Loperamide Hydrochloride
This medicine should always be taken exactly as described in the package leaflet or as directed by a doctor, pharmacist, or nurse.
Lopacut contains loperamide hydrochloride. It belongs to a group of anti-diarrheal medicines.
Lopacut is used:
Lopacut makes the stool harder and reduces the frequency of bowel movements.
A doctor may also prescribe this medicine for other conditions.
If there is no improvement or the patient feels worse after 2 days, they should consult their doctor.
Lopacut is not indicated for use in children under 12 years of age.
The patient should inform their doctor or pharmacist about all medicines they are currently taking or have recently taken, as well as any medicines they plan to take.
Some medicines may interact with Lopacut, and Lopacut may interact with other medicines if taken at the same time. Examples of such medicines include:
If the patient is taking any of the above medicines, they should consult their doctor before taking Lopacut.
If the patient is pregnant or breastfeeding, thinks they may be pregnant, or plans to have a child, they should consult their doctor or pharmacist before taking this medicine.
There is insufficient data on the use of loperamide in pregnancy, so medical consultation is necessary before taking the medicine if the patient is pregnant.
Loperamide passes into breast milk, so it is not recommended for use in breastfeeding mothers. The patient should consult their doctor before taking Lopacut if they are breastfeeding.
While taking Lopacut, the patient may experience drowsiness, dizziness, and sleepiness.
The patient should assess whether they can drive or perform tasks that require increased concentration. One of the factors that may affect the ability to drive or use machines is the effect or effects of the medicines being taken. The description of the effect and side effects of the medicine can be found in other sections of this leaflet. The patient should read the entire leaflet to know how to proceed. If the patient thinks the medicine affects their concentration, they should not drive or use machines.
If the patient has any doubts, they should consult their doctor or pharmacist.
This medicine should always be taken exactly as described in the package leaflet or as directed by a doctor or pharmacist. If in doubt, the patient should consult their doctor or pharmacist.
Initially 2 tablets, then 1 tablet after each loose stool, but not sooner than 2-3 hours after the initial dose. The maximum daily dose should not exceed 6 tablets in adults (maximum daily dose is 12 mg) and 4 tablets in adolescents (maximum dose is 8 mg). Lopacut should not be taken for more than 2 days without consulting a doctor.
If the patient has taken too much Lopacut, they should immediately consult a doctor or go to the hospital. The following symptoms may occur: rapid heart rate, irregular heart rhythm, changes in heart rhythm (these symptoms can have severe, life-threatening consequences), muscle stiffness, uncoordinated movements, drowsiness, difficulty urinating, and shallow breathing.
In children, the reaction to taking too much Lopacut is stronger than in adults. If a child takes too much Lopacut or experiences any of the above symptoms, they should immediately consult a doctor.
A double dose should not be taken to make up for a missed dose.
If the patient has any further doubts about taking this medicine, they should consult their doctor or pharmacist.
Like all medicines, Lopacut can cause side effects, although not everybody gets them.
The patient should stop taking Lopacut and consult their doctor immediatelyif they experience:
The following list of side effects is presented according to their frequency of occurrence.
Common (may affect up to 1 in 10 people)
Uncommon (may affect up to 1 in 100 people)
Rare (may affect up to 1 in 1,000 people)
Not known (frequency cannot be estimated from the available data)
If the patient experiences any side effects, including those not listed in the leaflet, they should inform their doctor, pharmacist, or nurse. Side effects can be reported directly to the Department of Drug Safety Monitoring 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.
Reporting side effects will help gather more information on the safety of the medicine.
The medicine should be stored out of sight and reach of children.
There are no special precautions for storing the medicine.
The medicine should not be taken after the expiry date stated on the blister and carton after EXP.
The expiry date refers to the last day of the month.
The medicine should not be taken if the tablets are damaged or have an unusual appearance.
Medicines should not be disposed of via wastewater or household waste. The patient should ask their pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
The active substance of Lopacut is loperamide hydrochloride, 2 mg per tablet.
The other ingredients of the medicine are:
Tablet core: microcrystalline cellulose, pregelatinized starch, sodium croscarmellose, colloidal anhydrous silica, and magnesium stearate.
Tablet coating: Opadry OY-S-28703: polydextrose, hypromellose, titanium dioxide (E 171), and macrogol 4000.
Appearance:
The tablets are white, round, and convex with the logo “6”. Diameter 8 mm.
Pack size:
8 and 10 coated tablets in a blister pack (PVC/Aluminum).
Vitabalans Oy
Varastokatu 8
FI-13500 Hämeenlinna
FINLAND
Phone: +358 (3) 615600
Fax: +358 (3) 6183130
Lopacut (CZ, DE, DK, EE, FI, HU, LT, LV, NO, PL, SE, SI, SK)
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