Lactulosum
This medicine should always be used exactly as described in this package leaflet for the patient or as directed by a doctor or pharmacist.
Keep this leaflet, you may need to read it again.
If you need advice or additional information, consult a pharmacist.
If you experience any side effects, including any possible side effects not listed in this leaflet, tell your doctor or pharmacist.
If after a few days there is no improvement or you feel worse, consult a doctor.
Lactulosum Polfarmex contains lactulose - a synthetic disaccharide that is not absorbed in the gastrointestinal tract. It inhibits putrefaction processes and the production of ammonia, and by lowering the pH of the colon environment, it reduces the absorption of ammonium salts, which are excreted in the stool.
As a result of osmosis, it leads to an increase in the volume of intestinal contents, stimulates intestinal peristalsis, and has a laxative effect.
Lactulosum Polfarmex is indicated for use:
If after a few days there is no improvement or the patient feels worse, consult a doctor.
Before starting to use Lactulosum Polfarmex, discuss it with your doctor or pharmacist.
In the case of long-term use, periodic monitoring of electrolyte levels in serum (potassium, chlorides) is recommended, especially in elderly patients.
Talk to your doctor, even if the above warnings refer to situations that have occurred in the past.
Tell your doctor or pharmacist about all medicines you are currently taking or have recently taken, as well as any medicines you plan to take.
Since lactulose lowers the pH in the colon, medicines whose release depends on pH may be inactivated.
If you are pregnant or breastfeeding, think you may be pregnant, or plan to have a child, consult your doctor or pharmacist before using this medicine.
The medicine may be used during pregnancy and breastfeeding only if necessary.
The medicine does not affect the ability to drive and use machines.
Ethanol
Lactulosum Polfarmex contains a mango aroma, liquid, whose component is ethanol (alcohol). This medicine contains 0.00963 g of alcohol (ethanol) in each 15 ml of syrup.
Laxative
Fructose
Lactulosum Polfarmex contains 0.075 g of fructose in each 15 ml of syrup.
Lactulosum Polfarmex contains 0.9 g of fructose in the maximum daily dose.
Fructose contained in the medicine may have a harmful effect on teeth.
Lactose
If the patient has previously been diagnosed with intolerance to some sugars, the patient should consult a doctor before taking the medicine. The medicine contains 0.75 g of lactose in 15 ml.
Lactulosum Polfarmex contains 9 g of lactose in the maximum daily dose. This should be taken into account in patients with diabetes.
Galactose
If the patient has previously been diagnosed with intolerance to some sugars, the patient should consult a doctor before taking the medicine.
The medicine contains 1.125 g of galactose in each 15 ml of syrup.
Lactulosum Polfarmex contains 13.5 g of galactose in the maximum daily dose.
Sulfites
The medicine may rarely cause severe hypersensitivity reactions and bronchospasm.
This medicine should always be taken as directed by a doctor or pharmacist. In case of doubt, consult a doctor or pharmacist.
Laxative:
orally, usually 30-45 ml (2-3 tablespoons) before breakfast or 15 ml (1 tablespoon) 3 times a day before meals. After achieving the effect - 15 ml of syrup on an empty stomach.
In liver failure:
orally, 100-180 ml per day in 4-6 doses.
Laxative:
initially, infants - 2.5 ml; children up to 3 years - 5 ml; over 3 years - 15 ml per day. Then the dose of the medicine can be gradually increased every 3 days until normal bowel movements are achieved. If abdominal bloating occurs, the dose should be reduced to a level tolerated by the child. It is recommended to administer the syrup with lactulose after diluting it with water or fruit juice.
There are no data on overdose of the medicine.
Do not take a double dose to make up for a missed dose.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
In the initial period of use, abdominal pain may occur. Sometimes, after using large doses, nausea, diarrhea, and bloating are observed.
Frequency not known (frequency cannot be estimated from the available data): allergic reactions, rash, itching, urticaria.
If you experience any side effects, including any possible side effects not listed in this leaflet, tell your doctor or pharmacist.
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
Phone: +48 22 49 21 301
Fax: +48 22 49 21 309
Website: https://smz.ezdrowie.gov.pl
Side effects can also be reported to the marketing authorization holder.
By reporting side effects, you can help provide more information on the safety of this medicine.
Keep the medicine out of the sight and reach of children.
Store in a temperature below 25°C.
Do not freeze.
Shelf life after opening the bottle: 3 months.
Do not use this medicine after the expiry date stated on the carton and bottle after the words "EXP". The expiry date refers to the last day of the month.
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.
The active substance of the medicine is lactulose. 15 ml of syrup contains 7.5 g of lactulose.
The other ingredients are: citric acid monohydrate, mango aroma, liquid (contains, among others, ethanol and butylhydroxyanisole), purified water.
The bottle contains 150 ml of syrup.
Polfarmex S.A.
ul. Józefów 9
99-300 Kutno
Poland (Poland)
Phone: 24 357 44 44
Fax: 24 357 45 45
e-mail: polfarmex@polfarmex.pl
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