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論文・技術情報

• • Profiles and influencing factors of pulmonary fibrosis associated with biologic and conventional disease-modifying antirheumatic drugs for autoimmune diseases: a disproportionality study based on FAERS and VigiAccess.
    タグ:

    • FAERS
    2025/10/13
  • FDA-Approved Biologics for CRSwNP: A Five-Year Analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/10/13
  • Venous thromboembolism events associated with tofacitinib in rheumatoid arthritis patients: a real-world study from FAERS database.
    タグ:

    • FAERS
    2025/10/11
  • Angioedema risk of thrombolytics: an integrated assessment using disproportionality analysis of the USFDA adverse event reporting system, case reviews and meta-analysis.
    タグ:

    • FAERS
    2025/10/11
  • Potential adverse events of fluoxetine: a real-world study based on the FAERS database.
    タグ:

    • FAERS
    2025/3/16
  • Signal mining and risk analysis of olanzapine adverse events in the FAERS database.
    タグ:

    • FAERS
    2024/11/17
  • Quality of Reports on Drug Toxicity in Eudravigilance: A Safety Physician’s Perspective.
    タグ:

    • EudraVigilance
    2025/10/17
  • Immune checkpoint inhibitors and metabolic events: results from a European safety analysis.
    タグ:

    • EudraVigilance
    2025/10/16
  • Fatal Outcomes in Use of Clozapine: A VigiBase Study of 6402 Women and 11,222 Men.
    タグ:

    • VigiBase
    2025/10/14
  • Neurological Adverse Events from COVID-19 Vaccination and It’s Associated Factors in Burkina Faso: Analysis of Spontaneous Reports from the National Database of Pharmacovigilance from 2021 to 2023.
    タグ:

    • VigiBase
    2025/10/13

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