Kanefron of N

General characteristics. Structure:

Active ingredients: the crushed medicinal vegetable raw materials: 18 mg of a centaury of a grass, 18 mg of a lyubistok medicinal root, 18 mg of rosemary of leaves.

Excipients: starch corn, silicon dioxide colloid, lactoses monohydrate, povidone.

Cover: ferrous oxide red, E 101 Riboflavinum, calcium a carbonate, a dextrose, starch corn, the starch corn modified wax mountain glycolic, povidone, castor oil, sucrose, shellac, talc, titanium dioxide.

Pharmacological properties:

Pharmacodynamics. The combined drug of a plant origin, renders diuretic, spasmolytic, antiinflammatory, antimicrobic action.

Indications to use:

Drug is used in complex therapy at treatment of persistent infections of a bladder (cystitis) and kidneys (pyelonephritis), at noninfectious chronic inflammations of kidneys (a glomerulonephritis, intersticial nephrite), as the means interfering formation of urinary stones (also after removal of urinary stones).

Route of administration and doses:

Inside, without chewing, washing down with water. Adult: on 2 dragees 3 times a day. To children of school age: on 1 dragee 3 times a day. After easing of sharpness of a disease it is necessary to continue treatment by drug within 2-4 weeks.

During treatment drug recommends consumption of a large amount of liquid.

Features of use:

At the hypostases caused by dysfunctions of heart or kidneys, consumption of a large amount of liquid is contraindicated.

At an impaired renal function it is not necessary to appoint drug as monotherapy. In case of an inflammatory disease of kidneys it is necessary to see a doctor behind consultation.

In case of availability of blood in urine, urodynias or at an acute ischuria it is necessary to see a doctor urgently. The acquired carbohydrates which are contained in one dragee make less than 0,04 "grain units" (GU).

Influence on ability of control of vehicles and mechanisms. Drug does not exert impact on ability to performance of potentially dangerous types of activity demanding the increased concentration of attention and speed of psychomotor reactions (including, control of vehicles, work with moving mechanisms).

Side effects:

Allergic reactions are possible. Disorders of digestive tract (nausea, vomiting, diarrhea) are possible.

At emergence of signs of allergic reaction it is necessary to stop administration of drug.

Interaction with other medicines:

The combination with antibacterial agents is possible and reasonable. Interactions with other medicines are at the moment unknown.

Contraindications:

Hypersensitivity to drug components. Children's age (up to 6 years). A peptic ulcer of a stomach and duodenum in an aggravation stage. Insufficiency of lactase, lactose intolerance, glyukozo-galaktozny malabsorption. Deficit of invertase/isomaltase, intolerance of fructose.

Overdose:

Currently data on overdose and intoxication are absent. In case of overdose of drug the symptomatic treatment is appointed.

Storage conditions:

To store in the dry, protected from light place, at a temperature not above 25 °C. To store in the place, unavailable to children. Period of validity 3 years. Not to use after the period of validity specified on packaging.

Issue conditions:

Without recipe

Packaging:

Dragee. On 20 dragees in the blister from aluminum foil (lower part) and polyvinylchloride / a polyvinylidene chloride film (an upper part). On 3 or 6 blisters together with the application instruction place in a folding cardboard box.