Duspatalin retard
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How to use Duspatalin retard
Package Leaflet: Information for the Patient
Warning! Keep the leaflet. Information on the immediate packaging in a foreign language.
Duspatalin Retard (Duspatalin 200 mg)
200 mg, prolonged-release hard capsules
Mebeverine hydrochloride
Duspatalin retard and Duspatalin 200 mg are different trade names for the same medicine.
Read the leaflet carefully before taking the medicine, as it contains important information for the patient.
- Keep this leaflet, so you can read it again if you need to.
- If you have any doubts, consult your doctor or pharmacist.
- This medicine has been prescribed specifically for you. Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same.
- If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor, pharmacist, or nurse. See section 4.
Table of Contents of the Leaflet
- 1. What is Duspatalin retard and what is it used for
- 2. Important information before taking Duspatalin retard
- 3. How to take Duspatalin retard
- 4. Possible side effects
- 5. How to store Duspatalin retard
- 6. Contents of the pack and other information
1. What is Duspatalin retard and what is it used for
What is Duspatalin retard
Duspatalin retard is a prolonged-release hard capsule. Duspatalin retard contains the active substance mebeverine hydrochloride. It belongs to a group of medicines called antispasmodics, which act on the intestine.
The intestine is part of the digestive tract. Its walls are made of muscles. Digested food passes through the intestine. If the muscles of the intestine contract too much, it causes pain. Duspatalin retard acts to relax the muscles and relieve pain.
What is Duspatalin retard used for
Duspatalin retard is used to treat the symptoms of irritable bowel syndrome. The symptoms of irritable bowel syndrome vary from person to person and may include:
- abdominal pain and cramps;
- bloating and gas;
- diarrhea, constipation, or both;
- small, hard stools in the shape of balls or ribbons.
2. Important information before taking Duspatalin retard
When not to take Duspatalin retard
Do not take Duspatalin retard if you are affected by the above statement. If you are unsure, consult your doctor or pharmacist before taking the medicine.
Duspatalin retard and other medicines
It is not expected that Duspatalin retard will affect the action of any other medicine you are taking. However, tell your doctor or pharmacist about all the medicines you are taking now or have taken recently, as well as any medicines you plan to take.
Pregnancy, breastfeeding, and fertility
If you are pregnant, breastfeeding, or think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before taking this medicine.
- Tell your doctor if you are pregnant or think you may be pregnant. Duspatalin retard is not recommended during pregnancy. Your doctor may advise you to stop taking Duspatalin retard or take a different medicine instead of Duspatalin retard.
- Tell your doctor if you are breastfeeding or plan to breastfeed. Duspatalin retard is not recommended for breastfeeding mothers. Your doctor may advise you to stop breastfeeding or take a different medicine while breastfeeding.
Driving and using machines
It is unlikely that Duspatalin retard will affect your ability to drive or use machines.
3. How to take Duspatalin retard
Always take this medicine exactly as your doctor or pharmacist has told you. If you are unsure, consult your doctor or pharmacist.
How to take the medicine
- Duspatalin retard can be taken by adults and children over 10 years of age.
- Swallow the capsules whole with a sufficient amount of water (at least 100 ml). Do not crush or chew the capsules.
- Try to take the capsules at the same time every day. This will help you remember to take them.
Dosage
Adults and children over 10 years of age
- The usual dose is 1 capsule of 200 mg twice a day.
- Take one capsule in the morning and one in the evening.
Do not give Duspatalin retard to children under 10 years of age.
Overdose
If you have taken more than the recommended dose of the medicine, contact your doctor or go to the hospital immediately. Take the packaging and the leaflet with you.
Missed dose
- If you miss a dose, take the next dose at the scheduled time. Miss the forgotten dose.
- Do not take a double dose to make up for the missed dose.
If you have any further doubts about taking the medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
After taking this medicine, the following side effects may occur:
Stop taking Duspatalin retard and contact your doctor immediately if you experience any of the following serious side effects. You may need urgent medical attention:
- Difficulty breathing, swelling of the face, neck, lips, tongue, or throat. This may be a severe allergic reaction (hypersensitivity) to the medicine. If you experience any of these symptoms, stop taking the medicine and contact your doctor immediately.
Other side effects
- Milder allergic reactions (hypersensitivity) to the medicine may occur, such as rash, red, itchy skin rashes.
Reporting side effects
If you experience any side effects, including any side effects not listed in this leaflet, tell your doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety, Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C
02-222 Warsaw
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
By reporting side effects, you can help gather more information on the safety of this medicine.
5. How to store Duspatalin retard
- Keep the medicine out of the sight and reach of children.
- Store in a temperature below 25°C. Store in the original packaging.
- Do not use the medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month stated.
- Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help protect the environment.
6. Contents of the pack and other information
What Duspatalin retard contains
- The active substance is mebeverine hydrochloride. Each capsule contains 200 mg of the active substance.
- The other ingredients are: magnesium stearate, polyacrylate dispersion 30%, hypromellose, talc, methacrylic acid, and ethyl acrylate copolymer (1:1), dispersion 30%, triacetin. Capsule shell: gelatin, titanium dioxide (E 171). Printing ink: shellac (E 904), propylene glycol, ammonia solution, potassium hydroxide, iron oxide black (E 172).
What Duspatalin retard looks like and contents of the pack
The capsules are opaque, white, hard gelatin capsules, size 1, with the imprint "245".
The capsules are packaged in PVC/Al blisters in a cardboard box.
The pack contains 30 or 60 capsules.
For more detailed information, consult the marketing authorization holder or the parallel importer.
Marketing authorization holder in Greece, the country of export:
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart, Dublin 15
Dublin, Ireland
Manufacturer:
Mylan Laboratories SAS
Châtillon sur Chalaronne
France
Parallel importer:
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Repackaged by:
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
License number in Greece, the country of export:
45598/14-09-2009
92996/14/04-11-2016
Parallel import license number: 300/11
Date of leaflet approval: 30.10.2024
[Information about the trademark]
- Country of registration
- Active substance
- Prescription requiredNo
- Marketing authorisation holder (MAH)Viatris Healthcare Limited
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
- Alternatives to Duspatalin retardDosage form: Capsules, 200 mgActive substance: mebeverineManufacturer: APL Swift Services (Malta) Ltd.Prescription requiredDosage form: Tablets, 135 mgActive substance: mebeverineManufacturer: Mylan Laboratoires SASPrescription not requiredDosage form: Capsules, 200 mgActive substance: mebeverineManufacturer: Mylan Laboratoires SASPrescription not required
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