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論文・技術情報

• • Neurological adverse events associated with baclofen: A disproportionality analysis based on FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/4/30
  • Pulmonary adverse events associated with monoclonal antibodies approved for multiple myeloma: a pharmacovigilance study based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/4/30
  • Risk of thromboembolic events in patients co-treated with factor Xa-inhibiting direct oral anticoagulants and anti-seizure medications: insights from pharmacovigilance data.
    タグ:

    • FAERS
    2025/4/30
  • Gastrointestinal adverse events associated with Lenvatinib versus Lenvatinib plus Pembrolizumab: A pharmacovigilance study in FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/4/30
  • Evaluating adverse events of pegvaliase-pqpz in phenylketonuria treatment: A comprehensive safety assessment.
    タグ:

    • FAERS
    2025/4/29
  • Establishment of a visualization platform for ADR query and analysis: an example of severe skin adverse reactions caused by sulfonylureas.
    タグ:

    • FAERS
    2025/4/29
  • Adverse Reactions With VEGF Inhibitors in Combination With NSAIDs: Disproportionality Analysis Using JADRE and FAERS.
    タグ:

    • JADER
    • FAERS
    2025/4/29
  • A Real-world Pharmacovigilance Study Of FDA Adverse Event Reporting System (FAERS) Events For Gender Of Voriconazole Drugs.
    タグ:

    • FAERS
    2025/4/29
  • Comparative Analysis of Adverse Event Profiles Among Seven Statins for Hypercholesterolemia Management Using the United States FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/4/28
  • A Real-World Pharmacovigilance Study of FDA Adverse Event Reporting System Events for Avelumab.
    タグ:

    • FAERS
    2025/4/28

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