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論文・技術情報

• • 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
  • The Association Between Dexmedetomidine and Bradycardia: An Analysis of FDA Adverse Event Reporting System (FAERS) Data and Transcriptomic Profiles.
    タグ:

    • FAERS
    2025/6/26
  • SGLT2 Inhibitors May Increase Creatinine Clearance: Data Mining Utilizing the FDA Adverse Event Report System Database and Pharmacokinetic Study with Rats.
    タグ:

    • FAERS
    2025/6/26
  • Real-world pharmacovigilance reports of hepatitis A inactivated and hepatitis B (recombinant) vaccine: insights from disproportionality analysis of the vaccine adverse event reporting system.
    タグ:

    • VAERS
    • FAERS
    2025/6/25

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