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論文・技術情報

• • A disproportionality analysis of nifedipine in the overall population and in pregnant women using the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2025/11/20
  • Adverse Event Profiles of Acetaminophen and Ibuprofen in Infants: A Food and Drug Administration Adverse Event Reporting System Database Retrospective Cohort Study.
    タグ:

    • FAERS
    2025/11/19
  • Association between oral JAK-1 inhibitors and infection risks in atopic dermatitis: a retrospective analysis of the FAERS database.
    タグ:

    • FAERS
    2025/11/19
  • Insights from pharmacovigilance databases, clinical cohorts and preclinical models into VEGF(R) inhibitor-induced arthritis in cancer.
    タグ:

    • VigiBase
    • FAERS
    2025/11/19
  • Reporting patterns of multiple sclerosis with immune checkpoint inhibitors: analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2025/11/21
  • A disproportionality analysis on proprotein convertase subtilisin/kexin type 9 inhibitors and hypersensitivity and anaphylaxis.
    タグ:

    • CVAR
    • FAERS
    2025/11/21
  • Cardiotoxicity of different 5-HT3 receptor antagonists analyzed using the FAERS database and pharmacokinetic study.
    タグ:

    • FAERS
    2025/11/21
  • Adverse events associated with single-ingredient folic acid in pregnancy: A descriptive analysis of the United States Food and Drug Administration Adverse Event Reporting System (2004-2025).
    タグ:

    • FAERS
    2025/11/20
  • Tiopronin safety in cystinuria: first real-world pharmacovigilance analysis using the FDA Adverse Event Reporting System (FAERS): an EAU YAU and Endourology sections review.
    タグ:

    • FAERS
    2025/11/20
  • Bridging pharmacovigilance and genetic insight: investigating drugs and indications for breast cancer risk in women with autoimmune diseases.
    タグ:

    • FAERS
    2025/11/22

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