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.
Flecainide was granted FDA approval on 31 October 1985.
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.
Cardiology Clinic, University Hospital of Patras, Patras, Achaia, Greece
1st Cardiology Clinic, National and Kapodistrian University of Athens, Athens, Attika, Greece
Cardilogy Clinic, University of Crete, Heraklion, Greece
Oslo University Hospital Rikshospitalet, Oslo, Norway
Athens Heart Center Amarousion, Athens, Attiki, Greece
Attikon General Hospital of Athens, Athens, Greece
First Department of Cardiology, Hippocration General Hospital, National and Kapodistrian University of Athens, Athens, Greece, Athens, Greece
Hopital Pitié Salpetrière, Paris, IDF, France
Wojewodzki Szpital Zespolony im. L. Rydygiera w Toruniu, Toruń, Poland
Bridgeport Hospital, Bridgeport, Connecticut, United States
University of Cincinnati College of Medicine, Cincinnati, Ohio, United States
Skylitseio General Hospital, Chios, Greece
Hämeenlinna Central Hospital, Hämeenlinna, Kanta-Häme, Finland
Sakunta Central Hospital, Pori, Satakunta, Finland
Central Finland Central Hospital, Jyväskylä, Central Finland, Finland
Isala hospital, Zwolle, Netherlands
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