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論文・技術情報

• • Post-marketing safety of pimavanserin: a real-world pharmacovigilance study based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/1/28
  • Overweight and glucose/lipid metabolism abnormality associated with SSRIs: a pharmacovigilance study based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/1/27
  • Antibiotics-induced pulmonary embolism: A disproportionality analysis in Food and Drug Administration database of Adverse Event Reporting System using data mining algorithms.
    タグ:

    • FAERS
    2025/1/27
  • Post-Marketing Safety of Temozolomide: A Pharmacovigilance Study Based on the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/1/27
  • Post-Marketing Pharmacovigilance of Canakinumab from the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/1/25
  • A Comprehensive 10-Year Nationwide Pharmacovigilance Surveillance on Antibacterial Agents in Korea: Data Mining for Signal Detection of Trends and Seriousness of Adverse Events.
    タグ:

    • KAERS
    • FAERS
    2025/1/25
  • Pharmacovigilance imbalance analysis of VEGFR-TKI-related taste and smell disorders.
    タグ:

    • FAERS
    2025/1/25
  • Analysis of postmarketing neuropsychiatric adverse events of avapritinib based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/1/25
  • Investigation of the total anticholinergic load of reported anticholinergic drug-related adverse events using the Japanese adverse drug event report database: a retrospective pharmacovigilance study.
    タグ:

    • JADER
    2025/1/31
  • BRAF and MEK inhibitors rechallenge after an adverse drug reaction in patients with cancer: A pharmacovigilance cohort study.
    タグ:

    • VigiBase
    2025/1/25

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