Package Leaflet: Information for the User
Nintedanib Eugia 100 mg Soft Capsules EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
Nintedanib Eugia contains the active substance nintedanib, a medicine that belongs to the class of drugs known as tyrosine kinase inhibitors, and is used to treat idiopathic pulmonary fibrosis (IPF), other chronic fibrosing interstitial lung diseases (ILD) with a progressive phenotype, and interstitial lung disease associated with systemic sclerosis (SSc-ILD) in adults.
Idiopathic Pulmonary Fibrosis (IPF)
IPF is a disease that causes thickening, hardening, and scarring of the lung tissue over time. As a result, scarring reduces the ability to transfer oxygen from the lungs to the bloodstream, making it difficult to breathe deeply. Nintedanib helps reduce the occurrence of further scarring and hardening of the lungs.
Other Chronic Fibrosing Interstitial Lung Diseases (ILD) with a Progressive Phenotype
In addition to IPF, there are other disorders in which the lung tissue becomes thickened, hardened, and scarred over time (pulmonary fibrosis) and continues to worsen (progressive phenotype). Some examples of these disorders include hypersensitivity pneumonitis, autoimmune ILD (such as ILD associated with rheumatoid arthritis), idiopathic nonspecific interstitial pneumonia, idiopathic unclassifiable interstitial pneumonia, and other ILD. Nintedanib reduces new scarring and hardening of the lungs.
Interstitial Lung Disease Associated with Systemic Sclerosis (SSc-ILD)
Systemic sclerosis (SSc), also known as scleroderma, is a rare chronic autoimmune disease that affects the connective tissue in many parts of the body. SSc causes fibrosis (scarring and hardening) of the skin and other internal organs, such as the lungs. When the lungs are affected by fibrosis, it is called interstitial lung disease (ILD), and the disease is called SSc-ILD. Fibrosis in the lungs reduces the ability to transfer oxygen to the bloodstream and reduces the ability to breathe. Nintedanib reduces new scarring and hardening of the lungs.
Do not takeNintedanib Eugia
Warnings and precautions
Talk to your doctor or pharmacist before starting to take nintedanib:
Based on this information, your doctor may perform some blood tests, for example, to check your liver function. Your doctor will discuss the results of these tests with you to decide if you can take nintedanib.
Tell your doctor immediately while taking this medicine:
Children and adolescents
Children and adolescents under 18 years should not take this medicine.
Other medicines andNintedanib Eugia
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, including herbal medicines and medicines obtained without a prescription.
Nintedanib may interact with other medicines. The following medicines may increase the levels of nintedanib in the blood and, therefore, increase the risk of side effects (see section 4):
The following medicines are examples that may decrease the levels of nintedanib in the blood and, thus, reduce its effectiveness:
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
Pregnancy
Do not take this medicine during pregnancy, as it may harm the fetus and cause congenital defects.
A pregnancy test should be performed to ensure you are not pregnant before starting treatment with nintedanib. Talk to your doctor.
Contraception
Breastfeeding
Do not breastfeed your baby during treatment with nintedanib, as it may harm the baby.
Driving and using machines
Nintedanib has a minor influence on the ability to drive and use machines. Do not drive or use machines if you feel dizzy.
Nintedanib Eugia contains soy lecithin
Do not use this medicine if you are allergic to peanuts or soy (see section 2).
Always take this medicine exactly as your doctor or pharmacist has told you. If you are not sure, check with your doctor or pharmacist.
Take the capsules twice a day, approximately 12 hours apart, and at about the same time each day; for example, one capsule in the morning and one capsule in the evening. This will help keep a constant level of nintedanib in your blood. Swallow the capsules whole with water, without chewing. It is recommended to take the capsules with food, i.e., during meals or immediately before or after meals. Do not open or split the capsule (see section 5).
Adults
The recommended dose is one 100 mg capsule twice a day (a total of 200 mg per day).
Do not take more than the recommended dose of two 100 mg nintedanib capsules per day.
If you do not tolerate the recommended dose of two 100 mg nintedanib capsules per day (see possible side effects in section 4), your doctor may recommend that you stop taking this medicine. Do not reduce the dose or stop treatment by yourself without consulting your doctor first.
If you take moreNintedanib Eugiathan you should
Contact your doctor or pharmacist immediately.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service, phone 91 562 04 20, indicating the medicine and the amount taken.
If you forget to takeNintedanib Eugia
Do not take two capsules together if you have missed your previous dose. You should take your next dose of 100 mg of nintedanib according to the schedule established and recommended by your doctor or pharmacist.
If you stop taking Nintedanib Eugia
Do not stop taking nintedanib without talking to your doctor first. It is important to take this medicine every day while your doctor prescribes it.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
You should pay special attention if you experience the following side effects during treatment with nintedanib:
Diarrhea(very common, may affect more than 1 in 10 people):
Diarrhea can cause dehydration: a loss of fluids and important salts (electrolytes, such as sodium or potassium) from the body. At the first symptoms of diarrhea, drink plenty of fluids and consult your doctor immediately. Start appropriate antidiarrheal treatment as soon as possible, for example, by taking loperamide.
The following side effects have also been observed during treatment with this medicine.
Talk to your doctor if you experience any type of side effect.
Idiopathic Pulmonary Fibrosis (IPF)
Very common side effects (may affect more than 1 in 10 people)
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Frequency not known (cannot be estimated from the available data)
Other Chronic Fibrosing Interstitial Lung Diseases (ILD) with a Progressive Phenotype
Very common side effects (may affect more than 1 in 10 people)
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Frequency not known (cannot be estimated from the available data)
Interstitial Lung Disease Associated with Systemic Sclerosis (SSc-ILD)
Very common side effects (may affect more than 1 in 10 people)
Common side effects (may affect up to 1 in 10 people)
Uncommon side effects (may affect up to 1 in 100 people)
Frequency not known (cannot be estimated from the available data)
Reporting of side effects
If you experience any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly to the Spanish Medicines Agency: www.notificaram.es. By reporting side effects, you can help provide more information on the safety of this medicine.
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 carton and blister, after "EXP". The expiry date is the last day of the month indicated.
Do not store above 25 °C.
Store in the original packaging to protect from moisture.
Do not use this medicine if you notice that the blister containing the capsules is open or that a capsule is broken. If you come into contact with the contents of the capsule, wash your hands immediately with plenty of water (see section 3).
Medicines should not be disposed of via wastewater or household waste. Dispose of the packaging and any unused medicines at the pharmacy's SIGRE collection point. Ask your pharmacist how to dispose of the packaging and medicines you no longer need. This will help protect the environment.
Composition ofNintedanib Eugia
Capsule content:medium-chain triglycerides, hard fat, lecithin (soy).
Capsule shell:gelatin, glycerol (85%), titanium dioxide (E171), yellow iron oxide (E172), red iron oxide (E172).
Printing ink:black iron oxide (E172), propylene glycol (E1520), and hypromellose 2910 (6 cp) (E464).
Appearance and Package Contents of the Product
Soft capsules.
A soft gelatin capsule with an elongated shape, opaque peach-colored, with "N100" printed in black ink, containing a bright yellow suspension.
Nintedanib Eugia soft capsules are available in blister packs of 30, 60, or 120 soft capsules.
Only some pack sizes may be marketed.
Marketing Authorization Holder and Manufacturer
Marketing Authorization Holder
Eugia Pharma (Malta) Limited
Vault 14, Level 2, Valletta Waterfront
Floriana, FRN 1914
Malta
Manufacturer
APL Swift Services (Malta) Limited
HF26, Hal Far Industrial Estate, Hal Far
Birzebbugia, BBG 3000
Malta
Or
Generis Farmacêutica, S.A.
Rua João de Deus, 19
2700-487 Amadora
Portugal
Or
Arrow Génériques
26 Avenue Tony Garnier
69007 Lyon
France
You can request more information about this medicine by contacting the local representative of the marketing authorization holder:
Aurovitas Spain, S.A.U.
Avda. de Burgos, 16-D
28036 Madrid
Spain
This medicine is authorized in the Member States of the European Economic Area under the following names:
Germany: Nintedanib Eugia 100 mg soft capsules
Belgium: Nintedanib Eugia 100 mg soft capsules / capsules molles / Weichkapseln
Spain: Nintedanib Eugia 100 mg soft capsules EFG
France: NINTEDANIB EUGIA PHARMA 100 mg, soft capsule
Italy: Nintedanib Eugia
Netherlands: Nintedanib Eugia 100 mg, soft capsules
Poland: Nintedanib Eugia
Portugal: Nintedanib Eugia
Date of the last revision of this leaflet: November 2024
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) (http://www.aemps.gob.es/).