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論文・技術情報

• • Characterizing bleeding adverse events associated with BCR-ABL tyrosine kinase inhibitors: insights from FAERS reports.
    タグ:

    • FAERS
    2026/9/24
  • Post-marketing safety signal profile of mavacamten in the FDA adverse event reporting system (FAERS): a disproportionality analysis.
    タグ:

    • FAERS
    2026/9/24
  • Comparative Pharmacovigilance Analysis of Safety Signals Among Advanced Prostate Cancer Therapies Using FAERS (FDA Adverse Event Reporting System).
    タグ:

    • FAERS
    2026/9/24
  • Drug-specific safety signal prioritization of antibody-drug conjugates in breast cancer: integrating FAERS pharmacovigilance, machine learning, and clinical contextualization.
    タグ:

    • FAERS
    2026/9/24
  • Pharmacovigilance and network toxicology analysis of risdiplam-associated adverse events in pediatric patients with spinal muscular atrophy.
    タグ:

    • FAERS
    2026/9/25
  • Zolbetuximab-associated adverse event reporting signals in gastric cancer: a FAERS disproportionality analysis.
    タグ:

    • FAERS
    2026/9/25
  • Pharmacovigilance of Androgen Receptor Pathway Inhibitors in Prostate Cancer: The Impact of Docetaxel Co-Reporting.
    タグ:

    • FAERS
    2026/9/26
  • Agent-Specific Clinical Profiles of Antibiotic-Associated Encephalopathy: A Dual-Database Pharmacovigilance Study Using JADER and FAERS.
    タグ:

    • JADER
    • FAERS
    2026/9/26
  • Comment on “Drug-induced liver injury: A real-world pharmacovigilance study using the FDA Adverse Event Reporting System database (2004-2024)”.
    タグ:

    • FAERS
    2026/9/25
  • Post-marketing safety of ensifentrine in COPD: A retrospective pharmacovigilance study using disproportionality analysis of FAERS/AEMS reports.
    タグ:

    • FAERS
    2026/9/26

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