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• • Response to Li et al., “Comment on Nie et al. (2026) ‘Suicidality Reports in Acne Patients Treated with Isotretinoin and Concomitant Antidepressants: A Descriptive Analysis of FDA Adverse Event Reporting System Data'”.
    タグ:

    • FAERS
    2026/7/7
  • Pharmacovigilance Analysis of Bleeding Events Associated With Selective Serotonin Reuptake Inhibitors (SSRIs) Using the US Food and Drug Administration Adverse Event Reporting System (FAERS).
    タグ:

    • FAERS
    2026/7/6
  • Postmarketing Safety Concerns With Caplacizumab: A Real-World Pharmacovigilance Study Based on the FDA Adverse Event Reporting System Database.
    タグ:

    • FAERS
    2026/7/7
  • Drug-induced paronychia: a disproportionality and time-to-onset pharmacovigilance study using FAERS and JADER.
    タグ:

    • FAERS
    • JADER
    2026/7/8
  • Multi-method statistical signal aggregation with machine learning for severity classification of neonatal adverse drug reactions.
    タグ:

    • FAERS
    2026/7/7
  • Pharmacovigilance analysis of severe cutaneous adverse reactions associated with antiseizure medications: a FAERS database study with time-to-onset evaluation.
    タグ:

    • FAERS
    2026/7/8
  • Evaluating the safety profile of poliomyelitis vaccines: insights from post-marketing surveillance.
    タグ:

    • VAERS
    • FAERS
    2026/7/8
  • Lorazepam during breastfeeding: a pharmacokinetic case report and exploratory pharmacovigilance assessment – a contribution from the ConcePTION project.
    タグ:

    • EudraVigilance
    • FAERS
    2026/7/9
  • Large Language Models for World Health Organization-Uppsala Monitoring Centre Drug-Adverse Event Causality Assessment Using Food and Drug Administration Adverse Event Reporting System Cases: Comparative Performance Study.
    タグ:

    • KAERS
    • FAERS
    2026/7/8
  • Adverse events associated with targeted therapy and immunotherapy for ovarian cancer: a FAERS pharmacovigilance study.
    タグ:

    • FAERS
    2026/7/8

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