Stalevo, 100 mg+25 mg+200 mg 30 pcs
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Stalevo is a combined anti-Parkinsonian drug that is a combination of levodopa, a metabolic precursor of dopamine, carbidopa, an aromatic amino acid decarboxylase inhibitor, and entacapone, a catechol-O-methyltransferase (COMT) inhibitor. Levodopa increases dopamine in the brain.
Dopamine is formed directly from levodopa with the participation of aromatic amino acid decarboxylase. The anti-Parkinsonian effect of levodopa is due to its conversion to dopamine directly in the CNS. Levodopa is rapidly decarboxylated in peripheral tissues, converting to dopamine, which, however, does not penetrate through the BBB.
Carbidopa inhibits the process of decarboxylation of levodopa and formation of dopamine in peripheral tissues, which indirectly leads to an increase in the amount of levodopa delivered to the CNS.
Levodopa is biotransformed with catechol-O-methyltransferase (COMT) into the potentially dangerous metabolite 3-O-methyldopa (3-OMD) as a result of dopa decarboxylase inhibition.
Entacapone is a reversible, specific COMT inhibitor of mainly peripheral action. Entacapone slows the clearance of levodopa from the bloodstream, resulting in increased bioavailability of levodopa, prolonging its therapeutic effect.
Indications
Parkinson’s disease and Parkinsonism (except drug-induced) where the use of levodopa + carbidopa combination is ineffective.
Composition
One coated tablet contains:
Levodopa 100 mg,
Carbidopa in monohydrate form 12.5 mg, entacapone 200 mg.
Auxiliary substances:
Corn starch,
Mannitol,
p> sodium croscarmellose,
povidone,
magnesium stearate.
Shell composition:
Hypromellose, sucrose, titanium dioxide, iron oxide yellow, iron oxide red, magnesium stearate, polysorbate 80, glycerin 85%.
How to take, the dosage
The drug is taken orally, regardless of meals, without dividing the tablet into parts. The optimal daily dose is determined by careful individual selection. We recommend one of three current dosages (50/12.5/200 mg, 100/25/200 mg, or 150/37.5/200 mg levodopa/carbidopa/entacapone).
Only 1 tablet of any dosage should be taken as a single dose. The maximum daily dose is 1.5 g of levodopa, 2 g of entacapone, 375 mg of carbidopa (corresponding to 10 tablets of Stalevo 150/37.5/200 mg).
If more levodopa is needed, reduce the interval between doses and/or transfer the patient to Stalevo treatment at a higher dosage (necessarily within the recommended dosage). If less levodopa is needed, increase the intervals between doses and/or transfer the patient to Stalevo treatment at a lower dosage.
If other medications containing levodopa are used concomitantly with Stalevo, the recommendations for the total daily dose of the medication should be carefully followed.
Interaction
Therapeutic effect of Stalevo is decreased when concomitant administration with dopamine receptor antagonists (some neuroleptics and antiemetics), phenytoin, papaverine.
Concomitant administration with iron preparations may decrease the effectiveness of Stalevo because levodopa and entacapone form chelated complexes with iron ions in the GI tract.
There should be a time interval of 2-3 h between doses of Stalevo and iron-containing drugs.
The therapeutic effect of Stalevo may decrease in patients receiving a high-protein diet due to the competing effects of levodopa and some amino acids. Stalevo is compatible with imisin and moclobemide, pyridoxine hydrochloride, diazepam, and ibuprofen.
Special Instructions
Stalevo is not intended to eliminate extrapyramidal reactions caused by medication. Prior to planned general anesthesia, the drug may be taken as long as the patient is allowed to take it orally.
In case of prolonged therapy with Stalevo, periodic monitoring of the liver, hematopoiesis system, renal, cardiovascular system functions is required. Control of cardiovascular system function is required during the whole period of initial dose adjustment of the drug.
The use of the drug in open-angle glaucoma is possible only with careful control of intraocular pressure. When replacing Stalevo with levodopa + carbidopa therapy (without entacapone), an increase in the levodopa dose will be required. Stalevo should be withdrawn slowly, increasing the levodopa dose as needed. Stalevo does not prevent the use of other anti-Parkinsonian drugs. The daily dose of seleginine in concurrent use with the drug Stalevo should not exceed 10 mg.
Impact on driving and operating machinery: Entacapone in combination with levodopa causes drowsiness and occasional momentary falling asleep. It is necessary to refrain from driving and working with machines and mechanisms while taking the drug Stalevo.
Contraindications
– Severe liver function abnormalities.
– Closed-angle glaucoma.
– Pheochromocytoma.
– Concomitant use with non-selective MAO inhibitors of types A and B (e.g., phenelzine, tranylcypromine).
– Concomitant use with selective MAO inhibitors of types A and B.
– Malignant neuroleptic syndrome and/or atraumatic acute rhabdomyolysis (including anamnesis).
– Childhood and adolescence under 18 years of age.
– Pregnancy.
– The period of lactation (breast-feeding).
– Hypersensitivity to the components of the drug.
The drug should be used with caution:
– Severe cardiovascular and pulmonary insufficiency.
– Bronchial asthma.
– Liver diseases.
– Kidney diseases.
– Diabetes mellitus and other decompensated endocrine diseases.
– Gastrointestinal erosive and ulcerative lesions.
– Seizures (in anamnesis).
– Myocardial infarction in the anamnesis (with persisting heart rhythm disorders).
– Psychosis in the anamnesis and/or during treatment.
– Depression with suicidal tendencies.
– Asocial behavior.
– Open-angle glaucoma.
Caution should be exercised when concomitant use of Stalevo with:
– Drugs that can cause orthostatic hypotension.
– With neuroleptics that block dopamine (especially dopamine D2-receptor antagonists).
– With tricyclic antidepressants, desipramine, maprolitin, venlafaxine.
– With warfarin and drugs metabolized by COMT (paroxetine).
Overdose
Symptoms: increased severity of side effects, except for allergic reactions, which are dose-dependent.
Treatment: hospitalization, gastric lavage, repeated administration of activated charcoal. Control of functions of the respiratory, cardiovascular and urinary systems; ECG-monitoring, if necessary – antiarrhythmic therapy.
Pyridoxine is ineffective in Stalevo overdose.
Pregnancy use
The drug is contraindicated in pregnancy (except when the potential positive effect of taking the drug exceeds the possible risk to the fetus) and during lactation.
Weight | 0.048 kg |
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Shelf life | 3 years |
Conditions of storage | At 15-25 °C |
Manufacturer | Orion Corporation, Finland |
Medication form | pills |
Brand | Orion Corporation |
Other forms…
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