MIGRENAZ – L

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Syrup of herbal extracts, brown viscous liquid with individual odor (may have light sediment and clouding) in the original vials of 100 ml with a protective seal – (1) cardboard packs with protective branded holographic label; (2) Spoon – dispenser; (3) instruction for use.

Composition:   

Common Valerian Extract (Valeriána officinális)
Brandy Mint Extract (Méntha piperíta)
Ginkgo Biloba Extract (Gīnkgo Biloba)
May Lily Extract (Convallária majális)
Field Caraway Extract (Fructus Carvi)
Blood-Red Hawthorn Extract (Crataégus sanguínea)

EFFECT OF THE MEDICINE
  • Improves cerebral blood circulation and brain oxygen supply;
  • Affects the metabolism of the cells, blood rheology and improves peripheral circulation and microcirculation;
  • Expressed anti-edema effect on the level of the brain and in peripheral tissues;
  • It has an anti-stress effect on the normalization of post-stress behavior, somatic-vegetative violations, restoration of the sleep-wake cycles, broken processes of learning and memory, and reducing degenerative
    morphological changes in different brain structures.
SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation.
Use of the medicine should be discontinued when hypersensitivity reactions occur.
The usage of the medicine must be informed to the doctor before the surgery.

SPECIAL INSTRUCTIONS

Before use, carefully shake the vial.
Keep the vial in a cool place after opening it. Do not heat and do not freeze.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS

Migrenaz – L is used in the treatment and prevention of the following:

  • Acute and chronic cerebral circulatory disorders;
  • Mild traumatic brain injury (Mild concussion);
  • Vegetative dystonia syndrome;
  • Mild cognitive impairment of atherosclerotic nature;
  • Disorders of memory and mental activity;
  • Vertigo, tinnitus, feelings of fear;
  • Violation of peripheral blood circulation and microcirculation (including arteriopathy of the lower limbs and pediatric orthopedics), Raynaud’s syndrome.
CONTRAINDICATIONS

Individual intolerance to certain ingredients of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

CHILDREN FROM 1 TO 3 YEARS OLD

CHILDREN FROM 4 TO 12 YEARS OLD

ADULTS AND CHILDREN FROM 12 YEARS OLD AND ABOVE

1.0-2.5 ml 2-3 times a day

3.0-5.0 ml 2-3 times a day

5.0-7.5 ml 2-3 times a day

For peroral use, 5-10 minutes before the meal. The course of treatment is at least 3 months (especially in elderly patients).
Courses can be repeated after consultation with the doctor.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.

Expiration date: 24 months

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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DOLGOJITEL №1

  • ABOUT PRODUCT
  • INSTRUCTIONS

DOLGOJITEL № 1 – FOR ATHLETES

COMPOSITION AND DOSAGE FORM

DOLGOJITEL №1, 0.25 gr. in each capsule, 60 pcs of capsules packaged in original bottles with a protective seal. (1) – cardboard pack with a protective holographic label; (2) – instruction for use;

Composition:

Dihydroquercetin (Taxifolin) 95% 40 mg.
Arabinogalactan 80 mg.
Acidum ascorbinicum 25 mg.
Starch 105 mg.
INDICATIONS
  • for athletes and people whose life is associated with great physical and emotional stress;
  • increases endurance and stamina;
  • improves efficiency;
  • helps to concentrate as much as possible on achieving a result.
SIDE EFFECTS

Usually, there are no side effects; in the majority of cases, the drug is well tolerated.
Use of the drug should be discontinued when hypersensitivity reactions occur.

CONTRAINDICATIONS

Hypersensitivity to one or more components of the agent.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

Dosage and Administration

The duration of treatment and the dose are determined by a physician for each patient individually.

PATIENTS BETWEEN 9 AND 18 YEARS OF AGE

PATIENTS ABOVE 19 YEARS OF AGE

1 capsule 2 times a day with meals.

1 capsule 3 times a day with meals.

Duration of admission

4-8 weeks.

Repeated course after 2 weeks.
Consult with your doctor before use.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light at a temperature from + 2° C to + 25°C.
Expiration date: 24 months

Not considered as a pharmaceutical medicine.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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GINKO CARDIOZEN

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets of herbs, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Ginkgo biloba (Ginkgo L.)
Elecampane (Inula helenium L.)
Midland hawthorn (Crataegus laevigata)
Valerian herb (Valeriana officinalis)
Lemon balm (Melissa officinalis)
Common yarrow (Achillea millefolium L)
Motherwort (Leonúrus)
Peppermint (Mentha piperita L.)

effect of the medicine
  • GINKO CARDIOZEN – a preparation of herbal origin. The medicine has a spasmolytic effect of myotropic nature (similar to the effect of papaverine), mainly in relation to coronary vessels.
  • 3-5 days after the intake of Ginko Cardiozen, the therapeutic effect of the medicine occurs – attenuation is observed or elimination of the manifestations of diseases (elimination or significant attenuation of chest pains, pain in the heart, etc.).
  • Treatment with Ginko Cardiozen significantly reduces and weakens the attacks of angina, patients less often resort to the use of nitroglycerin, Validol, and other vasodilators.
  • Contributes to the normalization of the heart rate. The medicine contributes to the normalization of the contractile function of the myocardium, improving conductivity, and provides nutrition to the heart muscle.
  • The main components of the medicine (hawthorn and motherwort) affect all the basic mechanisms that optimize the work of the heart, improves the nutrition of the heart muscle, by dilating the coronary vessels, improves metabolic processes in the myocardium at the cellular level, regulates the heart rate.
  • Moreover, possesses a sedative effect, which is important in the prevention of heart diseases.
SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation.
Use of the medicine should be discontinued when hypersensitivity reactions occur.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS

The medicine GINKO CARDIOZEN is prescribed for:

  • heart failure;
  • cardioneurosis;
  • cardio-psychoneurosis;
  • arterial hypertension;
  • cardiac ischemia;
  • chronic coronary insufficiency; (manifested by pain behind the sternum and in the region of the heart at rest or after physical exertion).
  • myocardial dystrophy of different genesis;
  • disorders of cerebral circulation;
CONTRAINDICATIONS
  • diagnosed gastritis of erosive type;
  • stomach ulcer;
  • peptic ulcer of the duodenum in the stage of exacerbation;
  • acute myocardial infarction;
  • stable low blood pressure – (Arterial hypotension);
  • disorders of cerebral circulation in an acute phase.
  • hypersensitivity to one or more components of the medicine.
DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually. GINKO CARDIOSEN is recommended to take:

Inside

1 tablet 2-3 times a day, for half an hour before meals.

The duration of treatment with the medicine (from 2 to 4 weeks) is determined by the patient’s individual response to treatment.
Repeated use of the medicine is recommended after the interval of 5-10 days. The medicine can be used not only in inpatient but also in outpatient basis.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 24 months.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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ANEMAK

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Syrup of herbal extracts, brown viscous liquid with individual odor (may have light sediment and clouding) in the original vials of 150 ml with a protective seal – (1) cardboard packs with protective branded holographic label; (2) Spoon – dispenser; (3) instruction for use.

Composition:

Common Nettle Extract (Urtica dioica L.)
Eleutherococcus Extract (Eleutherococcus senticosus)
Milfoil Extract (Achillea millefolium L.)
Aloe Extract (Aloe arborescens Mill.)
Trifid Bur-marigold Extract (Bidens Tripartita)
Excipients: purified water up to 100 ml, Sugar, Ethyl alcohol (95%)

EFFECT OF THE MEDICINE

– When using the medicine has a gradual regression effect on clinical and laboratory symptoms of anemia;
– Restores iron deficiency in the body and stimulates the synthesis of hemoglobin in iron deficiency anemia;
– Increases iron absorption in the intestine.
– It is a source of iron and essential amino acids;
– It helps overcome fatigue, depression, frequent tiredness, dizziness, increases the body defenses;

INDICATIONS

– Anemia (iron deficiency of different degrees of severity);
– Vitamin B12 deficiency anemia;
– Pregnancy and lactation (prevention of iron deficiency during pregnancy and lactation);
– Retardation of physical and mental development, and intensive growth;
– Sports and physical exercise, intense physical labor;
– Poor nutrition, unbalanced diet;
– Frequent acute respiratory viral infections and acute respiratory diseases (in the complex therapy);
– Donation of blood;
– For patients after various surgical measures;
– At prolonged bleeding;
– For children in adolescence and for adults (e.g., vegetarians and the elderly);
– Prevention of iron deficiency anemia in patients of a risk-group in the case where there is no possibility to ensure adequate intake of iron from food.

SPECIAL INSTRUCTIONS

Before use, carefully shake the vial. Keep the vial in a cool place after opening it. Do not heat and do not freeze.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

CONTRAINDICATIONS

Individual intolerance to certain ingredients of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.
Anemak is recommended to take:

ADULTS AND CHILDREN ABOVE 12 YEARS OF AGE

CHILDREN BETWEEN 3 AND 12 YEARS OF AGE

5 – 10 ml., 3 times a day with a meal

2,5 – 5 ml., 2-3 times a day with a meal

For peroral use, 5-10 minutes after the meal.
The course of administration is usually 30 days.

SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation. The use of the medicine should be discontinued when hypersensitivity reactions occur.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 24 months.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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VITALIT

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets, biconvex, light – brown, speckled tablets, 60 pieces. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Bird Cherry Fruits (Fructus Padus)
Rose Hips Fruits (Frūctūs Rosae)
Common Nettle (Urtica dioica L.)
Roseroot (Rhodiola rosae L)
Creeping Thyme (Thymus serpyllum L)
Walnut (Júglans régia)

effect of the medicine
  • VITALIT is a complex herbal vitamin medicine, consisting of vitamins, macro- and microelements and Bifida bacteria.
  • Compensates lack of vitamins and minerals in the body,  and it has antioxidant activity which normalizes intestinal micro-flora and increases a non-specific resistance of the organism.
  • It is recommended as a health improving agent to enhance the body’s defenses, resistance to infectious diseases and environmental hazards.
  • Contributes to the restoration and maintenance of the normal functioning of the gastrointestinal tract.
  • Helps in asthenic conditions, convalescence after infections and colds and other states, accompanied by vitamin deficiency, including the prevention of hypovitaminosis A, C, P, K (combination therapy).
INDICATIONS
  • The medicine beneficially effects overall health, improves physical and mental health;
  • Prevention of vitamin deficiencies, lack of minerals and micronutrients;
  • Increases the body’s resistance to adverse environmental effects;
  • Strengthens the immune system, it contributes to the prevention of infectious diseases;
  • Stimulates metabolism;
  • Increases the body’s resistance to stress, prevents depression;
  • Promotes excretion of salts of heavy metals and other toxic substances;
  • Compensates the deficiency of vitamins and minerals, caused by physical and mental work, poor nutrition;
  • For the period of pregnancy and lactation;
  • Reduces the negative effects of smoking and alcohol consumption.
INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

RECOMMENDATIONS

The medicine is recommended as a multivitamin, health improving agent for the prevention and in the complex therapy of diseases such as:
– Hypertension;
– Atherosclerosis;
– Thyroid gland dysfunction;
– Diabetes;
– Gastritis with low acidity;
– Kidney disease;
– Rheumatism;
– Radiation injuries and allergic diseases of the skin (eczema, dermatitis, neurodermatitis);
– Bleeding of various origins;
– Hypovitaminosis – and vitamin deficiency.

CONTRAINDICATIONS

Hypersensitivity to one or more components of the medicine.

DOSAGE

Dosage is determined individually.

ADULTS

CHILDREN BETWEEN 3 AND 12 YEARS OF AGE

2 tablets 2-3 times a day with the meal

1 tablet 2-3 times a day with the meal

The course of administration is 1-2 months. If necessary the treatment course can be repeated.

SIDE EFFECTS

Usually, there are no side effects. In the majority of cases, the medicine is well tolerated.
In the case of individual sensitivity to one or more components of the medicine, there may be allergic reactions, dyspeptic disorders of the gastrointestinal tract.
Use of the medicine should be discontinued when hypersensitivity reactions occur.

OVERDOSE

The cases of VITALIT overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.
Expiration date: 2 yearsю

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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NATUROSED

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND DOSAGE FORM

Round tablets of herbs, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:

Peppermint (Méntha piperíta)
Oregano (Origanum Vulgare L)
Common Valerian (Valeriána officinális L.)
Cowberry Leaves (Folium vitis-idaea L.)
Creeping Thyme (Thymus serpyllum L.)
Common Motherwort (Leonurus L.)
Hawthorn (Crataegus sanguinea)

EFFECT OF THE MEDICINE
  • improves the central nervous system functioning;
  • contributes to the improvement of the autonomic nervous system;
  • improves the psycho-emotional stability of the body, normalizes sleep;
  • contributes to the preservation of peace stressful situations;
  • strengthens the immune system and increases the body’s defenses.
SIDE EFFECTS

Usually does not occur, in most cases, the drug is tolerated well.
In the case of individual hypersensitivity to one or more of the components of the drug, allergic reactions, dyspepsia disorders on the part of the gastrointestinal tract are possible.
When developing a hypersensitivity reaction, the drug should be discontinued.

INTERACTION WITH OTHER PREPARATIONS

When prescribing with other medication adverse effects were not revealed.

INDICATIONS
  • Functional disorders of the central and autonomic nervous system;
  • The state of prolonged stress, significant mental and emotional stress;
  • Irritability, emotional lability;
  • Chronic fatigue, overwork;
  • Sleep disturbances;
  • Cardioneurosis;
  • Psychosomatic disorders;
  • Climacteric syndrome;
CONTRAINDICATIONS

Hypersensitivity to one or more of the components of the medicine.

DOSage

The duration of treatment and the dose are determined by a physician for each patient individually.

CHILDREN FROM 3 YEARS OF AGE

ADULTS

1 tablet 3 times a day.

1-2 tablets 3 times a day.

In stationary conditions, as an auxiliary sedative effect, 1 tablet 3 times a day.

Tablets are taken 10-15 minutes before meals.

Usually, for chronic diseases, the course of treatment is 20 – 30 days.

If necessary, a second course is possible.

OVERDOSE

No cases of overdose of Naturosed have been detected.

STORAGE CONDITIONS

The drug should be stored out of reach of children, protected from light, at a temperature of +2 ° C to + 25 ° C.

Expiration date: 24 months

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

3

MIGRENAZ-L

  • ABOUT PRODUCT
  • INSTRUCTIONS
COMPOSITION AND PACKING

Round tablets of herbs, with individual odor, biconvex, light – brown, speckled tablets. 60 pieces 0.5 g each. Polyethylene vials with a protective seal or packed in blisters. (1) – cardboard pack with protective holographic label, (2) – instruction for use.

Composition:
Valerian Extract (Valeriána officinális)
Brandy Mint Extract (Méntha piperíta)
Ginkgo Biloba Extract (Gīnkgo)
May Lily Extract (Convallária majális)
Field Caraway Extract (Fructus Carvi)
Blood-Red Hawthorn Extract (Crataégus sanguínea)
EFFECT OF THE MEDICINE
  • improves cerebral circulation and brain supply;
  • affects the metabolism in cells, the rheological properties of blood and improves peripheral circulation and microcirculation;
  • possesses a pronounced anti-edematous effect at the level of the brain and in peripheral tissues;
  • anti-stress action manifests itself in the normalization of post-stress behavior, somatovegetative disorders, restoration of sleep-wake cycles, disrupted learning and memory processes, reduction of dystrophic and
    morphological changes in various structures of the brain.
SIDE EFFECTS

There may be rarely allergic hypersensitivity to separate ingredients of the preparation.
Use of the medicine should be discontinued when hypersensitivity reactions occur.
The usage of the medicine must be informed to the doctor before the surgery.

INTERACTION WITH OTHER MEDICATION

When prescribing with other medication adverse effects were not revealed.

INDICATIONS

The medicine MIGRENAZ – L is prescribed for:
– acute and chronic disorders of cerebral circulation;
– light craniocerebral trauma; (light concussion of the brain)
– syndrome of vegetative-vascular dystonia (VSD, neurocirculatory dysfunction);
– light cognitive impairment of atherosclerotic origin;
– memory disorders and mental activity;
– dizziness, noise in the ears, a sense of fear;
– violation of peripheral circulation and microcirculation (including arteriopathy of the lower extremities and pediatric orthopedics), Raynaud’s syndrome.

CONTRAINDICATIONS

Individual intolerance to certain ingredients of the medicine.

DOSAGE

The duration of treatment and the dose are determined by the attending physician for each patient individually.

CHILDREN BETWEEN 4 AND 12 YEARS OF AGE

ADULTS AND CHILDREN OVER 12 YEARS OF AGE

1 tablet 3 times a day

1 tablet 3 times a day

For peroral use, 5-10 minutes before the meal.
The course of treatment is at least 3 months (especially in elderly patients).
Courses can be repeated after consultation with the doctor.

OVERDOSE

The cases of overdose were not reported.

STORAGE CONDITIONS AND EXPIRATION DATE

The medicine should be stored out of reach of children, protected from light, at a temperature from + 2° C to + 25°C.

Expiration date: 24 months.

The information presented on the site should not be used for self-diagnosis and treatment and can not serve as a substitute for a doctor's internal consultation.

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