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• • Constipation-predominant irritable bowel syndrome treatment options Linaclotide, Lubiprostone, Plecanatide, and Tenapanor: analysis of the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/6/12
  • Comparative pharmacological analysis of fam-trastuzumab deruxtecan-nxki and sacituzumab govitecan-hziy: Two recently developed chemotherapies in the crucial battle against breast cancer.
    タグ:

    • FAERS
    2025/6/12
  • Pharmacovigilance Analysis of Lifitegrast-Associated Adverse Events Using the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/6/12
  • Analysis of the relationship between histamine H1 receptor antagonists and broad dementia events using the FAERS, JADER, and CVAR databases.
    タグ:

    • CVAR
    • JADER
    • FAERS
    2025/6/12
  • Adverse event profile differences between maribavir and valganciclovir: findings from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/6/10
  • The real-world safety of Nivolumab: a pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/6/10
  • Post-marketing safety concerns with Tislelizumab: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/6/10
  • Drug-related visual blurring: findings from the U.S. Food and Drug Administration Adverse Event Reporting System database.
    タグ:

    • FAERS
    2025/6/10
  • Disproportionality analyses of Tapinarof-related adverse events based on the FAERS database.
    タグ:

    • FAERS
    2025/6/9
  • Exploring Ototoxicity Associated with Capmatinib: Insights from a Real-World Data Analysis of the FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2025/6/9

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