Incidence of potential drug-drug interactions with antidiabetic drugs

被引:4
作者
Samardzic, I.
Bacic-Vrca, V.
机构
[1] Gradska Ijekarna Zagreb, Community Pharm, Zagreb 10000, Croatia
[2] Univ Hosp Dubrava, Dept Clin Pharm, Zagreb, Croatia
来源
PHARMAZIE | 2015年 / 70卷 / 06期
关键词
TYPE-2; DIABETES-MELLITUS; ELDERLY-PATIENTS; BETA-BLOCKERS; GATIFLOXACIN; LEVOFLOXACIN; THERAPY; HYPERGLYCEMIA; HYPOGLYCEMIA; HYPERTENSION; COMBINATION;
D O I
10.1691/ph.2015.4777
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In an effort to achieve normoglycemia more than one antidiabetic agent is usually needed. Diabetes is associated with several comorbidities and patients with diabetes are often treated with multiple medications. Therefore, patients with diabetes are especially exposed to drug-drug interactions (DDIs). The aim of this study was to analyse the incidence and type of potential DDIs of antidiabetic drugs in patients with diabetes. This retrospective study analyzed pharmacy record data of 225 patients with diabetes mellitus. Both type 1 and type 2 diabetic patients who were taking at least one antidiabetic agent during the period of six months were included. We investigated associated therapy in that period in order to identify potential DDIs with antidiabetic therapy. Potential interactions were identified by Lexicomp (R) Lexi-Interact (TM) Online (Lexi-Comp, Inc., Hudson, USA) software which categorizes potential DDIs according to clinical significance in five types (A, B, C, D and X). Categories C, D and X are of clinical concern and always require medical attention (therapy monitoring, therapy modification or avoiding combination). We found that 80.9% of patients had at least one potential category C interaction while there were no D and X interactions. Most frequently encountered potential DDI (n = 176) included antidiabetic drugs and thiazide or thiazide like diuretics. Patients with diabetes are exposed to a large number of potential clinically significant DDIs that may require appropriate monitoring. Using databases of DDIs could be helpful in reducing the risk of potential clinically significant DDIs.
引用
收藏
页码:410 / 415
页数:6
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