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論文・技術情報

• • A pharmacovigilance study of FDA adverse events for sugammadex.
    タグ:

    • EudraVigilance
    • FAERS
    2024/6/17
  • Comprehensive signal detection of delirium-associated medication using the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/6/29
  • Comparing the Differences in Adverse Events among Chimeric Antigen Receptor T-Cell Therapies: A Real-World Pharmacovigilance Study.
    タグ:

    • FAERS
    2024/8/31
  • Adverse Event Profiles of the Third-Generation Aromatase Inhibitors: Analysis of Spontaneous Reports Submitted to FAERS.
    タグ:

    • FAERS
    2024/8/31
  • Profiling the Cardiovascular Toxicities of CDK4/6 Inhibitors: A Real-World Pharmacovigilance Study.
    タグ:

    • KAERS
    • FAERS
    2024/8/31
  • Co-Occurring Infections in Cancer Patients Treated with Checkpoint Inhibitors Significantly Increase the Risk of Immune-Related Adverse Events.
    タグ:

    • FAERS
    2024/8/31
  • A comprehensive assessment of the association between common drugs and psychiatric disorders using Mendelian randomization and real-world pharmacovigilance database.
    タグ:

    • FAERS
    2024/8/28
  • A safety signal for congenital strabismus associated with valproic acid: A pharmacovigilance analysis utilizing the FDA Adverse Event Reporting System database.
    タグ:

    • FAERS
    2024/7/31
  • Comparison of thrombotic adverse events in patients treated with factor VIII products and emicizumab using the 2018-2022 US Food and Drug Administration Adverse Event Reporting System data: comment from Berkowitz et al.
    タグ:

    • FAERS
    2024/8/23
  • Erythema multiforme associated with the immune checkpoint inhibitors: A disproportionality analysis using the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/8/22

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