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論文・技術情報

• • Central serous chorioretinopathy secondary to drugs: a real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/7/30
  • Safety assessment of Yasmin: Real-world adverse event analysis using the FAERS database.
    タグ:

    • FAERS
    2024/8/1
  • Post-marketing safety concern of PI3K inhibitors in the cancer therapies: an 8-year disproportionality analysis from the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/7/31
  • A disproportionality analysis of CDK4/6 inhibitors in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2024/7/31
  • A real-world disproportionality analysis of cyclosporine from the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2024/7/31
  • Vonoprazan-associated Clostridioides difficile infection: an analysis of the Japanese Adverse Drug Event Report and the FDA Adverse Event Reporting System.
    タグ:

    • JADER
    • FAERS
    2024/8/2
  • A systematic review and Bayesian analysis of the adverse effects of dienogest.
    タグ:

    • FAERS
    2024/8/2
  • Drug-associated porphyria: a pharmacovigilance study.
    タグ:

    • FAERS
    2024/8/2
  • Risk of Clostridioides difficile infection following different antibiotics: insights from multi-source medical data.
    タグ:

    • FAERS
    2024/8/2
  • Analysis of eplerenone in the FDA adverse event reporting system (FAERS) database: a focus on overall patient population and gender-specific subgroups.
    タグ:

    • FAERS
    2024/8/1

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