Vernakalant was developed by Cardiome Pharma as as an antiarrhythmic drug intended for rapid conversion of atrial fibrillation to sinus rhythm. It acts as an atypical class III antiarrhythmic drug that potentiates its effect in higher heart rates. Intravenous formulation was approved in Europe in September 2010 as Brinavess and in Canada in April 2017. It is an investigational drug under regulatory review by FDA.
Indicated for the rapid conversion of recent onset of atrial fibrillation to sinus rhythm in adults for non-surgery patients that lasts for less than 7 days of duration and post-cardiac surgery patients with atrial fibrillation lasting less than 3 days of duration.
University of Alberta Hospital, Edmonton, Alberta, Canada
Vancouver General Hospital, Vancouver, British Columbia, Canada
Montreal Heart Institute, Montreal, Quebec, Canada
Hospital Clínico Universitario San Carlos, Madrid, Madrid/Madrid, Spain
Maastricht University Hospital, Maastricht, Netherlands
Medical University of Vienna, Department of Emergency Medicine, Vienna, Austria
St-Vincenz Krankenhaus, Paderborn, Germany
Hospital Universitario Severo Ochoa, Madrid, Spain
Skanes Universistetssjukhus, Malmo, Sweden
Royal Perth Hospital Emergency Research, Perth, Western Australia, Australia
Gentofte Amtssygehus Kardiologisk afdeling, Hellerup, Denmark
Herlev Amtssygehus, Kardiologisk, Herlev, Denmark
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