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論文・技術情報

• • A real-world study of ublituximab based on the WHO-VigiAccess and U.S. food and drug administration’s adverse event reporting system databases.
    タグ:

    • FAERS
    2026/3/2
  • Thromboembolic adverse events associated with TPO-RA in ITP treatment: a pharmacovigilance analysis of the FDA Adverse Event Reporting System.
    タグ:

    • FAERS
    2026/3/2
  • Real-world safety assessment of burosumab: a pharmacovigilance study utilizing the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/2/28
  • Association of GnRH agonists with depression and suicide/self-injury: a FAERS pharmacovigilance study.
    タグ:

    • FAERS
    2026/3/2
  • A real-world study of adverse event profiles associated with the four key components of antibody-drug conjugates based on the FAERS database.
    タグ:

    • FAERS
    2026/3/2
  • Drug-related proteinuria: a vigilance analysis based on the FAERS database.
    タグ:

    • FAERS
    2026/3/4
  • Disproportionality analysis of adverse events associated with degarelix: a real-world study from the FDA Adverse Event Reporting System (FAERS) database.
    タグ:

    • FAERS
    2026/3/4
  • Pharmacovigilance study of INSTIs associated with weight gain and glucose/lipid metabolism adverse events based on the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/3/3
  • Descriptive analysis of anaphylactic events reported in the FDA Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2026/3/5
  • Appendicitis and multiple sclerosis disease-modifying therapies: a disproportionality analysis of the FDA adverse event reporting system.
    タグ:

    • FAERS
    2026/3/6

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