Blocks sodium channels on cardiomyocytes which leads to their reduced excitation. This reduces myocardial automaticity and slows down the impulse conduction as well as prolongs refractory period of cardiomyocytes.
Second effect is a block of potassium channels which lengthens the action potential in cardiomyocytes.
Indications and dose
Pharmacokinetics
Onset of action: 2–4 hours
Half-life of elimination:
13 hours after single dose
16 hours after multiple doses
Metabolism: Hepatic
Elimination: Kidneys (86 %), liver
Directions for administration
Should be taken at least one hour before food since food undesirably affects the absorption of the drug.
Medicinal forms
Pills – 50 mg, 100 mg
Side-effects
Arrhythmias (high risk in patients with structural heart disease)