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Merck

Long-acting carbidopa-levodopa in the management of moderate and advanced Parkinson's disease.

Neurology (1992-01-01)
J T Hutton, J L Morris
ABSTRACT

Parkinson's disease patients treated chronically with levodopa often develop fluctuations in motor response. Motor fluctuations can be attributed in part to oscillating plasma levodopa concentrations. A controlled-release formulation containing 200 mg of levodopa and 50 mg of carbidopa provides superior plasma levodopa profiles compared with the standard preparation. A multicenter, double-blind trial involving 202 patients with fluctuating motor response found controlled-release carbidopa-levodopa to be safe and tolerable, with improved efficacy compared with the standard formulation. Long-term exposure to the controlled-release formulation, at least for a period of 3 years, does not appear to be associated with any increase in the incidence of adverse side effects.

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USP
Carbidopa, United States Pharmacopeia (USP) Reference Standard
Carbidopa, European Pharmacopoeia (EP) Reference Standard