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p = 0.023) was an independent predictor for major bleeding. A post-hoc analysis of RE-LY trial comparing the safety of dabigatran with warfarin in subgroups of
Intracranial Hemorrhage in Atrial Fibrillation Patients During Anticoagulation With Warfarin or Dabigatran The RE-LY Trial
Pradaxa Bleeding & Other Side Effects. The RE-LY trial showed that Pradaxa was Emily Miller is an award-winning writer who has held editorial positions with
andRenalDrugsAdvisoryCommittee/UCM226009.pdf Concomitant use of P-glycoprotein inhibitors with dabigatran or warfarin in the RE-LY trial
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PDF. Not Available. Citations. With Atrial Fibrillation Receiving Dabigatran or Warfarin in Relation to the CHADS 2 Score: A Subgroup Analysis of the RE-LY Trial.
The RE-LY trial, a PROBE (prospective randomised, open-label, blinded endpoint) study, was designed to establish the non-inferiority of two masked doses of
IntraCoronary Treatment with Integrilin To Improve Fibrillation and Stroke Dabigatran RE-LY: A Non-inferiority Trial Trial Execution Baseline
LOS ANGELES — Data from an additional 2.3 years of follow-up from the dabigatran (Pradaxa, Boehringer Ingelheim) group in the RE-LY trial of AF patients suggest
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Analysis of Upper Gastrointestinal Adverse Events Among Patients Given Dabigatran in the RE-LY Trial the RE-LY trial (N during RE-LY per lower level term,
Analysis of Upper Gastrointestinal Adverse Events Among Patients Given Dabigatran in the RE-LY Trial the RE-LY trial (N during RE-LY per lower level term,
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Background— The Randomized Evaluation of Long-term Anticoagulation Therapy (RE-LY) trial showed that dabigatran etexilate 150 mg BID was superior and dabigatran
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