Dabigatran is an oral anticoagulant that does not require monitoring of prothrombin time (INR).
In one open trial comparing warfarin, dabigatrin 150 mg/12h showed a lower incidence of stroke or embolic events, and a similar incidence of severe bleeding. Dabigatran 110 mg/12h showed a lower incidence of severe bleeding and no differencein the incidence of stroke or embolic events.
In centres with adequate INR control there were no differences on the incidence of stroke, embolic events or severe bleeding vs warfarin.
After commercialization there have been various alerts on the risk of bleeding and there are data on the possible increase in the incidence of myocardial infarctions.
There are no available headto- head comparisons with other new oral anticoagulants.