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論文・技術情報

• • Triptans and serious adverse vascular events: data mining of the FDA Adverse Event Reporting System database.
    タグ:

    • FAERS
    2013/08/08
  • Standardizing drug adverse event reporting data.
    タグ:

    • FAERS
    2013/08/08
  • Building a knowledge base of severe adverse drug events based on AERS reporting data using semantic web technologies.
    タグ:

    • FAERS
    2013/08/08
  • Physicians’ knowledge and attitude towards adverse event reporting system and result to intervention–randomized nested trial among Bulgarian physicians.
    タグ:

    • FAERS
    2013/7/31
  • Dabigatran-dronedarone interaction in a spontaneous reporting system.
    タグ:

    • FAERS
    2013/7/31
  • Neuropsychiatric adverse effects of oseltamivir in the FDA Adverse Event Reporting System, 1999-2012.
    タグ:

    • FAERS
    2013/7/25
  • Use of case reports and the Adverse Event Reporting System in systematic reviews: overcoming barriers to assess the link between Crohn’s disease medications and hepatosplenic T-cell lymphoma.
    タグ:

    • FAERS
    2013/7/6
  • Toxicity assessments of nonsteroidal anti-inflammatory drugs in isolated mitochondria, rat hepatocytes, and zebrafish show good concordance across chemical classes.
    タグ:

    • FAERS
    2013/7/3
  • Neurological events with tumour necrosis factor alpha inhibitors reported to the Food and Drug Administration Adverse Event Reporting System.
    タグ:

    • FAERS
    2013/06/28
  • Pneumothorax as an adverse drug event: an exploratory aggregate analysis of the US FDA AERS database including a confounding by indication analysis inspired by Cornfield’s condition.
    タグ:

    • FAERS
    2013/6/27

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