Jak stosować INDOBUFENE EG
Treść ulotki
INDOBUFENE EG 200 mg tablets
Generic Equivalent Medicine
Read this leaflet carefully before taking this medicine as it contains
important information for you.
- Keep this leaflet. You may need to read it again.
- If you have any questions, ask your doctor or pharmacist.
- This medicine has been prescribed for you only. Do not give it to other people, even if their symptoms are the same as yours, as it could be harmful.
- If any side effects occur, including those not listed in this leaflet, tell your doctor or pharmacist. See section 4.
Contents of this leaflet:
- 1. What INDOBUFENE EG is and what it is used for
- 2. What you need to know before you take INDOBUFENE EG
- 3. How to take INDOBUFENE EG
- 4. Possible side effects
- 5. How to store INDOBUFENE EG
- 6. Contents of the pack and other information
1. What is INDOBUFENE EG and what is it used for
INDOBUFENE EG contains the active ingredient indobufene, belonging to the class of medicines
called antiplatelet agents, which improve blood circulation, preventing the
formation of blood clots (thrombi), which can block circulation.
INDOBUFENE EG is used:
- to prevent narrowing of the bypasses of the heart arteries (coronary arteries);
- for the treatment of movement difficulties due to problems with blood circulation (intermittent claudication);
2. What you need to know before taking INDOBUFENE EG
Do not take INDOBUFENE EG
- if you are allergic to the active ingredient or to any of the other ingredients of this medicine (listed in section 6);
- if you have lesions of the stomach and intestines (gastro-duodenal ulcer);
- if you have inflammation of the stomach accompanied by bleeding (hemorrhagic gastritis);
- if you have severe liver and/or kidney disorders;
- if you are prone to bleeding (hemorrhagic diathesis);
- if, in the past, after taking acetylsalicylic acid (aspirin) or other non-steroidal anti-inflammatory drugs (NSAIDs), you have experienced breathing difficulties (asthma), allergic rhinitis (hay fever) and skin irritation (urticaria).
Warnings and precautions
Consult your doctor or pharmacist before taking INDOBUFENE EG.
Use this medicine with caution in the following cases:
- if you have kidney problems (renal insufficiency), in which case it may be necessary to reduce the dose;
- if you have had lesions of the stomach or intestines;
- if you are using non-steroidal anti-inflammatory drugs (NSAIDs) or medicines that increase blood fluidity (antiplatelet agents).
Inform your doctor if you notice the appearance of the following conditions, as it may be
necessary to reduce the dosage or discontinue treatment with this medicine:
- skin irritation (urticaria);
- pain in the center of the abdomen (epigastric pain) and a burning sensation in the stomach (heartburn), a condition called dyspepsia and relating to digestive disorders.
Other medicines and INDOBUFENE EG
Tell your doctor or pharmacist if you are taking, have recently taken or might take
any other medicine.
If you suffer from diabetes and are taking oral medicines (by mouth) that lower blood sugar levels (hypoglycemic agents), such as sulfonylureas, you should have your blood sugar levels checked periodically.
If you are taking medicines, orally, that increase blood fluidity (oral anticoagulants), such as coumarin derivatives and/or heparin, you should have the following tests to check
blood coagulation:
- prothrombin time;
- other coagulation tests.
Pregnancy, breastfeeding and fertility
If you are pregnant, suspect you are pregnant or are planning a pregnancy, or if you are breastfeeding
with breast milk, ask your doctor or pharmacist for advice before taking this medicine.
The use of this medicine is not recommended in case of confirmed or suspected pregnancy, and
during breastfeeding with breast milk.
Driving and using machines
This medicine does not affect the ability to drive vehicles and operate machinery.
INDOBUFENE EG contains lactose monohydrate
If your doctor has diagnosed you with intolerance to certain sugars, contact him/her before taking
this medicine.
3. How to take INDOBUFENE EG
Take this medicine following exactly the instructions of your doctor. If you have any doubts
consult your doctor or pharmacist.
The recommended dose is 400 mg per day, to be taken in two separate doses, one every 12 hours.
Take one tablet in the morning after breakfast and one in the evening after dinner.
Elderly patients and/or patients with kidney problems
The doctor will adjust the dosage based on your kidney function assessed by the value of
creatinine clearance.
In elderly patients over 65 years of age, the dose must be evaluated by the doctor.
If you take more INDOBUFENE EG than you should
No cases of overdose with this medicine have been reported.
In case of accidental ingestion of an excessive dose, contact your doctor immediately or go to
the nearest hospital.
If you forget to take INDOBUFENE EG
Do not take a double dose to make up for the missed tablet.
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.
The most common side effects concern the gastrointestinal tract and consist of:
- difficulty in digestion (dyspepsia);
- heartburn (pyrosis);
- stomach pain (epigastric and abdominal pain);
- constipation or diarrhoea;
- abdominal bloating;
- nausea and vomiting.
Rarely, the following have been reported
- skin irritations of an allergic type;
- purpura associated with thrombocytopenia, which is a skin disorder associated with bleeding lesions due to a decrease in platelets;
- severe headache (cephalalgia).
Very rarely, cases of
- inflammation of the stomach and/or intestine, accompanied by lesions (erosive peptic ulcer and/or haemorrhagic gastritis), also associated with the presence of blood in vomit or stools and cases of cerebral haemorrhage.
Cases of the following have been observed:
- itching (frequency not known);
- nosebleeds (epistaxis);
- minor bleeding from gums, lower part of the eye (conjunctiva), lips, bladder and anus (rectum);
- outflow of blood from the mouth, often after a coughing fit (hemoptysis);
- alteration of some parameters of liver function (increase in levels of transaminases and azotaemia);
- alteration of some parameters of kidney function (decrease in creatinine clearance).
Reporting of side effects
If you get any side effects, even 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:
http://www.agenziafarmaco.gov.it/it/responsabili. By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store INDOBUFENE EG
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.
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 INDOBUFENE EG contains
- The active ingredient is indobufene. Each tablet contains 200 mg of indobufene
- The other ingredients are lactose monohydrate, microcrystalline cellulose, sodium carboxymethyl starch (type A), sodium lauryl sulfate, magnesium stearate.
Description of the appearance of INDOBUFENE EG and contents of the pack
Pack of 30 divisible tablets.
Marketing Authorisation Holder
EG S.p.A.
Via Pavia, 6
20136 Milano
Italy
Manufacturer
Doppel Farmaceutici S.r.l.
Via Volturno 48
Quinto de’ Stampi, Rozzano (Milano)
Italy

- Kraj rejestracji
- Postać farmaceutycznaTablet, 200 MG
- Kod ATCB01AC10
- Substancja czynna
- Wymaga receptyTak
- Producent
- Te treści mają charakter wyłącznie informacyjny i nie zastępują konsultacji lekarskiej.
- Zamienniki INDOBUFENE EGPostać farmaceutyczna: Tablet, 200 MGSubstancja czynna: indobufenProducent: PFIZER ITALIA S.R.L.Wymaga receptyPostać farmaceutyczna: Enteric-coated tablet, 100 MGSubstancja czynna: acetylsalicylic acidProducent: AUROBINDO PHARMA (ITALIA) S.R.L.Wymaga receptyPostać farmaceutyczna: Enteric-coated tablet, 100 MGSubstancja czynna: acetylsalicylic acidProducent: DOC GENERICI SRLWymaga recepty
Odpowiedniki INDOBUFENE EG w innych krajach
Leki z tą samą substancją czynną dostępne w innych krajach.
Odpowiednik INDOBUFENE EG w Hiszpania
Lekarze online w sprawie INDOBUFENE EG
Omów stosowanie INDOBUFENE EG, bezpieczeństwo i ocenę zasadności recepty zgodnie z obowiązującymi przepisami.
Uzyskaj receptę na INDOBUFENE EG online
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Często zadawane pytania
INDOBUFENE EG wymaga recepty w Włochy. Możesz skonsultować się z lekarzem online, aby sprawdzić, czy ten lek może być odpowiedni w Twojej sytuacji.
Substancją czynną w INDOBUFENE EG jest indobufen. Informacja ta pomaga rozpoznać leki o tym samym składzie, ale pod różnymi nazwami handlowymi.
INDOBUFENE EG jest produkowany przez EG 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 INDOBUFENE EG 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 INDOBUFENE EG 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 (indobufen) to m.in. IBUSTRIN, AKIDO AKETILSALIKILIKO AUROBINDO, AKIDO AKETILSALIKILIKO DOK JENERIKI. Mogą one różnić się nazwą handlową lub postacią, ale zawierają ten sam składnik terapeutyczny. Przed zmianą lub rozpoczęciem nowego leku skonsultuj się z lekarzem.
















