Fortrans
Ask a doctor about a prescription for Fortrans
How to use Fortrans
LEAFLET INCLUDED IN THE PACKAGING: INFORMATION FOR THE PATIENT
Warning! Keep the leaflet, the information on the immediate packaging is in a foreign language!
Fortrans
powder for oral solution, in a sachet
macrogol 4000, anhydrous sodium sulfate, sodium bicarbonate, sodium chloride, potassium chloride
You should carefully read the contents of the leaflet before using the medicine, as it contains important information for the patient.
- You should keep this leaflet, so that you can read it again if you need to.
- In case of any doubts, you should consult a doctor or pharmacist.
- This medicine has been prescribed specifically for you. Do not pass it on to others. The medicine may harm another person, even if their symptoms are the same.
- If the patient experiences any side effects, including any side effects not listed in this leaflet, they should tell their doctor, pharmacist, or nurse. See section 4.
Table of contents of the leaflet:
- 1. What is Fortrans and what is it used for
- 2. Important information before using Fortrans
- 3. How to use Fortrans
- 4. Possible side effects
- 5. How to store Fortrans
- 6. Contents of the packaging and other information
1. What is Fortrans and what is it used for
Fortrans is used in adults to cleanse the intestine before an examination or surgical procedure in the intestine.
Fortrans is a laxative with an osmotic effect containing macrogol with a high molecular weight (polyethylene glycol, PEG) and additional salts. Fortrans increases the amount of fluid in the intestine, causing more frequent bowel movements with a watery stool, which ultimately leads to the cleansing of the intestines.
2. Important information before using Fortrans
When not to use Fortrans:
- if the patient is allergic to macrogol (PEG), anhydrous sodium sulfate, sodium bicarbonate, sodium chloride, potassium chloride, or any of the other ingredients of this medicine (listed in section 6);
- if the patient has severe heart failure;
- if the patient is in a severe general condition, e.g., is dehydrated;
- if the patient is in an advanced stage of cancer or has another disease that leads to excessive fragility of the mucous membrane;
- if the patient has an acute phase of inflammatory bowel disease, including Crohn's disease and ulcerative colitis;
- if the patient has a perforation of the gastrointestinal tract wall or there is an increased risk of perforation of the gastrointestinal tract wall;
- if the patient has colitis or toxic colitis;
- if the patient has intestinal obstruction or suspected intestinal obstruction;
- if the patient has gastric emptying disorders (such as gastroparesis - slowed gastric emptying);
- in children and adolescents under 18 years of age.
Warnings and precautions
In elderly patients in poor general condition, the medicine should be used only under medical supervision.
This medicine contains macrogol. Allergic reactions (including rash, itching, and severe allergic reaction with sudden swelling of the face, lips, tongue, or throat, or difficulty breathing or dizziness) have been reported after taking products containing macrogol.
Diarrhea caused by the use of Fortrans may significantly disrupt the absorption of other medicines taken at the same time (see "Fortrans and other medicines").
If the patient is at risk of changes in electrolyte levels (electrolyte imbalance), e.g., in patients with renal failure, heart failure, or taking diuretics, the doctor may decide to monitor electrolyte levels in the blood before and after using the medicine. Caution should be exercised when using in patients with a tendency to develop electrolyte imbalance.
Before taking Fortrans, you should consult a doctor or pharmacist if:
- the patient has heart disease (including heart failure);
- the patient has kidney disease;
- the patient has swallowing disorders or a risk of aspiration (food or fluid entering the airways);
- the patient is bedridden;
- the patient is taking diuretics (medicines that increase urine production).
If, during the use of Fortrans for bowel cleansing, the patient experiences sudden abdominal pain or rectal bleeding, they should contact their doctor or seek medical help immediately.
Children and adolescents
Fortrans is not intended for use in patients under 18 years of age. The safety and efficacy of use in this group have not been established.
Fortrans and other medicines
You should 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.
Diarrhea caused by the use of Fortrans may cause significant disruption to the absorption of other medicines taken at the same time. The absorption of other medicines, such as digoxin (a medicine used for heart conditions), antiepileptic medicines, coumarins (blood-thinning medicines), and immunosuppressive medicines (used, for example, in the treatment of cancer and after organ transplants), may be temporarily reduced during use with Fortrans, which may reduce their effectiveness.
Pregnancy, breastfeeding, and fertility
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, you should consult a doctor or pharmacist before using this medicine.
Fortrans contains sodium and potassium
The medicine contains 2.890 g of sodium (the main component of common salt) in each sachet. This corresponds to 144.5% of the maximum recommended daily intake of sodium in the diet for adults. This should be taken into account in patients on a strict low-sodium diet.
Fortrans contains 393 mg of potassium in one sachet, which should be taken into account in patients with reduced kidney function and in patients controlling their potassium intake.
3. How to use Fortrans
Fortrans should always be used in accordance with the doctor's recommendations. In case of doubts, you should contact your doctor or pharmacist.
Fortrans is intended for use only in adults. The recommended dose is approximately one liter of solution per 15 to 20 kg of body weight, which corresponds to an average dose of 3 to 4 liters of solution.
To obtain one liter of solution, the contents of one sachet should be dissolved in one liter of water. Mix until the powder is completely dissolved. After dissolving the powder, you should start taking the solution immediately. One liter of solution should be taken within one hour.
Fortrans can be administered:
- in divided doses:
- either 2 liters in the evening before the examination or procedure and 1-2 liters in the morning on the day of the examination or procedure;
- or 3 liters in the evening before the examination or procedure and 1 liter in the morning on the day of the examination or procedure;
in a single dose:
- 3-4 liters in the evening before the examination or procedure, with a possible 1-hour break after drinking 2 liters of solution.
According to the doctor's recommendation, you should drink one 250 ml glass of solution every 10 to 15 minutes.
It is recommended that the patient takes the last part of the solution 3-4 hours before the examination or procedure.
Taking more than the recommended dose of Fortrans
If you think you have taken too much Fortrans, you should inform your doctor and drink enough water or clear fluids to prevent dehydration.
4. Possible side effects
After taking the medicine, frequent bowel movements with a watery stool will occur. This is normal and indicates the effective action of the medicine. You should stay near a toilet until the effect of the medicine has passed.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
In case of any of the following symptoms, you should stop using Fortrans and contact your doctor or the Emergency Department of the nearest hospital immediately. You should take the packaging of the medicine with you to inform the doctor which medicine you have taken:
the medicine that has been taken:
- Allergic reaction - symptoms may include skin rash, itching, or hives.
- Severe allergic reaction causing swelling of the face or throat (angioedema) or difficulty breathing or dizziness (anaphylactic reaction).
Other side effects include:
Very common (may affect more than 1 in 10 people)
- Nausea
- Bloating or abdominal pain
Common (may affect up to 1 in 10 people)
- Vomiting
Frequency not known (cannot be estimated from the available data)
- Allergic reactions (including rash, hives, and severe allergic reaction with sudden swelling of the face, lips, tongue, or throat, or difficulty breathing or dizziness)
Reporting side effects
If you experience any side effects, including any side effects not listed in the leaflet, you should 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, you can help provide more information on the safety of this medicine.
5. How to store Fortrans
The medicine should be stored out of sight and reach of children.
There are no special precautions for storage.
Do not use this medicine after the expiry date stated on the packaging. The expiry date refers to the last day of the month stated.
Medicines should not be disposed of via wastewater or household waste. You should ask your pharmacist how to dispose of medicines that are no longer needed. This will help protect the environment.
6. Contents of the packaging and other information
What Fortrans contains
- The active substances of the medicine are macrogol 4000, anhydrous sodium sulfate, sodium bicarbonate, sodium chloride, potassium chloride.
- The excipient is sodium saccharin.
What Fortrans looks like and what the packaging contains
Paper/Aluminum/PE sachets in a cardboard box.
The packaging contains 4 sachets of 73.69 g of powder.
For more detailed information, you should contact the marketing authorization holder or the parallel importer.
Marketing authorization holder in Romania, the country of export:
IPSEN Consumer HealthCare
65 Quai Georges Gorse
92100 Boulogne-Billancourt
France
Manufacturer:
Beaufour Ipsen Industrie
Rue d’Ethe Virton
28 100 Dreux
France
Parallel importer:
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
Repackaged by:
Medezin Sp. z o.o.
ul. Zbąszyńska 3
91-342 Łódź
CEFEA Sp. z o.o. Sp. komandytowa
ul. Działkowa 56
02-234 Warszawa
Pharma Innovations Sp. z o.o.
ul. Jagiellońska 76
03-301 Warszawa
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 Romania, the country of export: 1992/2009/01
Parallel import authorization number: 256/22
Date of leaflet approval: 23.06.2022
[Information about the trademark]
- Country of registration
- Active substance
- Prescription requiredYes
- Marketing authorisation holder (MAH)Ipsen Consumer HealthCare
- This information is for reference only and does not constitute medical advice. Always consult a licensed doctor before taking any medication. Oladoctor is not responsible for medical decisions based on this content.
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