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論文・技術情報

• • Comprehensive Post-marketing safety analysis of Tildrakizumab: insights from the FDA adverse event Reporting system.
    タグ:

    • FAERS
    2025/6/13
  • Carpal Tunnel Syndrome Attributed to Medication Use: A Pharmacovigilance Study.
    タグ:

    • FAERS
    2025/6/13
  • Cardiovascular Safety Profile of BRAF and MEK Inhibitors in Melanoma: FAERS Data Through a Retrospective Disproportionality Analysis (2014-2023).
    タグ:

    • FAERS
    2025/6/13
  • Gender and age disparities in cardiac immune-related adverse events associated with immune checkpoint inhibitors: a pharmacovigilance analysis of the FAERS database.
    タグ:

    • FAERS
    2025/6/13
  • A real-world population-based study on the association between cataracts and antipsychotics.
    タグ:

    • FAERS
    2025/6/13
  • 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

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