Uronephron tablets 500 mg, 60 pcs.

Diseases that cause bladder dysfunction in children and adults are diagnosed quite often. The risk group usually includes people with low immunity and concomitant diseases of the reproductive system. Treatment should be comprehensive, including the use of antibacterial drugs and natural remedies that improve overall well-being and saturate the tissues with flavonoids. Uronefril copes well with the latter task. Buying the supplement is not difficult at a regular pharmacy; customer reviews are good.

Indications for use

The instructions note that Uronefril tablets can be used to replenish arbutin, which contains flavonoids and other beneficial microelements.

The natural remedy is used in complex treatment:

  • glomerulonephritis;
  • cystitis, urethritis;
  • pyelonephritis.

In addition, the drug is actively used to prevent urolithiasis and rehabilitation after long-term pharmacotherapy with antibiotics.

Uronephron tablets 500 mg, 60 pcs.

Uronephron® is a combination preparation of plant origin. It has anti-inflammatory, diuretic, antispasmodic and antimicrobial effects. The diuretic effect is due to flavone derivatives, inositol, saponins and silicates. The latter also enhance the excretion of uric acid due to urate deposits in the kidneys. The drug prevents the crystallization of mineral components in the urinary tract, has a beneficial effect on maintaining the balance between colloids and crystalloids in urine. Saponins reduce surface tension, form protective colloids and emulsify pathogenic components of urine, preventing the formation of sand and kidney stones. Promotes the removal of sand and small stones, prevents the increase of stones and the appearance of new ones. The effect of Uronephron on the tubular and glomerular system of the kidneys leads to a decrease in protein secretion during proteinuria.

Onion peel contains essential oil (up to 0.15%), Vitamin C, riboflavin, thiamine, carotenoids, phytic, citric and malic acid, sugars (glucose, fructose, sucrose), flavonoids, potassium compounds, iron, manganese, zinc and cobalt Has an anti-inflammatory effect.

Birch leaves contain essential oils, saponins, tannins, resins, ascorbic and nicotinic acids. The main effect is diuretic, choleretic, antispasmodic, anti-inflammatory.

Creeping wheatgrass. The rhizome contains polysaccharides, sugars, alcohols, glycosides, vitamins, essential and fatty oils, and organic acids. The main effect is diuretic, regulating metabolism.

Curly parsley roots contain aponil, myristicin, and flavonoids. The main effect is diuretic, anti-inflammatory, litholytic.

Fenugreek seeds contain trigonelin, nicotinic acid, rutin, steroid saponins and phytosterols, flavonoids, essential oils. The main effect is anti-inflammatory, restorative, wound healing.

Common goldenrod herb contains flavonoids: kaempferol, quercetin and their glycosides - astragalin, rutin. The main effect is diuretic, antibacterial, anti-inflammatory.

Horsetail contains flavonoids: apigenin derivatives, luteolin, kaempferol, quercetin, and also contains phenolcarboxylic acids, tannins, saponins. The main effect is diuretic, anti-inflammatory, litholytic, detoxification.

Common knotweed grass contains flavonoids, phenolic acids, carotene, ascorbic acid, and tannins. The main effect is diuretic, hemostatic.

Lovage officinalis. The aboveground mass and roots of lovage contain essential oil (in fresh roots - 0.1-0.2%, in dry roots - 0.6-1.0%), sugars, organic acids, minerals, resins, starch. The composition of the essential oil includes terpineol, cineole, acetic, isovaleric and benzoic acids. The main effect is diuretic, anti-inflammatory.

The components that make up the herbal medicine Uronefron® exhibit complex activity, which is manifested in the anti-inflammatory effect and elimination of spasms of the urinary tract, diuretic, vasodilating effects, and also determine the effectiveness of the antimicrobial effect of the drug.

Contraindications to treatment

Uronefril is considered a relatively safe drug, rarely causing side effects. At the same time, the instructions note that taking pills is prohibited if:

  • individual intolerance or hypersensitivity to components;
  • pregnancy at any stage, breastfeeding;
  • renal failure, liver dysfunction;
  • peptic ulcer during exacerbation;
  • severe pathologies of the cardiovascular system.

It is necessary to stop therapy if skin rashes, local increases in body temperature, peristalsis disturbances (diarrhea), nausea, and vomiting appear.

URONEPHRON (CANEPHRON) TAB No. 60

Instructions

Trade name of the drug: Canephron® n (Canephron N)
Active ingredients: Comb.drug (centaurii herba, levistici radix, posmarini folia)*

Pharmacotherapeutic group: Diuretics, Diuretics.

Release form:

Dragees: blisters of 20 dragees each. Package sizes: 60 and 120 tablets.

Dosage form:

Oral solution 100 ml (bottles). Dragee N60 (3×20), N120 (6×20) (blisters)

Compound:

1 tablet contains crushed medicinal raw materials (powder) from: Centaury herb (Centaurii herba) 18 mg Lovage medicinal root (Levistici radix) 18 mg Rosemary leaves (Rosmarini folia) 18 mg

Pharmacological properties:

The drug has anti-inflammatory, antioxidant, antispasmodic and analgesic effects. The herbal components of the drug have an antibacterial and diuretic effect.

Pharmacokinetics:

The drug is used in standard and complex therapy of acute and chronic bladder infections (cystitis). The drug is used in the complex therapy of pyelonephritis, glomerulonephritis, interstitial nephritis; as a prophylaxis against the formation of urinary stones (also after removal of urinary stones).

Mode of application:

Dosage Patients single dose daily dose Adults and adolescents from 12 years of age 2 tablets 6 tablets School-age children 1 tablet 3 tablets Method of administration Take a single dose in the morning, afternoon and evening. The dragee should be taken without chewing and washed down with liquid. Due to its good tolerability, the drug can be used for long-term therapy. Irrigation therapy: take with plenty of liquid.

Side effects:

Allergic reactions (rash, itchy skin), gastrointestinal disorders (vomiting, mild diarrhea) may occur. At the first appearance of allergic reactions, use of the drug should be discontinued. Allergic reactions (rash, itchy skin), gastrointestinal disorders (vomiting, mild diarrhea) may occur. At the first appearance of allergic reactions, use of the drug should be discontinued.

Contraindications:

- hypersensitivity to the components of the drug, to other plants of the umbelliferous family (for example, anise, fennel), to anethole (i.e. to a component of essential oils, for example, anise, fennel); - gastric and duodenal ulcers in the acute period; - children under 6 years of age.

Drug interactions:

Combination with antibacterial drugs is possible and advisable. At the moment, there is no information on interactions with other drugs.

Special instructions:

If you suspect inflammatory kidney disease and/or impaired renal function, you should consult your doctor before using the drug. In addition, the acceptable amount of fluid intake for patients suffering from renal or heart failure should be determined by a physician. If, while taking the drug, complaints such as high fever, cramps, blood in the urine, urinary problems or acute urinary retention occur, you should consult your doctor. This medicine contains glucose, sucrose and lactose. In case of intolerance to glucose, sucrose and lactose, the use of the drug Canephron® tablets is possible only after consultation with a doctor. The medicine does not affect the ability to drive a car or operate machinery. Use during pregnancy and lactation The use of Canephron® N during pregnancy and lactation is possible only as prescribed by a doctor and after assessing the risk-benefit ratio, with strict adherence to the instructions for use. Note for diabetics: The digestible carbohydrates contained in one tablet are approximately 0.02 bread units (BRU). The drug should not be used after the expiration date and should be stored out of the reach of children. Use during pregnancy and lactation The use of Canephron® N during pregnancy and lactation is possible only as prescribed by a doctor and after assessing the risk-benefit ratio, with strict adherence to the instructions by application. Note for diabetics: The digestible carbohydrates contained in one tablet are approximately 0.02 bread units (BRU). The drug should not be used after the expiration date and should be stored out of the reach of children.

Overdose:

At the moment, there is no data on overdose. Treatment is symptomatic. At the moment, there is no data on overdose. Treatment is symptomatic. At the moment, there is no data on overdose. Treatment is symptomatic.

Storage conditions: Store in a dry place, protected from light, at a temperature not exceeding 30°C.

Shelf life: 4 years

Conditions of release: without prescription

Manufacturer: Bionorica SE, Germany

Descriptions: round-shaped dragee, with a biconvex, smooth surface of orange color.

Operating principle

The instructions for use note that Uronefril is able to accelerate the recovery of the body during the treatment of diseases that disrupt the functioning of the genitourinary system. Provided the correct dosage and time of administration, you can quickly compensate for the deficiency of flavonoids and normalize bladder function.

A big plus of the drug is the correct composition. All components are natural, relatively safe, but quite effective when combined to influence the causes of the pathological condition:

  • bearberry (leaves);
  • centaury grass;
  • lovage roots;
  • medicinal rosemary.

The film coating consists of cellulose and auxiliary microelements.

Uronephron

Name: Uronephron Pharmacological action: Uronephron is a combination drug with diuretic, antimicrobial, antispasmodic and anti-inflammatory effects. The composition of the drug Uronephron includes components of plant origin, the biologically active substances of which determine the effect of the drug.

Uronephron increases diuresis and also increases the excretion of uric acid in patients with urate stones in the kidneys, resulting in the washing out of sand and small stones, as well as a reduction in the size of large stones. In addition, Uronephron prevents the crystallization of mineral components and the formation of stones and sand in the urinary tract, and also regulates the balance of colloids and crystalloids in urine. The drug normalizes metabolic processes, reduces the intensity of the inflammatory process of the urinary tract, and has some choleretic and restorative effects.

The pharmacokinetics of the drug Uronephron is not presented.

Indications for use: Uronephron is prescribed as part of complex therapy for patients suffering from infectious and inflammatory diseases of the urinary system, which are accompanied by urolithiasis. Uronephron is also effective in preventing relapses of urolithiasis.

Directions for use: Uronephron syrup: The drug is administered orally. It is recommended to take the syrup undiluted after meals, measuring the required amount of the drug using a measuring spoon. The syrup can be washed down with a small amount of drinking water. The duration of therapy and dose of the drug Uronefron is determined by the doctor. The recommended single dose of syrup is 5 ml. The recommended daily dose of syrup is 15-20 ml.

Oral drops Uronefron: The drug is intended for oral administration. Immediately before use, the required number of drops should be diluted in 100 ml of drinking water. It is recommended to take Uronefron drops after meals. The duration of the course of treatment and the dose of Uronefron is determined by the doctor. The recommended single dose is 25-30 drops. Usually 3-4 doses of the drug are prescribed per day.

Gel for oral use Uronephron: The drug is intended for oral administration. Immediately before use, the required amount of gel should be dissolved in 100 ml of warm drinking water. It is recommended to take Uronefron after meals. The duration of administration and dose of the gel is determined by the doctor. The recommended single dose is 5 g of gel (1 teaspoon). The recommended daily dose is 15-20 g of gel (3-4 teaspoons). Regardless of the form of release of the drug Uronefron, the course of treatment usually ranges from 2 to 6 weeks. If necessary, after some time, a second course of treatment with Uronefron is carried out.

Side effects: Uronephron is in most cases well tolerated by patients. Isolated cases of photosensitivity, changes in taste and nausea have been reported during therapy with Uronefron. The possibility of developing allergic reactions during the use of the drug Uronefron cannot be ruled out.

Contraindications: Uronephron is not prescribed to patients with known individual sensitivity to the components of the drug. Uronephron is not used to treat patients suffering from acute nephritis, phosphate lithiasis, nephrosis, as well as impaired renal function and heart failure. Uronephron is not used in pediatric practice to treat children under 15 years of age.

Pregnancy: Should not be prescribed to lactating and pregnant women due to the lack of necessary clinical studies of the drug Uronephron in this category of patients.

Interaction with other drugs: Uronephron, due to its diuretic effect, can reduce the half-life of drugs that are excreted by the kidneys. The drug Uronefron, when used simultaneously, potentiates the effect of hypoglycemic agents, monoamine oxidase inhibitors, non-narcotic analgesics and anticoagulant drugs.

When used in combination with the drug Uronefron, it is possible to increase the duration of the therapeutic effect of paracetamol and pentabarbital. Uronephron may reduce the absorption of alpha-tocopherol, cholesterol and beta-carotene in the small intestine.

Overdose: There is no data on overdose of the drug Uronefron.

Release form: Syrup for oral administration Uronefron 100 ml in dark glass bottles, 1 bottle is included in a cardboard box. Uronefron drops for oral administration, 25 ml in dark glass bottles, 1 bottle included in a cardboard box. Uronefron gel for oral administration, 100 g in tubes, 1 tube is included in a cardboard box.

Storage conditions: Uronefron oral syrup and drops can be used within 2 years after release. Uronefron oral gel can be used for 3 years after release. Regardless of the form of release, Uronefron should be stored in rooms with a temperature not exceeding 25 degrees Celsius.

Composition: 5 ml of Uronefron syrup contains: Thick phytoextract (in terms of dry residue) – 0.6 g; Additional ingredients including sorbitol.

The thick phytoextract is obtained from: 5 parts of onion peel; 5 parts goldenrod herb; 10 parts lovage roots; 10 parts of birch leaves; 10 parts horsetail herb; 12.5 parts wheatgrass root; 15 parts fenugreek seeds; 15 parts of knotweed herb; 17.5 parts parsley root.

1 bottle of oral Uronefron drops contains: Liquid phytoextract (1:5.8) – 25 ml; Additional ingredients. 1 ml = 27 drops

The liquid phytoextract was obtained by extraction with 45% ethyl alcohol from plant materials: Onion peels; Goldenrod herbs; Lovage roots; Birch leaves; Horsetail herbs; Wheatgrass root; Fenugreek seeds; Polygonum herbs; Parsley root.

100 g of Uronefron gel contain: Thick phytoextract – 12 g; Additional ingredients include peppermint, mountain pine, sage and orange oils.

Thick phytoextract obtained from: Onion peel; Goldenrod herbs; Lovage roots; Birch leaves; Horsetail herbs; Wheatgrass root; Fenugreek seeds; Polygonum herbs; Parsley root.

Attention! The description of the drug " Uronefron " on this page is a simplified and expanded version of the official instructions for use. Before purchasing or using the drug, you should consult your doctor and read the instructions approved by the manufacturer. Information about the drug is provided for informational purposes only and should not be used as a guide to self-medication. Only a doctor can decide to prescribe the drug, as well as determine the dose and methods of its use.

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