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論文・技術情報

• • Comparison of Adverse Events Among Angiotensin Receptor Blockers in Hypertension Using the United States Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/5/9
  • Pharmacovigilance analysis of small bowel bleeding associated with NSAIDs.
    タグ:

    • JADER
    • FAERS
    2025/5/8
  • Real-World Safety Profile of Cenegermin Per FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/5/7
  • Dupilumab Use in Eosinophilic Esophagitis: Analysis of the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2025/5/6
  • Challenges with Using the FDA Adverse Event Reporting System to Evaluate the Risk of Benzoyl Peroxide-Containing Products.
    タグ:

    • FAERS
    2025/5/6
  • Identification of drug combinations to reduce the risk of pioglitazone-related bladder cancer using the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/5/5
  • Corneal Complications: Drug-Induced Deposits and Food and Drug Administration Adverse Event Reporting System Data Insights-A Retrospective Study.
    タグ:

    • FAERS
    2025/5/5
  • Pharmacovigilance and Stevens-Johnson Syndrome (SJS)/Toxic Epidermal Necrolysis (TEN): 55 Years of Retrospective Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/5/5
  • Risk factors for drug-related non-infectious pneumonia: insights from the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/5/5
  • Focusing on spinal stenosis: emerging discoveries concerning Alendronate-induced risks and genetic drug targets.
    タグ:

    • FAERS
    2025/5/5

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