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論文・技術情報

• • Novel insights into post-marketing AEs associated with leuprorelin: A comprehensive analysis utilizing the FAERS database.
    タグ:

    • FAERS
    2024/8/19
  • Characteristics of eye disorders induced by atypical antipsychotics: a real-world study from 2016 to 2022 based on Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/8/19
  • Catatonia related to tacrolimus: a real world pharmacovigilance study of FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2024/8/17
  • Real-world pharmacovigilance analysis of galsulfase: a study based on the FDA adverse event reporting system (FAERS) database.
    タグ:

    • FAERS
    2024/8/20
  • What’s the harm? Results of an active surveillance adverse event reporting system for chiropractors and physiotherapists.
    タグ:

    • FAERS
    2024/8/19
  • Adverse drug reactions of intravesical instillation therapy for bladder cancer: based on FDA adverse event reporting system.
    タグ:

    • VAERS
    • FAERS
    2024/8/19
  • Safety of proteasome inhibitor drugs for the treatment of multiple myeloma post-marketing: a pharmacovigilance investigation based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/8/19
  • Post-marketing safety of finerenone: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/8/21
  • Data mining and safety analysis of dual orexin receptor antagonists (DORAs): a real-world pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS
    2024/8/21
  • Multiple Adverse Reactions Associated With the Use of Second-Generation Antipsychotics in People With Alzheimer’s Disease: A Pharmacovigilance Analysis Based on the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2024/8/21

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