The potential for drug interactions with statin therapy in Ireland

被引:32
|
作者
Heerey A. [1 ]
Barry M. [1 ]
Ryan M. [1 ]
Kelly A. [1 ]
机构
[1] Department of Pharmacology and Therapeutics, University of Dublin, Trinity College, Dublin
关键词
Statin; Simvastatin; Atorvastatin; Itraconazole; Pravastatin;
D O I
10.1007/BF03167690
中图分类号
学科分类号
摘要
Background. Seven per cent of acute hospital admissions result from adverse drug reactions, of which 25% are due to drug interactions. Adverse effects of statin drugs occur in 3% of patients, mainly due to co-prescribing with other lipid-lowering agents or agents that alter their metabolism. Aim. The aim of this study was to investigate co-prescribing of the frequently-used statin medications with interacting drugs. Methods. Data from the General Medical Services (GMS) scheme of the Eastern Health Board from January to December 1998 were used in this study. Using the coding index for statins, co-prescribing was identified when concomitant medications were administered under the same GMS claim number. Results. Of 7,602 patients prescribed statins, co-prescribing of simvastatin, atorvastatin and fluvastatin with competing substrates or inhibitors of their metabolism occurred in 32, 26 and 13.4% of prescriptions issued. Thirty-four per cent of patients on simvastatin, 28% on atorvastatin and 16% on fluvastatin were prescribed medications with drug interaction potential. Conclusion. Co-prescribing of statins with competing substrates or inhibitors of their metabolism occurred in up to one-third of prescriptions issued. When statins are co-prescribed with recognised inhibitors of drug metabolism, pravastatin, which does not undergo significant hepatic metabolism, is the statin of choice.
引用
收藏
页码:176 / 179
页数:3
相关论文
共 50 条
  • [41] Incidence of statin-drug interactions in Croatian community pharmacy
    Samardzic, I.
    Benkovic, I.
    Vrca, V. Bacic
    PHARMAZIE, 2017, 72 (03): : 187 - 191
  • [42] Potential drug interactions with cyclosporine
    Katz, HI
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 1997, 36 : 18 - 24
  • [43] Potential drug interactions with melatonin
    Papagiannidou, Eleni
    Skene, Debra J.
    Ioannides, Costas
    PHYSIOLOGY & BEHAVIOR, 2014, 131 : 17 - 24
  • [44] Terbinafine and potential drug interactions
    Kaplan, DL
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 43 (05) : 882 - 882
  • [45] DRUG UTILIZATION AND POTENTIAL DRUG-DRUG INTERACTIONS
    LAVENTURIER, MF
    TALLEY, RB
    HEFNER, DL
    KENNARD, LH
    JOURNAL OF THE AMERICAN PHARMACEUTICAL ASSOCIATION, 1976, 16 (02): : 77 - 81
  • [46] THE POTENTIAL FOR DRUG-INTERACTIONS
    KARAS, S
    ANNALS OF EMERGENCY MEDICINE, 1981, 10 (12) : 627 - 630
  • [47] Potential Drug Interactions Forgotten
    Regenthal, Ralf
    DEUTSCHES ARZTEBLATT INTERNATIONAL, 2019, 116 (05): : 71 - 72
  • [48] Concomitant device and drug therapy: Current trends, potential benefits, and adverse interactions
    Marchlinski, FE
    Zado, ES
    Deely, MP
    Saligan, J
    Ashar, M
    Nayak, H
    AMERICAN JOURNAL OF CARDIOLOGY, 1999, 84 (9A): : 69R - 75R
  • [49] Potential drug–drug interactions in deceased inpatients
    Alfredo Jose Pardo-Cabello
    Victoria Manzano-Gamero
    Esperanza Del Pozo
    Francisco Javier Gómez Jiménez
    Juan de Dios Luna
    Emilio Puche Cañas
    Internal and Emergency Medicine, 2019, 14 : 325 - 328
  • [50] Consider potential drug interactions when starting combination therapy with antiepileptic drugs
    Adis Medical Writers
    Drugs & Therapy Perspectives, 2018, 34 (8) : 368 - 371