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Effectiveness and safety of ranolazine (Ranexa) were investigated in a 5-dose, randomized, double-blind, placebo-controlled trial involving 24 client-owned dogs with atrial flutter or fibrillation (AF). On day 1, dogs received ranolazine (1.5, 3.0, 4.5, 6.0, or 7.5 mg/kg PO) or placebo (PL) and were evaluated for 12 h. On day 2, dogs received ranolazine (1.5, 3.0, 4.5, or 7.5 mg/kg PO) or PL and were evaluated for 6 h. Dogs with inducible AF were treated with the same dosage and evaluated for 6 h. Dogs not inducible after 2 h of treatment were treated with doses escalated to a maximal dosage of 12.0 mg/kg PO. Effects on sinus rate, inducible AF, and adverse effects were evaluated. In a dose-dependent manner, ranolazine decreased sinus rate to less than 30% of baseline over the first 6 h of treatment and to less than 50% of baseline over the entire 12-h study period. In 27 dogs, 12 were inducible, and all inducible dogs were successfully treated with a single ranolazine dosage (mean dosage, 6.5 mg/kg PO). No adverse effects were identified. These findings suggest that single-dose ranolazine effectively decreases AF rate in a dose-dependent manner, with no adverse effects.Q:
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