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.
Also has a weak effect as beta-blocker which may be clinically significant in high doses.
Indications and dose
Pharmacokinetics
Onset of action:
within 2–3 hours
steady state after 3–4 days
Half-life of elimination: 2–10 hours (up to 32 hours for slow metabolizers)
Metabolism: Hepatic
Elimination: Kidneys
Directions for administration
Peroral: increase of dosage should be undertaken after at least three days of original treatment.