Package Leaflet: Information for the Patient
LIVTENCITY 200 mg Film-Coated Tablets
maribavir
This medicine is subject to additional monitoring, which will allow for quick identification of new safety information. You can help by reporting any side effects you may get. The last section of section 4 will tell you how to report side effects.
Read all of this leaflet carefully before you start taking this medicine, because it contains important information for you.
Contents of the Package Leaflet
LIVTENCITY is an antiviral medicine that contains the active substance maribavir.
It is a medicine used to treat adults who have received an organ or bone marrow transplant and have developed a cytomegalovirus (CMV) infection that has not gone away or has come back after taking another antiviral medicine.
CMV is a virus that many people have without symptoms and normally remains in the body without causing any harm. However, if the immune system is weakened after receiving an organ or bone marrow transplant, you may be at a higher risk of becoming ill due to CMV.
Do not take LIVTENCITY
Do not take LIVTENCITY if any of the above applies to you. If you are unsure, consult your doctor, pharmacist, or nurse before taking LIVTENCITY.
Warnings and precautions
Consult your doctor or pharmacist before taking LIVTENCITY if you are already being treated with ciclosporin, tacrolimus, sirolimus, or everolimus (medicines to prevent transplant rejection). You may need to have extra blood tests to check the levels of these medicines in your blood. High levels of these medicines can cause serious side effects.
Children and adolescents
LIVTENCITY should not be used in children and adolescents under 18 years of age, as LIVTENCITY has not been tested in this age group.
Other medicines and LIVTENCITY
Tell your doctor or pharmacist if you are taking, have recently taken, or might take any other medicines, as LIVTENCITY may affect how other medicines work, and other medicines may affect how LIVTENCITY works. Your doctor or pharmacist will tell you if it is safe to take LIVTENCITY with other medicines.
There are some medicines that you should not take with LIVTENCITY. See the list "Do not take LIVTENCITY".
Tell your doctor if you are taking any of the following medicines, as your doctor may need to change your medicines or adjust the dose of them:
You can ask your doctor, pharmacist, or nurse for a list of medicines that may interact with LIVTENCITY.
Pregnancy
If you are pregnant, think you may be pregnant, or are planning to have a baby, ask your doctor for advice before taking this medicine. It is not recommended to use LIVTENCITY during pregnancy, as it has not been studied in pregnancy and it is not known whether LIVTENCITY can harm your baby while you are pregnant.
Breast-feeding
If you are breast-feeding or plan to breast-feed, ask your doctor for advice before taking this medicine. It is not recommended to breast-feed during treatment with LIVTENCITY, as it is not known whether LIVTENCITY passes into breast milk or whether it could affect your baby.
Driving and using machines
LIVTENCITY has no influence on the ability to drive and use machines.
LIVTENCITY contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per tablet; this is essentially "sodium-free".
Always take this medicine exactly as your doctor, pharmacist, or nurse has told you. If you are unsure, ask your doctor, pharmacist, or nurse.
The recommended dose is 400 mg twice a day. This means you should take two 200 mg tablets of LIVTENCITY in the morning and two 200 mg tablets in the evening. You can take this medicine with or without food, as a whole tablet or crushed.
If you take more LIVTENCITY than you should
If you take too much LIVTENCITY, tell your doctor immediately.
If you forget to take LIVTENCITY
If you miss a dose and it is 3 hours or less before your next dose, skip the missed dose and go back to your regular schedule. Do not take a double dose to make up for missed doses.
If you stop taking LIVTENCITY
Even if you feel better, do not stop taking LIVTENCITY without talking to your doctor first. Taking LIVTENCITY as recommended should give you the best chance of getting rid of the CMV infection and/or disease.
If you have any other questions about 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.
Tell your doctor, pharmacist, or nurse if you notice any of the following side effects:
Very common(may affect more than 1 in 10 people):
Common(may affect up to 1 in 10 people):
Reporting of side effects
If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the European Medicines Agency website: http://www.ema.europa.eu. 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 on the label of the bottle after EXP. The expiry date refers to the last day of that month.
Do not store above 30°C.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of LIVTENCITY
Appearance of the product and pack size
LIVTENCITY 200 mg film-coated tablets are blue, oval, and convex, with "SHP" engraved on one side and "620" on the other.
The tablets are packaged in high-density polyethylene (HDPE) bottles with child-resistant caps and contain 28, 56, or 112 (2 bottles of 56) film-coated tablets.
Not all pack sizes may be marketed.
Marketing authorisation holder
Takeda Pharmaceuticals International AG Ireland Branch
Block 2 Miesian Plaza
50-58 Baggot Street Lower
Dublin 2
D02 HW68
Ireland
Manufacturer
Takeda Ireland Limited
Bray Business Park
Kilruddery
Co. Wicklow
Ireland
You can get more information about this medicine by contacting the local representative of the marketing authorisation 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 | |
Ceská republika Takeda Pharmaceuticals Czech Republic s.r.o. Tel: + 420 234 722 722 medinfoEMEA@takeda.com | Magyarország Takeda Pharma Kft. Tel.: +36 1 270 7030 medinfoEMEA@takeda.com |
Danmark Takeda Pharma A/S Tlf: +45 46 77 10 10 medinfoEMEA@takeda.com | Malta Τakeda HELLAS S.A. Tel: +30 210 6387800 medinfoEMEA@takeda.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 AS Tel: +372 6177 669 medinfoEMEA@takeda.com | Norge Takeda AS Tlf: +47 800 800 30 medinfoEMEA@takeda.com |
Ελλáδα Τakeda ΕΛΛΑΣ Α.Ε. Tηλ: +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 Tél: + 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 |
Κúπρος Τakeda ΕΛΛΑΣ Α.Ε. Τηλ.: +30 210 6387800 medinfoEMEA@takeda.com | 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) 2830 640 902 medinfoEMEA@takeda.com |
Date of last revision of this leaflet: 02/2023
Other sources of information
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu.