Kanefron N, 100 ml
€16.08 €15.88
Clinico-pharmacological group
Diuretic drug of plant origin.
Pharmacological action
The combined drug has diuretic, antispasmodic, anti-inflammatory, antimicrobial action.
Pharmacokinetics
Pharmacokinetic data are not available.
Indications
Kanefron is used in adults and children in the treatment of complex therapy:
Composition
The oral solution is clear or slightly cloudy, yellowish-brown in color, with an aromatic odor; slight precipitation is possible during storage.
100 g of the solution contains:
Active substances:
aqueous-alcoholic extract from medicinal herbal raw materials: 29 g;
Goldenberry herb 600 mg;
Lulubostoc medicinal root 600 mg;
Rosemary leaves 600 mg.
Auxiliary substances:
Purified water 71 g.
In a bottle with a dropper dispenser 50 or 100 ml of solution. There is 1 vial in the carton pack.
How to take, the dosage
Dosage and administration
Internal, diluted in a small amount of water or with water.
Dosing regimen for different age groups
After the acute disease has subsided, the drug should be continued for 2-4 weeks. If necessary, for example, to soften the bitter taste for children, the drug may be taken together with other liquids. It is recommended to drink plenty of fluids during therapy. Shake well before use!
Interaction
Combination with antibacterial agents is possible and appropriate.
Interactions with other drugs are currently unknown.
Special Instructions
Precautionary measures when taking the drug
In case of edema caused by impaired heart or renal function, large amounts of fluid are contraindicated.
In case of impaired renal function, the drug should not be prescribed as monotherapy.
In case of inflammatory kidney disease, a physician should be consulted. If there is blood in the urine, pain during urination or acute retention of urine, a physician should be seen urgently.
A slight clouding or precipitation may occur during storage; this does not affect the effectiveness of the drug.
Impact on ability to drive vehicles and other mechanisms requiring high concentration
The content of ethyl alcohol in the drug is from 16.0 to 19.5% (by volume). During the period of the drug treatment, caution must be exercised while driving motor transport and engaging in other potentially hazardous activities which require increased concentration and quick psychomotor reactions.
Interaction with alcohol
Alcoholic beverages should be avoided while taking the drug.
Prescription conditions from pharmacies
Without prescription.
Contraindications
The contraindication to the use of Canefron N is:
With caution: liver disease, brain injury, brain disease, childhood (over 1 year) (use only after consulting a physician) – due to the content of ethanol.
Side effects
When using the drug, allergic reactions are possible:
Allergic reactions (if signs of allergic reactions appear, discontinue the drug), dyspeptic disorders (nausea, vomiting, diarrhea).
Overdose
There are currently no data on overdose and intoxication.
In case of overdose, symptomatic treatment is indicated.
Pregnancy use
The use of the drug during pregnancy and lactation 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.
It is contraindicated in children under 1 year of age.
Weight | 0.215 kg |
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Shelf life | 3 years |
Conditions of storage | In a dry, light-protected place at a temperature not exceeding 25 °C |
Manufacturer | Bionorica SE, Germany |
Medication form | oral solution |
Brand | Bionorica SE |
Other forms…
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