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論文・技術情報

• • Exploration of adverse event profiles for glofitamab: A disproportionality analysis using the FDA adverse event reporting system.
    タグ:

    • FAERS
    2025/11/4
  • Comparative Analysis of Adverse Drug Reactions Between Oritavancin Diphosphate and Oritavancin-HPbetaCD Using FAERS Data.
    タグ:

    • FAERS
    2025/11/4
  • Post-market surveillance data demonstrate high mortality associated with enfortumab vedotin skin toxicity, not worsened by immune checkpoint inhibitors or corticosteroids.
    タグ:

    • FAERS
    2025/11/4
  • Pharmacokinetic prediction and dosage adjustment of enoxaparin administration in pregnant women with renal insufficiency: A FAERS-PBPK modeling study.
    タグ:

    • FAERS
    2025/11/4
  • Risk Factors for Drug-Induced Acute Generalized Exanthematous Pustulosis(AGEP) from 2004 to 2024: A Real-World Study Based on the FAERS.
    タグ:

    • FAERS
    2025/11/3
  • Pregnancy-Related Adverse Events with Tyrosine Kinase Inhibitor Use in Chronic Myeloid Leukemia: A FAERS Pharmacovigilance Analysis (2001-2024).
    タグ:

    • FAERS
    2025/11/3
  • Safety of COMT-inhibitors in parkinson’s disease: a phase-IV comparative study on adverse events of Tolcapone, Entacapone and Opicapone.
    タグ:

    • FAERS
    2025/11/1
  • Anti-Osteoporotic Medication-Related Jaw Osteonecrosis: A Descriptive Analysis of the European EudraVigilance Database.
    タグ:

    • EudraVigilance
    2025/11/8
  • Tremelimumab Plus Durvalumab in Advanced Hepatocellular Carcinoma Treatment: A Pharmacovigilance Comparative Analysis Between Eudravigilance and HIMALAYA Study.
    タグ:

    • EudraVigilance
    2025/11/4
  • Respiratory Disorders Associated with Antibody-Drug Conjugates: A Combined Analysis of the French and the WHO Pharmacovigilance Databases.
    タグ:

    • FPVD
    • VigiBase
    2025/11/7

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