Cerepro caps 400mg #28

Cerepro instruction

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Composition

One capsule of Cerepro contains 0.4 g of glycerylphosphoryl choline hydrate. In addition, the composition of the product includes additional components: methylparaben, gelatin, propylparaben, glycerin, water prepared, sorbitol, iron oxide red, titanium dioxide.
In 1 ampoule Cerepro contains INN glycerylphosphoryl choline hydrate (1000 mg), as well as water as an additional component.

Form of issue

Cerepro can be purchased in capsules and ampoules. Capsules have an oblong shape, they are soft, made of gelatin. The color of the ampoules is reddish-brown, inside is a transparent oily liquid, which can be slightly colored or colorless. Capsules are packed in blisters (10 or 14 pcs.) Or in jars (10 or 14 pcs.).
A solution in ampoules is a clear liquid without color. Ampoules are packaged in contour packs of 3, 5 or 10 ampoules.

pharmachologic effect

The active substance of the drug is glycerylphosphoryl choline hydrate. Due to the enzymatic cleavage of this substance, choline and glycerophosphate are delivered to the cells of the body. Choline is a substrate for the synthesis of acetylcholine, glycerophosphate provides synthesis of phosphotidylcholine membranes of neurons. As a consequence, metabolism and blood flow in the central nervous system are activated in the body under the influence of the drug, synaptic transmission improves, cholinergic activity decreases. The drug improves plasticity and restores the integrity of previously damaged neuronal membranes at the cellular level.
As a result, the use of the drug improves cognitive and behavioral responses, normalizes brain activity, notes the involution of the psycho-organic syndrome in people who are experiencing the post-traumatic period, as well as those who have problems with the vessels of the brain. The drug also normalizes the space-time characteristics of spontaneous brain activity. Cerepro does not affect reproductive function and does not have mutagenic and tetragonal effects.

Pharmacokinetics and pharmacodynamics

Absorption of the active substance is 88%. The substance easily penetrates the BBB. Excretion of the drug in the form of carbon dioxide is carried out through the lungs, no more than 15% of the active substance is excreted through the intestine and kidneys.

Indications for use Cerepro

Indications for use Cerepro are as follows:
    consequences of craniocerebral trauma (acute period);
    recovery from head injuries;
    acute period after an ischemic stroke;
    Post-stroke period after a hemorrhagic stroke, in which there is focal symptomatology, and there are symptoms of brain stem damage;
    involutional and degenerative changes in the brain, in which there is a psycho-organic symptomatology;
    insufficiency of blood flow in the brain;
    dementia;
    senile pseudomelanchia;
    encephalopathy;
    cognitive disorders;
    manifestation of cerebrovascular disease;
    violation of orientation;
    state of demoralization, apathy;
    intracranial trauma and its consequences.

Contraindications

Cerepro preparation can not be administered to patients under the following conditions:
    acute form of hemorrhagic brain damage;
    pregnancy, breast-feeding;
    high sensitivity to the components of the remedy.

Side effects

In the treatment of these drugs, the patient may exhibit some adverse reactions:
    allergic reactions;
    dyspepsia;
    symptoms of gastritis;
    peptic ulcer;
    feeling of dryness of the oral mucosa;
    pharyngitis;
    state of aggression, anxiety, sleep problems;
    dizziness, headache;
    hyperkinesia;
    convulsions;
    frequent urination.
With the administration of the drug, the patient may feel pain, and also manifestations of postinjectinone local soreness.

Instructions for use Cerepro (Method and dosage)

If a patient is prescribed acute conditions for Cerepro, the instructions for use provide that the injections are administered intramuscularly or intravenously, and the dose is 1 g per day.
The drug in parenteral form is prescribed for 10-15 days, after which the patient should take another oral form of Cerepro for 6 months. In this case, the daily dose of the drug is 1200 mg.
Instructions for use Cerepro contains a note that capsules should not be taken in the evening, as this can lead to problems with sleep.
Capsules are preferably taken in the morning (800 mg) and at lunch time (400 mg). Take the drug you need before eating. If the remedy is well tolerated by the patient, then 400 mg can be administered thrice. If a patient has a chronic condition, then treatment begins with the taking of capsules, with a dosage of 1200 mg / day.

Overdose

If the dosage of the drug has been exceeded, the patient may experience dyspepsia, and side effects may also increase. In this case, symptomatic treatment is practiced.

Interaction

There was no significant interaction with the application of Cerepro and other drugs.

Terms of sale

To buy Cerepro online you don't need a prescription.

Storage conditions

Keep Cerepro at a temperature of up to 25 degrees Celsius.
Shelf life - 2 years.

special instructions

If in the treatment of drugs in a person there are constant attacks of nausea, you need to reduce the dose.
The speed of the reactions does not have a significant effect on the drug intake.

Children

In pediatric practice, Cerepro is not used. It is possible to use only as directed by a doctor.

In pregnancy and lactation

It is not applied at any time of pregnancy, nor is it given to nursing mothers.

Reviews about Cerepro

Those patients who used to treat Cerepro, reviews on the forums leave mostly positive. The doctors' testimonies also testify that this drug is highly effective in various pathologies of the brain. Side effects in the treatment of this drug are rare, so Cerepro is well tolerated and is often used for prolonged therapy. For children, the drug is used only in cases when the doctor confirms the expediency of the appointment. In the reviews marked positive effect of drugs in the treatment of children.