ACTOVEGIN 10 ml 5amp - Blood Extract 40mg/ml
Release form: 40 mg/ml injection solution 10 ml ampoules 5 pcs.
ACTOVEGIN activates tissue metabolism, improves trophism and stimulates the regeneration process.
Actovegin is an antihypoxant that has three types of effects: metabolic, neuroprotective and microcirculatory. Actovegin* increases the absorption and utilization of oxygen; The phospho-oligosaccharides contained in the preparation inositol have a positive effect on the transport and utilization of glucose, which leads to an improvement in the energy metabolism of cells and a decrease in the formation of lactate under ischemic conditions.
Several ways to implement the neuroprotective mechanism of action of the preparation are being considered.
Actovegin® prevents the development of apoptosis induced by beta-amyloid peptide (Ap25-35).
Actovegin modulates the activity of nuclear factor kappa B (NF-kB), which plays an important role in the regulation of apoptosis and inflammation in the central and peripheral nervous system.
Another mechanism of action involves the nuclear enzyme poly(ADP-ribose) polymerase (PARP). PARP plays an important role in the detection and repair of single-stranded DNA damage, but excessive activation of the enzyme can trigger cell death in conditions such as cerebrovascular disease and diabetic polyneuropathy. Actovegin' inhibits PARP activity, which leads to functional and morphological improvement in the central and peripheral nervous system.
The positive effects of the preparation Actovegin®, affecting microcirculation processes and the endothelium, are an increase in the speed of capillary blood flow, a decrease in the pericapillary zone, a decrease in the myogenic tone of precapillary arterioles and capillary sphincters, a decrease in the degree of arteriovenular shunt blood flow with preferential blood circulation in the capillary bed and stimulation of the function of endothelial synthase nitric oxide, which affects the microvasculature.
In the course of various studies, it was found that the effect of the preparation Actovegin® occurs no later than 30 minutes after taking it. The maximum effect is observed 3 hours after parenteral and 2-6 hours after oral administration.
Directions:
As part of complex therapy:
- cognitive impairment, including post-stroke cognitive impairment and dementia;
- peripheral circulatory disorders and their consequences;
- diabetic polyneuropathy.
Ingredients:
Actovegin® concentrate (in terms of dry deproteinized hemoderivative of calf blood)
1 ml = 40 mg
1 amp = 400 mg
Dosage:
The preparation is used intravenously, intravenously (including as an infusion) and intramuscularly.
Depending on the severity of the clinical picture, first, 10-20 ml of the preparation should be administered intravenously or intravenously daily;
then - 5 ml intravenously or intramuscularly slowly, daily or several times a week.
For infusion, from 10 to 50 ml of the preparation should be added to 200-300 ml of the stock solution (isotonic sodium chloride solution or 5% glucose solution). The infusion rate is about 2 ml / min.
For intramuscular injections, no more than 5 ml of the preparation is used, that should be injected slowly, since the solution is hypertonic.
In the acute period of ischemic stroke (starting from 5-7 days) - 2000 mg / day intravenous drip up to 20 infusions with the transition to taking tablets of 2 tablets.
3 times / day (1200 mg / day). The total duration of treatment is 6 months.
With dementia - 2000 mg / day IV drip. The duration of treatment is up to 4 weeks.
In case of violations of peripheral circulation and their consequences - 800-2000 mg / day intravenously or intravenously drip. The duration of treatment is up to 4 weeks.
With diabetic polyneuropathy - 2000 mg / day intravenous drip 20 infusions with the transition to taking tablets of 3 tablets. 3 times / day (1800 mg / day). The duration of treatment is from 4 to 5 months.
Instructions for using breakpoint ampoules:
Place the tip of the aampoule point up.
Gently tapping with your finger and shaking the ampoule, let the solution flow down from the tip of the ampoule.
Holding the ampoule with the tip up in one hand, break off the tip of the ampoule with the other hand along the break point.
Form release:
Solution for injection 40 mg/1 ml.
Amp. 10 ml 5 Pcs.

Guarantee:
ТАКЕДА ФАРМАСЬЮТИКАЛС (Russian Federation)
Development and production:
ТАКЕДА ФАРМАСЬЮТИКАЛС (Russian Federation)



