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論文・技術情報

• • Safety analysis of romiplostim, eltrombopag, and avatrombopag post-market approval: a pharmacovigilance study based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/2/28
  • Comprehensive analysis of adverse events associated with T-cell engagers using the FAERS database.
    タグ:

    • FAERS
    2025/2/21
  • Safety of edaravone in real-world use: analysis based on FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/2/21
  • Safety assessment of rosuvastatin-fenofibrate combination in the treatment of hyperlipidemia based on FDA’s adverse event reporting system database.
    タグ:

    • FAERS
    2025/2/21
  • Adverse events associated with inclisiran: a real-world pharmacovigilance study of FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/2/21
  • A pharmacovigilance study of olanzapine/samidorphan based on FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/2/21
  • Postmarketing safety surveillance of adalimumab, secukinumab, and infliximab in hidradenitis suppurativa: an analysis of the FDA adverse events reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/2/21
  • Drug-induced hypokalemia: an analytical study based on real-world drug monitoring data.
    タグ:

    • FAERS
    2025/2/20
  • Adverse event profiles of CDK4/6 inhibitors: a disproportionality analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/2/20
  • A real-world pharmacovigilance analysis of hepatitis B vaccine using the U.S. Vaccine Adverse Event Reporting System (VAERS) database.
    タグ:

    • VAERS
    • FAERS
    2025/2/20

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