Flecainide is a Class I anti-arrhythmic agent like encainide and propafenone. Flecainide’s development began in 1966 and was first synthesized in 1972 as an attempt to generate new anesthetics. It is used to prevent supraventricular and ventricular arrhythmias, as well as paroxysmal atrial fibrillation and flutter.
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In New Zealand and America, flecainide is indicated to prevent supraventricular arrhythmias and ventricular arrhythmias. In the United States, it is also indicated to prevent paroxysmal atrial fibrillation and flutter.
Oslo University Hospital Rikshospitalet, Oslo, Norway
Hopital Pitié Salpetrière, Paris, IDF, France
Hämeenlinna Central Hospital, Hämeenlinna, Kanta-Häme, Finland
Sakunta Central Hospital, Pori, Satakunta, Finland
Central Finland Central Hospital, Jyväskylä, Central Finland, Finland
Division of Cardiology, Department of Internal Medicine, Kyungpook National University Hospital, Daegu, Korea, Republic of
Seoul Asan Medical Center, Seoul, Korea, Republic of
Severance Cardiovascular Hospital, Seoul, Korea, Republic of
Imelda, Bonheiden, Belgium
OLVG, Amsterdam, Netherlands
Deventer Ziekenhuis, Deventer, Netherlands
Hospital Clínico Universitario San Carlos, Madrid, Madrid/Madrid, Spain
Jesse Brown VA Medical Center, Chicago, Illinois, United States
Rush University Medical Center, Chicago, Illinois, United States
University of Illinois at Chicago, Chicago, Illinois, United States
Carina Blomström Lundqvist, Uppsala, Sweden
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