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論文・技術情報

• • Psychiatric adverse events associated with GLP-1 receptor agonists: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System database.
    タグ:

    • FAERS
    2024/2/23
  • Cardiovascular toxicities associated with bispecific T-cell engager therapy.
    タグ:

    • FAERS
    2024/2/23
  • Major cardiovascular events under biologic psoriasis therapies: a 19-year real-world analysis of FAERS data.
    タグ:

    • FAERS
    2024/2/22
  • A pharmacovigilance study on antibody-drug conjugate (ADC)-related neurotoxicity based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/2/22
  • Short-Term Reported Urologic Adverse Events Following COVID-19 Immunization: A Vaccine Adverse Event Reporting System Analysis.
    タグ:

    • VAERS
    • FAERS
    2024/2/20
  • Thromboembolic Events Associated with Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors: A Pharmacovigilance Analysis of the US FDA Adverse Event Reporting System (FAERS) Database.
    タグ:

    • FAERS
    2024/2/20
  • A Real-World Pharmacovigilance Study of Ceftazidime/Avibactam: Data Mining of the Food and Drug Administration Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2024/2/20
  • Detection of potential safety signals related to the use of remdesivir and tocilizumab in the COVID era during pregnancy, resorting to open data from the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/2/19
  • Administration of the GSK Respiratory Syncytial Virus Vaccine to Pregnant Persons in Error.
    タグ:

    • VAERS
    • FAERS
    2024/2/23
  • Clinical Utilization of Generic Drugs and Biosimilars for Ulcerative Colitis Treatment: Insights from a Nationwide Database Study in Japan.
    タグ:

    • DeSC
    2024/2/12

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