Actovegin, 200 mg 50 pcs.
€44.56 €44.15
A drug that activates tissue metabolism, reduces tissue hypoxia, improves trophism and stimulates the regeneration process. It is a hemoderivate, which is obtained by dialysis and ultrafiltration (penetrates compounds with a molecular weight of less than 5000 daltons).
Positively affects the transport and utilization of glucose, stimulates oxygen consumption (which leads to stabilization of plasma cell membranes during ischemia and reduction of lactate formation) thus having an antihypoxic effect.
Actovegin not only increases intracellular glucose content but also improves oxidative metabolism, this improves cellular energy supply as evidenced by increased concentration of direct free energy transporters such as ATP, ADP, phosphocreatine and amino acids such as glutamate, aspartate and GABA.
In disorders of metabolism and blood supply to the brain, such as cerebral insufficiency syndrome (dementia), the transport of glucose through the BBB and its utilization by cells is impaired. PDH activity and acetylcholine concentration also decrease. Administration of Actovegin helps to normalize these figures, improves glucose transport and utilization, with increased oxygen consumption.
Actovegin has been shown to have the same effect in peripheral (arterial, venous) circulatory disorders and the corresponding consequences of such disorders (arterial angiopathy, ulcers of the lower extremities) as well as when used to accelerate wound healing. In case of ulcers of various etiology, trophic disorders (bedsores), burns and radiation injuries Aktovegin improves not only morphological but also biochemical parameters of granulation, for example, concentration of DNA, hemoglobin and hydroxyproline increases.
The effect of Actovegin starts to show no later than 30 min after oral administration and reaches a maximum on average in 3 h (2-6 h).
Indications
Active ingredient
Composition
1 tablet contains:
Active substances:
deproteinized hemoderivate from calf blood – 200 mg.
Additional Ingredients:
magnesium stearate – 2.0 mg,
talc – 3.0 mg.
Shell composition:
Acacia gum – 6.8 mg,
mountain glycol wax – 0.1 mg,
hypromellose phthalate – 29.45 mg,
diethyl phthalate – 11.8 mg,
quinoline yellow varnish aluminum dye – 2.0 mg,
macrogol-6000 – 2.95 mg,
povidone-K 30 – 1.54 mg,
sucrose – 52.3 mg,
talc – 42.2 mg,
titanium dioxide – 0.86 mg.
How to take, the dosage
Prescribe 1-2 tablets. 3 times a day before meals.
The tablet is not chewed, drink a small amount of water.
The duration of treatment is 4-6 weeks.
Interaction
Special Instructions
Contraindications
With cautiousness the drug should be prescribed in cases of heart failure stage II-III, pulmonary edema, oliguria, anuria, hyperhydration, diabetes mellitus, hyperglycemia.
Side effects
Overdose
Weight | 0.024 kg |
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Shelf life | 3 years. Do not use after the expiration date. |
Conditions of storage | The drug should be kept out of reach of children, protected from light at a temperature not exceeding 25°C. |
Manufacturer | Takeda Pharmaceuticals LLC, Russia |
Medication form | pills |
Brand | Takeda Pharmaceuticals LLC |
Other forms…
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