Ropinirole hydrochloride
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Classification: Antiparkinson agent See Also: See also Antiparkinson Agents. Action/Kinetics: Mechanism is not known but believed to involve stimulation of postsynaptic D 2 dopamine receptors in caudate-putamen in brain. Causes decreases in both systolic and diastolic BP at doses above 0.25 mg. Rapidly absorbed. Peak plasma levels: 1-2 hr. Food reduces maximum concentration. t 1/2, elimination: 6 hr. First pass effect; extensively metabolized in liver. Uses: Treat signs and symptoms of idiopathic Parkinson's disease, both as initial therapy and adjunctive therapy with levodopa. Contraindications: Lactation. Special Concerns: Safety and efficacy have not been determined in children. Side Effects: CNS: Hallucinations, cause and/or exacerbate pre-existing dyskinesia. CV: Syncope (sometimes with bradycardia), postural hypotension. Overdose Management: Symptoms: Agitation, increased dyskinesia, grogginess, sedation, orthostatic hypotension, chest pain, confusion, N&V.; Treatment: General suppportive measures. Maintain vital signs. Gastric lavage.
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How Supplied: Tablets: 0.25 mg, 0.5 mg, 1 mg, 2 mg, 4 mg, 5 mg
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