SINEMET® is widely prescribed for the treatment of Parkinson's disease and some Parkinson's_Plus syndromes.
Active ingredients[edit | edit source]
Carbidopa, is an inhibitor of aromatic amino acid decarboxylation, and is a white, crystalline compound, slightly soluble in water, with a molecular weight of 244.3. It is designated chemically as (—)-L-α-hydrazino-α-methyl-β-(3,4-dihydroxybenzene) propanoic acid monohydrate. Its empirical formula is C10H14N2O4•H2O.
Levodopa, an aromatic amino acid, is a white, crystalline compound, slightly soluble in water, with a molecular weight of 197.2. It is designated chemically as (—)-L-α-amino-β-(3,4-dihydroxybenzene) propanoic acid. Its empirical formula is C9H11NO4.
Inactive ingredients[edit | edit source]
SINEMET 10-100 and 25-250 Tablets also contain:-
FD&C Blue #2/lndigo Carmine AL.
SINEMET 25-100 Tablets also contain:-
D&C Yellow #10 Lake.
Most common adverse reactions to SINEMET[edit | edit source]
Less common adverse reactions to SINEMET[edit | edit source]
Body as a Whole
Back pain, shoulder pain, muscle cramps.
Psychotic episodes including delusions, hallucinations, and paranoid ideation, neuroleptic malignant syndrome, bradykinetic episodes ("on-off" phenomenon), confusion, agitation, dizziness, somnolence, dream abnormalities including nightmares, insomnia, paresthesia, headache, depression with or without development of suicidal tendencies, dementia, pathological gambling, increased libido including hypersexuality, impulse control symptoms.
Dyspnea, upper respiratory infection.
Rash, increased sweating, alopecia, dark sweat.
Urinary tract infection, urinary frequency, dark urine.
Drug interactions[edit | edit source]
Symptomatic postural hypotension has occurred when SINEMET was added to the treatment of a patient receiving antihypertensive drugs.
Severe orthostatic hypertenson can occur for patients receiving MAO inhibitors (Type A or B).
There have been rare reports of adverse reactions, including hypertension and dyskinesia, resulting from the concomitant use of tricyclic antidepressants and SINEMET.
Dopamine D2 receptor antagonists (e.g. phenothiazines, butyrophenones, risperidone) and isoniazid may reduce the therapeutic effects of levodopa. In addition, the beneficial effects of levodopa in Parkinson's disease have been reported to be reversed by phenytoin and papaverine.
Iron salts may reduce the bioavailability of levodopa and carbidopa.
Although metoclopramide may increase the bioavailability of levodopa by increasing gastric emptying, metoclopramide may also adversely affect disease control by its dopamine receptor antagonistic properties.
Further Reading[edit | edit source]
Block et al carried out a multi-centre trial over 5 years comparing the effects of Sinemet (immediate Release) and Sinemet CR (Controlled Release) and found favourably for the latter.
|Search the scientific literature (Sinemet)|
References[edit | edit source]
- Block, G,; Liss, C.; Reines, S.; Irr. I. and Nibbelink, D. AbstractEur. Neurol. 37 (1) 23 – 27 Comparison of Immediate-Release and Controlled Release Carbidopa/Levodopa in Parkinson’s Disease http://www.karger.com/Article/Abstract/117399