Effects of renal impairment on the pharmacokinetics, pharmacodynamics and safety of rivaroxaban, an oral, direct Factor Xa inhibitor.

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Published in Br J Clin Pharmacol on November 01, 2010

Authors

Dagmar Kubitza1, Michael Becka, Wolfgang Mueck, Atef Halabi, Haidar Maatouk, Norbert Klause, Volkmar Lufft, Dominic D Wand, Thomas Philipp, Heike Bruck

Author Affiliations

1: Clinical Pharmacology, Bayer Schering Pharma AG, 42096 Wuppertal, Germany. dagmar.kubitza@bayerhealthcare.com

Associated clinical trials:

Oral Direct Factor Xa Inhibitor Rivaroxaban in Patients With Acute Symptomatic Pulmonary Embolism - The EINSTEIN PE Study | NCT00439777

Oral Direct Factor Xa Inhibitor Rivaroxaban in Patients With Acute Symptomatic Deep Vein Thrombosis - The EINSTEIN DVT Study | NCT00440193

Once - Daily Oral Direct Factor Xa Inhibitor Rivaroxaban In The Long-Term Prevention Of Recurrent Symptomatic Venous Thromboembolism In Patients With Symptomatic Deep-Vein Thrombosis Or Pulmonary Embolism. The Einstein-Extension Study | NCT00439725

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