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論文・技術情報

• • Skin toxicity associated with immune checkpoint inhibitors based on the FDA adverse event reporting system 2011 – 2023 data.
    タグ:

    • FAERS
    2025/7/22
  • Efficacy and safety of bisphosphonates in pediatric glucocorticoid-induced osteoporosis: a meta-analysis and pharmacovigilance study.
    タグ:

    • FAERS
    2025/7/22
  • Pharmacovigilance and signal detection of adverse drug events associated with proteasome inhibitors in multiple myeloma: a real-world analysis using the FAERS database.
    タグ:

    • FAERS
    2025/7/22
  • Post-marketing safety signals of anifrolumab in systemic lupus erythematosus: a pharmacovigilance study based on FAERS.
    タグ:

    • FAERS
    2025/7/22
  • An in-depth investigation of NAs-induced osteoporosis adverse events: a real-world, network toxicology and molecular docking analysis.
    タグ:

    • FAERS
    2025/7/21
  • National Pharmacovigilance Assessment of Oral Adverse Events Following COVID-19 Vaccination in Germany (2020-2023).
    タグ:

    • FAERS
    • VAERS
    2025/7/21
  • Comparative safety of nivolumab plus ipilimumab versus nivolumab plus relatlimab in advanced melanoma: a pharmacovigilance study based on the FDA adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2025/7/20
  • Drug-induced sinusoidal obstruction syndrome: a real-world pharmacovigilance study based on the FDA Adverse Event Reporting System (FEARS).
    タグ:

    • FAERS
    2025/7/19
  • Data mining and safety analysis of FGFR tyrosine kinase inhibitors based on the FAERS database.
    タグ:

    • FAERS
    2025/7/19
  • Trends in the use of sodium-glucose cotransporter-2 inhibitors and characteristics of adverse event reporting in patients with heart failure in Japan: reports from the medical administration database and the adverse event reporting database.
    タグ:

    • JMDC
    • JADER
    2025/7/25

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