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countries globally once these new trials are completed.Current Experience with PRADAXAPRADAXA is approved to reduce the risk of stroke and systemic embolism in patients with NVAF, for the treatment of deep venous thrombosis (DVT) and pulmonary embolism (PE) in patients who have been treated with a parenteral anticoagulant for five to 10 days and to reduce the risk of recurrent DVT and PE in patients who have been previously treated. since its approval in October of 2010.PRADAXA 150 mg twice daily is the only oral anticoagulant to demonstrate superior reduction of ischemic stroke compared to warfarin in patients with NVAF. PRADAXA also demonstrated a similar rate of major bleeding events. Ischemic strokes are the most common type of stroke that NVAF patients experience.The efficacy and safety of PRADAXA in NVAF were established in the RE LY trial, one of the largest stroke prevention clinical studies ever conducted with NVAF patients. The 18,113 patient RE LY trial showed that, compared to well controlled warfarin (N=6,022), PRADAXA 150 mg (N=6,076) significantly reduced the risk of stroke and systemic embolism by 35 percent (primary efficacy endpoint: 134 [2.2%] vs. 202 [3.4%] events, HR: 0.65, 95% CI [0.52, 0.81], P=0.0001), ischemic stroke by 25 percent (103 [1.7%] vs. 134 [2.2%] events, HR: 0.75, 95% CI [0.58, 0.97], P=0.0296) and hemorrhagic stroke by 74 percent (12 [0.2%] vs.

Nike Air Max 90 Size 9

Information contained on this page is provided by an independent third party content provider. WorldNow and this Station make no warranties or representations in connection therewith. in 2013. For most AFib patients, taking an anticoagulant is essential because their irregular heart beat increases their risk of an ischemic, or clot based, stroke by up to five times. Reducing the risk of blood clots during ablation is extremely important, because the procedure itself can temporarily increase the risk of blood clots in patients."Currently there are no international guidelines regarding the specific use of novel oral anticoagulants (NOACs) during ablation procedures, despite their wide use in patients with NVAF," said Dr. Hugh Calkins, Chairman of the RE CIRCUIT Study Steering Committee and Professor of Cardiology and Director of the Electrophysiology Laboratory and Arrhythmia Service, Johns Hopkins Hospital, Baltimore, Maryland. Nike Air Max 90 Size 9 "This study will provide valuable insights regarding the practical management of NVAF patients requiring anticoagulation during these procedures."In RE CIRCUIT, treatment will be equally and randomly split between 610 NVAF patients from 80 international sites who will receive either PRADAXA 150 mg twice Nike Air Max 90 Mens Size 9.5

Nike Air Max 90 Size 9

Nike Air Max 90 Size 9

Nike Air Max 90 Size 9

Nike Air Max 90 Size 9

daily or warfarin at an International Normalized Ratio (INR) of 2.0 to 3.0. Patients will be followed for 90 days following their procedure. Results of the study are expected in 2016.RE CIRCUIT is part of Boehringer Ingelheim extensive clinical trial program, RE VOLUTION. With the recently announced RE DUAL PCI and RE Nike Air Max 90 Ultra White And Black

Nike Air Max 90 Size 9

SPECT ESUS studies, the entire program will include 15 clinical trials involving over 55,000 patients in more than 44 Air Max 90 For Women Red

Nike Air Max 90 Size 9

Nike Air Max 90 Size 9

dabigatran etexilate mesylate in NVAF Patients Undergoing Ablation

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