PROPAFENONE (SUBGROUP 1C)
Propafenone
has some structural similarities to propranolol and possesses weak β-blocking activity.
Its spectrum of action is very similar to that of quinidine, but it does not
prolong the action potential. Its sodium channel-blocking kinetics are similar
to that of flecainide. Propafenone is metabolized in the liver, with an average half-life of 5–7 hours. The usual
daily dosage of propafenone is 450–900 mg in three divided doses. The drug is
used primarily for supraventricular arrhythmias. The most com-mon adverse
effects are a metallic taste and constipation; arrhyth-mia exacerbation can
also occur.
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