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.
Kyung Hee University Medical Center, Seoul, Dongdaemun-gu, Korea, Republic of
Maastricht University Hospital, Maastricht, Netherlands
University of California Los Angeles, Los Angeles, California, United States
Nationwide Children's Hospital, Columbus, Ohio, United States
MetroHealth Medical Center, Cleveland, Ohio, United States
Hospital Puerta de Hierro, Madrid, Spain
Hospital Donostia, Donostia, Guipuzcoa, Spain
Hospital La Fe, Valencia, Spain
Patrick KOHAN, 18 rue de la Commanderie, Nancy, France
Department of Cardiology, MHAT Burgas AD, 73 Stefan Stambolov blvd, Burgas, Bulgaria
Hôpital St.-Joseph, Rue de la Duchère 6, Gilly, Belgium
Piedmont Hospital, Atlanta, Georgia, United States
Lahey Clinic, Burlington, Massachusetts, United States
Stony Brook University Hospital, Stony Brook, New York, United States
CCOP - Kalamazoo, Kalamazoo, Michigan, United States
CCOP - Cedar Rapids Oncology Project, Cedar Rapids, Iowa, United States
CCOP - Sioux Community Cancer Consortium, Sioux Falls, South Dakota, United States
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