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Posted on 13.05.2018 in the General category

Requip xl has also been evaluated in 2 postmarketing, randomized, double-blind, multicenter, fixed-dose, dose-response clinical trials conducted in advanced and early parkinson s disease patients study 2 and study 4, respectively .

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in two phase 2 studies in patients with rls, 14 of 55 patients 25 receiving requip experienced an adverse event of hypotension or orthostatic hypotension compared with none of the 27 patients receiving placebo.

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during the premarketing development of requip pd hydrochloride tablets, patients received requip pd hydrochloride tablets either without l-dopa early parkinson s disease studies or as concomitant therapy with l-dopa advanced parkinson s disease studies .

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requip xl is designed to release medication over a 24-hour period.

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