Urolesan capsules blister No. 40

Instructions for Urolesan capsules blister No. 40

Composition

active ingredients: 1 capsule contains thick extract of Urolesan, calculated on moisture content 10% - 10.70 mg (contains dry residue: wild carrot fruit (Fructi Dauci carotae) (1: 1) - 1.84 mg (extractant ethanol 96%), hop cones (Fructi Strobuli lupuli) (1: 1) - 6.33 mg (extractant ethanol 96%), oregano herb (Herba Origani) (1: 1) - 1.46 mg (extractant ethanol 96%)); peppermint oil - 7.46 mg; fir oil - 25.50 mg;

other ingredients: magnesium aluminometasilicate; castor oil; heavy magnesium carbonate; talc; lactose monohydrate; disodium edetate (Trilon B); potato starch.

Dosage form

Capsules.

Main physicochemical properties: hard gelatin capsules numbered "0", green body and cap. Capsule contents - granular powder and/or compacted mass from yellow-gray to gray-brown with a greenish tint with inclusions and the smell of peppermint and fir. The presence of agglomerates that crumble when pressed is allowed.

Pharmacotherapeutic group

Means used in urology.

ATX code G04B X.

Pharmacological properties

A combined herbal preparation. The components of Urolesan® reduce inflammation in the urinary tract and kidneys, promote increased blood circulation in the kidneys and liver, have a diuretic, antibacterial, choleretic effect, form a protective colloid in the urine, and normalize the tone of the smooth muscles of the upper urinary tract.

Urolesan® increases the excretion of urea and chlorides, promotes the excretion of small stones and sand from the bladder and kidneys.

Indication

Acute and chronic infections of the urinary tract and kidneys (cystitis and pyelonephritis); urolithiasis and uric acid diathesis (prevention of the formation of stones after their removal); chronic cholecystitis (including calculous), biliary dyskinesia, cholelithiasis.

Contraindication

- hypersensitivity to the components of the drug;

- gastritis (except gastritis with secretory insufficiency), gastric and duodenal ulcers.

Interaction with other medicinal products and other types of interactions

Didn't study.

Application features

Do not use the drug if the diameter of the stones exceeds 3 mm.

The drug contains the excipients lactose and potato starch, therefore patients with rare hereditary forms of galactose intolerance, lactase deficiency, glucose-galactose malabsorption syndrome or with hypersensitivity or intolerance to gluten should not use this medicinal product.

Use during pregnancy or breastfeeding

The use of the drug during pregnancy or breastfeeding has not been studied.

Ability to influence reaction speed when driving vehicles or other mechanisms

Didn't study.

Method of administration and doses

The drug should be taken orally before meals.

Recommended doses for adults and children over 14 years of age: 1 capsule 3 times a day. In acute conditions (including renal and hepatic colic), the duration of the course of therapy is from 5 to 7 days, in chronic conditions from 7 days to 1 month. In the event of renal and hepatic colic, the single dose can be increased to 2 capsules at a time, then return to the usual single dose (1 capsule) at the next dose.

Children

Children under 14 years of age should be prescribed Urolesan in syrup or liquid form.

Overdose

Overdose may cause nausea, dizziness, and increased sedative effect of the drug.

Therapy is symptomatic. Intensive warm drinking, rest, activated charcoal, atropine sulfate (0.0005-0.001 g).

Adverse reactions

Urolesan is usually well tolerated. When using the drug, the following are possible:

Gastrointestinal: dyspeptic disorders (including nausea, vomiting);

allergic reactions, including flushing, urticaria, itching, facial flushing, skin rashes, angioedema (including a feeling of tightness in the throat, difficulty breathing, swelling of the face and tongue);

from the central and peripheral nervous system: dizziness, general weakness;

Cardiovascular system: arterial hypertension, hypotension, pain in the heart area.

Expiration date

3 years.

Storage conditions

Store in original packaging at temperatures above 25°C. Keep out of the reach of children.

Packaging

10 capsules in a blister, 4 blisters in a pack.

Vacation category

Without a prescription.

Producer

PJSC "Kyivmedpreparat".

Location of the manufacturer and its business address

Ukraine, 01032, Kyiv, Saksaganskoho St., 139.