Kanefron N, 120 pcs.

Pharmacotherapeutic group

Diuretic agent of plant origin.

Pharmacological properties

A combination drug of plant origin, has diuretic, antispasmodic, anti-inflammatory, antimicrobial action.

Indications

The drug is used in the treatment of chronic urinary bladder (cystitis) and kidney infections (pyelonephritis), non-infectious chronic kidney inflammations (glomerulonephritis, interstitial nephritis), as a means of preventing the formation of urinary stones (also after removal of urinary stones).

Active ingredient

Goldenseal herb, Lycium cinereum roots, Rosemary leaves

Composition

Active ingredients:

crushed medicinal herbal raw materials:

Goldense herb 18 mg

Lubistock medicinal root 18 mg

Rosemary common leaves 18 mg

Excipients: lactose monohydrate, magnesium stearate, corn starch, povidone K 25, colloidal anhydrous silica.

Wrapper: calcium carbonate, castor oil, glucose, iron oxide red dye (E 172), corn starch, dextrin, mountain glycol wax, povidone K 30, riboflavin, shellac, sucrose, talc, titanium dioxide

How to take, the dosage

Inside, without chewing, with water. Adults: 2 tablets 3 times a day. Children of school age: 1 tablet 3 times a day. After relieving the severity of the disease should continue treatment for 2 – 4 weeks. During treatment with the drug it is recommended to drink plenty of fluids.

Interaction

Combination with antibacterial agents is possible and reasonable. Interactions with other drugs are currently unknown.

Special Instructions

In case of edema caused by cardiac or renal disorders, consumption of large amounts of fluid is contraindicated.

The drug should not be prescribed as monotherapy if renal function is impaired. If there is inflammatory kidney disease, a physician should be consulted.

If there is blood in the urine, pain during urination, or if there is severe urinary retention, a physician should be seen immediately.

The digestible carbohydrates in one tablet are less than 0.04 “bread units” (BE).

Influence on driving and operating ability

The drug does not affect the ability to perform potentially hazardous activities requiring increased concentration and quick psychomotor reactions (including driving vehicles and operating moving machinery).

Synopsis

Orange, round, biconvex, coated tablets with a smooth surface.

Contraindications

Hypersensitivity to the components of the drug. Childhood age (under 6 years). Gastric and duodenal ulcer in the acute stage. Lactase deficiency, lactose intolerance, glucose-galactose malabsorption. Sucrose/isomaltase deficiency, fructose intolerance.

Side effects

Allergic reactions are possible. Gastrointestinal tract disorders (nausea, vomiting, diarrhea) are possible. If signs of an allergic reaction occur, stop taking the drug.

Overdose

To date, there are no data on overdose and intoxication. In case of overdose, symptomatic treatment is prescribed

Pregnancy use

Use of the drug during pregnancy and breast-feeding is possible only by prescription, in strict accordance with the recommendations for use and after evaluation by the attending physician of the risk/benefit ratio.

Similarities

Nephrostene