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Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects

Direct oral anticoagulants (DOACs) have predictable pharmacokinetics and pharmacodynamics, limited potential for drug to drug interactions, and can be given at fixed doses without the need for routine coagulation monitoring, which makes them a very attractive alternative to vitamin K antagonists. DO...

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Detalles Bibliográficos
Autor principal: Bratsos, Sosipatros
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713240/
https://www.ncbi.nlm.nih.gov/pubmed/31489274
http://dx.doi.org/10.7759/cureus.5484
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author Bratsos, Sosipatros
author_facet Bratsos, Sosipatros
author_sort Bratsos, Sosipatros
collection PubMed
description Direct oral anticoagulants (DOACs) have predictable pharmacokinetics and pharmacodynamics, limited potential for drug to drug interactions, and can be given at fixed doses without the need for routine coagulation monitoring, which makes them a very attractive alternative to vitamin K antagonists. DOACs act by specifically targeting a single coagulation factor, such as Factor Xa or thrombin. Rivaroxaban is a direct Factor Xa inhibitor and has been approved for use in several thromboembolic disorders, such as the prevention of stroke and systemic embolism in adults with non-valvular atrial fibrillation and the prevention of recurrent deep vein thrombosis and pulmonary embolism in adult patients. This review aimed to provide an overview of the mechanism of action of rivaroxaban and outline its pharmacokinetic properties (absorption, distribution, metabolism, and excretion) in healthy adult subjects.
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spelling pubmed-67132402019-09-05 Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects Bratsos, Sosipatros Cureus Cardiology Direct oral anticoagulants (DOACs) have predictable pharmacokinetics and pharmacodynamics, limited potential for drug to drug interactions, and can be given at fixed doses without the need for routine coagulation monitoring, which makes them a very attractive alternative to vitamin K antagonists. DOACs act by specifically targeting a single coagulation factor, such as Factor Xa or thrombin. Rivaroxaban is a direct Factor Xa inhibitor and has been approved for use in several thromboembolic disorders, such as the prevention of stroke and systemic embolism in adults with non-valvular atrial fibrillation and the prevention of recurrent deep vein thrombosis and pulmonary embolism in adult patients. This review aimed to provide an overview of the mechanism of action of rivaroxaban and outline its pharmacokinetic properties (absorption, distribution, metabolism, and excretion) in healthy adult subjects. Cureus 2019-08-25 /pmc/articles/PMC6713240/ /pubmed/31489274 http://dx.doi.org/10.7759/cureus.5484 Text en Copyright © 2019, Bratsos et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Cardiology
Bratsos, Sosipatros
Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title_full Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title_fullStr Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title_full_unstemmed Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title_short Pharmacokinetic Properties of Rivaroxaban in Healthy Human Subjects
title_sort pharmacokinetic properties of rivaroxaban in healthy human subjects
topic Cardiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6713240/
https://www.ncbi.nlm.nih.gov/pubmed/31489274
http://dx.doi.org/10.7759/cureus.5484
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