Product Information for the Patient
Bylvay 200 micrograms Hard Capsules
Bylvay 400 micrograms Hard Capsules
Bylvay 600 micrograms Hard Capsules
Bylvay 1200 micrograms Hard Capsules
odevixibat
This medicine is subject to additional monitoring, which will facilitate the detection of new information about its safety. You can contribute by reporting any adverse effects you may experience. The final part of section 4 includes information on how to report these adverse effects.
Read this leaflet carefully before starting to take this medicine, as it contains important information for you.
Bylvay contains the active ingredient odevixibat. Odevixibat is a medication that increases the elimination of the body of certain substances called bile acids. Bile acids are components of the digestive fluid called bile, which is produced by the liver and secreted into the intestine. Odevixibat blocks the mechanism that normally reabsorbs them from the intestine after they have done their work. In this way, they can be eliminated from the body through feces.
Bylvay is used to treat progressive familial intrahepatic cholestasis (PFIC) in patients 6 months or older. PFIC is a liver disease caused by the accumulation of bile acids (cholestasis) that worsens over time and is often accompanied by severe itching.
Do not take Bylvay
Warnings and precautions
Consult your doctor or pharmacist before starting to take Bylvay:
Consult your doctor if you experience diarrhea while taking Bylvay. Patients with diarrhea should drink enough liquid to avoid dehydration.
During treatment with Bylvay, elevated levels of liver enzymes may be observed in liver function tests. Before starting to take Bylvay, your doctor will measure your liver function to check the functioning of your liver. Your doctor will perform regular checks to monitor your liver function.
Your doctor may recommend an evaluation of your blood levels of vitamins A, D, and E and the blood clotting value known as INR before and during treatment with Bylvay.
Children
Bylvay is not recommended for use in babies under 6 months of age, as it is not known if the medicine is safe and effective in this age group.
Use of Bylvay with other medicines
Inform your doctor or pharmacist if you are using, have used recently, or may need to use any other medicine.
Treatment with odevixibat may affect the absorption of fat-soluble vitamins, such as vitamins A, D, and E, and some medicines.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor before using this medicine.
Bylvay is not recommended during pregnancy or in women of childbearing potential who are not using contraceptive methods.
It is not known if odevixibat can pass into breast milk and affect the baby. Your doctor will help you decide whether to stop breastfeeding or avoid treatment with Bylvay, taking into account the benefits of breastfeeding for the baby and Bylvay for the mother.
Driving and operating machines
The influence of Bylvay on the ability to drive and use machines is negligible or insignificant.
Follow exactly the administration instructions for this medication as indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Treatment should be initiated and supervised by a doctor experienced in the treatment of progressive liver disease with reduced bile flow.
The dose of Bylvay depends on your weight. Your doctor will calculate the correct number of capsules you should take and their concentration.
The recommended dose is
No alternative doses are recommended for adults.
Method of use
Take the capsules once a day in the morning, with or without food.
All capsules can be swallowed whole with a glass of water or opened and sprinkled over some food or a suitable liquid for the age (for example, breast milk, infant formula, or water).
The larger capsules, 200 and 600 micrograms, are designed to be opened and sprinkled over some food or a suitable liquid for the age, but can be swallowed whole. The smaller capsules, 400 and 1,200 micrograms, are designed to be swallowed whole, but can be opened and sprinkled over some food or a suitable liquid for the age.
You will find detailed instructions on how to open the capsules and sprinkle the content over some food or a liquid at the end of this leaflet.
If your condition does not improve after 6 months of continuous daily treatment, your doctor will recommend an alternative treatment.
If you take more Bylvay than you should
Inform your doctor if you think you have taken too much Bylvay.
The possible symptoms of an overdose are diarrhea and stomach and intestinal problems.
If you forget to take Bylvay
Do not take a double dose to make up for the missed dose. Take the next dose at the usual time.
If you interrupt treatment with Bylvay
Do not stop taking Bylvay without first talking to your doctor.
If you have any other questions about the use of this medication, ask your doctor or pharmacist.
Like all medications, this medication may produce adverse effects, although not everyone will experience them.
Adverse effects may appear with the following frequencies:
Very Frequent(may affect more than 1 in 10 people)
Frequent(may affect up to 1 in 10 people)
•diarrhea, including bloody stools, soft stools
•abdominal pain
•enlargement of the liver
Reporting Adverse Effects
If you experience any type of adverse effect, consult your doctor or pharmacist, even if it is a possible adverse effect not listed in this prospectus. You can also report them directly through theSpanish System for Pharmacovigilance of Medicinal Products for Human Use: https://www.notificaRAM.es.By reporting adverse effects, you can contribute to providing more information about the safety of this medication.
Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the box and the bottle after EXP. The expiration date is the last day of the month indicated.
Store in the original packaging to protect it from light. Do not store at a temperature above 25 °C.
Medicines should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the containers and medications that you no longer need. This will help protect the environment.
Composition of Bylvay
Each hard capsule of Bylvay 200 micrograms contains 200 micrograms of odevixibat (as sesquihydrate).
Each hard capsule of Bylvay 400 micrograms contains 400 micrograms of odevixibat (as sesquihydrate).
Each hard capsule of Bylvay 600 micrograms contains 600 micrograms of odevixibat (as sesquihydrate).
Each hard capsule of Bylvay 1 200 micrograms contains 1 200 micrograms of odevixibat (as sesquihydrate).
The other components are:
Microcrystalline cellulose Hypromellose
Hard capsule coating
Bylvay 200 micrograms and 600 micrograms hard capsules
Hypromellose
Titanium dioxide (E171)
Yellow iron oxide (E172)
Bylvay 400 micrograms and 1 200 micrograms hard capsules
Hypromellose
Titanium dioxide (E171)
Yellow iron oxide (E172) Red iron oxide (E172)
Printing ink
Lacquer
Propylene glycol
Black iron oxide (E172)
Appearance of the product and contents of the pack
Bylvay 200 micrograms hard capsules:
Size 0 capsules (21.7 mm × 7.64 mm) with a white opaque body and a beige opaque cap; with the inscription "A200" in black ink.
Bylvay 400 micrograms hard capsules:
Size 3 capsules (15.9 mm × 5.82 mm) with a white opaque body and an orange opaque cap; with the inscription "A400" in black ink.
Bylvay 600 micrograms hard capsules:
Size 0 capsules (21.7 mm × 7.64 mm) with a white opaque body and a beige opaque cap; with the inscription "A600" in black ink.
Bylvay 1 200 micrograms hard capsules:
Size 3 capsules (15.9 mm × 5.82 mm) with a white opaque body and an orange opaque cap; with the inscription "A1200" in black ink.
The hard capsules of Bylvay are packed in a plastic bottle with a polypropylene closure, with a safety seal and child-resistant. Pack size: 30 hard capsules.
Marketing authorisation holder
Ipsen Pharma
65 quai Georges Gorse
92100 Boulogne-Billancourt
France
Responsible person for manufacturing
Almac Pharma Services Limited
Seagoe Industrial EstatePortadown, Craigavon
County Armagh
BT63 5UA
United Kingdom (Northern Ireland)
For further information about this medicinal product, please contact the representative in your country of the marketing authorisation holder:
België/Belgique/Belgien/Luxembourg/ Luxemburg Ipsen NV België/Belgique/Belgien Tél/Tel: +32 9 243 96 00 | Italia Ipsen SpA Tel: + 39 02 39 22 41 |
Latvija Ipsen Pharma representative office Tel: + 371 67622233 | |
Lietuva Ipsen Pharma SAS Lietuvos filialas Tel: +370 700 33305 | |
Danmark, Norge, Suomi/Finland, Sverige, Ísland Institut Produits Synthèse (IPSEN) AB Sverige/Ruotsi/Svíþjóð Tlf/Puh/Tel/Sími: +46 8 451 60 00 | Magyarország IPSEN Pharma Hungary Kft. Tel.: + 36 1 555 5930 |
Deutschland, Österreich Ipsen Pharma GmbH Deutschland Tel: +49 89 2620 432 89 | Nederland Ipsen Farmaceutica B.V. Tel: +31 (0) 23 554 1600 |
Eesti Centralpharma Communications OÜ Tel: +372 60 15 540 | Polska Ipsen Poland Sp. z o.o. Tel.: + 48 22653 68 00 |
Ελλ?δα, Κ?προς, Malta Ipsen Μονοπρ?σωπη EΠΕ Ελλ?δα Τηλ: +30 210 984 3324 | Portugal Ipsen Portugal - Produtos Farmacêuticos S.A. Tel: + 351 21 412 3550 |
España Ipsen Pharma, S.A.U. Tel: +34 936 858 100 | România Ipsen Pharma România SRL Tel: + 40 21 231 27 20 |
France Ipsen Pharma Tél: +33 1 58 33 50 00 | Slovenija Swixx Biopharma d.o.o. Tel: + 386 1 2355 100 |
Hrvatska Swixx Biopharma d.o.o. Tel: +385 1 2078 500 | Slovenská republika Ipsen Pharma, organizacná zložka Tel: + 420 242481 821 |
Ireland, United Kingdom (Northern Ireland) Ipsen Pharmaceuticals Limited Tel: +44 (0)1753 62 77 77 |
Fecha of the last revision of this leaflet:
This medicinal product has been authorised under «exceptional circumstances». This type of authorisation means that due to the rarity of this disease, it has not been possible to obtain complete information about this medicinal product.
The European Medicines Agency will review annually any new information about this medicinal product that may become available and this leaflet will be updated as necessary.
Otras fuentes de información
The detailed information about this medicinal product is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
There are also links to other websites about rare diseases and orphan medicinal products.
Instrucciones
Instrucciones para abrir las cápsulas y espolvorear el contenido sobre algún alimento:
Step1. Put a small amount of a soft food in a bowl (2cucharadas/30ml of yoghurt, apple sauce, mashed banana, chocolate pudding, rice pudding or oatmeal). The food should be at room temperature or cooler.
Step2: • Hold the capsule horizontally by both ends and twist in opposite directions. | |
Step3: • Separate them to empty the contents into the bowl containing the soft food. • Gently tap the capsule to ensure all the granules come out. • Repeat the step above if more than one capsule is needed for the dose. | |
Step4: • Mix the contents of the capsule gently with the soft food. | |
• Take the full dose immediately after mixing it. Do not save the mixture for later use. • Drink a glass of water after the dose. • Dispose of the empty capsule shells. |
Instrucciones para abrir las cápsulas y espolvorear el contenido en un líquido adecuado para la edad:
Do not administer the medicinal product through a bottle or a baby cup, as the granules will not pass through the opening. The granules will not dissolve in liquids.
Consult your pharmacist if you do not have an oral syringe suitable for administering the medicinal product at home.
Step1: • Hold the capsule horizontally by both ends and twist in opposite directions. • Separate them to empty the contents into a small cup or a glass. Gently tap the capsule to ensure all the granules come out. Repeat this step if more than one capsule is needed for the dose. • Add 1cucharadita (5ml) of an appropriate liquid for the age (e.g. breast milk, infant formula or water). • Let the granules settle in the liquid for about 5minutes to allow them to become fully moistened (the granules will not dissolve). | |
Step2: • After 5minutes, insert the tip of the oral syringe into the mixture cup. • Pull the plunger of the syringe upwards slowly to extract the liquid and granule mixture into the syringe. Press the plunger downwards gently to return the liquid and granule mixture to the mixture cup. Repeat this process 2 or 3 times to ensure complete mixing of the granules in the liquid. | |
Step3: • Extract all the contents into the oral syringe by pulling the plunger to the end of the syringe. | |
Step4: • Place the tip of the oral syringe in the front of the baby's mouth between the tongue and the side of the mouth and, then, press the plunger gently to administer a jet of the liquid and granule mixture between the tongue and the side of the baby's mouth. Do not administer a jet of the liquid and granule mixture at the back of the baby's throat, as this could cause vomiting or choking. • If there are any remaining liquid and granule mixture in the mixture cup, repeat steps3 and 4 until the full dose has been administered. | |
• Administer the full dose immediately after mixing it. Do not save the liquid and granule mixture for later use. • Give the baby breast milk, infant formula or another appropriate liquid for the age to drink after the dose. • Dispose of the empty capsule shells. |
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