Composition, form of production and packaging
Solution for intravenous administration of 1 ml
fraction of polysaccharides obtained from fresh potato sprouts 0.5 g
Excipients: sodium chloride, water d / and.
1 ml - ampoules (3) - packings of cellular contour (1) - packs cardboard.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2011.
PHARMACHOLOGIC EFFECT
Has the ability to activate regenerative and reparative processes in the mucosa of the gastrointestinal tract.
PHARMACOKINETICS
Not studied.
INDICATIONS
- Stomach ulcer and duodenal ulcer in the phase of exacerbation.
DOSING MODE
In / in 1 ml of the solution 0.5 mg / ml.
Single dose: 0.5 mg (1 injection) in 7 days. The course of treatment is 3 injections for 14 days.
SIDE EFFECT
There may be a brief burning sensation and pain at the injection site. Allergic reactions are possible.
CONTRAINDICATIONS
- the period of pregnancy and lactation;
- children's age till 14 years;
hypersensitivity to the drug.
PREGNANCY AND LACTATION
Contraindicated in pregnancy and lactation.
APPLICATION FOR CHILDREN
Contraindicated in children under 14 years.
DRUG INTERACTION
Not found.
TERMS OF RELEASE FROM PHARMACY
On prescription.
TERMS AND CONDITIONS OF STORAGE
Keep out of reach of children, protected from light, at a temperature of 2 В° to 10 В° C. Protect from freezing. Shelf life - 3 years.
