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• • A Real-World Disproportionality Analysis of Histamine H2-Receptors Antagonists (Famotidine): A Pharmacovigilance Study Based on Spontaneous Reports in the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/1/17
  • Real-world safety of maribavir: a retrospective study based on signal detection in the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/1/17
  • Hepatic adverse events associated with ketamine and esketamine: A population-based disproportionality analysis.
    タグ:

    • FAERS
    2025/1/17
  • Masking in Active Comparator Designs in Pharmacovigilance: A Retrospective Bias Analysis on the Spontaneous Reporting of Thiazolidinediones and Cardiovascular Events.
    タグ:

    • CVAR
    • FAERS
    2025/1/15
  • Romosozumab adverse event profile: a pharmacovigilance analysis based on the FDA Adverse Event Reporting System (FAERS) from 2019 to 2023.
    タグ:

    • FAERS
    2025/1/14
  • A Comprehensive Study on Adverse Reactions of Benzoyl Peroxide (BPO) in Dermatological Aesthetics Utilizing the FAERS Database.
    タグ:

    • FAERS
    2025/1/14
  • A retrospective analysis of medications associated with pityriasis rosea reported in the FDA adverse events reporting system.
    タグ:

    • FAERS
    2025/1/13
  • Drug use and acute kidney injury: a Drug-Wide Association Study (DWAS) in Denmark and Sweden.
    タグ:

    • FAERS
    2025/1/13
  • Unveiling unexpected adverse events: post-marketing safety surveillance of gilteritinib and midostaurin from the FDA Adverse Event Reporting database.
    タグ:

    • FAERS
    2025/1/13
  • Unveiling the safety profile of lecanemab: A comprehensive analysis of adverse events using FDA adverse event reporting system data.
    タグ:

    • FAERS
    2025/1/13

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