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• • Capecitabine-associated gastrointestinal ulceration, haemorrhage, and obstruction: a pharmacovigilance analysis based on the FAERS.
    タグ:

    • FAERS
    2024/7/1
  • Risk of immune system and skin and subcutaneous tissue related adverse events associated with oxaliplatin combined with immune checkpoint inhibitors: a pharmacovigilance study.
    タグ:

    • FAERS
    2024/7/1
  • Pharmacovigilance of esketamine nasal spray: an analysis of the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2024/7/1
  • Comparative analysis of adverse events among intravesical drugs in bladder cancer: a real-world study on FAERS database.
    タグ:

    • FAERS
    2024/7/1
  • Dermatologic adverse events associated with chimeric antigen receptor T-cell therapy: a pharmacovigilance analysis of the FDA reporting system.
    タグ:

    • FAERS
    2024/7/1
  • Cutaneous T-cell lymphoma following dupilumab use – A real-world pharmacovigilance study of the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2024/7/1
  • Safety evaluation of bempedoic acid: A pharmacovigilance analysis using FDA adverse event reporting system data.
    タグ:

    • FAERS
    2024/6/30
  • Recommendations for the selection of nucleoside analogues as antihuman herpesvirus drugs: a real-world analysis of reported cases from the FDA adverse event reporting system.
    タグ:

    • FAERS
    2024/6/29
  • Antidepressants and fetal death: A systematic review and disproportionality analysis in the WHO safety database (VigiBase(ⓁE).
    タグ:

    • VigiBase
    2024/7/4
  • PCSK9 Inhibitors and Infection-Related Adverse Events: A Pharmacovigilance Study Using the World Health Organization VigiBase.
    タグ:

    • VigiBase
    2024/7/2

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