmacovigilance study.
    タグ:

    • FAERS
    2025/12/30
  • Adverse events following measles, mumps, rubella and varicella virus vaccine live (PROQUAD((R))) reported to the vaccine adverse event reporting system (VAERS), 2015-2025.
    タグ:

    • FAERS
    • VAERS
    2025/12/30
  • A 20-year FAERS analysis of hypersensitivity reports to chlorhexidine and povidone-iodine (2004-2024).
    タグ:

    • FAERS
    2025/12/29
  • Disproportionality analysis of safety signals for milnacipran and levomilnacipran: a pharmacovigilance study using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/12/29
  • Real-world disproportionality analysis of sleep disturbances associated with antiseizure medications in epilepsy: a pharmacovigilance study.
    タグ:

    • FAERS
    2025/12/29
  • Intrahepatic cholestasis of pregnancy associated with azathioprine: first quantitative disproportionality analysis using the FDA adverse event reporting system.
    タグ:

    • KAERS
    • FAERS
    2026/1/1
  • Assessment of Drug Induced Thyroid Dysfunction Risk Using the United States Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/1/1
  • Drug-Induced Liver Injury Associated With Moxifloxacin: A Pharmacovigilance Analysis of the FDA Adverse Event Reporting System and a Real-World Retrospective Study.
    タグ:

    • FAERS
    2025/12/31
  • Disproportionality Analysis of Adverse Events Associated with IL-1 Inhibitors in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/12/31

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