Intravenous and oral lorcainide: assessment of central nervous system toxicity and antiarrhythmic efficacy.
@article{Vlay1986IntravenousAO, title={Intravenous and oral lorcainide: assessment of central nervous system toxicity and antiarrhythmic efficacy.}, author={S. Vlay and G. Mallis}, journal={American heart journal}, year={1986}, volume={111 3}, pages={ 452-5 } }
Twenty-eight subjects underwent evaluation of drug toxicity and antiarrhythmic efficacy with oral and intravenous lorcainide. Lorcainide, a new type 1C antiarrhythmic drug, has an active metabolite, norlorcainide, which accumulates after oral but not significantly after intravenous administration. Group 1 consisted of 14 subjects who received intravenous lorcainide with an initial bolus of 2 mg/kg at a rate of 2 mg/min followed by 0.14 mg/min or 200 mg/24 hours. The lorcainide level after bolus… CONTINUE READING
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