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MUCOSOLVAN 30mg x 20 tabl

Code :

8571

Brand:

Manufacturer :

SANOFI-AVENTIS

лекарствена информация
5.06 € / 9.90 лв
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MUCOSOLVAN 30mg x 20 tabl

MUCOSOLVAN tab. 30 mg. * 20

Leaflet: information for the user
MUCOSOLVAN 30 mg tablets
Ambroxol hydrochloride
MUCOSOLVAN 30 mg tablets
Ambroxol hydrochloride
Read all of this leaflet carefully before you start taking this medicine because 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.
Keep this leaflet. You may need to read it again.
If you need further information or advice, ask your doctor or pharmacist.
If you get any side effects, please tell your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.
If you do not feel better after 4-5 days or your condition worsens, you should seek medical attention.

What this leaflet contains
1) What is MUCOSOLVAN and what is it used for?
2) What you need to know before taking MUCOSOLVAN
3) How to take MUCOSOLVAN
4) Possible side effects
5) How to store MUCOSOLVAN
6) Package contents and additional information

1. What MUCOSOLVAN is and what it is used for
Ambroxol, the active ingredient of MUCOSOLVAN, promotes mucus secretion in the respiratory tract, facilitates expectoration and relieves coughing.
MUCOSOLVAN is used for secretolytic treatment of acute and chronic diseases of the bronchi and lungs, occurring with abnormal bronchial secretion and impaired transport of secretions (phlegm).

2. What you need to know before you take MUCOSOLVAN
Do not take MUCOSOLVAN if:

you are allergic to ambroxol hydrochloride or any of the other ingredients of this medicine (listed in section 6);
you have rare congenital diseases that may lead to incompatibilities with any of the ingredients of this medicine (see also “MUCOSOLVAN contains lactose”).

Warnings and precautions
Talk to your doctor or pharmacist before taking MUCOSOLVAN:

If you have impaired kidney function or severely impaired liver function.

There have been reports of severe skin reactions associated with the use of ambroxol hydrochloride. If you develop a skin rash (including lesions of the mucous membranes, e.g. mouth, throat, nose, eyes, genitals), stop using MUCOSOLVAN and call your doctor immediately.

Other medicines and MUCOSOLVAN
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
The use of ambroxol hydrochloride with cough suppressant medicinal products is not recommended.
No clinically significant adverse interactions with other medicinal products have been reported.

Pregnancy, breastfeeding and fertility
If you are pregnant or breast-feeding, think you may be pregnant or are planning to become pregnant, ask your doctor or pharmacist for advice before using this medicine.
The use of MUCOSOLVAN is not recommended during pregnancy, especially during the first three months of pregnancy.
The use of MUCOSOLVAN is not recommended in breastfeeding women, as ambroxol hydrochloride passes into breast milk.

Driving and using machines
There is no evidence from post-marketing data regarding an effect on the ability to drive and use machines. No studies have been performed on the effects on the ability to drive and use machines.

MUCOSOLVAN contains lactose
Talk to your doctor before using this medicine if you know that you have an intolerance to some sugars.
One tablet contains 171 mg lactose, which corresponds to 684 mg lactose in the maximum recommended daily dose (120 mg). It is not recommended to use this medicine if you have galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption.

3. How to take MUCOSOLVAN
Always take this medicine exactly as described in this leaflet. If you are not sure, ask your doctor or pharmacist.

The recommended dose is:

Adults and children over 12 years of age: 1 tablet 3 times daily.

The therapeutic effect can be enhanced by taking 2 tablets twice a day.
This dosage is suitable for the treatment of acute respiratory tract diseases and for initial therapy of chronic conditions for up to 14 days.
If in the case of an acute respiratory illness, your symptoms do not improve after 4-5 days of treatment with MUCOSOLVAN, you should seek medical attention.
The tablets should be taken with liquid.
You can take MUCOSOLVAN with or without food.

If you take more MUCOSOLVAN than you should
If you have taken more than the required dose of MUCOSOLVAN, contact your doctor or pharmacist for advice. No specific symptoms of overdose in humans have been reported so far. The symptoms observed in reports of accidental overdose or improper use correspond to the known adverse reactions when using MUCOSOLVAN in recommended doses and may require symptomatic treatment.

If you forget to take MUCOSOLVAN
If you forget to take a dose, take it as soon as you remember. Do not take a double dose to make up for a forgotten dose. Take the next dose as usual.

If you stop taking MUCOSOLVAN
MUCOSOLVAN should be taken only when needed, and its use should be discontinued after symptoms subside.

If you have any further questions on the use of this medicine, ask your doctor or pharmacist.

4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.

Common (may affect up to 1 in 10 people):

nausea.

Uncommon (may affect up to 1 in 100 people):

diarrhea;
vomiting;
digestive disorders;
stomach pain.

Rare (may affect up to 1 in 1,000 people):

hypersensitivity reactions;
rash;
urticaria (hives).

Not known (frequency cannot be estimated from the available data):

anaphylactic reactions, including anaphylactic shock, angioedema (rapidly developing swelling of the skin, subcutaneous tissue, mucous membranes or submucosal layer) and pruritus;
severe skin adverse reactions (including erythema multiforme, Stevens-Johnson syndrome/toxic epidermal necrolysis and acute generalized exanthematous pustulosis).

Reporting side effects
If you get any side effects, please tell your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly by:

Executive Agency for Medicines,
8 Damyan Gruev Street,
1303 Sofia,
Tel.: +3592 8903417
website: www.bda.bg.

By reporting side effects, you can help provide more information about the safety of this medicine.

5. How to store MUCOSOLVAN
Keep out of the reach of children.
Do not use MUCOSOLVAN after the expiry date which is stated on the carton after "EXP".
The expiry date refers to the last day of that month.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to dispose of medicines you no longer use. This will help to protect the environment.

6. Contents of the pack and other information
What MUCOSOLVAN contains
The active substance is: ambroxol hydrochloride (1 tablet contains 30 mg ambroxol hydrochloride).
The other ingredients are: Lactose monohydrate, dry corn starch, colloidal anhydrous silica, magnesium stearate.

What MUCOSOLVAN looks like and what the pack contains
MUCOSOLVAN tablets are round, white, smooth on both sides, with beveled edges. On one side they are engraved with “67C” below and above the score, and on the other side the company symbol is depicted.
MUCOSOLVAN tablets are available in PVC/aluminum blister packs placed in cardboard boxes.
The package contains 20 tablets.

Marketing Authorisation Holder:
SANOFI BULGARIA EOOD, Bulgaria.

Manufacturer:
Delpharm Reims, France;
Boehringer Ingelheim Ellas AE, Greece

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MUCOSOLVAN 30mg x 20 tabl