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論文・技術情報

• • Risk of medication-induced lactic acidosis and hyperlactatemia: a pharmacovigilance study of the United States Food and Drug Administration’s Adverse Event Reporting System database.
    タグ:

    • FAERS
    2025/4/23
  • Post-marketing safety profile of ganirelix in women: a 20-year pharmacovigilance analysis of global adverse drug event databases (2004-2024).
    タグ:

    • JADER
    • FAERS
    2025/4/23
  • Post-market safety profile and suicide/self-injury risk signals of dextromethorphan/bupropion: a real-world pharmacovigilance study.
    タグ:

    • FAERS
    2025/4/23
  • A Drug Similarity-Based Bayesian Method for Early Adverse Drug Event Detection.
    タグ:

    • FAERS
    2025/4/22
  • Identifying signals of disproportionate reporting for calcitonin gene-related peptide inhibitors: real-world evidence from the FDA adverse event reporting system.
    タグ:

    • KAERS
    • FAERS
    2025/4/22
  • A real-world pharmacovigilance study of netarsudil based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/4/22
  • Immune Checkpoint Inhibitor-induced Uveitis: Disproportionality and Timing Analyses of the Japanese Pharmacovigilance Database.
    タグ:

    • JADER
    2025/4/29
  • HIF-PHIs associated with embolic and thrombotic events: a real-world pharmacovigilance study based on the Japan Adverse Drug Event Report database.
    タグ:

    • JADER
    2025/4/23
  • H1 antihistamine-induced adverse events and time to onset: A retrospective analysis using the Japanese Adverse Drug Event Report Database.
    タグ:

    • JADER
    2025/4/22
  • Disproportionality analysis of European safety reports on autoimmune and rheumatic diseases following COVID-19 vaccination.
    タグ:

    • EudraVigilance
    2025/4/28

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