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• • Real-world safety assessment of Ixekizumab based on the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/5/23
  • Calcium supplementation and the risk of type 2 diabetes.
    タグ:

    • FAERS
    2025/5/23
  • Psychiatric disorders with antiseizure medications in children: an analysis of the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/5/23
  • Retrospective analysis of pembrolizumab-related adverse reactions and death outcomes based on the FAERS database.
    タグ:

    • FAERS
    2025/5/23
  • Evaluation of post-market adverse events of lubiprostone: a real-world adverse event analysis from the FAERS database.
    タグ:

    • FAERS
    2025/5/23
  • Signal detection of ferric carboxymaltose-induced serious adverse events: disproportionality analysis of FAERS and VigiBase data and systematic review of case reports.
    タグ:

    • FAERS
    • VigiBase
    2025/5/22
  • Drug-Associated Tendinopathies and Ligament Disorders: Results from a Retrospective Pharmacovigilance Study Using Disproportionality Analysis.
    タグ:

    • VAERS
    • FAERS
    2025/5/22
  • Assessing the association between drug use and ischaemic colitis: a retrospective pharmacovigilance study using FDA Adverse Event data.
    タグ:

    • FAERS
    2025/5/22
  • Safety Profile of Istradefylline in Parkinson’s Disease: A Meta-Analysis of Randomized Controlled Trials and Disproportionality Analysis Using FAERS.
    タグ:

    • FAERS
    2025/5/21
  • Adverse events associated with amlodipine: a pharmacovigilance study using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/5/21

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