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論文・技術情報

• • Tirzepatide safety in type 2 diabetes: a disproportionality analysis of adverse events using the FDA FAERS database.
    タグ:

    • FAERS
    2025/7/9
  • Immune Checkpoint Inhibitors as Independent and Synergistic Drivers of SJS/TEN: An Analysis of FAERS.
    タグ:

    • FAERS
    2025/7/9
  • Comprehensive safety analysis of adverse events associated with eptinezumab in migraine treatment.
    タグ:

    • FAERS
    2025/7/9
  • Post-marketing safety signals of imatinib: pharmacovigilance insights from the FDA Adverse Event Reporting System (FAERS) and implications for clinical practice.
    タグ:

    • FAERS
    2025/7/8
  • Apixaban- and Rivaroxaban-Associated Bleeding: A Retrospective Analysis Using the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/7/8
  • Assessing post-marketing safety of PDE5Is in erectile dysfunction: real-world evidence from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/7/8
  • Safety profile of ramelteon from the perspective of physicians and pharmacists: a 20-year real-world pharmacovigilance analysis based on the FAERS database.
    タグ:

    • FAERS
    2025/7/8
  • Cardiovascular safety of propranolol oral solution in infantile hemangiomas: a disproportionality analysis based on the FAERS database.
    タグ:

    • FAERS
    2025/7/8
  • Mifepristone-related foetal cardiac adverse events: findings from the postmarketing safety reports.
    タグ:

    • FAERS
    2025/7/7
  • HER2-targeted agents and interstitial lung disease: A real-world pharmacovigilance analysis using FAERS data.
    タグ:

    • FAERS
    2025/7/7

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