The instruction for medical use
of UROLESAN® medicine
the Trade name
the International unlicensed name
Is not present
the Dosage form
of the Structure One Capsule Capsule contains
active agent: Urolesanum of extract dense, in terms of moisture of 10% 1 – 10.70 mg, peppermint oils – 7.46 mg, fir oils – 25.50 mg,
excipients: magnesium alyumometasilikat, castor oil, magnesium carbonate heavy, talc, lactoses monohydrate (tablettoza-80), dinatrium edetat (Trilonum B), potato starch,
Structure of the body of the capsule: blue patent V (E 131), yellow quinolinic (E 104), titan dioxide (E 171), iron oxide yellow (E 172), gelatin,
Structure of a lid of the capsule: blue patent V (E 131), yellow quinolinic (E 104), the titan dioxide (E 171), iron oxide yellow (E 172),
gelatin 1 – Urolesanum extract dense contains the dry rest: carrots wild fruits – 1.84 mg, hop of cones – 6.33 mg, a grass marjoram – 1.46 mg
Solid gelatin capsules number 0, the body and a lid of green color. Contents of capsules – powder from yellow-gray till gray-brown color with a greenish shade with impregnations and a smell of oils of a peppermint and fir.
Other drugs for urological diseases.
ATX G04BX code
Combined Drug of Plant Origin properties. Components of the drug Urolesan® reduce the inflammatory phenomena in urinary tract and kidneys, promote the strengthened blood supply of kidneys and a liver, have diuretic, antibacterial, bile-expelling effect, form protective colloid in urine and normalize a tone of smooth muscles of upper uric ways and a gall bladder.
Уролесан® increases discharge of urea and chlorides, promotes removal of small concrements and sand from a bladder and kidneys.
– acute and persistent infections of urinary tract and kidneys (cystitis and pyelonephritises)
– an urolithiasis and urate diathesis (prevention of formation of concrements after their removal)
– chronic cholecystitises (including calculous), dyskinesia of bilious ways, cholelithiasis.
The route of administration and doses
take the Drug inside to food.
The recommended doses for adults on 1 capsule 3 times a day. At acute conditions (including in renal and hepatic gripes) duration of a course of therapy is from 5 to 7 days, at chronicities – from 7 days to 1 month. When developing renal and hepatic gripes the single dose can be raised once to 2 capsules, then on the subsequent reception to return to a usual single dose (1 capsule).
– the dispepsichesky phenomena (nausea, vomiting)
– allergic reactions (feeling of an itching, face reddening, skin rash, a Quincke’s disease, feeling of irritation in a throat, breath difficulty, edema of face, language)
– dizziness, the general weakness
– arterial hypertension,
– hypersensitivity to drug components
– gastritises (except gastritises with secretory insufficiency), a peptic ulcer of a stomach and duodenum
– pregnancy and the period of a lactation
– children’s age up to 18 years
Interaction with other medicines is not known.
not to use drug if diameter of concrements exceeds 3 mm.
Features of influence of medicine on ability to run the vehicle or potentially dangerous mechanisms.
Considering a possibility of development of side effects, it is necessary to be careful.
Symptoms: nausea, dizziness.
Treatment: plentiful warm drink, rest, activated carbon, Atropini sulfas (0.0005-0.001g).
The form of release and packing
On 10 capsules place in blister strip packaging from a film of the polyvinylchloride and printing aluminum foil varnished.
On the 4th blister strip packagings together with the instruction for medical use in the state and Russian languages put in a pack from cardboard.
To Store storage conditions in original packing at a temperature not above 25 °C.
To store out of children’s reach!
not to apply a period of storage after the expiry date specified on packing!
Ukraine JSC Kiyevmedpreparat Producer, 01032, Kiev, Saksagansky St., 139
the Name and the country of the owner of the registration certificate
of JSC Kiyevmedpreparat, Ukraine
the Address of the organization accepting in the territory of the Republic of Kazakhstan claims from consumers on quality of products:
Representative office of Arterium corporation in
Republic of Kazakhstan 050060, Almaty, Al-Farabi Avenue 97, 3 entrance, office 54
Ph. / fax: 8 (727) 315-82-09, 8 (727) 315-82-10,