Combitropil

Overdose

Data on the overdose of the drug is not provided.

Contraindications

hypersensitivity,

severe hepatic insufficiency,

severe renal failure,

parkinsonism,

pregnancy,

lactation period,

children under 5 years of age.

With caution:

Parkinson's disease,

renal and / or hepatic insufficiency.

Incompatibilities

Combarel® increases the effects of drugs, CNS depressants, ethanol, as well as nootropic and antihypertensive agents.

Improves the tolerance of antipsychotic drugs (neuroleptics) and tricyclic antidepressants.

Vasodilating drugs enhance the effect of Combitropil®.

Pharmaceutical form

Gelatin capsules, size No. 0, white, the contents of the capsules are white or almost white powder.

Undesirable effects

From the central nervous system and peripheral nervous system: irritability, sleep disturbance, headache, tremor of the extremities.

From the digestive system: dyspepsia, epigastric pain, dry mouth.

Allergic reactions: skin rash.

Special instructions

During treatment, liver function should be monitored.

At the beginning of treatment, the patient should refrain from taking alcohol.

Due to the content of cinnarizine, the drug can cause a positive reaction when conducting a doping test in athletes.

The drug should be used with caution in cases of increased intraocular pressure.

Influence on the ability to drive vehicles and manage mechanisms

During the treatment period, care should be taken when driving a car and engaging in activities that require increased concentration and speed of psychomotor reactions.

Therapeutic indications

disorders of cerebral circulation (including atherosclerosis of the cerebral vessels, ischemic stroke, during the post-treatment period after hemorrhagic stroke, after TBI),

encephalopathies of various origins,

and subcomittee comatose state after intoxication and injury of the brain,

diseases of the central nervous system, accompanied by a decrease in intellectual and mnestic functions,

labirintovaya of different Genesis (accompanied by dizziness, tinnitus, nystagmus, nausea and vomiting), Meniere's syndrome,

depression,

psycho-organic syndrome with prevalence of signs of fatigue and weakness,

asthenia of psychogenic origin,

prevention of migraines and kinetoses,

impaired memory, mental function, and concentration,

backlog of intellectual development in children.

Pharmacotherapeutic group

  • Nootropics in combinations

Pharmacodynamic properties

It has a pronounced antihypoxic (mutually potentiated components), nootropic and vasodilating effect. Promotes a significant increase in blood flow in the brain.

Piracetam - nootropic agent. It has a positive effect on the metabolic processes of the brain: increases the concentration of ATP in the brain tissue, increases the synthesis of RNA and phospholipids, stimulates glycolytic processes, increases the utilization of glucose.

It improves the integrative activity of the brain, promotes memory consolidation, and facilitates the learning process.

Changes the rate of propagation of arousal in the brain, improves microcirculation, without having a vasodilating effect, suppresses the aggregation of activated platelets.

It has a protective effect on brain damage caused by hypoxia, intoxication, electric shock, increases α - and β-activity, reduces δ-activity on the EEG, reduces the severity of vestibular nystagmus.

Improves interneuronal transmission and synaptic conduction in neocortical structures, increases mental performance, improves brain blood flow.

The effect develops gradually. Almost does not have a sedative and stimulating effect.

The therapeutic effect of piracetam is manifested in 1-6 hours.

Cinnarizine - selective BCC, reduces the intake of calcium ions into the cells and reduces its content in the depot of the plasmolemma, reduces the tone of the smooth muscles of the arterioles, reduces their reaction to biogenic vasoconstrictors (including epinephrine, norepinephrine, dopamine, angiotensin, vasopressin, serotonin).

It has a vasodilating effect (especially in relation to the blood vessels of the brain, increasing the antihypoxic effect of piracetam), does not significantly affect blood pressure.

It shows moderate antihistamine activity, reduces the excitability of the vestibular apparatus, lowers the tone of the sympathetic nervous system.

In patients with peripheral circulatory disorders, it improves blood supply to organs and tissues (including the myocardium), increases postischemic vasodilation.

Increases the elasticity of the membranes of red blood cells, their ability to deform, reduces the viscosity of the blood.

The toxicity of the combination does not exceed the toxicity of the individual components of the drug.

Pharmacokinetic properties

The drug is quickly and completely absorbed from the gastrointestinal tract.

Piracetam

Suction

The bioavailability of piracetam is 95%. Cmax piracetam is reached in 2-6 hours.

Distribution

Piracetam does not bind to plasma proteins. Penetrates through the BBB, the placental barrier. It accumulates in the brain tissue 1-4 hours after ingestion. It is removed from the cerebrospinal fluid much more slowly than from other tissues.

Metabolism and excretion

Piracetam is practically not metabolized. T1/2 piracetam from blood plasma-4.5 h, T1/2 from the brain-an average of 7.7 hours. It is mainly excreted by the kidneys (more than 95% of the dose taken in 30 hours).

Cinnarizine

Suction

Withmax cinnarizine is reached in 1-4 hours.

Distribution

Cmax cinnarizine after 1-4 hours is noted not only in the blood, but also in the liver, kidneys, heart, lungs, spleen and brain. Binding to plasma proteins — 91%.

Metabolism and excretion

Cinnarizine is completely metabolized in the liver (by disalkylation). T1/2 cinnarizine — 4 hours. It is excreted as metabolites (1/3-by the kidneys with urine, 2/3-through the intestine with feces).

Special precautions for storage

In a place protected from light, at a temperature not exceeding 25 °C.

Keep out of reach of children.

The shelf life of the drug Combarel®3 года.

Do not use after the expiration date indicated on the package.

Nature and contents of container

Capsules 1 caps.
piracetam 400 mg
cinnarizine 25 mg
excipients: MCC, lactose (milk sugar), magnesium stearate, talc  
shell: titanium dioxide, methyl parahydroxybenzoate, propyl parahydroxybenzoate, acetic acid, gelatin  

in a contour cell package of 10 pcs. , in a pack of cardboard 3 or 6 packages, or in polymer cans of 20 or 60 pcs., in a pack of cardboard 1 bank.

Fertility, pregnancy and lactation

Contraindicated in pregnancy. Breastfeeding should be discontinued for the duration of treatment.

Nosological classification (ICD-10)

  • F06. 6 Organic emotionally labile [asthenic] disorder
  • F07. 9 Organic personality and behavior disorder caused by brain disease, damage or dysfunction, unspecified
  • F32 Depressive episode
  • F33 Recurrent depressive disorder
  • F79 Mental retardation, unspecified
  • F90. 0 Disturbance of activity and attention
  • G43. 9 Migraine, unspecified
  • G93. 4 Encephalopathy, unspecified
  • G98 Other disorders of the nervous system, not classified elsewhere (residual effects of traumatic brain injuries)
  • H55 Nystagmus and other involuntary eye movements
  • H81 Vestibular function disorders
  • H81. 0 Meniere's disease
  • H83. 2 Labyrinth dysfunction
  • H83. 3 Inner ear noise effects
  • H93. 1 Tinnitus (subjective)
  • I61 Intracerebral hemorrhage
  • I63 Brain infarction
  • I67. 2 Cerebral atherosclerosis
  • I67. 9 Cerebrovascular disease, unspecified
  • R40. 2 Coma, unspecified
  • R41. 3. 0* Reduced memory
  • R41. 8. 0* Intellectual-mnestic disorders
  • T75. 3 Motion sickness
  • T90. 5 Consequences of intracranial trauma

Dosage (Posology) and method of administration

Inside.

Adults-1-2 caps. 3 times a day for 1-3 months, depending on the severity of the disease.

Children over the age of 5 years — 1-2 caps. 1-2 times a day for 1-3 months.

Courses of treatment are carried out 2-3 times a year.

In chronic renal failure (creatinine Cl <60 ml / min), it is necessary to reduce the dose or increase the interval between doses of the drug.

ATC - Anatomical and therapeutic chemical classification

N06BX Other psychostimulants and nootropic drugs