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• • Toxicity profiles of immune checkpoint inhibitors in nervous system cancer: a comprehensive disproportionality analysis using FDA adverse event reporting system.
    タグ:

    • FAERS

    2024/9/9
  • Assessing the risk of tumor lysis syndrome associated with the use of antineoplastic agents: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database.
    タグ:

    • FAERS

    2024/9/9
  • Comprehensive understanding of the adverse effects associated with temozolomide: a disproportionate analysis based on the FAERS database.
    タグ:

    • FAERS

    2024/9/9
  • Dexmedetomidine: a real-world safety analysis based on FDA adverse event reporting system database.
    タグ:

    • FAERS

    2024/9/9
  • Assessment of Cardiovascular Events Caused by New-Generation Androgen Receptor Pathway Inhibitors Used for Prostate Cancer: A Real-World Study in Japan.
    タグ:

    • FAERS

    2024/9/9
  • Differences in the Adverse Event Burden of Corticosteroid Use in Inflammatory Bowel Disease as Reported Between Adverse Event Reporting Systems and a Patient Questionnaire.
    タグ:

    • VigiBase
    • FAERS

    2024/9/7
  • Adverse events associated with Atogepant: a FAERS-based pharmacovigilance analysis.
    タグ:

    • FAERS

    2024/9/7
  • Syncope after live attenuated influenza vaccine: Reports to the Vaccine Adverse Event Reporting System (2003-2024).
    タグ:

    • VAERS
    • FAERS

    2024/9/7
  • Bisphosphonate- and disumab-related gingival disorders: case analysis from the U.S. Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS

    2024/9/6
  • Analysis of publicly available adverse events reported for pediatric patients treated with Janus kinase inhibitors.
    タグ:

    • CVAR
    • FAERS

    2024/9/5

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