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• • A real-world pharmacovigilance analysis of potential ototoxicity associated with sacubitril/valsartan based on FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2024/12/31
  • Fatal outcome related to drug reaction with eosinophilia and systemic symptoms: a disproportionality analysis of FAERS database and a systematic review of cases.
    タグ:

    • FAERS
    2024/12/31
  • Gastrointestinal Perforations Associated With JAK Inhibitors: A Disproportionality Analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/12/30
  • Drug-induced retinal vein occlusion: a disproportionality analysis from the FDA adverse event reporting system (2004-2023).
    タグ:

    • FAERS
    2024/12/30
  • A real-world pharmacovigilance study of Sorafenib based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/1/1
  • Cardiovascular and Metabolic Adverse Events of Endocrine Therapies in Women with Breast Cancer: A Disproportionality Analysis of Reports in the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/1/1
  • Data mining of adverse drug event signals with Nirmatrelvir/Ritonavir from FAERS.
    タグ:

    • FAERS
    2025/1/1
  • Drug-Induced Spontaneous Intramural Hematoma of the Gastrointestinal Tract: A Real-World Pharmacovigilance Analysis.
    タグ:

    • FAERS
    2025/1/1
  • Real-world individual and comparative analysis of adverse event reporting for adalimumab and etanercept using public FDA adverse event reporting system data.
    タグ:

    • FAERS
    2025/1/1
  • Using multiple drug similarity networks to promote adverse drug event detection.
    タグ:

    • FAERS
    2025/1/3

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