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論文・技術情報

• • Post-bariatric surgery nutritional follow-up in primary care: a population-based cohort study.
    タグ:

    • THIN
    2021/4/8
  • Lower heart failure and chronic kidney disease risks associated with sodium-glucose cotransporter-2 inhibitor use in Japanese type 2 diabetes patients without established cardiovascular and renal diseases.
    タグ:

    • MDV
    2021/4/10
  • Healthcare resource utilization after initiation of sodium-glucose co-transporter-2 inhibitors versus dipeptidyl peptidase-4 inhibitors or other glucose-lowering drugs in Japanese patients with type 2 diabetes.
    タグ:

    • MDV
    2021/4/10
  • Measuring the complexity of general practice consultations: a Delphi and cross-sectional study in English primary care.
    タグ:

    • CPRD
    2021/4/8
  • Causality assessment between reported fatal cerebral haemorrhage and suspected drugs: developing a new algorithm based on the analysis of the Japanese Adverse Event Report (JADER) database and literature review.
    タグ:

    • JADER
    2021/4/9
  • Cases of clozapine-induced gastrointestinal hypomotility in Europe: Outcomes and fatality risk factors based on EudraVigilance data.
    タグ:

    • EudraVigilance
    2021/4/8
  • Adverse Event Reporting with Immune Checkpoint Inhibitors in Older Patients: Age Subgroup Disproportionality Analysis in VigiBase.
    タグ:

    • VigiBase
    2021/4/4
  • Geographic variations in rheumatoid arthritis treatment in Japan: A nationwide retrospective study using the national database of health insurance claims and specific health checkups of Japan.
    タグ:

    • NDB
    2021/4/6
  • Decreased Administration of Life-Sustaining Treatment just before Death among Older Inpatients in Japan: A Time-Trend Analysis from 2012 through 2014 Based on a Nationally Representative Sample.
    タグ:

    • NDB
    2021/4/4
  • Authors’ Reply to Michael Auerbach’s Comment on: “Frequency and Associated Costs of Anaphylaxis- and Hypersensitivity-Related Adverse Events for Intravenous Iron Products in the USA: An Analysis Using the US Food and Drug Administration Adverse Event Reporting System”.
    タグ:

    • FAERS
    2021/4/10

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