Patient Information Leaflet
Entyvio 300 mg powder for concentrate for solution for infusion
vedolizumab
Read this leaflet carefully before you start using this medicine, because it contains important information for you.
1.What Entyvio is and what it is used for
2.What you need to know before you receive Entyvio
3.How you will receive Entyvio
4.Possible side effects
5.Storage of Entyvio
6. Contents of the pack and additional information.
What is Entyvio
Entyvio contains the active ingredient “vedolizumab”. Vedolizumab belongs to a group of biologic medications known as monoclonal antibodies (mAbs).
How Entyvio works
Entyvio blocks a protein on the surface of white blood cells (leukocytes) that causes inflammation in ulcerative colitis, Crohn's disease, and pyelonephritis, thereby reducing inflammation.
What Entyvio is indicated for
Entyvio is used to treat 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 medications. If you do not respond satisfactorily or cannot tolerate these medications, your doctor may prescribe Entyvio to reduce the symptoms of the disease.
Crohn's Disease
Crohn's disease is a disease that causes inflammation of the digestive system. If you have Crohn's disease, you will first be given other medications. If you do not respond satisfactorily or cannot tolerate these medications, your doctor may prescribe Entyvio to reduce the symptoms of the disease.
Pyelonephritis
Pyelonephritis is a disease that causes inflammation of the lining of the reservoir created during surgery to treat ulcerative colitis. If you have pyelonephritis, you may first be given antibiotics. If you do not respond sufficiently to antibiotics, your doctor may prescribe Entyvio to reduce the symptoms of the disease.
Do not use Entyvio:
Warnings and precautions
Consult your doctor or nurse before receiving Entyvio.
Inform your doctor or nurse immediatelywhen you receive this medication for the first time, during treatment and between doses:
Children and adolescents
Entyvio is not recommended for use in children and adolescents (under 18years of age) due to the lack of information on the use of this medication in this age group.
Other medications and Entyvio
Inform your doctor or nurse if you are taking, have taken recently or may need to take any other medication.
Inform your doctor if you have previously been administered:
Your doctor will have to decide if it is possible to administer Entyvio.
Pregnancy and breastfeeding
If you are pregnant or breastfeeding, or think you may be pregnant, consult your doctor before using this medication.
Pregnancy
The effects of Entyvio on pregnant women are unknown. Therefore, it is not recommended to use this medication during pregnancy. You and your doctor must decide if the benefit for you is clearly greater than the potential risk to you and your baby.
If you are a fertile woman, it is recommended that you avoid becoming pregnant during the use of Entyvio. You should use appropriate contraceptive methods during treatment and for at least 4.5months after receiving the last dose.
Breastfeeding
Inform your doctor if you are breastfeeding or intend to be. Entyvio passes into breast milk. There is not enough information about the effects this may have on your baby and milk production. It will be necessary to decide whether to interrupt breastfeeding or the Entyvio treatment, for which an evaluation of the benefits of breastfeeding for your baby and the benefits of treatment for you will be required.
Driving and operating machinery
The effects of this medication on the ability to drive and operate machinery or tools are small. A reduced number ofpatients have felt dizzy after receiving Entyvio. If you feel dizzy, do not drive or use tools or machinery.
How Much Entyvio Will Be Administered
The treatment with Entyvio is the same for ulcerative colitis, Crohn's disease, and sclerosing cholangitis.
The recommended dose is 300 mg of Entyvio, which will be administered as follows (see table):
Treatment Number (Infusion) | Treatment Time (Infusion) |
Treatment 1 | 0 weeks |
Treatment 2 | 2 weeks after Treatment 1 |
Treatment 3 | 6 weeks after Treatment 1 |
Subsequent Treatments | Every 8 weeks |
Your doctor may decide to modify this treatment schedule based on how you respond to Entyvio treatment.
What to Do If You Forget or Miss a Treatment Appointment for Entyvio
If you forget or miss a treatment appointment to receive the infusion, schedule another appointment as soon as possible.
What to Do If You Interrupt Entyvio Treatment
Do not stop using Entyvio without first talking to your doctor.
If you have any other questions about using this medication, ask your doctor or nurse.
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Severe side effects
Inform your doctorimmediatelyif you notice any of the following symptoms:
Other side effects
Inform your doctoras soon as possibleif you notice any of the following symptoms:
Frequent side effects(can affect more than 1 in 10 patients)
Common side effects(can affect up to 1 in 10 patients)
Uncommon side effects(can affect up to 1 in 100 patients)
Rare side effects(can affect up to 1 in 10,000 patients)
Unknown frequency(frequency cannot be estimated from available data)
Reporting side effects
If you experience any type of side effect, consult your doctor or nurse,even if it is a possible side effect that does not appear in this leaflet.You can also report them directly through thenational notification system included in theAppendix V. By reporting side effects, you can contribute to providing more information on the safety of this medicine.
Keep this medication out of the reach and sight of children.
Do not use this medication after the expiration date that appears on the carton and on the label, after "CAD." The expiration date is the last day of the month indicated.
Entyvio is administered by a doctor or nurse. Patients should not store or handle it.
Entyvio is for single use only.
Sealed vial:Store in the refrigerator (between 2°C and 8°C).Store the vial in the original carton to protect it from light.
Reconstituted and diluted solutions:Use immediately. If this is not possible, the reconstituted solution in the vial can be stored for up to 8 hours between 2°C and 8°C.The diluted solution in a sodium chloride 9 mg/ml (0.9%) solution for injection can be stored for up to 12 hours at room temperature equal to or below 25°C, for up to 24 hours in the refrigerator (between 2°C and 8°C), or for up to 12 hours at room temperature in the refrigerator (between 2°C and 8°C). The 24-hour period may include up to 8 hours in the case of the reconstituted solution in the vial between 2°C and 8°C and up to 12 hours in the case of the diluted solution in the infusion bag at a temperature between 20°C and 25°C.However, the infusion bag should be stored in the refrigerator (between 2°C and 8°C) for the remainder of the 24-hour period.The time the reconstituted solution is maintained in the vial should be subtracted from the time the solution is maintained in the infusion bag.
Do not freeze.
Do not use this medication if you observe the presence of particles in the liquid or discoloration (the solution should be transparent or opalescent, colorless, or with a yellowish tint) before administration.
Medicines should not be disposed of through the drains or in the trash. Ask your pharmacist how to dispose of the containers and medicines that you no longer need. This will help protect the environment.
Composition of Entyvio
Aspect of the product and content of the packaging
Holder of the marketing authorization
Takeda Pharma A/S
Delta Park 45
2665 Vallensbaek Strand
Denmark
Responsible for manufacturing
Takeda Austria GmbH
St. Peter‑Straße 25
A‑4020Linz
Austria
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
België/Belgique/Belgien Takeda Belgium NV Tel./Tel.: +32 2 464 06 11 | Lietuva Takeda, UAB Tel.: +370 521 09 070 |
Luxembourg/Luxemburg Takeda Belgium NV Tél./Tel.: +32 2 464 06 11 | |
Ceská republika Takeda Pharmaceuticals Czech Republic s.r.o. Tel: + 420 234 722 722 | Magyarország Takeda Pharma Kft. Tel.: +361 2707030 |
Danmark Takeda Pharma A/S Tlf: +45 46 77 10 10 | Malta Drugsales Ltd Tel.: +356 2141 9070 |
Deutschland Takeda GmbH Tel.: +49 (0) 800 825 3325 | Nederland Takeda Nederland B.V. Tel.:+31 20 203 5492 |
Eesti Takeda PharmaOÜ Tel.: +372 6177 669 | Norge Takeda AS Tlf: +47 800 800 30 |
Ελλάδα TAKEDAΕΛΛΑΣ Α.Ε. Τηλ.:+30 210 6387800 | Österreich Takeda Pharma Ges.m.b.H. Tel.: +43 (0) 800 20 80 50 |
España Takeda Farmacéutica España, S.A. Tel.: +34 917 90 42 22 | Polska Takeda Pharma Sp. z o.o. Tel.: +48223062447 |
France Takeda France SAS Tel.:+33 1 40 67 33 00 | Portugal Takeda Farmacêuticos Portugal, Lda. Tel.: +351 21 120 1457 |
Hrvatska Takeda Pharmaceuticals Croatia d.o.o. Tel: +385 1 377 88 96 | România Takeda Pharmaceuticals SRL Tel.: +40 21 335 03 91 |
Ireland Takeda Products Ireland Ltd. Tel.: 1800 937 970 | Slovenija Takeda Pharmaceuticals farmacevtska družba d.o.o. Tel.: +386 (0) 59 082 480 |
Ísland Vistor hf. Simi: +354 535 7000 | 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 | Suomi/Finland Takeda Oy Puh/Tel: 0800 774 051 |
Κύπρος A.POTAMITIS MEDICARE LTD Τηλ: +357 22583333 | Sverige Takeda PharmaAB Tel: 020 795 079 |
Latvija Takeda Latvia SIA Tel.: +371 67840082 | United Kingdom (Northern Ireland) Takeda UK Ltd Tel.: +44 (0) 3333 000 181 |
Last review date of this leaflet: 03/2025
Other sources of information
This leaflet is available in a format suitable for patients who are blind or have reduced vision and can be requested from the local representative of the marketing authorization holder.
The detailed information about this medication is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
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This information is intended solely for healthcare professionals:
Traceability
In order to improve the traceability of biological medicines, the name and batch number of the administered medicine must be clearly recorded.
Instructions for reconstitution and infusion
The reconstituted solution should be used as soon as possible.
Storage conditions | ||
Refrigerator (2°C‑8°C) | 20°C‑25°C | |
Solution reconstituted in the vial | 8hours | Do not store1 |
Diluted solution in a sodium chloride9mg/ml (0.9%) solution for injection | 24hours2,3 | 12hours2 |
1This time is allowed for reconstitution, up to 30minutes.
2This time assumes that the reconstituted solution is immediately diluted in the sodium chloride 9mg/ml (0.9%) solution for injection and is stored only in the infusion bag. The time the reconstituted solution is stored in the vial should be subtracted from the time the solution can be stored in the infusion bag.
3This period of time may include up to 12hours at 20°Cand25°C.
Do not freeze. Do not store unused solution for reutilization.
Each vial is for single use.
The disposal of unused medication and all materials that have come into contact with it will be carried out in accordance with local regulations.
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