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論文・技術情報

• • Cardiovascular Adverse Events of JAK versus TNF Inhibitors using the Korean Pharmacovigilance Database.
    タグ:

    • KAERS
    • FAERS
    2026/1/30
  • Evaluation of Dexmedetomidine-Associated Bradycardia and Related Drug-Drug Interactions Using Electronic Health Record (EHR) and miRNA Target Analysis.
    タグ:

    • FAERS
    2026/1/30
  • Beyond the label: real-world gastrointestinal adverse events associated with vedolizumab – a decade of FAERS pharmacovigilance.
    タグ:

    • FAERS
    2026/1/30
  • Post-marketing safety concerns with trofinetide: a disproportionality analysis of the first therapeutic agent for Rett syndrome based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2026/1/30
  • Disproportionality analysis of satralizumab in FDA adverse event reporting system and Japanese adverse drug event report: a pharmacovigilance study.
    タグ:

    • JADER
    • FAERS
    2026/1/30
  • Exploring adverse events associated with vosoritide monotherapy: Insights from the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/1/29
  • Post-marketing safety surveillance of tarlatamab: a real-world pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS
    2026/1/29
  • Pharmacovigilance study and genetic target prediction analysis of FDA adverse event reporting system for anticancer drug-associated interstitial lung disease.
    タグ:

    • FAERS
    2026/1/29
  • Electronic Health Record Intervention and Deprescribing for Older Adults: A Randomized Clinical Trial.
    タグ:

    • FAERS
    2026/1/29
  • Hemorrhagic risk of concomitant direct oral anticoagulants and fluoroquinolones: integration of pharmacovigilance and therapeutic drug monitoring.
    タグ:

    • FAERS
    2026/1/29

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