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Treść ulotki
PACKAGE
LEAFLET
patient
Canephron
coated tablets
Active ingredients: centaury powder; lovage root powder; rosemary leaf powder
Read this leaflet carefully before taking this medicine as it contains important information for you.
Always take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you.
to do.
- Keep this leaflet. You may need to read it again.
- Consult your pharmacist if you want more information or advice,
- If any undesirable effects occur, including effects not listed in this leaflet, consult your doctor or pharmacist. See section 4.
- Consult your doctor if you do not notice any improvement or if your symptoms worsen after 3 days.
Contents of this leaflet
- 1. What Canephron is and what it is used for
- 2. What you need to know before taking Canephron
- 3. How to take Canephron
- 4. Possible side effects
- 5. How to store Canephron
- 6. Contents of the pack and other information
1. What is Canephron and what is it used for
Canephron is a traditional medicine of plant origin.
- for supportive treatment and as an adjunct to specific measures in case of mild disorders (such as frequent urination, burning during urination and increased urinary urgency) caused by inflammatory diseases of the efferent urinary tract;
- for washing the urinary tract in order to reduce the deposition of kidney sand (so-called renal grit). The use of this traditional medicine of plant origin, for the indicated therapeutic indications, is based exclusively on many years of use experience.
Consult a doctor or qualified healthcare professional if symptoms persist during use of the
2. What you need to know before taking Canephron
Do not take Canephron
- if you are allergic to the active ingredients, to other plants of the Apiaceae (Umbelliferae) family (e.g. anise, fennel), to anethole (a component of essential oils) or to any of the other ingredients of this medicine (listed in section 6);
- if you suffer from peptic ulcer;
- in case of edema due to impaired cardiac or renal function and/or if the doctor has recommended reducing fluid intake. Warnings and precautionsImmediately consult your doctor if you have persistent fever, lower abdominal pain, spasms, blood in the urine, difficulty urinating and acute urinary retention.
Children and adolescents
There is insufficient data on the use of this medicine in children under 12 years of age.
Urinary tract disorders in children require medical intervention (they must be
diagnosed, treated and monitored by a doctor). Therefore, Canephron should not be used in
children under 12 years of age.
Canephron should be used in adolescents under 18 years of age only after a doctor
has ruled out serious illnesses.
Other medicines and Canephron
Tell your doctor or pharmacist if you are taking, have recently taken or might
take any other medicine.
No interactions with other medicines are known to date. No clinical interaction studies
have been conducted.
Pregnancy, breastfeeding and fertility
If you are pregnant, suspect you are pregnant or are planning a pregnancy, ask
your doctor or pharmacist for advice before taking this medicine.
The use of Canephron can be considered during pregnancy if deemed necessary
by the treating physician.
It is not known whether Canephron or its active ingredients/metabolites are excreted in breast milk. Canephron
should not be used during breastfeeding.
No data are available regarding effects on human fertility.
Driving and operating machinery
No studies have been conducted with Canephron regarding effects on the ability to drive
vehicles and operate machinery.
Canephron contains glucose, sucrose and lactose sugars
If your doctor has told you that you have an intolerance to certain sugars, consult your doctor
before taking this medicine.
Note for diabetics:
one coated tablet contains an average of 0.3 g of available carbohydrates.
3. How to take Canephron
Take this medicine exactly as described in this leaflet or as your doctor or pharmacist has told you. If you have any doubts, consult your doctor or pharmacist.
The recommended dose is:
Adults and adolescents aged 12 years and over: 1 coated tablet 3 times a day.
Use in children and adolescents
There is insufficient data on the use of this medicine in children under 12 years of age. Urinary tract disorders in children require medical intervention (they must be diagnosed, treated and monitored by a doctor).
Therefore, Canephron should not be used in children under 12 years of age. Canephron should only be used in adolescents under 18 years of age after a doctor has ruled out serious illnesses.
There is insufficient data to issue specific dosage recommendations in case of impaired renal/hepatic function.
Method of administration:
Take a single dose of Canephron 3 times a day (morning, noon, evening). Canephron should be swallowed whole (not chewed) and it is best to take it with some liquid, for example a glass of water.
Drinking plenty of fluids during the treatment phase supports the therapy.
If symptoms worsen or do not improve within 3 days, consult a doctor or qualified healthcare professional. The medicine should not be used for more than 2 weeks in self-medication.
If you take more Canephron than you should
If you have taken a dose of Canephron higher than you should have, inform your doctor.
The doctor will decide on the necessary measures. It is possible that the side effects listed below may be more intense.
No cases of overdose have been reported so far.
If you forget to take Canephron
Do not take a double dose to make up for a missed dose.
If you have any doubts about using this medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
manifest.
Common side effects(may affect up to 1 in 10 people):
Gastrointestinal disorders (nausea, vomiting, diarrhea).
Not known(frequency cannot be estimated from available data)
Hypersensitivity reactions (rash, itching, facial edema).
If you experience any side effects, stop treatment and consult a doctor immediately. The doctor can
assess the severity and decide on any further necessary measures.
Reporting of side effects
If you get any side effects, talk to your doctor or pharmacist. You can also report side effects directly
through the national reporting system http://www.agenziafarmaco.gov.it/content/come-segnalare-una-sospetta-
reazione-avversa .
Reporting side effects helps provide more information on the safety of
this medicine.
5. How to store Canephron
Do not store above 30 °C.
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the package and the container
(blister). The expiry date refers to the last day of that month.
Do not dispose of any medicine in waste water or household waste. Ask your pharmacist how
to eliminate medicines that you no longer use. This will help protect the environment.
6. Package contents and other information
What Canephron contains
The active ingredients are:
1 coated tablet contains:
Centaurium erythraeaRafn s.l., herb (powdered lesser centaury) 36 mg; Levisticum officinale
Koch., root (powdered lovage root) 36 mg; Rosmarinus officinalisL., leaf (powdered
rosemary leaf) 36 mg.
The other ingredients are:
Tablet core: lactose monohydrate; magnesium stearate (Ph.Eur.) [of vegetable origin];
corn starch; povidone K 25; anhydrous colloidal silica
Coating: calcium carbonate; virgin castor oil; iron(III) oxide (E172); dextrin (from
corn starch); atomized glucose syrup; montanglicole wax; povidone K 30; sugar
(sucrose); shellac (without wax); talc; riboflavin (E101); titanium dioxide (E171).
Description of the appearance of Canephron and package contents
The coated tablets are orange in color, round, biconvex with a smooth surface. One
coated tablet has a diameter of 10.2-10.6 mm in packs of 30, 60 and 90 coated tablets.
Not all pack sizes may be marketed.
Marketing authorisation holder and manufacturer
BIONORICA SE
Kerschensteinerstraße 11-15
92318 Neumarkt
Germany
Telephone: +49(0)9181 / 231-90
Fax: +49(0)9181 / 231-265
E-mail: [email protected]
This medicinal product is authorised in the Member States of the European Economic Area with the
following denominations:
Canephron
Canephron Uno
Canephron
France
Germany
Italy

- Kraj rejestracji
- Postać farmaceutycznaCoated tablet
- Wymaga receptyNie
- Producent
- Te treści mają charakter wyłącznie informacyjny i nie zastępują konsultacji lekarskiej.
- Zamienniki KANEPRONPostać farmaceutyczna: Hard capsule, 100 MGSubstancja czynna: pentosan polysulfate sodiumProducent: BENE-ARZNEIMITTEL GMBHWymaga receptyPostać farmaceutyczna: Film-coated tablet, 30 MGSubstancja czynna: dapoxetineWymaga receptyPostać farmaceutyczna: Film-coated tablet, 20 MGSubstancja czynna: tadalafilProducent: ELI LILLY NEDERLAND B.V.Wymaga recepty
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KANEPRON jest produkowany przez BIONORICA SE. Nazwy handlowe i opakowania mogą się różnić w zależności od dystrybutora.
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