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論文・技術情報

• • Post-marketing drug safety surveillance of enfortumab vedotin: an observational pharmacovigilance study based on a real-world database.
    タグ:

    • FAERS
    2024/9/5
  • 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
  • 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
  • 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
  • Semaglutide-associated kidney injury.
    タグ:

    • FAERS
    2024/9/11
  • High-risks drug adverse events associated with Cetirizine and Loratadine for the treatment of allergic diseases: A retrospective pharmacovigilance study based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/9/11
  • A real-world pharmacovigilance study of esketamine nasal spray.
    タグ:

    • FAERS
    2024/9/10

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