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論文・技術情報

• • Pain and Sedative Medication Use Among Individuals With Inflammatory Bowel Disease: A Nationwide Population-Based Cohort Study.
    タグ:

    • CPRD
    2025/7/2
  • Response to Lavin et al (2025)’s Paper: Cutaneous T-Cell Lymphoma after Dupilumab Use: A Real-World Pharmacovigilance Study of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/7/3
  • Response to “Stevens-Johnson syndrome and toxic epidermal necrolysis associated with the use of immune checkpoint inhibitors: A disproportionality analysis using the FDA Adverse Event Reporting System database”.
    タグ:

    • FAERS
    2025/7/1
  • Fluoroquinolones and risk of nightmares: A literature review and disproportionality analysis using individual case safety reports from Food and Drug Administration Adverse Event Reporting System database.
    タグ:

    • FAERS
    2025/6/27
  • Adverse event profiles of four monomethyl auristatin E-conjugated antibody drug conjugates: a disproportionality analysis based on the US FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/6/27
  • Identifying Predictors of Serious Adverse Events in Antidepressant Treatment from a Decade-Long Nationwide Pharmacovigilance Study: Impact of Dementia and Parkinson’s Disease Treatment.
    タグ:

    • KAERS
    • FAERS
    2025/6/27
  • Explaining Uncertain Hepatoprotective Effects: When Silibinin Co-Administered with Other Drugs.
    タグ:

    • FAERS
    2025/6/26
  • Towards interpretable drug interaction prediction via dual-stage attention and Bayesian calibration with active learning.
    タグ:

    • FAERS
    2025/6/26
  • Drug adverse events associated with temozolomide administration: A real-world pharmacovigilance study using the FAERS database from 2014 to 2024.
    タグ:

    • FAERS
    2025/6/26
  • Malignant melanoma and multiple sclerosis therapies: A disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/6/26

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