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Sinemet
Combination product
Pronunciation: kar-bi-DOE-pa and lee-voe-DOE-pa
What it is Dopamine precursor plus peripheral dopa-decarboxylase inhibitor; Parkinson disease motor symptoms.
Why this one The most effective symptomatic Parkinson drug; carbidopa cuts peripheral conversion, nausea and levodopa dose.
What limits it Within 5–8 years most develop wearing-off, on-off swings and dyskinesia; gait, speech and cognition stop responding.
Pearls Dietary protein competes for absorption; separate doses from high-protein meals. Controlled-release tablets: do not split, crush or chew. Rytary ER capsules are not dose-interchangeable with other formulations. Advanced disease: enteral suspension infused 16 h/day via PEG-J.
Visual mnemonic: Sinemet mascot(Carly and Levi) Dopey Cinema
Components (2)
FDA label
Read the full label on DailyMed ↗
FDA dosing Population Start Target Max
Parkinson's disease, post-encephalitic parkinsonism, and symptomatic parkinsonism (carbon monoxide or manganese intoxication) Adults 1 tablet carbidopa/levodopa 25-100 TID (75 mg carbidopa/day) Individualized; provide >=70–100 mg carbidopa/day 8 tablets/day
Titration Increase by 1 tablet every day or every other day as needed
Renal Use with caution; periodic renal function evaluation recommended during extended therapy
Hepatic Use with caution; periodic hepatic function evaluation recommended during extended therapy
Tablets of 1:4 (25-100) and 1:10 (10-100, 25-250) ratios may be combined to individualize dose; 25-250 no longer marketed by this manufacturer
Instructions Individualize by careful titration When transferring from levodopa alone, discontinue levodopa >=12 h before and start Sinemet at ~25% of the prior levodopa dose Do not abruptly reduce/discontinue (risk of hyperpyrexia, confusion, NMS-like syndrome) Evaluate vitamin B6 levels before and periodically during treatment; supplement if low
Available strengths
tab 10/100, 25/100, 25/250 mgER cap 23.75/95, 35/140, 36.25/145, 48.75/195, 52.5/210, 61.25/245, 70/280, 87.5/350 mgER tab 25/100, 50/200 mgODT 10/100, 25/100, 25/250 mgsusp 4.63/20 mg/mL
Contraindications Concurrent use of nonselective MAO inhibitors (discontinue >=2 weeks before); MAO-B-selective inhibitors at recommended doses may be co-administered Narrow-angle glaucoma
Cautions Depression with suicidal tendencies Severe cardiovascular/pulmonary disease, asthma; arrhythmias post-MI Upper GI hemorrhage (history of peptic ulcer) Vitamin B6 deficiency and seizures Falling asleep during activities of daily living/somnolence Hallucinations/psychotic-like behavior Impulse control/compulsive behaviors Melanoma risk
Adverse reactions Dyskinesias (choreiform, dystonic, involuntary movements) Nausea Orthostatic hypotension Hallucinations/confusion Somnolence
Pregnancy No adequate human data; visceral and skeletal malformations seen in rabbits and reduced pup survival in rats; use only if benefit justifies risk.
Lactation Undefined
Clinical profile
Therapeutic safety burden 2 / 4
Sedation liability 2 / 4
Direct muscarinic antagonism 0 / 4
Embryofetal risk 2 / 4
Part D rank #135.
Self-check What movement complication is listed with cumulative carbidopa–levodopa exposure? Dyskinesia.What response-pattern complication also accumulates? Motor fluctuation.
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