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• • Comprehensive safety analysis of the clinical spectrum of adverse events associated with immune checkpoint inhibitors based on FAERS.
    タグ:

    • FAERS
    2026/5/18
  • Hypothesis-Generating Analysis of Four Immunosuppressive Regimens After Simultaneous Pancreas-Kidney Transplantation Using the United States Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/5/18
  • Pharmacovigilance analysis of vonoprazan: a disproportionality analysis based on the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2026/5/18
  • Interstitial lung disease associated with antiandrogen agents: a pharmacovigilance study based on FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/5/19
  • Medication-related nephrotic syndrome: a real-world study from 2004 to 2024 based on the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/5/19
  • Post-marketing safety concerns with foscarbidopa/foslevodopa: A pharmacovigilance study with disproportionality analysis based on FAERS.
    タグ:

    • FAERS
    2026/5/19
  • Hematological toxicities in bevacizumab associated with ovarian cancer: A pharmacovigilance study using FDA adverse event reporting system database.
    タグ:

    • FAERS
    2026/5/19
  • Antibiotic use and immune-related adverse events in patients treated with immune checkpoint inhibitors: analysis of the FAERS database.
    タグ:

    • FAERS
    2026/5/21
  • Characterization of Safety Signals for Spinal Muscular Atrophy Treatments in Children Aged 0 to 3 Years Potential Safety Patterns for Further Investigation.
    タグ:

    • FAERS
    2026/5/21
  • Sex-specific risk profiles of drug-associated joint stiffness and deformity: a FAERS-based pharmacovigilance study with Canadian Vigilance Adverse Reaction Database validation.
    タグ:

    • FAERS
    2026/5/19

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