Leaflet: information for the patient
Colpermin 187 mg hard gastro-resistant capsules
Piperine mint essential oil
Read this leaflet carefully before you start taking this medicine, because it contains important information for you.
Follow exactly the administration instructions contained in this leaflet or those given by your doctor or pharmacist.
1. What isColperminand what it is used for
2. What you need to know before starting to takeColpermin
3. How to takeColpermin
4. Possible side effects
5. Storage ofColpermin
6. Contents of the pack and additional information
Colpermin is a plant-based medication containing peppermint essential oil.
Colpermin capsules are indicated for the symptomatic relief of mild gastrointestinal spasms, flatulence, and abdominal pain, particularly in patients with irritable bowel syndrome.
Do not take Colpermin
Colpermin contains oil ofArachis hypogaeaL. (peanut oil)
Do not use this medication if you are allergic to peanuts or soy.
Warnings and precautions
Consult your doctor or pharmacist before starting to take Colpermin.
Inform your doctor or pharmacist if you have heartburn or hiatal hernia (a condition in which a portion of the stomach protrudes into the thoracic cavity). In these cases, the use of this medication may worsen symptoms and treatment may need to be discontinued.
Colpermin capsules should be swallowed whole, without breaking or chewing, and should not be taken with meals. This may cause premature release of peppermint essential oil and cause irritation in the mouth and upper part of the digestive tube (esophagus).
Children
This medication is recommended for use in children from 8 years old and should not be used in children under this age (8 years).
Other medications and Colpermin
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medication.
The simultaneous administration of other medications used to reduce stomach acid (such as H2 receptor antagonists and proton pump inhibitors) or antacids may cause premature release of peppermint essential oil, therefore they should be taken at least 2 hours before or after taking this medication.
Use of Colpermin with food and drinks
The simultaneous consumption of food may cause premature release of peppermint essential oil. Therefore, this medication should be taken at least 30 minutes before or after meals.
Pregnancy and breastfeeding
Lack of sufficient data, this medication is not recommended for use during pregnancy and breastfeeding, or in women of childbearing age who are not using contraceptive methods.
If you are pregnant or breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
Driving and operating machines
The influence of this medication on your ability to drive and operate machines is negligible or insignificant.
Follow exactly the medication administration instructions contained in this leaflet or those indicated by your doctor or pharmacist. If in doubt, consult your doctor or pharmacist again.
Use in adults and elderly people
The recommended dose is 1 capsule 3 times a day. The dose may be increased to a maximum of 2 capsules 3 times a day, if necessary.
Use in adolescents 12 to 17 years old
The recommended dose is 1 capsule 3 times a day.
Use in children 8 to 11 years old
The recommended dose is 1 capsule 2 times a day.
Children under 8 years old
This medication should not be used in children under 8 years old.
Special populations
No data are available on the dosage in cases of renal insufficiency.
The administration route is oral. Colpermin capsules should be swallowed whole with a sufficient amount of liquid to allow the capsule to pass comfortably. Do not chew, crush, or break the capsules.
Be careful when removing the capsules from the blister pack.
Colpermin should be taken at least 30 minutes before or after a meal.
The usual duration of treatment is 1 or 2 weeks. The maximum duration of treatment is 3 months per course of treatment. If symptoms persist, inform your doctor or pharmacist.
If you take more Colpermin than you should
The symptoms of an overdose may be:
In case of overdose, seek advice from your doctor or pharmacist.
If you forgot to take Colpermin
If you forget to take a dose at the right time, simply take the next dose in the usual way. Do not take a double dose to make up for the missed doses.
If you have any further questions about the use of this medication, ask your doctor or pharmacist.
If you interrupt the treatment with Colpermin
No rebound effect is expected.
Take Colpermin for the time your doctor or pharmacist has indicated. If you have any other doubts about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication may produce adverse effects, although not everyone will experience them.
Stop treatment with this medication and seek urgent medical assistance
If you develop severe allergic reactions, including anaphylactic shock (a severe, sudden allergic reaction with symptoms such as a drop in blood pressure and difficulty breathing), which requires immediate medical treatment, mild or intense tremors, movement disorders with balance problems, decreased heart rate, and red skin rash. The frequency of these reactions is unknown.
The following adverse effects have been described with the approximate frequencies indicated:
Frequent:may affect up to 1 in 10 people
Headache, heartburn (acid reflux, burning), anal discomfort, abnormal-smelling stools, dry mouth, feeling of unease, and stomach discomfort and nausea, and vomiting.
Rare:may affect up to 1 in 100 people
Allergic hypersensitivity, skin itching, gastric hemorrhage, and blurred vision.
Unknown frequency: cannot be estimated from available data
Pain around the anus, diarrhea, difficulty and pain urinating, inflammation of the head of the penis (glans), and abnormal-smelling urine.
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through the Spanish System for Pharmacovigilance of Medicinal Products for Human Use:https://www.notificaram.es. By reporting adverse effects, you can contribute to providing more information on the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the box and on the blister pack after CAD. The expiration date is the last day of the month indicated.
Do not store above 25°C. Store in the original packaging to protect it from light and moisture.
Medicines should not be disposed of through drains. Ask your pharmacist how to dispose of the containers and medications that you no longer need. This will help protect the environment.
Composition of Colpermin
Content of the capsule:
Capsule shell:
Appearance of the product and contents of the package
The body of the gastro-resistant hard capsule Colpermin is opaque, light blue; the cap is opaque, blue, with a dark blue band between the body and the cap.
Colpermin capsules are packaged in blister strips of 10 capsules and each box may contain 30 or 100 hard gastro-resistant capsules (3 or 10 blister strips). Some package sizes may only be marketed.
Marketing Authorization Holder
Tillotts Pharma GmbH
Warmbacher Strasse 80
79618 Rheinfelden, Germany
Responsible for manufacturing
Tillotts Pharma GmbH
Warmbacher Strasse 80
79618 Rheinfelden,
Germany
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
TILLOTTS PHARMA SPAIN, S.L.U.
Gran Via de les Corts Catalanes 680,1st 1st
08010 Barcelona
Spain
This medicinal product is authorized in the Member States of the EEA with the following names:
Belgium, Denmark, Finland, France, Germany, Iceland, Luxembourg, Netherlands, Norway, Portugal, Spain, Sweden: Colpermin
Austria: Pfefferminzöl Tillotts 187 mg gastro-resistant hard capsules
Last review date of this leaflet:September 2022
Other sources of information
The detailed and updated information on this medicinal product is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es/
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