Gekoven solution for inf. quarrystone. 200 ml

Solution for infusions Gekoven is shown at the hypovolemia caused by sharp blood loss in cases when use only of crystalloids is considered insufficient.

Structure

Active ingredients: hydroxyethylstarch 130/0.4; sodium chloride;

100 ml of solution is contained: hydroxyethylstarch 130/0.4 (the average molecular weight 130000, extent of molar substitution 0.4) in terms of dry matter of 6.0 g, sodium of chloride of 0.9 g;

Excipient: water for injections.

Contraindication

Sepsis, serious illness of a liver; the known increased individual sensitivity to hydroxyethyl starch; clinical diseases where the volume overload is a potential problem, especially in case of a fluid lungs and stagnant heart failure; dehydration; already available disturbances of coagulation and fibrillation; intracranial bleeding; renal failure or replacement renal therapy; heavy hypernatremia or heavy hyperchloremia.

It is contraindicated to patients with burns, with transplanted organs and to critically sick patients because of risk of damage of kidneys and a lethal outcome.

Route of administration

Only for intravenous administration.

Daily dose and speed of infusion depend on the volume of blood loss, maintenance or restoration of a hemodynamics and on hemodilution (effect of dilution). Gekoven it is possible to enter repeatedly within several days.

First 10–20 ml of medicament needs to be entered slowly. The patient has to be under fixed observation because of possible anaphylactic/anaphylactoid reactions.

Feature of use

Pregnant

Gekoven can be applied during pregnancy only in cases when the expected advantage of treatment outweighs possible risk for a fruit.

Children

Use of GEK to teenagers from 12 years is confirmed by data of the corresponding controlled researches of medicament at adults.

Drivers

Gekoven does not influence speed of response at control of motor transport or work with other mechanisms.

Overdose

As well as at administration of other plasma substituting solutions, Gekoven's overdose can lead to a blood circulatory system overload (for example, to a fluid lungs). In this case infusion should be stopped immediately and, if necessary, to enter diuretic.

Side effects

• from blood and lymphatic system: at high doses, at administration of hydroxyethyl starch because of effect of cultivation fibrillation disturbances which depend on a dose can be observed.
• from the immune system: the medicines containing hydroxyethyl starch (GEK) can cause anaphylactic/anaphylactoid reactions (hypersensitivity, weak grippopodobny symptoms, bradycardia, tachycardia, a bronchospasm, not cardial fluid lungs). If there were reactions of hypersensitivity administration of medicament it is necessary to stop and hold immediately relevant medical and supporting activities until symptoms are eliminated.
• from skin and hypodermic fabric: long introduction of high doses of hydroxyethyl starch can cause an itching which is the known side effect of GEK.

Cases of interaction of Gekoven with other medicines are unknown to

.

during administration of medicament the amylase level in blood serum can temporarily increase that can influence definition of the diagnosis of pancreatitis.

effects of cultivation can lead

At high doses to decrease in level of blood-coagulation factors and other proteins of blood plasma and reduction of a hematocrit.

Storage conditions

to Store

at a temperature not above 25 °C out of children's reach.

At storage not to allow medicament freezing.

Expiration date - 3 years.