40 mg/ml, oral drops, emulsion
Simeticone
Espumisan and Espumisan L 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 to treat gastrointestinal disorders, reducing foaming of the gastrointestinal tract contents and as an auxiliary agent in diagnostic tests.
It can be used in all age groups.
The active substance of the drug, simeticone, causes the rupture 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, the patient should discuss it with their doctor or pharmacist.
Espumisan should not be taken by infants under 1 month of age.
In the event of new and/or persistent gastrointestinal symptoms, the patient should consult their doctor to determine the cause of the symptoms and possibly diagnose the underlying disease.
No interactions with other medicines are known.
During treatment with Espumisan, the patient should 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 the bottle with milk or food, or given on a spoon before or after breastfeeding.
Before taking any medicine, the patient should consult their 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 it is considered "sodium-free".
This medicine should always be taken as described in the leaflet or as advised by a doctor. In case of doubts, the patient should consult their 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 bloating and infantile colic in infants over 1 month of age:
Age group | Dose |
Infants over 1 month of age | 1-2 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 the bottle with milk or given on a spoon before or after breastfeeding. |
Children from 1 to 6 years of age | 1 ml (25 drops), which corresponds to 40 mg of simeticone, 3 to 5 times a day. |
Children from 6 to 14 years of age | 1-2 ml (25-50 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 in the postoperative period.
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.
For preparation for diagnostic tests of the abdominal cavity:
2 ml (50 drops) of Espumisan 3 times a day on the day before the examination and 2 ml (50 drops) of Espumisan in the morning on the day of the examination, on an empty stomach.
For double-contrast imaging, 4 to 8 ml (100 to 200 drops) of Espumisan are used per 1 liter of contrast fluid.
Prior to endoscopy, 4-8 ml (corresponding to 100-200 drops).
If necessary, a few ml of the emulsion can be instilled through the instrumental channel of the endoscope during the examination to reduce foaming of the gastrointestinal tract contents.
As an antidote in detergent (surface-active substance) poisonings:
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 ingestion of a detergent, the patient should immediatelyconsult a doctor!
In case of any doubts or feelings that the effect of Espumisan is too strong or too weak, the patient should consult their doctor or pharmacist.
Shake before use.
Dosing using a dropper:
To measure the correct number of drops, the bottle should be held 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 excluded. 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 recur.
In case of any further doubts related to the use of this medicine, the patient should consult their 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, the patient should inform their 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
Reporting side effects can help gather more information on the safety of the medicine.
Store in a place invisible and inaccessible to children.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the given month.
No special storage precautions are required.
After the first opening of the packaging, the medicine retains its potency for 6 months.
Medicines should not be disposed of via wastewater or household waste containers. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
Milky white to yellowish emulsion, slightly viscous. Oral drops, emulsion.
Packaging: 30 ml glass bottle with a PP cap and a PE dropper, in a cardboard box, containing 30 ml of oral drops, emulsion.
For more detailed information, the patient should contact the marketing authorization holder or the parallel importer:
Berlin-Chemie AG
(Menarini Group)
Glienicker Weg 125
D-12489 Berlin, Germany
Berlin-Chemie AG
(Menarini Group)
Glienicker Weg 125
D-12489 Berlin, Germany
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Delfarma Sp. z o.o.
ul. Św. Teresy od Dzieciątka Jezus 111
91-222 Łódź
Marketing authorization number in Latvia, the country of export: 00-0568
[Information about the trademark]
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