Universal reference book for medicines
Product name: ECDISTEN (ECDISTEN)

Active substance: nonappropriate

Type: drug with restorative action

Manufacturer: ВИФИТЕХ (Russia)
Composition, form of production and packaging
Tablets are
round, flat-cylindrical with a chamfer, from white to white with a yellowish hue of color.

1 tab.

ecdystene 0.005 g

Auxiliary substances: sugar (sucrose) 0.089 g, potato starch 0.005 g, calcium stearate 0.001 g.

10 pieces.
- packings cellular planimetric (3) - packs cardboard.
10 pieces.
- packings cellular planimetric (5) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2011.

PHARMACHOLOGIC EFFECT

Natural connection of the steroid structure from the roots and rhizomes of levzeya safflower;
has a tonic effect, promotes the enhancement of protein synthesis in the body. Increases mental and physical performance.
INDICATIONS

- asthenic syndrome associated with the weakening of protein-synthesizing processes;

- with prolonged intoxications, infections;

mental and physical overwork;

- for athletes, as a medicine that increases the speed and strength in the period of preparation for the competition.

DOSING MODE

Inside, to 0.005-0.01 g (1-2 tables.) 3 times / day after eating;
course of treatment - 15-20 days; on the recommendation of a doctor, a repeat course of treatment can be performed in 1-2 weeks; in sports medicine apply to 0.01 g (2 tab.) 3 times / day for 2-3 weeks; the maximum single dose - 0.01 g (2 tab.), the highest daily dose - 0.03 g (6 tab.).
SIDE EFFECT

Possible insomnia, increased blood pressure, pain in the epigastric region.

If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.

CONTRAINDICATIONS

- nervous excitement;

- Insomnia;

- arterial hypertension;

- epilepsy;

- hyperkinesis;

- Stomach ulcer and duodenal ulcer (in the stage of exacerbation);

- congenital intolerance to fructose;

- glucose-galactose malabsorption;

- deficiency of sugar / isomaltase;

- Pregnancy;

- lactation period;

- age up to 18 years;

- increased individual sensitivity to the components of the drug.

If you have any of these diseases, consult a doctor before taking the drug.

Be wary of a diabetic patient and those on a diet with a reduced carbohydrate content.

PREGNANCY AND LACTATION

The drug is contraindicated in pregnancy and lactation.

APPLICATION FOR CHILDREN

Contraindicated in children under 18 years.

SPECIAL INSTRUCTIONS

To achieve the effect simultaneously with the use of the drug, it is necessary to obtain adequate amounts of proteins, fats, carbohydrates, vitamins and minerals with food.

In case of side effects, incl.
to avoid disturbance of sleep, it is advisable to reduce the dose or stop the evening intake of the drug.
Patients with diabetes should take into account that one tablet contains about 0.094 grams of carbohydrates (0.008 XE).

Impact on the ability to drive vehicles and manage mechanisms

The use of the drug does not affect the ability to drive vehicles and engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

OVERDOSE

Symptoms: Possible increase in dose-dependent adverse reactions.

Treatment: symptomatic.

DRUG INTERACTION

With simultaneous use, it is possible to increase the effect of stimulants and analeptics (caffeine, camphor, phenamine).

The drug is an antagonist of drugs that depress the central nervous system (including neuroleptics, barbiturates, tranquilizers, anticonvulsant drugs).

TERMS OF RELEASE FROM PHARMACY

The drug is released by prescription.

TERMS AND CONDITIONS OF STORAGE

The drug should be stored in a dry, dark place at a temperature of no higher than 25 ° C.
Keep out of the reach of children.
Shelf life - 2 years.

Do not use after the expiration date.

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