Product Information for the Patient
Venclyxto 10 mg Film-Coated Tablets
Venclyxto 50 mg Film-Coated Tablets
Venclyxto 100 mg Film-Coated Tablets
venetoclax
Read this entire product information carefully before starting to take this medicine, as it contains important information for you.
1.What is Venclyxto and for what it is used
2.What you need to know before starting to take Venclyxto
3.How to take Venclyxto
4.Possible side effects
5.Storage of Venclyxto
6.Contents of the pack and additional information
What is Venclyxto
Venclyxtois a cancer medicationthatcontains the active ingredient venetoclax. It belongs to a group of medications called “BCL-2 inhibitors”.
What is Venclyxto used for
Venclyxto is used to treat adults with:
CLL is a type of cancer that affects a type of white blood cells called lymphocytes, and the lymph nodes. In CLL, lymphocytes multiply too quickly and live too long, resulting in an excess of these cells in the blood.
AML is a type of cancer that affects a type of white blood cells called myeloid cells. In AML, myeloid cells multiply and grow very quickly in the bone marrow and blood, resulting in too many of them and not enough red blood cells in the blood.
How Venclyxto works
Venclyxto acts by blocking a protein in the body called “BCL-2”. This protein is present in high amounts in some cancer cells and helps cancer cells to survive. Blocking this protein facilitates the destruction of cancer cells and reduces their number. It also delays the worsening of the disease
Do not take Venclyxto if:
Once the Venclyxto dose has been increased to the standard full dose, consult your doctor if you can start taking these medicines again.
It is essential to inform your doctor, pharmacist, or nurse about all the medicines you are taking, including those available over-the-counter, prescription medicines, vitamins, and herbal supplements. Your doctor may ask you to stop taking certain medicines when starting Venclyxto and during the first few days or weeks, during the dose increase to the standard full dose.
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting Venclyxto if:
If you are in any of the above circumstances, or are unsure, consult your doctor, pharmacist, or nurse before taking this medicine.
Tumor Lysis Syndrome (TLS)
Some people may experience an unusual amount of certain salts in the blood (such as potassium and uric acid) due to the rapid breakdown of cancer cells during treatment. This situation can cause kidney function abnormalities, abnormal heart rhythms, or seizures. The condition is called Tumor Lysis Syndrome (TLS). The risk of TLS occurs in the first few days or weeks of treatment with Venclyxto, when the dose is increased.
If you have CLL
Your doctor, pharmacist, or nurse will perform blood tests to detect the presence of TLS.
Before starting treatment with Venclyxto, your doctor will administer medicines to help prevent the accumulation of uric acid in the body.
Drinking plenty of water, at least 1.5 to 2 liters per day, helps to eliminate waste products from cancer cells through urine and may reduce the risk of TLS (see section 3).
Inform your doctor, pharmacist, or nurse immediately if you experience any of the TLS symptoms listed in section 4.
If you are at risk of TLS, you may receive treatment in the hospital to administer intravenous fluids if necessary, perform more frequent blood tests, and monitor for adverse effects. This precaution is taken to ensure you can safely continue taking this medicine.
If you have Lymphoma
You may receive treatment in the hospital, and your doctor or nurse will ensure you have enough water or fluids, administer medicines to prevent uric acid accumulation in your body, and perform blood tests before starting Venclyxto, during dose increases, and when starting the full dose.
Children and Adolescents
Venclyxto should not be used in children and adolescents.
Other Medicines and Venclyxto
Inform your doctor or pharmacist if you are taking any of the following medicines, as they may increase or decrease the amount of venetoclax in the blood:
Your doctor may change your Venclyxto dose.
Inform your doctor if you are taking any of the following medicines, as Venclyxto may affect their functioning:
Inform your doctor or pharmacist if you are taking, have taken recently, or may need to take any other medicine. This includes over-the-counter medicines, herbal supplements, and vitamins. You should do this because Venclyxto may affect how some medicines work. Additionally, other medicines may affect how Venclyxto works.
Taking Venclyxto with Food and Drinks
Do not take products containing grapefruit, Seville oranges (bitter oranges, often used in marmalades), or starfruit while taking Venclyxto - do not eat them, drink their juice, or take supplements that may contain them. This is because they may increase the amount of venetoclax in the blood.
Pregnancy
Contraception
Breastfeeding
Do not breastfeed your child while taking this medicine. The active ingredient of Venclyxto may pass into breast milk.
Fertility
Based on animal studies, Venclyxto may cause male infertility (low or no sperm count). This may affect your ability to have children. Consult your doctor about sperm storage before starting treatment with Venclyxto.
Driving and Using Machines
After taking Venclyxto, you may feel tired or dizzy, which may affect your ability to drive and use tools or machines. If this happens, do not drive or use any tools or machines.
Venclyxto contains sodium.
This medicine contains less than 1 mmol of sodium (23 mg) per dose; it is essentially "sodium-free."
Follow exactly the administration instructions of this medication indicated by your doctor, pharmacist or nurse. In case of doubt, consult your doctor, pharmacist or nurse again.
Amount to take
If you have CLL
You will start treatment with Venclyxto at a low dose for 1 week. Your doctor will gradually increase the dose over the next 4 weeks to the standard full dose. During the first 4 weeks, you will receive a new package every week.
You may need a dose adjustment due to adverse effects. Your doctor will indicate what dose you should take.
If you have LMA
You will start treatment with Venclyxto at a lower dose. Your doctor will gradually increase the dose each day for the first 3 days. After 3 days, you will take the standard full dose. The dose (tablets) is taken once a day.
Doses are indicated in the following table
Day | Daily dose of Venclyxto |
1 | 100 mg (one 100 mg tablet) |
2 | 200 mg (two 100 mg tablets) |
3 and subsequent | 400 mg (four 100 mg tablets) |
Your doctor will administer Venclyxto in combination with another medication (azacitidine or decitabine).
You will continue to take the full dose of Venclyxto until your LMA worsens or you cannot take Venclyxto because it is causing severe adverse effects.
How to take Venclyxto
If you vomit after taking Venclyxto, do not take an additional dose that day. Take the next dose at the usual time the next day. If you have trouble taking this medication, inform your doctor.
Drink plenty of water
If you have CLL
It is very important that you drink plenty of water while taking Venclyxto during the first 5 weeks of treatment. This will help eliminate the waste products of cancer cells from the blood through urine.
You should start drinking at least 1.5 to 2 liters of water per day, two days before starting Venclyxto. You can also include non-caffeinated and non-alcoholic beverages in this amount, but do not drink grapefruit, bitter orange or starfruit juice. You should continue to drink at least 1.5 to 2 liters of water per day two days before the dose increase and on that day.
If your doctor considers that you are at risk of developing TLS, you may receive treatment in the hospital to administer additional intravenous fluids, if necessary, perform more frequent blood tests and check for adverse effects. This precaution is taken to determine if you can safely continue taking this medication.
If you have LMA
It is very important that you drink plenty of water while taking Venclyxto, especially when starting treatment and when increasing the dose. Drinking water will help eliminate the waste products of cancer cells from the blood through urine. If you are in the hospital, your doctor or nurse will administer intravenous fluids if necessary to ensure this occurs.
If you take more Venclyxto than you should
If you take more Venclyxto than you should, consult your doctor, pharmacist or nurse or go to the hospital immediately. Bring the tablets and this leaflet with you.
If you forget to take Venclyxto
If you interrupt treatment with Venclyxto
Do not interrupt treatment with this medication unless your doctor tells you to. If you have any other questions about the use of this medication, ask your doctor, pharmacist or nurse.
Like all medicines, this medicine can cause side effects, although not everyone will experience them. This medicine can cause the following serious side effects:
Tumour Lysis Syndrome (TLS)(frequent-can affect up to 1 in 10people)
Stop taking Venclyxto and seek medical attention immediately if you notice any of the symptoms of TLS:
Decrease in white blood cell count (neutropenia) and infections(very frequent-can affect more than 1 in 10people)
Your doctor will check the blood cell count during treatment with Venclyxto. The decrease in white blood cells may increase the risk of infections. The signs may be fever, chills, weakness, or confusion, cough, pain, or burning sensation while urinating. Some infections such as pneumonia or blood infection (sepsis) can be severe and cause death. Inform your doctor immediately if you have signs of infection during treatment with this medicine.
Inform your doctor if you notice any of the following side effects:
If you have CLL
Very frequent(can affect more than 1 in 10 people)
The following may also be observed in the blood test:
Frequent(can affect up to 1 in 10 people)
The following may also be observed in the blood test:
If you have LMA
Very frequent(can affect more than 1 in 10people)
The blood tests may show:
Frequent(can affect up to 1 in 10people)
Reporting of side effects
If you experience any type of side effect, consult your doctor, pharmacist, or nurse, even if it is a possible side effect that does not appear in this leaflet. You can also report them directly through thenationalnotification 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 thelabelof the blister pack and the container, after CAD.
No special storage conditions are required.
Medicines should not be disposed of through drains or in the trash. Ask your pharmacist how to dispose of the containers and medications that you no longer need. By doing so, you will help protect the environment.
Composition of Venclyxto
The active ingredient is venetoclax.
The other components are:
On the film coating:
Appearance of the product and contents of the pack
Venclyxto 10 mg film-coated tablet is pale yellow, round, 6 mm in diameter, marked with a V on one face and 10 on the other.
Venclyxto 50 mg film-coated tablet is beige, oblong, 14 mm long, marked with a V on one face and 50 on the other.
Venclyxto 100 mg film-coated tablet is pale yellow, oblong, 17.2 mm long, marked with a V on one face and 100 on the other.
Venclyxto tablets are presented in blisters or bottles contained in the following packs:
Venclyxto 10mgfilm-coated tablets:
Venclyxto 50mg film-coated tablets:
Venclyxto 100mg film-coated tablets:
Only some pack sizes may be marketed.
Marketing authorisation holder and responsible manufacturer
AbbVie Deutschland GmbH & Co. KG
Knollstrasse
67061 Ludwigshafen
Germany
AbbVieS.r.l.
S.R. 148 Pontina, km 52 SNC
04011 Campoverde di Aprilia (Latina)
Italy
For further information about this medicinal product, please contact the local representative of the marketing authorisation holder:
België/Belgique/Belgien AbbVie SA Tél/Tel: +32 10 477811 | Lietuva AbbVie UAB Tel: +370 5205 3023 |
Luxembourg/Luxemburg AbbVie SA Belgique/Belgien Tél/Tel: +32 10 477811 | |
Ceská republika AbbVie s.r.o. Tel: +420 233 098 111 | Magyarország AbbVie Kft. Tel:+36 1 455 8600 |
Danmark AbbVie A/S Tlf: +45 72 30‑20‑28 | Malta V.J.Salomone Pharma Limited Tel: +356 22983201 |
Deutschland AbbVie Deutschland GmbH & Co.KG Tel: 00800 222843 33 (free of charge) Tel: +49 (0) 611/1720‑0 | Nederland AbbVie B.V. Tel: +31 (0)88 322 2843 |
Eesti AbbVie OÜ Tel: +372 623 1011 | Norge AbbVie AS Tlf: +47 67 81 80 00 |
Ελλ?δα AbbVie ΦΑΡΜΑΚΕΥΤΙΚΗ Α.Ε. Τηλ: +30 214 4165 555 | Österreich AbbVie GmbH Tel: +43 1 20589‑0 |
España AbbVie Spain, S.L.U. Tel: +34 91 384 09 10 | Polska AbbVie Sp. z o.o. Tel.: +48 22 372 78 00 |
France AbbVie Tél: +33 (0) 1 45 60 13 00 | Portugal AbbVie, Lda. Tel: +351 (0)21 1908400 |
Hrvatska AbbVie d.o.o. Tel: + 385 (0)1 5625 501 | România AbbVie S.R.L. Tel: +40 21 529 30 35 |
Ireland AbbVie Limited Tel: +353 (0)1 4287900 | Slovenija AbbVie Biofarmacevtska družba d.o.o. Tel: +386 (1)32 08 060 |
Ísland Vistor hf. Tel: +354 535 7000 | Slovenská republika AbbVie s.r.o. Tel: +421 2 5050 0777 |
Italia AbbVie S.r.l. Tel: +39 06 928921 | Suomi/Finland AbbVie Oy Puh/Tel: +358 (0)10 2411 200 |
Κ?προς Lifepharma (Z.A.M.)Ltd Τηλ: +357 22 34 74 40 | Sverige AbbVie AB Tel: +46 (0)8 684 44 600 |
Latvija AbbVie SIA Tel: +371 67605000 |
Last update of this leaflet:
Other sources of information
The detailed information on this medicinal product is available on the website of the European Medicines Agencyhttp://www.ema.europa.eu.
The website of the European Medicines Agency may be consulted for this leaflet in all languages of the European Union/European Economic Area.
To listen to this leaflet or request a copy in Braille, large print or audio, please contact the local representative of the marketing authorisation holder.
Есть вопросы по этому лекарству или вашим симптомам? Свяжитесь с лицензированным врачом для получения помощи и персонализированного ухода.