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論文・技術情報

• • Safety assessment of sildenafil use in neonates: a real-world data analysis based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/7/23
  • Evaluation of anticancer therapy-related dermatologic adverse events: Insights from Food and Drug Administration’s Adverse Event Reporting System dataset.
    タグ:

    • FAERS
    2024/7/23
  • Assessment of adverse events related to anti-interleukin-6 receptor monoclonal antibodies using the FDA adverse event reporting system: a real-world pharmacovigilance study.
    タグ:

    • FAERS
    2024/7/26
  • Polypharmacy and Elevated Risk of Severe Adverse Events in Older Adults Based on the Korea Institute of Drug Safety and Risk Management-Korea Adverse Event Reporting System Database.
    タグ:

    • KAERS
    • FAERS
    2024/7/26
  • The atypical antipsychotics and sexual dysfunction: a pharmacovigilance-pharmacodynamic study.
    タグ:

    • FAERS
    2024/7/24
  • Neurological adverse events associated with oxaliplatin: A pharmacovigilance analysis based on FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/7/24
  • Pharmacovigilance study of GLP-1 receptor agonists for metabolic and nutritional adverse events.
    タグ:

    • FAERS
    2024/7/23
  • Hypersensitivity Reactions Induced by Iodinated Contrast Media in Radiological Diagnosis: A Disproportionality Analysis Based on the FAERS Database.
    タグ:

    • FAERS
    2024/7/26
  • Immune-Related Adverse Events Associated with Atezolizumab: Insights from Real-World Pharmacovigilance Data.
    タグ:

    • FAERS
    2024/7/26
  • Evaluating drug withdrawal syndrome risks through food and drug administration adverse event reporting system: a comprehensive disproportionality analysis.
    タグ:

    • FAERS
    2024/7/26

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