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論文・技術情報

• • Gastrointestinal stromal tumors with the use of ripretinib and sunitinib: real-world adverse event analysis based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/7/11
  • Drug-associated hearing impairment in children: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/7/11
  • Predicting Drug-Side Effect Relationships From Parametric Knowledge Embedded in Biomedical BERT Models: Methodological Study With a Natural Language Processing Approach.
    タグ:

    • KAERS
    • FAERS
    2025/7/10
  • A pharmacovigilance study of adverse events associated with polycythemia vera treatments using the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/7/10
  • Exploring Clinical Studies and the FDA Adverse Event Reporting System (FAERS) Database for nirogacestat-related Adverse Events.
    タグ:

    • FAERS
    2025/7/10
  • Pharmacovigilance study for the identification of mogamulizumab-induced immune-related adverse events using a real-world database.
    タグ:

    • FAERS
    • VigiBase
    2025/7/10
  • Age-stratified pharmacovigilance of azithromycin: a multimethod signal detection analysis in the FAERS database.
    タグ:

    • FAERS
    2025/7/10
  • Real-world FDA database analysis unveiling cardiovascular adverse events associated with bispecific T cell engagers in multip myeloma.
    タグ:

    • FAERS
    2025/7/10
  • A Justification to Using the FDA Adverse Event Reporting System for Hypothesis Generation Regarding Benzoyl Peroxide.
    タグ:

    • FAERS
    2025/7/10
  • Hepatotoxicity associated with statins: A retrospective pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS
    2025/7/9

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