Posaconazole-digoxin drug-drug interaction mediated by inhibition of P-glycoprotein

被引:13
|
作者
Shumaker, Abby C. [1 ]
Bullard, Heather M. [2 ]
Churpek, Jane [3 ]
Knoebel, Randall W. [2 ]
机构
[1] Blessing Hosp, Dept Pharm, Quincy, IL USA
[2] Univ Chicago Med, Dept Pharm, Chicago, IL USA
[3] Univ Chicago Med, Dept Med, Sect Hematol Oncol, Chicago, IL USA
关键词
Digoxin; interaction; posaconazole; ITRACONAZOLE;
D O I
10.1177/1078155218801055
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Drug-drug interactions between digoxin and the triazole antifungal agents, mediated via various cytochrome P450 isozymes, have been described in the literature. Posaconazole is not extensively metabolized by these isozymes but is both a p-glycoprotein (P-gp) substrate and inhibitor. To our knowledge, there have been no published cases of clinically significant posaconazole-digoxin drug-drug interactions. We report an interaction between posaconazole (300 mg by mouth daily) and digoxin (0.25 mg by mouth daily, Monday through Friday) resulting in atrial fibrillation with slow ventricular response and degenerating into polymorphic ventricular tachycardia.
引用
收藏
页码:1758 / 1761
页数:4
相关论文
共 50 条
  • [21] Cardiovascular Ion Channel Inhibitor Drug-Drug Interactions with P-glycoprotein
    Ledwitch, Kaitlyn V.
    Roberts, Arthur G.
    AAPS JOURNAL, 2017, 19 (02): : 409 - 420
  • [22] Cardiovascular Ion Channel Inhibitor Drug-Drug Interactions with P-glycoprotein
    Kaitlyn V. Ledwitch
    Arthur G. Roberts
    The AAPS Journal, 2017, 19 : 409 - 420
  • [23] Clinical Drug-Drug Interaction Assessment of Ivacaftor as a Potential Inhibitor of Cytochrome P450 and P-glycoprotein
    Robertson, Sarah M.
    Luo, Xia
    Dubey, Neeraj
    Li, Chonghua
    Chavan, Ajit B.
    Gilmartin, Geoffrey S.
    Higgins, Mark
    Mahnke, Lisa
    JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 55 (01): : 56 - 62
  • [24] Evaluation of the Cytochrome P450 3A and P-glycoprotein Drug-Drug Interaction Potential of Futibatinib
    Yamamiya, Ikuo
    Hunt, Allen
    Takenaka, Toru
    Sonnichsen, Daryl
    Mina, Mark
    He, Yaohua
    Benhadji, Karim A.
    Gao, Ling
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2023, 12 (10): : 966 - 978
  • [25] Evaluation of Potential Drug-Drug Interaction Risk of Pexidartinib With Substrates of Cytochrome P450 and P-Glycoprotein
    Zahir, Hamim
    Kobayashi, Fumiaki
    Zamora, Cynthia
    Gajee, Roohi
    Gordon, Michael S.
    Babiker, Hani M.
    Wang, Qiang
    Greenberg, Jonathan
    Wagner, Andrew J.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2021, 61 (03): : 298 - 306
  • [26] Predicting Drug-Drug Interactions Involving the Inhibition of Intestinal CYP3A4 and P-Glycoprotein
    Tachibana, Tatsuhiko
    Kato, Motohiro
    Takano, Junichi
    Sugiyama, Yuichi
    CURRENT DRUG METABOLISM, 2010, 11 (09) : 762 - 777
  • [27] Tocilizumab and mesenteric arterial thrombosis: drug-drug interaction with anticoagulants metabolized by CYP 450 and/or by P-glycoprotein
    B. Clarivet
    P. Robin
    Y. M. Pers
    R. Ferreira
    J. Lebrun
    C. Jorgensen
    D. Hillaire-Buys
    V. Brés
    J. L. Faillie
    European Journal of Clinical Pharmacology, 2016, 72 : 1413 - 1414
  • [28] Tocilizumab and mesenteric arterial thrombosis: drug-drug interaction with anticoagulants metabolized by CYP 450 and/or by P-glycoprotein
    Clarivet, B.
    Robin, P.
    Pers, Y. M.
    Ferreira, R.
    Lebrun, J.
    Jorgensen, C.
    Hillaire-Buys, D.
    Bres, V.
    Faillie, J. L.
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2016, 72 (11) : 1413 - 1414
  • [29] Application of Permeability-Limited Physiologically-Based Pharmacokinetic Models: Part II - Prediction of P-Glycoprotein Mediated Drug-Drug Interactions with Digoxin
    Neuhoff, Sibylle
    Yeo, Karen Rowland
    Barter, Zoe
    Jamei, Masoud
    Turner, David B.
    Rostami-Hodjegan, Amin
    JOURNAL OF PHARMACEUTICAL SCIENCES, 2013, 102 (09) : 3161 - 3173
  • [30] Longitudinal assessment of a P-glycoprotein-mediated drug interaction of valspodar on digoxin
    Kovarik, JM
    Rigaudy, L
    Guerret, M
    Gerbeau, C
    Rost, KL
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 1999, 66 (04) : 391 - 400