Prospect: information for the patient
Kaftrio 37,5mg/25mg/50mg film-coated tablets
Kaftrio75mg/50mg/100mg film-coated tablets
ivacaftor/tezacaftor/elexacaftor
This medicine is subject to additional monitoring, which will speed up the detection of new information about its safety. You can contribute by reporting any adverse effects you may experience. The final part of section4 includes information on how to report these adverse effects.
Read this prospect carefully before starting to take this medicine, as it contains important information for you.
Kaftrio contains three active principles:ivacaftor, tezacaftor and elexacaftor. This medication helps lung cells function better in some patients with cystic fibrosis (CF). CF is a hereditary condition in which the lungs and digestive system can become obstructed with thick and sticky mucus.
Kaftrio taken with ivacaftor is forpatients aged 6or older who suffer from CF withat least one F508del mutationin the CFTR gene(cystic fibrosis transmembrane conductance regulator).Kaftriois designed as a long-term treatment.
Kaftrio acts on a protein called CFTR. The protein is damaged in some people with CF, if they have a mutation in theCFTRgene.
Kaftrio is usually taken with another medication,ivacaftor. Ivacaftor makes the protein function better while tezacaftor and elexacaftor increase the amount of protein on the cell surface.
Kaftrio (taken together with ivacaftor) helps you breathe better by improving your lung function. You may also notice that you get sick less often or that it is easier for you to gain weight.
Do not takeKaftrio
Consult your doctorand do not take the tablets if this is the case.
Warnings and precautions
Inform your doctor immediatelyif you have any symptoms indicative of liver problems. These are listed in section4.
Childrenunder 6years
Do not give this medication to children under 6years old as the safety and efficacy of Kaftrio tablets in this age group are unknown.
Other medications andKaftrio
Inform your doctor or pharmacistif you are taking, have taken recently, or may need to take any other medication. Some medications may affect the functioning of Kaftrio or increase the likelihood of adverse effects. In particular, consult your doctor if you are taking any of the medications listed below. Your doctor may change the dose of one of the medications if you are taking some of these.
TakingKaftrio withfood and drinks
Avoid foods or drinks containing grapefruit during treatment as they may increasethe adverse effects of Kaftrio by increasing the amount of Kaftrio in the body.
Pregnancy and breastfeeding
Driving and operating machinery
Kaftrio may cause dizziness. If you feel dizzy, do not drive, ride a bike, or operate machinery unless you are sure it will not affect you.
Kaftrio contains sodium
This medicationcontainsless than23mg of sodium (1mmol)per dose; this is, essentially “sodium-free”.
Follow exactly the administration instructions of this medication indicated by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again..
Your doctor will determine the correct dose for you.
Kaftrio is usually taken with ivacaftor.
Recommended dose for patients 6 years or older
Age | Weight | Morning dose | Evening dose |
6 years to <12 yearsyears | Twotablets of 37.5mg of ivacaftor/25mg of tezacaftor/50mg of elexacaftor | Onetablet of 75mg of ivacaftor | |
6 years to <12 yearsyears | ≥30kg | Twotablets of 75mg of ivacaftor/50mg of tezacaftor/100mg of elexacaftor | Onetablet of 150mg of ivacaftor |
12 years or older | - | Twotablets of 75mg of ivacaftor/50mg of tezacaftor/100mg of elexacaftor | Onetablet of 150mg of ivacaftor |
Take the morning and evening tablets with an interval of about 12 hours.
The tablets are taken orally.
Take the Kaftrio and ivacaftor tablets with foods that contain fats.Meals or snacks that contain fats are those prepared with butter or oils or those that contain eggs. Examples of other foods that contain fats are:
Avoid meals and drinks that contain grapefruit while taking Kaftrio. SeeTaking Kaftrio with food and drinksin section2 for more information.
Swallow the tablets whole.Do not chew, crush, or break the tablets before swallowing.
You should continue taking all other medications, unless your doctor tells you to stop taking them.
If you have liver problems,whether moderate or severe, your doctor may reduce your dose of tablets or decide to suspend treatment with Kaftrio. SeeWarnings and precautionsin section2.
If you take moreKaftriothan you should
Consult your doctor or pharmacist.If possible, bring the medication and this leaflet. You may experience adverse effects, including those listed in section4 below.
If you forget to takeKaftrio
If you forget a dose, calculate how much time has passed since the time you were supposed to take the dose.
Do nottake a double dose to make up for the missed tablets.
If you interrupt treatment withKaftrio
Your doctor will tell you for how long you need to take Kaftrio. It is essential that you take this medication consistently. Do not make changes unless your doctor tells you to.
If you have any other questions about the use of this medication, ask your doctor or pharmacist..
Like all medicines, this medicine can cause side effects, although not everyone will experience them.
Severe side effects
Possible signs of liver problems
Liver damage and worsening of liver functionin people with severe liver disease. Worsening of liver function can be severe and may require a transplant.
The increase in liver enzymes in the blood is frequent in patients with FQ. The following may be signs of liver problems:
Depression.The signs include sadness or mood alteration, anxiety, emotional discomfort.
Inform your doctor immediatelyif you experience any of these symptoms.
Very common side effects(may affect more than 1 in 10people)
Inform your doctor immediatelyif you experience a skin rash.
Other side effectsobserved with Kaftrio:
Very common(may affect more than 1 in 10people)
Common(may affect up to 1 in 10people)
Uncommon(may affect up to 1 in 100people)
Frequency not known(cannot be estimated from available data)
Additional side effectsin adolescents
The side effects observed in adolescents are similar to those observed in adults.
Reporting of side effects
If you experience any type of side effect, consult your doctor or pharmacist, 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 sight and reach of children.
Do not use this medication after the expiration date that appears on the box and on the blister afterEXP.The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medicines should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the packaging and medications that you no longer need. In this way, you will help protect the environment.
Composition ofKaftrio
Kaftrio 37,5mg/25mg/50mg film-coated tablets
Each film-coated tablet contains 37.5mg of ivacaftor, 25mg of tezacaftor, and 50mg of elexacaftor.
Kaftrio75mg/50mg/100mg film-coated tablets
Each film-coated tablet contains 75mg of ivacaftor, 50mg of tezacaftor, and 100mg of elexacaftor.
See the end of section 2 for important information on the contents of Kaftrio.
Appearance of the product and contents of the pack
Kaftrio37,5mg/25mg/50mgfilm-coated tablets are orange-yellow capsules with the imprint “T50” on one side and smooth on the other.
Kaftrio75mg/50mg/100mg film-coated tablets are orange capsules with the imprint “T100” on one side and smooth on the other.
Kaftrio is available in pack sizes of 56film-coated tablets (4blister packs of 14film-coated tablets each).
Marketing Authorization Holder
Vertex Pharmaceuticals (Ireland) Limited
Unit 49, Block 5, Northwood Court, Northwood Crescent, ,
Dublin 9, D09 T665,
Ireland
Responsible Person
Almac Pharma Services (Ireland) Limited
Finnabair Industrial Estate
Dundalk
Co. Louth
A91 P9KD
Ireland
Almac Pharma Services Limited
Seagoe Industrial Estate
Craigavon
County Armagh
BT63 5UA
United Kingdom (Northern Ireland)
For further information about this medicinal product, please contact the local representative of the marketing authorization holder:
België/Belgique/Belgien,????????,Ceská republika, Danmark, Deutschland, Eesti, France, Hrvatska, Ireland, Ísland, Κ?προς, Latvija, Lietuva, Luxembourg/Luxemburg, Magyarország, Malta, Nederland, Norge, Österreich, Polska, Portugal, România, Slovenija, Slovenská republika, Suomi/Finland, Sverige Vertex Pharmaceuticals (Ireland) Limited Tél/Tel/Te?/Tlf/Sími/Τηλ/Puh: +353 (0) 1 761 7299 | España Vertex Pharmaceuticals Spain, S.L. Tel: + 34 91 7892800 |
Ελλ?δα VertexΦαρμακευτικ? Μονοπρ?σωπη Αν?νυμη Εταιρ?α Τηλ: +30 (211) 2120535 | Italia Vertex Pharmaceuticals (Italy) S.r.l. Tel: +39 0697794000 |
Date of the last revision of this leaflet:
Other sources of information
The detailed information on this medicinal product isavailable on the website of the European Medicines Agency:https://www.ema.europa.eu.There are also links to other websites on rare diseases and orphan medicinal products.
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