INGELHEIM, Germany-- (BUSINESS WIRE)--The RE-DUAL PCI™ trial explored anticoagulation with Pradaxa ® (dabigatran etexilate) dual therapy without aspirin in non-valvular atrial fibrillation (AF) ...
FDA Approves Pradaxa® (dabigatran etexilate mesylate) for Treatment and Reduction in the Risk of Recurrence of Deep Venous Thrombosis and Pulmonary Embolism Three pivotal trials showed PRADAXA as ...
New Sub-Analyses Report Pradaxa® (dabigatran etexilate mesylate) May Be Associated With Better Patient Outcomes After a Major Bleeding Event Compared to Warfarin RIDGEFIELD, Conn., Dec. 8, 2012 -- ...
RIDGEFIELD, Conn., March 19, 2017 /PRNewswire/ -- Important new data from the RE-CIRCUIT® study show a better safety profile for Pradaxa® (dabigatran etexilate mesylate) compared to warfarin in atrial ...
RIDGEFIELD, Conn., July 21, 2011 /PRNewswire/ --Boehringer Ingelheim Pharmaceuticals, Inc. (BIPI) today announced that Pradaxa® (dabigatran etexilate mesylate) capsules has been added to hospital ...
Presentations to include research around antidote for dabigatran, a post-hoc analysis of data from the RE-LY® trial and data from the GLORIA™-AF registry RIDGEFIELD, Conn. -- Boehringer Ingelheim ...
Ingelheim, Germany – Boehringer Ingelheim wants to set the record straight following misleading statements that the British Medical Journal (BMJ) published today regarding Pradaxa® (dabigatran ...
The FDA announced today that it was initiating a safety review of dabigatran (Pradaxa, Boehringer Ingelheim). The review was prompted by reports of serious bleeding events in people taking the drug.
On 15 March, the National Institute for Health and Clinical Excellence (NICE) has issued final guidance recommending the novel oral anticoagulant, Pradaxa ® (dabigatran etexilate) 2 as a ...
For media outside of the US, the UK & Canada only Over 100 countries have now approved Boehringer Ingelheim’s Pradaxa® for the prevention of stroke and systemic embolism for adult patients with the ...
Dabigatran is an oral anticoagulant (blood thinner) approved by the US FDA in 2010 to lower the risk of stroke and prevent systemic embolism in persons with nonvalvular atrial fibrillation. Unlike ...