
Ask a doctor about a prescription for CLEBORIL 500 micrograms tablets
Package Leaflet: Information for the User
Cleboril 500 micrograms tablets
clebopride
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack:
Cleboril contains clebopride and belongs to a group of medicines called prokinetics, which regulate gastrointestinal motility.
Cleboril is indicated for:
Do not take Cleboril:
Warnings and precautions
Consult your doctor or pharmacist before taking Cleboril:
Children and adolescents
In children, adolescents, and elderly people, the use of higher doses than recommended may increase the possibility of extrapyramidal reactions (alterations in muscle tone, posture, and appearance of involuntary movements).
In newborns, cases of acquired methemoglobinemia (a blood disorder that affects its ability to transport oxygen) due to orthopramides (the group of medicines to which Cleboril belongs) have been described.
Other medicines and Cleboril
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines.
It is especially important that you inform your doctor if you are taking any of the following medicines:
Taking Cleboril with alcohol
Avoid taking alcohol while being treated with Cleboril, as it may potentiate its sedative effects.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
There is not enough information on the use of this medicine in pregnant women or whether it is excreted in breast milk. For this reason, as a precautionary measure, it is preferable to avoid its use during pregnancy, especially during the first three months, and during breastfeeding.
Driving and using machines
During treatment with Cleboril, you should avoid situations that require a special state of alertness, such as driving vehicles or handling dangerous machinery.
Cleboril contains lactose and sodium
This medicine contains lactose. If your doctor has told you that you have an intolerance to some sugars, consult them before taking this medicine.
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; it is essentially "sodium-free".
Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
The recommended dose in adults is 1 tablet (500 micrograms of clebopride) 3 times a day, before each meal.
The recommended dose in adolescents (from 12 years to less than 18 years) is half a tablet (250 micrograms of clebopride) 3 times a day, before each meal.
This medicine is for oral administration.
The tablet can be divided into equal doses.
Take your dose with the help of some liquid, preferably water.
If you take more Cleboril than you should
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately, or call the Toxicology Information Service, phone 91 5620420, indicating the medicine and the amount taken.
In case of overdose, drowsiness, disorientation, and extrapyramidal reactions (alterations in muscle tone, posture, and appearance of involuntary movements) may appear, which usually disappear when treatment is discontinued.
If symptoms persist, stomach lavage and symptomatic medication will be performed. Extrapyramidal reactions are controlled with the administration of appropriate medicines.
If you forget to take Cleboril
Do not take a double dose to make up for forgotten doses.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
The following side effects have been reported in clinical trials and during post-marketing experience:
Rare side effects (may affect up to 1 in 1,000 people)
Very rare side effects (may affect up to 1 in 10,000 people)
These side effects have been reported after prolonged treatments
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist, even if it is possible side effects not listed in this leaflet. You can also report side effects directly through the Spanish Pharmacovigilance System for Human Use Medicines: https://www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
Keep this medicine out of the sight and reach of children.
No special storage conditions are required.
Do not use this medicine after the expiry date which is stated on the carton after EXP. The expiry date is the last day of the month shown.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of Cleboril
Appearance and packaging of the product
Cleboril is presented in the form of white, flat, circular, and scored tablets, in PVC/Aluminum blister packs, containing 30 or 60 tablets.
Marketing authorization holder and manufacturer
Marketing authorization holder
Almirall, S.A.
General Mitre, 151
08022 – Barcelona
Manufacturer
Industrias Farmacéuticas Almirall, S.A.
Ctra. de Martorell, 41-61
08740 Sant Andreu de la Barca - Barcelona (Spain)
Date of last revision of this leaflet:November 2023
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es
The average price of CLEBORIL 500 micrograms tablets in October, 2025 is around 3.33 EUR. Prices may vary depending on the region, pharmacy, and whether a prescription is required. Always check with a local pharmacy or online source for the most accurate information.
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