Patient Leaflet Updated 12-Feb-2024 | Bayer plc
VITRAKVI 20 mg/mL oral solution (Strawberry flavour)
Due to regulatory changes, the content of the following Patient Information Leaflet may vary from the one found in your medicine pack. Please compare the 'Leaflet prepared/revised date' towards the end of the leaflet to establish if there have been any changes.
If you have any doubts or queries about your medication, please contact your doctor or pharmacist.
VITRAKVI 20 mg/mL oral solution
larotrectinib
▼This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See the end of section 4 for how to report side effects.
1. What VITRAKVI is and what it is used for
2. What you need to know before you take VITRAKVI
3. How to take VITRAKVI
4. Possible side effects
5. How to store VITRAKVI
6. Contents of the pack and other information
VITRAKVI contains the active substance larotrectinib.
It is used in adults, adolescents and children to treat solid tumours (cancer) in various parts of the body that are caused by a change in the NTRK gene (neurotrophic tyrosine receptor kinase).
VITRAKVI is only used when
Before you are given VITRAKVI, your doctor will do a test to check if you have the change in the NTRK gene.
In patients whose cancer is due to an altered NTRK gene, the change in the gene causes the body to make an abnormal protein called TRK fusion protein, which can lead to uncontrolled cell growth and cancer. VITRAKVI blocks the action of TRK fusion proteins and so may slow or stop the growth of the cancer. It may also help to shrink the cancer.
If you have any questions on how VITRAKVI works or why it has been prescribed for you, ask your doctor, pharmacist or nurse.
VITRAKVI can increase the amount of the liver enzymes ALT and AST and bilirubin in your blood. Your doctor will do blood tests before and during treatment to check the level of ALT, AST and bilirubin and check how well your liver is working.
Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines. This is because some medicines may affect the way VITRAKVI works or VITRAKVI may affect how other medicines work.
In particular, tell your doctor, pharmacist or nurse if you are taking any of the following medicines:
If any of the above apply to you (or you are not sure), talk to your doctor, pharmacist or nurse.
Do not eat grapefruit or drink grapefruit juice while taking VITRAKVI. This is because it may increase the amount of VITRAKVI in your body.
Pregnancy
If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.
You should not use VITRAKVI during pregnancy since the effect of VITRAKVI on the unborn is not known.
Breast-feeding
Do not breast-feed while taking this medicine and for 3 days after the last dose. This is because it is not known if VITRAKVI passes into breast milk.
You should avoid getting pregnant while taking this medicine.
If you are able to become pregnant, your doctor should do a pregnancy test before you start treatment.
You must use effective methods of contraception while taking VITRAKVI and for at least 1 month after the last dose, if
Ask your doctor about the best method of contraception for you.
VITRAKVI may make you feel dizzy or tired. If this happens, do not drive, cycle or use any tools or machines.
Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor, pharmacist or nurse if you are not sure.
Adults (from 18 years)
Children and adolescents
If necessary, VITRAKVI may be administered via a nasogastric feeding tube. For details how to do so, please ask your doctor, pharmacist or nurse.
Talk to your doctor, pharmacist or nurse or go to a hospital straight away. Take the medicine pack and this leaflet with you.
Do not take a double dose to make up for a forgotten dose or if you vomit after taking this medicine. Take your next dose at the usual time.
Do not stop taking this medicine without talking to your doctor first. It is important to take VITRAKVI for as long as your doctor tells you.
If you are not able to take the medicine as your doctor prescribed talk to your doctor straight away.
If you have 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.
You should immediately contact your doctor if you experience any of the following serious side effects:
Your doctor may decide to lower the dose, or pause or stop the treatment.
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):
Not known (not known how often they occur)
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 (see details below). By reporting side effects you can help provide more information on the safety of this medicine.
or search for MHRA Yellow Card in the Google Play or Apple App Store.
The active substance is larotrectinib.
Each mL of oral solution contains 20 mg of larotrectinib (as sulfate).
The other ingredients are:
See “VITRAKVI contains” in section 2 for more information.
VITRAKVI is a colourless to yellow or orange or red or brownish oral solution.
Each carton contains 2 child-resistant glass bottles containing 50 mL oral solution each.
For any information about this medicine, please contact Bayer plc, Tel. 0118 206 3000.
This leaflet was last revised in March 2023.
Product licence number: PLGB 00010/0741
This medicine has been given ‘conditional approval’. This means that there is more evidence to come about this medicine.
The Medicines and Healthcare products Regulatory Agency (MHRA) will review new information on this medicine at least every year and this leaflet will be updated as necessary.
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