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Pincainide is a calcium channel inhibitor.1,2 It reduces norepinephrine-induced calcium influx and increases calcium efflux in isolated rat aortic strips.1 Pincainide reduces phasic and tonic contractions induced by norepinephrine (IC50s = 880 and 780 µM, respectively) and high potassium (IC50s = 620 and 670 µM, respectively) in isolated rat aortic strips. It also decreases heart rate, contractile force, and the maximum following frequency in isolated rat right atria.2 Infiltration of pincainide (1% solution) induces local anesthesia in rabbits with a duration of 240 minutes.3
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