Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10158420 | Clinical Therapeutics | 2018 | 9 Pages |
Abstract
The aim of the study was to examine the extent to which patients with type 2 diabetes mellitus (T2DM) initiating a dipeptidyl peptidase 4 (DPP-4) inhibitor, who had no recorded objective evidence to justify dose adjustment, were initiated on the manufacturer-specified dose. Adopting a cross-sectional study design and using data from the UK General Practice, this study showed that at least 10% of patients with T2DM and a creatinine clearance level >50 mL/min initiating treatment with a DPP-4 inhibitor were prescribed a dose lower than specified in the Summary of Product Characteristics. This study provides further insights regarding DPP-4 inhibitor dose selection with respect to manufacturer specification in relation to renal function.
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Authors
Dionysis PhD, Brendan MPharm, MRPharmS, Michael Dr.med, MSc, Toni BPharm, MRPharmS, Chris PhD,