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• • Multi-database pharmacovigilance assessment of GLP-1 receptor agonist-related ophthalmic risks using advanced signal detection in FAERS and vigibase.
    タグ:

    • VigiBase
    • FAERS
    2025/9/29
  • Pharmacovigilance assessment of drug-induced aplastic anemia: analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/9/29
  • Safety assessment of gemtuzumab ozogamicin: real-world adverse event analysis based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/9/29
  • Auditory system adverse events with sacubitril/valsartan: an active-comparator restricted disproportionality analysis using the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/9/29
  • Psychiatric disorders associated with newer antiseizure medications: A real-world disproportionality analysis of FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/9/29
  • Improving Large Language Models for Clinical Named Entity Recognition via Prompt Engineering.
    タグ:

    • VAERS
    • FAERS
    2024/1/25
  • Evaluation of Intraocular Anti-vascular Endothelial Growth Factor (VEGF) Drug-Associated Adverse Events Using Spontaneous Reporting Databases.
    タグ:

    • JADER
    2025/10/3
  • Changes in the trend and quality of adverse drug reaction reports in the Japanese Adverse Drug Event Report database and the impact of COVID-19-related reports.
    タグ:

    • JADER
    2025/9/27
  • Analysis of drug-drug interactions in spontaneous adverse drug reaction reports from EudraVigilance focusing on psychiatric drugs and somatic medication.
    タグ:

    • EudraVigilance
    2025/10/3
  • Antibiomania: A Systematic Review of Clarithromycin-Associated Manic Episodes.
    タグ:

    • EudraVigilance
    2025/9/29

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