Simeticone
Espumisan and Espumisan Emulsion are different trade names for the same drug.
This medicine should always be taken exactly as described in the patient leaflet or as advised by a doctor or pharmacist.
Espumisan contains the active substance simeticone, which is used in gastrointestinal disorders, reducing foaming of the gastrointestinal contents and as an auxiliary in diagnostic tests.
It can be used in all age groups.
The active substance of the drug, simeticone, causes the bursting of gas bubbles contained in food masses and in the mucus of the gastrointestinal tract. This allows the gases released in this way to be absorbed through the intestinal wall or removed from the gastrointestinal tract as a result of intestinal peristalsis.
Espumisan is used:
If there is no improvement or the patient feels worse, they should consult their doctor.
Before starting to take Espumisan, discuss it with your doctor or pharmacist.
Espumisan should not be taken by infants under 1 month of age.
In case of new and/or persistent gastrointestinal symptoms, consult a doctor to determine the cause of the symptoms and possibly diagnose the underlying disease.
No interactions with other medicines are known.
While taking Espumisan, avoid consuming carbonated beverages. Espumisan can be taken directly before, during, or after a meal, and if necessary, also before bedtime.
Infants
Espumisan should be added to a bottle with milk and/or food or given on a spoon before or after breastfeeding.
Before taking any medicine, consult a doctor or pharmacist.
There are no restrictions on the use of Espumisan in pregnant and breastfeeding women.
No special precautions are required.
The medicine contains less than 1 mmol (23 mg) of sodium per ml, which means the medicine is considered "sodium-free".
This medicine should always be taken in accordance with the leaflet or as advised by a doctor. In case of doubt, consult a doctor or pharmacist.
The dose can be measured using a dropper.
More detailed information on using the dropper can be found in the "Method of administration" section.
The recommended dose is:
Symptomatic treatment of gastrointestinal disorders associated with excessive gas accumulation, such as, for example: bloating and infantile colic in infants over 1 month of age:
Age group | Dose |
Infants over 1 month of age | 1 ml - 2 ml (25 - 50 drops), which corresponds to 40 - 80 mg of simeticone, per day in 2 (2 times a day, 13 - 25 drops) to 4 (4 times a day, 6 - 13 drops) divided doses; the total daily dose should not exceed 80 mg; Espumisan should be added to a bottle with milk or given on a spoon before or after breastfeeding. |
The total daily dose should not exceed 80 mg; Espumisan should be added to a bottle with milk or given on a spoon before or after breastfeeding. | |
Children from 1 to 6 years | 1 ml (25 drops), which corresponds to 40 mg of simeticone, 3 to 5 times a day. |
Children from 6 to 14 years | 1 ml (25 drops) - 2 ml (50 drops), which corresponds to 40 - 80 mg of simeticone, 3 to 5 times a day. |
Adolescents and adults | 2 ml (50 drops), which corresponds to 80 mg of simeticone, 3 to 5 times a day. |
Note: Espumisan can also be given to patients post-operatively.
Espumisan can be taken during or after a meal, and if necessary, also before bedtime.
Treatment should be continued until the symptoms disappear. If necessary, Espumisan can be taken for a longer period.
In preparation for abdominal cavity tests:
As an antidote in detergent (surface-active substance) poisoning:
Dosage in adults
Depending on the severity of the poisoning, 10 to 20 ml (approximately 1/3 to 2/3 of the contents of the 30 ml bottle) of Espumisan are used.
Dosage in children
Depending on the severity of the poisoning, 2.5 to 10 ml (65 drops to approximately 1/3 of the contents of the 30 ml bottle) of Espumisan are used.
Note: If Espumisan is used as a first-aid measure after ingesting detergent, you should immediatelyconsult a doctor!
In case of any doubts or feelings that the effect of Espumisan is too strong or too weak, consult a doctor or pharmacist.
Shake before use.
Dosage using a dropper:
To measure the correct number of drops, hold the bottle vertically, with the opening facing down.
25 drops (1 ml of oral drops, emulsion) contain 40 mg of simeticone.
No cases of overdose have been reported so far.
Simeticone is a chemically and physiologically completely inert substance that is not absorbed from the gastrointestinal tract, so the possibility of poisoning can be practically ruled out. Even large doses of Espumisan are well tolerated.
In such a case, the missed dose can be taken at any time.
In such a case, the symptoms may return.
In case of any further doubts related to the use of this medicine, consult a doctor or pharmacist.
No side effects related to the use of Espumisan have been reported so far.
If any side effects occur, 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 Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products
Al. Jerozolimskie 181C, 02-222 Warsaw
tel.: +48 22 49 21 301
fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
By reporting side effects, more information can be collected on the safety of the use of the medicine.
Store in a place out of sight and reach of children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the specified month.
Do not store above 30°C.
After opening the packaging, Espumisan remains stable for 4 weeks.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substance of Espumisan is simeticone.
1 ml (25 drops) of oral drops, emulsion contains 40 mg of simeticone.
The other ingredients of the medicine are: macrogol 1500 stearate, glycerol monostearate, sorbic acid, hydroxypropyl cellulose, sodium cyclamate, sodium saccharin, purified water.
Milky white to yellowish emulsion, slightly viscous. Oral drops, emulsion.
Packaging: orange glass bottle with a screw cap and dropper, in a cardboard box, containing 30 ml of oral drops, emulsion.
To obtain more detailed information, consult the marketing authorization holder or parallel importer.
Berlin-Chemie AG
Glienicker Weg 125
12489 Berlin
Germany
Berlin-Chemie AG
Glienicker Weg 125
12489 Berlin
Germany
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
CEFEA Sp. z o.o. Sp. komandytowa
ul. Działkowa 56
02-234 Warsaw
Pharma Innovations Sp. z o.o.
ul. Jagiellońska 76
03-301 Warsaw
SHIRAZ PRODUCTIONS Sp. z o.o.
ul. Tymiankowa 24/28
95-054 Ksawerów
CANPOLAND SPÓŁKA AKCYJNA
ul. Beskidzka 190
91-610 Łódź
Marketing authorization number in Germany, the country of export: 36478.00.00
Parallel import authorization number: 425/22
Date of leaflet approval: 09.12.2022
[Information about the trademark]
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