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論文・技術情報

• • What does real-world data reveal about cangrelor’s safety? An analysis of FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2025/2/20
  • Assessment of adverse events of the novel antiepileptic drug lamotrigine: a real-world pharmacovigilance study based on FAERS.
    タグ:

    • FAERS
    2025/2/18
  • Drug-induced skin ulcer: real-world pharmacovigilance analysis based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/2/18
  • Potential risk analysis of antipsychotics-related constipation from the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/2/18
  • Novel insights into post-marketing AEs associated with bempedoic acid: a comprehensive analysis utilizing the FAERS database.
    タグ:

    • FAERS
    2025/2/17
  • Hepatic adverse events with CDK4/6 inhibitors: a systematic review combining meta-analysis and FAERS database.
    タグ:

    • FAERS
    2025/2/17
  • Toxicity spectrum of taxanes: A safety analysis from pre-marketing to post-marketing.
    タグ:

    • FAERS
    2025/2/17
  • Effect of erythropoiesis-stimulating agents on malignant neoplasms: FAERS database and Mendelian randomization.
    タグ:

    • FAERS
    2025/2/17
  • Disproportionality analysis of Raynaud’s phenomenon associated with calcitonin gene-related peptide inhibitors using the Food and Drug Administration adverse event reporting system.
    タグ:

    • KAERS
    • FAERS
    2025/2/16
  • A pharmacovigilance analysis of abrocitinib-related skin adverse events based on the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2025/2/16

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