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論文・技術情報

• • Mining and analysis of dizziness adverse event signals in postoperative analgesia patients based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/2/28
  • Real-world pharmacovigilance investigation of imipenem/cilastatin: signal detection using the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/2/28
  • Disproportionality analysis of vibegron-associated adverse events using the FDA adverse event reporting system (FAERS): a real-world pharmacovigilance study.
    タグ:

    • FAERS
    2025/2/28
  • 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

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