PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 31332769-10 2019 Recently, there has been a resurgence of its use due to the US Food and Drug Administration approval of an extended-release (ER) amantadine formulation for treatment of L-dopa-induced dyskinesia. Levodopa 169-175 epiregulin Homo sapiens 125-127 6953463-4 1982 After levodopa treatment, only patients with left symptomatology responded to the attention task with an enlargement of EP components, largely in the noninvolved hemisphere. Levodopa 6-14 epiregulin Homo sapiens 120-122 28236251-4 2017 A new extended-release (ER) carbidopa-levodopa capsule product (also referred to as IPX066) was developed and approved in the US as Rytary and in the EU as Numient . Levodopa 38-46 epiregulin Homo sapiens 24-26 28236251-6 2017 Phase III studies of this ER carbidopa-levodopa capsule formulation in patients with PD have shown a significant reduction in "off" time compared with IR carbidopa-levodopa and carbidopa-levodopa-entacapone. Levodopa 39-47 epiregulin Homo sapiens 26-28 28236251-7 2017 We present a review of the clinical pharmacokinetics and pharmacodynamics of this ER product of carbidopa-levodopa in healthy subjects and in patients with PD. Levodopa 106-114 epiregulin Homo sapiens 82-84 26692288-2 2016 Carbidopa/levodopa ER capsules contain beads of carbidopa and levodopa, designed to release the drugs at different rates in the gastrointestinal tract and provide constant therapeutic levodopa concentrations that are maintained for 4-5 h (after an initial peak at 1 h). Levodopa 10-18 epiregulin Homo sapiens 19-21 26692288-2 2016 Carbidopa/levodopa ER capsules contain beads of carbidopa and levodopa, designed to release the drugs at different rates in the gastrointestinal tract and provide constant therapeutic levodopa concentrations that are maintained for 4-5 h (after an initial peak at 1 h). Levodopa 62-70 epiregulin Homo sapiens 19-21 26692288-3 2016 In randomized phase III trials, oral carbidopa/levodopa ER was significantly more effective than placebo with regard to improving motor symptoms and activities of daily living in patients with early PD after 30 weeks" treatment, and provided significantly greater reductions in daily "off-time" in patients with advanced PD than immediate-release (IR) carbidopa/levodopa or carbidopa/levodopa IR plus entacapone after a treatment period of 13 and 2 weeks, respectively, without increasing troublesome dyskinesia. Levodopa 47-55 epiregulin Homo sapiens 56-58