Package Leaflet: Information for the Patient
Entyvio 108mg solution for injection in pre-filled syringe
vedolizumab
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
What is Entyvio
Entyvio contains the active substance “vedolizumab”. Vedolizumab belongs to a group of biological medicines called monoclonal antibodies (MAb).
How Entyvio works
Entyvio blocks a protein on the surface of white blood cells (leucocytes) that causes inflammation in ulcerative colitis and Crohn's disease, thereby reducing inflammation.
What Entyvio is used for
Entyvio is used to treat signs and symptoms in adults with:
Ulcerative Colitis
Ulcerative colitis is a disease that causes inflammation of the large intestine. If you have ulcerative colitis, you will first be given other medicines. If you do not respond satisfactorily or cannot tolerate these medicines, your doctor may prescribe Entyvio to reduce the signs and symptoms of the disease.
Crohn's Disease
Crohn's disease is a disease that causes inflammation of the digestive tract. If you have Crohn's disease, you will first be given other medicines. If you do not respond satisfactorily or cannot tolerate these medicines, your doctor may prescribe Entyvio to reduce the signs and symptoms of the disease.
Do not use Entyvio
Warnings and precautions
Talk to your doctor, pharmacist, or nurse before using Entyvio.
Tell your doctor, pharmacist, or nurse immediatelywhen you start using this medicine for the first time, during treatment, and between doses:
Children and adolescents
Entyvio is not recommended for use in children and adolescents (under 18 years of age) due to a lack of information on the use of this medicine in this age group.
Other medicines and Entyvio
Tell your doctor, pharmacist, or nurse if you are taking, have recently taken, or might take any other medicines.
Tell your doctor if you have previously been given:
Your doctor will have to decide whether it is possible to administer Entyvio.
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before using this medicine.
Pregnancy
The effects of Entyvio in pregnant women are not known. Therefore, this medicine is not recommended during pregnancy. You and your doctor must decide whether the benefit to you is clearly greater than the potential risk to you and your baby.
If you are a woman of childbearing potential, you are advised to avoid becoming pregnant during use of Entyvio. You should use adequate contraceptive methods during treatment and for at least 4.5 months after receiving the last dose.
Breast-feeding
Tell your doctor if you are breast-feeding or plan to breast-feed. Entyvio passes into breast milk. There is not enough information on the effects this may have on your baby and on milk production. A decision must be made whether to discontinue breast-feeding or to discontinue/abstain from Entyvio therapy, taking into account the benefit of breast-feeding for the child and the benefit of therapy for you.
Driving and using machines
The effects of this medicine on the ability to drive and use machines or tools are small. A small number of patients have felt dizzy after receiving Entyvio. If you feel dizzy, do not drive or use tools or machines.
Entyvio 108mg solution for injection contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per dose; this is essentially “sodium-free”.
Follow exactly the instructions for administration of this medicine given by your doctor or pharmacist. If you are unsure, ask them again.
You or your caregiver will receive training on the use of subcutaneous injections (injections under the skin) of Entyvio.
How much Entyvio will you be given
Treatment with Entyvio is the same for ulcerative colitis and Crohn's disease.
The recommended dose is 108 mg of Entyvio administered by subcutaneous injection once every 2 weeks.
How to inject Entyvio
You can give yourself the subcutaneous injections or a caregiver can give them to you after receiving training. At the end of this leaflet, you will find instructions on how to proceed with the subcutaneous injection.
If you miss or omit an Entyvio injection
If you miss or omit a dose, inject the next dose as soon as possible and then every 2 weeks.
If you stop treatment with Entyvio
Do not stop using Entyvio without talking to your doctor first.
If you have any further questions on the use of this medicine, ask your doctor, pharmacist, or nurse.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
Serious side effects
Tell your doctor immediatelyif you notice any of the following symptoms:
Other side effects
Tell your doctor as soon as possibleif you notice any of the following symptoms:
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)
Rare side effects(may affect up to 1 in 10,000 people)
Frequency not known(frequency cannot be estimated from the available data)
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist, or nurse, including any possible side effects not listed in this leaflet. You can also report side effects directly through the national reporting system listed in Appendix V. By reporting side effects, you can help provide more information on the safety of this medicine.
Store in a refrigerator (between 2°C and 8°C). Store the pre-filled syringe(s) in the original carton to protect from light. If necessary, a single pre-filled syringe can be stored out of the refrigerator, protected from light, at room temperature (up to 25°C) for a maximum of 7 days. Do not use the syringe if it has been out of the refrigerator for more than 7 days.
Composition of Entyvio
Appearance of the Product and Container Contents
Marketing Authorization Holder
Takeda Pharma A/S
Delta Park 45
2665 Vallensbaek Strand
Denmark
Manufacturer
Takeda Austria GmbH
St. Peter-Straße 25
A-4020 Linz
Austria
You can request more information about this medicinal product from the local representative of the marketing authorization holder:
België/Belgique/Belgien Takeda Belgium NV Tel.: +32 2 464 06 11 medinfoEMEA@takeda.com | Lietuva Takeda, UAB Tel.: +370 521 09 070 medinfoEMEA@takeda.com |
Luxembourg/Luxemburg Takeda Belgium NV Tel.: +32 2 464 06 11 medinfoEMEA@takeda.com | |
Česká republika Takeda Pharmaceuticals Czech Republic s.r.o. Tel: +420 234 722 722 medinfoEMEA@takeda.com | Magyarország Takeda Pharma Kft. Tel.: +361 2707030 medinfoEMEA@takeda.com |
Danmark Takeda Pharma A/S Tlf: +45 46 77 10 10 medinfoEMEA@takeda.com | Malta Drugsales Ltd Tel.: +356 2141 9070 safety@drugsalesltd.com |
Deutschland Takeda GmbH Tel.: +49 (0) 800 825 3325 medinfoEMEA@takeda.com | Nederland Takeda Nederland B.V. Tel.: +31 20 203 5492 medinfoEMEA@takeda.com |
Eesti Takeda Pharma OÜ Tel.: +372 6177 669 medinfoEMEA@takeda.com | Norge Takeda AS Tlf.: +47 800 800 30 medinfoEMEA@takeda.com |
Ελλάδα ΤΑΚΕДА ΕΛΛΑΣ Α.Ε. Τηλ.: +30 210 6387800 medinfoEMEA@takeda.com | Österreich Takeda Pharma Ges.m.b.H. Tel.: +43 (0) 800 20 80 50 medinfoEMEA@takeda.com |
España Takeda Farmacéutica España, S.A. Tel.: +34 917 90 42 22 medinfoEMEA@takeda.com | Polska Takeda Pharma Sp. z o.o. Tel.: +48223062447 medinfoEMEA@takeda.com |
France Takeda France SAS Tel.: +33 1 40 67 33 00 medinfoEMEA@takeda.com | Portugal Takeda Farmacêuticos Portugal, Lda. Tel.: +351 21 120 1457 medinfoEMEA@takeda.com |
Hrvatska Takeda Pharmaceuticals Croatia d.o.o. Tel: +385 1 377 88 96 medinfoEMEA@takeda.com | România Takeda Pharmaceuticals SRL Tel.: +40 21 335 03 91 medinfoEMEA@takeda.com |
Ireland Takeda Products Ireland Ltd. Tel.: 1800 937 970 medinfoEMEA@takeda.com | Slovenija Takeda Pharmaceuticals farmacevtska družba d.o.o. Tel.: +386 (0) 59 082 480 medinfoEMEA@takeda.com |
Ísland Vistor hf. Sími: +354 535 7000 medinfoEMEA@takeda.com | Slovenská republika Takeda Pharmaceuticals Slovakia s.r.o. Tel.: +421 (2) 20 602 600 medinfoEMEA@takeda.com |
Italia Takeda Italia S.p.A Tel.: +39 06 502601 medinfoEMEA@takeda.com | Suomi/Finland Takeda Oy Puh./Tel.: 0800 774 051 medinfoEMEA@takeda.com |
Κύπρος A.POTAMITIS MEDICARE LTD Τηλ: +357 22583333 a.potamitismedicare@cytanet.com.cy | Sverige Takeda Pharma AB Tel: 020 795 079 medinfoEMEA@takeda.com |
Latvija Takeda Latvia SIA Tel.: +371 67840082 medinfoEMEA@takeda.com | United Kingdom (Northern Ireland) Takeda UK Ltd Tel.: +44 (0) 3333 000 181 medinfoEMEA@takeda.com |
Date of Last Revision of this Leaflet: 03/2025
Other Sources of Information
This leaflet is available in a format suitable for blind or partially sighted patients and can be requested from the local representative of the marketing authorization holder.
Detailed information on this medicinal product is available on the European Medicines Agency website: http://www.ema.europa.eu.
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This information is intended only for healthcare professionals:
Traceability
In order to improve the traceability of biological medicinal products, the name and batch number of the administered product should be clearly recorded.
Instructions for Use:
Read and follow these instructions before proceeding with the injection. Your doctor, nurse, or pharmacist should show you how to use the Entyvio prefilled syringe before you use it for the first time.
Your Entyvio Single-Use Prefilled Syringe
Before Use | |||
Needle Shield | Medicine | Needle | |
Purple Plunger | Wings | Spring | Needle Cap |
After Use | |||
Needle Shield | |||
Covered Needle | |||
Each prefilled syringe has a needle shield that automatically covers the needle after you press the plunger all the way down and release it. |
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| Wait 30minutes |
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