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論文・技術情報

• • Neuropsychiatric Adverse Events with Monoclonal Antibodies Approved for Multiple Myeloma: An Analysis from the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/10/26
  • Exploration of the potential association between newer antiseizure medications and arrhythmias: Integrating pharmacovigilance and bioinformatics evidence.
    タグ:

    • FAERS
    2024/10/26
  • Immune checkpoint inhibitor-associated bullous pemphigoid: A retrospective and real-world study based on the United States Food and Drug Administration adverse event reporting system.
    タグ:

    • FAERS
    2024/10/26
  • Drug-associated glaucoma: A real-world study based on the Food and Drug Administration adverse event reporting system database.
    タグ:

    • FAERS
    2024/10/26
  • Comprehensive evaluation of leuprorelin-associated adverse events: insights from FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/10/29
  • Psychiatric disorders associated with fluoroquinolones: a pharmacovigilance analysis of the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/10/29
  • Hepatotoxicity of antipsychotics: an exploratory pharmacoepidemiologic and pharmacodynamic study integrating FAERS data and in vitro receptor-binding affinities.
    タグ:

    • FAERS
    2024/10/29
  • A real-world pharmacovigilance study of FDA adverse event reporting system events for Lutetium-177-PSMA-617.
    タグ:

    • FAERS
    2024/10/29
  • Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/10/27
  • Evaluation of tolvaptan-associated hepatic disorder using different national pharmacovigilance databases.
    タグ:

    • JADER
    • FAERS
    2024/10/30

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