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論文・技術情報

• • Drug-induced hearing loss: a real-world pharmacovigilance study using the FDA adverse event reporting system database.
    タグ:

    • FAERS
    2025/4/7
  • Safety surveillance of respiratory syncytial virus (RSV) vaccine among pregnant individuals: a real-world pharmacovigilance study using the Vaccine Adverse Event Reporting System.
    タグ:

    • CVAR
    • VAERS
    • FAERS
    2025/4/6
  • Characteristics of second primary malignancies following bispecific antibodies therapy.
    タグ:

    • FAERS
    2025/4/6
  • Safety assessment of proteasome inhibitors real world adverse event analysis from the FAERS database.
    タグ:

    • FAERS
    2025/4/5
  • Deduplicating the FDA adverse event reporting system with a novel application of network-based grouping.
    タグ:

    • FAERS
    2025/4/5
  • Safe CAR-T: shedding light on CAR-related T-cell malignancies.
    タグ:

    • FAERS
    2025/3/1
  • Paroxysmal sympathetic hyperactivity and cerebral salt wasting post management of arteriovenous malformation in a pediatric patient: A case report.
    タグ:

    • JADER
    2025/4/10
  • Basophil activation test and lymphocyte transformation test in cefuroxime-induced anaphylactic reactions.
    タグ:

    • EudraVigilance
    2025/4/11
  • Utilising the Benefit Risk Assessment of Vaccines (BRAVE) toolkit to evaluate the benefits and risks of Vaxzevria in the EU: a population-based study.
    タグ:

    • EudraVigilance
    2025/4/10
  • Lymphopenia associated with sphingosine 1-phosphate receptor modulators (S1PRMs) in multiple sclerosis: analysis of European pharmacovigilance data.
    タグ:

    • EudraVigilance
    2025/4/9

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