Composition, form of production and packaging
? The pills are orange, round, biconvex, with a smooth surface.
1 dragee
crushed medicinal plant raw materials:
herb of the arsenal of 18 mg
roots love drug 18 mg
leaves of rosemary 18 mg
Excipients: corn starch - 15 mg, silicon dioxide colloid - 5.5 mg, lactose monohydrate - 45 mg, povidone - 9 mg.
The composition of the shell: iron oxide red - 0.049 mg, riboflavin (E101) - 0.243 mg, calcium carbonate - 17.222 mg, dextrose - 0.972 mg, corn starch - 2.5 mg, corn starch modified - 2.14 mg, wax mountain glycol - 0.075 mg, povidone - 0.103 mg, castor oil - 0.025 mg, sucrose - 57.182 mg, shellac - 0.615 mg, talc - 43.541 mg, titanium dioxide - 0.333 mg.
20 pcs. - blisters (3) - cardboard boxes.
20 pcs. - blisters (6) - cardboard boxes.
INSTRUCTION FOR THE SPECIALIST.
Description of the drug approved by the manufacturer for the printed edition of 2016.
PHARMACHOLOGIC EFFECT
Diuretic agent of plant origin. The drug has a diuretic, antispasmodic, anti-inflammatory, antimicrobial effect.
INDICATIONS
In complex therapy in the treatment of:
- chronic infections of the bladder (cystitis) and kidneys (pyelonephritis);
- non-infectious chronic inflammation of the kidneys (glomerulonephritis, interstitial nephritis).
As a means of preventing the formation of urinary stones (also after removal of urinary stones).
DOSING MODE
The drug is taken orally, without chewing, with water.
Adults - 2 tablets 3 times / day, children of school age - 1 tablet 3 times / day.
After weakening the severity of the disease should continue treatment with the drug for 2-4 weeks.
During the treatment with the drug, consumption of a large amount of liquid is recommended.
SIDE EFFECT
Perhaps: allergic reactions (if signs of an allergic reaction appear, you should stop taking the drug), gastrointestinal disorders (nausea, vomiting, diarrhea).
CONTRAINDICATIONS
- Stomach ulcer and duodenal ulcer in the stage of exacerbation;
- Lactase insufficiency, lactose intolerance, glucose-galactose malabsorption;
- deficiency of sugar / isomaltase, intolerance to fructose;
- children's age till 6 years;
- Hypersensitivity to the components of the drug.
PREGNANCY AND LACTATION
The use of the drug during pregnancy and during breastfeeding is possible only according to the doctor's prescription after assessing the risk-benefit ratio, in strict accordance with the recommendations for use.
APPLICATION FOR CHILDREN
Contraindicated the use of the drug in childhood to 6 years.
SPECIAL INSTRUCTIONS
When edema caused by impaired cardiac function or kidneys, the consumption of large amounts of fluid is contraindicated.
If the renal function is impaired, the drug should not be given as monotherapy. In the case of inflammatory kidney disease, you should consult a doctor for advice.
In the case of blood in the urine, pain during urination, or with acute urinary retention, you should urgently consult a doctor.
The digestible carbohydrates contained in a single dragee are less than 0.04 bread units (XE).
Impact on the ability to drive vehicles and manage mechanisms
The drug does not affect the ability to perform potentially hazardous activities requiring increased concentration of attention and speed of psychomotor reactions (including vehicle management, work with moving mechanisms).
OVERDOSE
At the moment there is no evidence of overdose or intoxication.
Treatment: in case of an overdose of the drug, symptomatic treatment is prescribed.
DRUG INTERACTION
Combination with antibacterial agents is possible and expedient.
Interaction with other drugs is currently unknown.
TERMS OF RELEASE FROM PHARMACY
The drug is approved for use as a means of OTC.
TERMS AND CONDITIONS OF STORAGE
The drug should be stored in a dry, protected from light, out of reach of children at a temperature of no higher than 25 В° C. Shelf life - 3 years.
