


Ask a doctor about a prescription for MUCOSAN RETARD 75 mg PROLONGED-RELEASE CAPSULES
Leaflet:information for the user
Mucosan Retard 75 mg prolonged-release capsules
Ambroxol hydrochloride
Read the entire leaflet carefully before starting to takethis medication, as it contains important information for you.
Follow the administration instructions of the medication contained in this leaflet or as indicated by your doctor or pharmacist.
Contents of the leaflet
Ambroxol, the active ingredient of this medication, belongs to a group of medications called mucolytics, which act by decreasing the viscosity of mucus, fluidizing it, and facilitating its elimination.
This medication is indicated to facilitate the elimination of excess mucus and phlegm in colds and flu, for adults.
You should consult a doctor if it worsens or does not improve after 5 days.
Do not take Mucosan
Warnings and precautions
Consult your doctor or pharmacist before starting to take Mucosan.
If you have problems related to kidney or liver function, consult your doctor before using this medication.
There have been reports of severe skin reactions associated with the administration of ambroxol hydrochloride. If you experience a skin rash (including lesions of the mucous membranes, such as the mouth, throat, nose, eyes, and genitals), stop using Mucosan and consult your doctor immediately.
Children
It is not indicated for use in children.
Other medications and Mucosan
Use of Mucosan with other medications
Inform your doctor or pharmacist if you are using, have recently used, or may need to use any other medication.
TakingMucosan with food and drinks
Mucosan can be taken with or without food.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or plan to become pregnant, consult your doctor or pharmacist before using this medication.
No harmful effects have been observed during pregnancy. However, the usual precautions regarding the use of medications during pregnancy should be followed. The use of Mucosan is not recommended, especially during the first trimester of pregnancy.
Animal studies have shown that the active ingredient of this medication, ambroxol hydrochloride, passes into breast milk, and although no harmful effects are expected in the breastfed infant, its use should be avoided during breastfeeding.
Studies in animals do not indicate direct or indirect harmful effects on fertility.
No clinical data are available on fertility for ambroxol hydrochloride.
Driving and using machines
No effects have been observed on the ability to drive and use machinery.
Follow the administration instructions of the medication contained in this leaflet or as indicated by your doctor or pharmacist. In case of doubt, ask your doctor or pharmacist.
The recommended dose is:
Adults: 1 capsule (75 mg of ambroxol hydrochloride) daily.
How to take:
Mucosan is taken orally.
The capsule should be swallowed whole with a little liquid, without opening and without chewing. It is recommended to drink a glass of water after administration and plenty of liquid during the day.
In exceptional cases, remnants of the excipient particles may be found in the feces, which no longer contain the active ingredient and are therefore of no importance.
You should consult a doctor if it worsens or does not improve after 5 days of treatment.
If you take more Mucosan than you should
If you have taken more Mucosan than you should, you may experience nausea or any other side effect described in section 4 Possible side effects. In case of overdose or accidental ingestion, consult your doctor or pharmacist, or call the Toxicology Information Service, phone 915 620 420, indicating the medication and the amount ingested.
In case of massive accidental administration, symptomatic treatment is recommended.
Like all medications, this medication can cause side effects, although not everyone experiences them.
The following side effects may occur:
Reporting of side effects:
If you experience any side effects, consult your doctor or pharmacist, even if they are possible side effects not listed in this leaflet. You can also report them directly through the Spanish Medicines Monitoring System: http://www.notificaram.es. By reporting side 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 store above 30°C.
Do not use this medication after the expiration date shown on the packaging after CAD. The expiration date is the last day of the month indicated.
Medications should not be disposed of through wastewater or household waste. Deposit the packaging and medications you no longer need at the SIGRE point in the pharmacy. Ask your pharmacist how to dispose of the packaging and medications you no longer need. This will help protect the environment.
Composition of Mucosan
Appearance of the product and package contents
Mucosan is available in boxes of 10 or 30 hard prolonged-release capsules.
They are hard gelatin capsules, elongated, with the upper part red and the lower part orange.
Marketing authorization holder
Opella Healthcare Spain, S.L.
C/ Rosselló i Porcel, 21
08016 – Barcelona
Spain
Sanofi Group
Manufacturer:
Delpharm Reims, S.A.S.
10 Rue Colonel Charbonneaux
51100 Reims
France
Detailed information about this medication is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es/.
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for MUCOSAN RETARD 75 mg PROLONGED-RELEASE CAPSULES – subject to medical assessment and local rules.