Jak stosować FLUIFORT
Treść ulotki
Fluifort 2.7 g granules for oral solution
Carbocisteine lysine salt monohydrate
Read this leaflet carefully before taking this medicine as it contains
important information for you.
Always take this medicine exactly as described in this leaflet, or as your
doctor or pharmacist has told you.
- Keep this leaflet. You may need to read it again.
- If you want more information or advice, ask your pharmacist.
- If any side effects occur, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
- See a doctor if you do not feel better or if your symptoms worsen after 14 days.
Contents of this leaflet:
- 1. What Fluifort is and what it is used for
- 2. What you need to know before you take Fluifort
- 3. How to take Fluifort
- 4. Possible side effects
- 5. How to store Fluifort
- 6. Contents of the pack and other information
1. What is Fluifort and what is it used for
Fluifort contains the active ingredient carbocisteine lysine salt monohydrate, which belongs to
a group of medicines for cough and colds called mucolytics
used to facilitate the elimination of mucus from the respiratory tract.
This medicine is indicated for the treatment of cough and acute and chronic diseases
of the respiratory system.
See your doctor if you do not feel better or if you feel worse after 14 days.
2. What you need to know before taking Fluifort
Do not take Fluifort
- if you are allergic to carbocisteine lysine salt monohydrate or to any of the other ingredients of this medicine (listed in section 6);
- if you suffer from gastroduodenal ulcer, a problem that can affect the stomach or the first part of the intestine;
- if you are pregnant or breastfeeding (see section “Pregnancy and breastfeeding”). Do not administer this medicine to children under 11 years of age (see section “Children”).
Warnings and precautions
Talk to your doctor or pharmacist before taking Fluifort.
No phenomena of reduced efficacy of the medicine have been reported after prolonged treatment or phenomena of dependence (need to continue taking the medicine) with the use of Fluifort.
Caution is recommended in elderly patients, asthmatic patients with a history of severe respiratory problems, debilitated patients, those with a history of gastroduodenal ulcers, or those who are taking medicines known to cause gastrointestinal bleeding. You must stop treatment with carbocisteine in case of gastrointestinal bleeding.
This medicine should not be used in association with cough suppressants and/or medicines that inhibit bronchial secretion.
Consult your doctor if the disorder occurs repeatedly or if you notice any recent change in its characteristics.
Fluifort does not affect weight, so you can take it if you are following a low-calorie diet or if you suffer from diabetes.
The medicine does not contain gluten, therefore it can be used by celiac patients.
Children
Fluifort should not be taken by children under 11 years of age (see section “Do not take Fluifort”).
Other medicines and Fluifort
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
No disturbances caused by the association with medicines used for the treatment of upper and lower respiratory tract diseases have been reported.
Pregnancy and breastfeeding
If you are pregnant, suspect you are pregnant, are planning to become pregnant, or are breastfeeding with breast milk, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
Do not take Fluifort during pregnancy.
Breastfeeding
Do not take Fluifort if you are breastfeeding.
Driving and using machines
Fluifort does not alter the ability to drive vehicles or use machines.
Fluifort contains aspartame.
This medicine contains 30 mg of aspartame per dose, equivalent to 6 mg/g. Aspartame is a source of phenylalanine. It may be harmful if you have phenylketonuria, a rare genetic disorder that causes the accumulation of phenylalanine because the body cannot dispose of it properly.
3. How to take Fluifort
Take this medicine following the instructions provided in this leaflet or as directed by your doctor or pharmacist. If you have any doubts, consult your doctor or pharmacist.
The recommended dose is1 sachet per day.
Dissolve the contents of the sachet in about half a glass of water, mixing well.
Caution: do not exceed the indicated doses.
Fluifort can also be taken for prolonged periods. However, if symptoms do not resolve after 14 days of treatment, it is recommended to consult a doctor.
If you have kidney or liver problems, you can take Fluifort and it is not necessary to adjust the dose.
If you take more Fluifort than you should
Symptoms reported in case of overdose may include: headache, nausea, vomiting,
diarrhea, stomach pain, skin reactions, altered senses.
In case of accidental ingestion/intake of an excessive dose of Fluifort, immediately notify your doctor or go to the nearest hospital.
If you forget to take Fluifort
Do not take a double dose to make up for a missed dose.
If you stop taking Fluifort
If you have any doubts about the use of this medicine, consult your doctor or pharmacist.
4. Possible side effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Contact your doctor if you experience any of the following side effects:
Frequency not known (the frequency cannot be estimated from available data):
- irritations and skin diseases (Stevens-Johnson Syndrome; bullous dermatitis; erythema multiforme; toxic skin rash). (In such cases, discontinue treatment and consult your doctor to establish appropriate therapy).
- gastrointestinal bleeding (In such cases, discontinue treatment and consult your doctor to establish appropriate therapy).
- skin manifestations (rash, urticaria, erythema, dermatitis), with the presence of spots, blisters or bubbles (exanthem, bullous exanthem/erythema), itching, swelling due to fluid accumulation around the eyes, mouth, tongue and throat, with possible difficulty breathing (angioedema).
- abdominal pain, nausea, vomiting, diarrhea.
- dizziness.
- difficulty breathing (dyspnea).
- redness.
Reporting of side effects
If you experience any side effects, including those not listed in this leaflet, please
tell your doctor or pharmacist. You can also report side effects directly
through the national reporting system at
https://www.aifa.gov.it/content/segnalazioni-reazioni-avverse.
By reporting side effects you can help provide more information on the
safety of this medicine.
5. How to store Fluifort
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the packaging after
Exp. The expiry date refers to the last day of that month. The expiry date
refers to the product in intact packaging, correctly stored.
This medicine does not require any particular storage conditions.
Do not dispose of any medicine in wastewater or household waste. Ask your pharmacist
how to dispose of medicines you no longer use. This will help protect the environment.
6. Contents of the pack and other information
What Fluifort contains
- The active ingredient is carbocisteine lysine salt monohydrate. 1 sachet of 5 grams contains 2.7 g of carbocisteine lysine salt.
- The other ingredients are: citric acid, mannitol, povidone, natural cedar aroma, natural orange aroma, orange juice, aspartame, maltodextrins.
Description of the appearance of Fluifort and contents of the pack
Fluifort is presented as granules for oral solution.
Fluifort is available in packs of 10, 20 and 30 sachets.
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Dompé farmaceutici S.p.A. - Via San Martino, 12 - 20122 Milano
Manufacturer
Dompé farmaceutici S.p.A. - Via Campo di Pile - L'Aquila

- Kraj rejestracji
- Postać farmaceutycznaGranules for oral solution, 2.7 G
- Kod ATCR05CB03
- Substancja czynna
- Wymaga receptyNie
- Producent
- Te treści mają charakter wyłącznie informacyjny i nie zastępują konsultacji lekarskiej.
- Zamienniki FLUIFORTPostać farmaceutyczna: Granules for oral solution, 2.7 GSubstancja czynna: carbocisteineProducent: IPSO PHARMA S.R.L.Wymaga receptyPostać farmaceutyczna: Granules for oral solution, 2.7 gSubstancja czynna: carbocisteineProducent: IPSO PHARMA S.R.L.Wymaga receptyPostać farmaceutyczna: Syrup, 250 MG/5 MLSubstancja czynna: carbocisteineBez recepty
Odpowiedniki FLUIFORT w innych krajach
Leki z tą samą substancją czynną dostępne w innych krajach.
Odpowiednik FLUIFORT w Hiszpania
Odpowiednik FLUIFORT w Polska
Odpowiednik FLUIFORT w Ukraina
Lekarze online w sprawie FLUIFORT
Omów stosowanie FLUIFORT, bezpieczeństwo i ocenę zasadności recepty zgodnie z obowiązującymi przepisami.
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FLUIFORT nie wymaga recepty w Włochy. Możesz skonsultować się z lekarzem online, aby sprawdzić, czy ten lek może być odpowiedni w Twojej sytuacji.
Substancją czynną w FLUIFORT jest carbocisteine. Informacja ta pomaga rozpoznać leki o tym samym składzie, ale pod różnymi nazwami handlowymi.
FLUIFORT jest produkowany przez DOMPE' FARMACEUTICI S.P.A.. Nazwy handlowe i opakowania mogą się różnić w zależności od dystrybutora.
Lekarze, tacy jak Lekarze rodzinni, Psychiatrzy, Dermatolodzy, Kardiolodzy, Endokrynolodzy, Gastroenterolodzy, Pulmonolodzy, Nefrolodzy, Reumatolodzy, Hematolodzy, Zakaźnicy, Alergolodzy, Geriatrzy, Pediatrzy, Onkolodzy, mogą ocenić, czy stosowanie FLUIFORT jest odpowiednie w Twoim przypadku, w zależności od sytuacji klinicznej i lokalnych przepisów. Możesz umówić konsultację online, aby omówić objawy i możliwe dalsze kroki.
Polska posiada dobrze rozwiniętą infrastrukturę ochrony zdrowia w dużych miastach, takich jak Warszawa, Kraków, Wrocław i Gdańsk. Apteki są łatwo dostępne i działają zgodnie z obowiązującymi przepisami, zapewniając dostęp do leków na receptę.
Możesz kupić FLUIFORT w Warszawie, Krakowie, Wrocławiu lub Gdańsku w każdej aptece, posiadając ważną receptę.
Aby uzyskać receptę, możesz skorzystać z Oladoctor:
Inne leki zawierające tę samą substancję czynną (carbocisteine) to m.in. BRONKOLIB, KARBOKISTEINA IPSO PARMA, KORYFIN TOSSE MUKOLITIKO. Mogą one różnić się nazwą handlową lub postacią, ale zawierają ten sam składnik terapeutyczny. Przed zmianą lub rozpoczęciem nowego leku skonsultuj się z lekarzem.
















