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論文・技術情報

• • Adverse events associated with acute pancreatitis caused by immune checkpoint inhibitors: a pharmacovigilance analysis of the FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/3/28
  • Post-marketing safety associated with sodium zirconium cyclosilicate: a pharmacovigilance study based on the FDA reporting system.
    タグ:

    • FAERS
    2025/3/28
  • The Association Between Statin Drugs and Rhabdomyolysis: An Analysis of FDA Adverse Event Reporting System (FAERS) Data and Transcriptomic Profiles.
    タグ:

    • FAERS
    2025/3/28
  • Drug-associated hyperprolactinemia: a comprehensive disproportionality analysis based on the FAERS database.
    タグ:

    • FAERS
    2025/3/28
  • Real-world safety profile of elexacaftor/tezacaftor/ivacaftor: a disproportionality analysis using the U.S. FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/3/27
  • Adverse event reporting of faricimab: a disproportionality analysis of FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/3/27
  • Cardiac arrhythmias of BCR-ABL inhibitors with or without triazole antifungal agents: A real-world pharmacovigilance study based on the food and drug administration adverse event reporting system database.
    タグ:

    • FAERS
    2025/3/27
  • Development of a Medication-Related Osteonecrosis of the Jaw Prediction Model Using the FDA Adverse Event Reporting System Database and Machine Learning.
    タグ:

    • FAERS
    2025/3/27
  • Assessing the Real-World Safety of Regadenoson for Myocardial Perfusion Imaging: Insights from a Comprehensive Analysis of FAERS Data.
    タグ:

    • FAERS
    2025/3/27
  • Evaluation of atypical antipsychotics associated rhabdomyolysis using the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/3/27

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