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• • Reply: [Post-marketing safety concerns with Lecanemab: a disproportionality analysis using the FDA adverse event reporting system].
    タグ:

    • FAERS

    2025/4/9
  • Analysis of adverse events induced by fluconazole based on FAERS database.
    タグ:

    • FAERS

    2025/4/9
  • Real-world safety of deucravacitinib: insights from the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS

    2025/4/9
  • Ophthalmotoxicity induced by antibody-drug conjugates: a pharmacovigilance study of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS

    2025/4/9
  • The adverse reactions of bevacizumab in combination with the FOLFOX chemotherapy regimen in metastatic colorectal cancer.
    タグ:

    • FAERS

    2025/4/8
  • Real-World Pharmacovigilance Analysis of Adverse Events Associated with Liposomal Bupivacaine and Bupivacaine.
    タグ:

    • FAERS

    2025/4/8
  • Efficacy and safety and analysis of thrombopoietin receptor agonists for the treatment of immune thrombocytopenia in adults: analysis of a systematic review and network meta-analysis of randomized controlled trials and results of real-world safety data.
    タグ:

    • FAERS

    2025/4/8
  • A Retrospective Comparative Analysis of Cutaneous Adverse Reactions in GLP-1 Agonist Therapies.
    タグ:

    • FAERS

    2025/4/8
  • Diarrhea-predominant irritable bowel syndrome treatment options eluxadoline, rifaximin, and alosetron: analysis of the FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS

    2025/4/8
  • Drug-induced hearing loss: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
    タグ:

    • FAERS

    2025/4/7

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