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論文・技術情報

• • Immune-Related Adverse Events Associated with Atezolizumab: Insights from Real-World Pharmacovigilance Data.
    タグ:

    • FAERS
    2024/7/26
  • Evaluating drug withdrawal syndrome risks through food and drug administration adverse event reporting system: a comprehensive disproportionality analysis.
    タグ:

    • FAERS
    2024/7/26
  • Safety of tildrakizumab: a disproportionality analysis based on the FDA adverse event reporting system (FAERS) database from 2018-2023.
    タグ:

    • FAERS
    2024/7/26
  • The real-world safety of oseltamivir and baloxavir marboxil in children: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/7/26
  • Descriptive Analysis of Adverse Events Reported for New Multiple Myeloma Medications Using FDA Adverse Event Reporting System (FAERS) Databases from 2015 to 2022.
    タグ:

    • FAERS
    2024/7/27
  • Real-World Data-Derived Pharmacovigilance on Drug-Induced Cognitive Impairment Utilizing a Nationwide Spontaneous Adverse Reporting System.
    タグ:

    • KAERS
    • FAERS
    2024/7/27
  • Neuronal toxicity of monoclonal antibodies (mAbs): an analysis of post-marketing reports from FDA Adverse Event Reporting System (FAERS) safety database.
    タグ:

    • FAERS
    2024/7/26
  • Cytokine release syndrome associated with immune checkpoint inhibitors: a pharmacovigilance study based on spontaneous reports in FAERS.
    タグ:

    • FAERS
    2024/7/26
  • Eye disorders associated with selective serotonin reuptake inhibitors: a real-world disproportionality analysis of FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/7/26
  • A replication study using the World Health Organization pharmacovigilance database (VigiBase(R)) to evaluate whether an association between ketamine and esketamine and alcohol and substance misuse exists.
    タグ:

    • VigiBase
    • FAERS
    2024/7/20

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