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論文・技術情報

• • Early Evaluation of the Food and Drug Administration (FDA) Adverse Event Monitoring System (AEMS): An Analysis of Over 32 Million Pharmacovigilance Reports.
    タグ:

    • FAERS
    2026/5/4
  • Five year of post-marketing safety of teprotumumab: A disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/5/6
  • A retrospective pharmacovigilance analysis based on the FAERS database reveals sex-associated differences in toxicities of CAR T-cell therapy.
    タグ:

    • FAERS
    2026/5/6
  • Comparative Analysis of Potential Side Effects of Targeted Oral Hypoglycemic Agents Using Spontaneous Adverse Event Reports and Social Media Data.
    タグ:

    • KAERS
    • FAERS
    2026/5/5
  • Posterior Reversible Encephalopathy Syndrome (PRES) Associated With Lenvatinib: A Disproportionality Analysis.
    タグ:

    • FAERS
    2026/5/4
  • Risk factors for drug-related gestational diabetes mellitus: a real-world pharmacovigilance study based on the FAERS database.
    タグ:

    • FAERS
    2026/5/7
  • Divergent neuropsychiatric and systemic toxicity profiles of abemaciclib and palbociclib: a triangulation study integrating pharmacovigilance, genetic epidemiology, and multi-omics profiling.
    タグ:

    • FAERS
    2026/5/7
  • Mining safety signals of PD-1/PD-L1 inhibitor-related adrenal insufficiency: a study based on the FAERS database.
    タグ:

    • FAERS
    2026/5/6
  • Posterior Reversible Encephalopathy Syndrome with Angiogenesis Inhibitors for Solid Tumours: Clues from a Disproportionality Analysis of the FDA Adverse Event Reporting System and Pharmacodynamics.
    タグ:

    • FAERS
    2026/5/6
  • Immune-Mediated upper gastrointestinal toxicities reported With immune checkpoint inhibitors: An analysis of the food and drug administration adverse event reporting system (FAERS).
    タグ:

    • FAERS
    2026/5/6

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