SOTALOL HYDROCHLORIDESotacor |
Reviewed by Dr Patricia Clarkson, Dr Jon Skinner (October 1999), Brenda Hughes, Lejla Brkic, Robyn Wilkinson |
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January 1999 Administration updated August 2002 |
IV
Oral
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Bradycardia and hypotension (mechanism not established). Monitor for haemodynamic depression |
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Diuretics |
May induce hypokalaemia or hypomagnesemia therefore increasing the risk of Torsades de Pointes |
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Flecainide |
Bradycardia, AV block, cardiac arrest (allow a gap of several days before starting flecainide) |
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Hypotension |
Sotalol has both beta adrenergic receptor blockade and antiarrhythmic properties. It is a non-selective beta adrenergic blocking agent affecting both beta1 and beta2 receptors. It has no intrinsic sympathomimetic activity or membrane stabilising activity. It inhibits renin release. Its beta adrenergic activity causes a reduction in heart rate (negative chronotropic effect) and a limited reduction in the force of contraction (negative inotropic effect). This leads to a decrease in myocardial oxygen consumption and cardiac work. Sotalol's antiarrhythmic activity causes a prolongation of the action potential in cardiac tissue by delaying the repolarisation phase.
When given orally its absorption is minimally affected by food. Sotalol undergoes very little first pass hepatic metabolism and, in adults, exhibits almost 100% bioavailability after oral dosing. It is not protein bound, and is hydrophilic with a low incidence of severe CNS adverse effects. Elimination is primarily by the kidneys with 75% of a dose excreted unchanged in the urine.