| Literature DB >> 32477689 |
Jin Wang1,2, Chih-Lin Chi1,3,2, Wendy L St Peter4, Angie Carlson4, Matt Loth1,3,2, Prajwal Mani Pradhan1,2, Yue Liang1,2, Wei-Yu Chen5,2, Tatiana Lenskaia6,2, Jennifer G Robinson7, Terrence J Adam1,4.
Abstract
Simvastatin is a commonly used medication for lipid management and cardiovascular disease, however, the risk of adverse events (AEs) with its use increases via drug-drug interaction (DDI) exposures. Patients were extracted if initially diagnosed with cardiovascular disease and newly initiated simvastatin therapy. The cohort was divided into a DDI-exposed group and a non-DDI exposed group. The DDI-exposed group was further divided into gemfibrozil, clarithromycin, and erythromycin exposure groups. The outcome was defined as a composite of predefined AEs. Our results show that the simvastatin-DDI group had a higher illness burden with longer simvastatin exposure time and more medical care follow-up compared with the simvastatin-non-DDI exposed group. AEs occurred more frequently in subjects exposed to interacting drugs with a higher risk for clarithromycin and erythromycin exposed subjects than for gemfibrozil subjects. ©2020 AMIA - All rights reserved.Entities:
Year: 2020 PMID: 32477689 PMCID: PMC7233072
Source DB: PubMed Journal: AMIA Jt Summits Transl Sci Proc