Prospect: Information for the Patient
Aybintio 25 mg/ml Concentrate for Solution for Infusion
bevacizumab
This medicine is subject to additional monitoring, which will expedite the detection of new information about its safety. You can contribute by reporting any adverse effects you may experience. The final part of section 4 includes information on how to report these adverse effects.
Read this prospect carefully before starting to use this medicine, because it contains important information for you.
The active ingredient of Aybintio is bevacizumab, a humanized monoclonal antibody (a type of protein that is normally produced by the immune system to help the body defend itself against infections and cancer). Bevacizumab selectively binds to a protein called vascular endothelial growth factor (VEGF, English acronym), which is located in the walls of blood and lymphatic vessels of the body. The VEGF protein causes blood vessels to grow within the tumor, which supplies it with nutrients and oxygen. When bevacizumab binds to VEGF, it prevents tumor growth by blocking the growth of blood vessels, which provide the necessary nutrients and oxygen for the tumor.
Aybintio is a medication used for the treatment of adult patients with advanced colorectal or rectal cancer. Aybintio will be administered in combination with a chemotherapy regimen containing a fluoropyrimidine medication.
Aybintio is also used for the treatment of adult patients with metastatic breast cancer. When used in patients with breast cancer, it will be administered with a chemotherapy medication called paclitaxel or capecitabine.
Aybintio is also used for the treatment of adult patients with advanced non-small cell lung cancer. Aybintio will be administered along with a platinum-based chemotherapy regimen.
Aybintio is also used for the treatment of adult patients with advanced non-small cell lung cancer when cancer cells have specific mutations in a protein called the epidermal growth factor receptor (EGFR). Aybintio will be administered in combination with erlotinib.
Aybintio is also used for the treatment of adult patients with advanced renal cancer. When used in patients with renal cancer, it will be administered with another type of medication called interferon.
Aybintio is also used for the treatment of adult patients with advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer. When used in patients with epithelial ovarian, fallopian tube, or primary peritoneal cancer, it will be administered in combination with carboplatin and paclitaxel.
When used in adult patients with advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer who have had a recurrence of their disease of at least 6 months since their last treatment with a platinum-based chemotherapy regimen, Aybintio will be administered in combination with carboplatin and gemcitabine or with carboplatin and paclitaxel.
When used in adult patients with advanced epithelial ovarian, fallopian tube, or primary peritoneal cancer who have had a recurrence of their disease of at least 6 months since their last treatment with a platinum-based chemotherapy regimen, Aybintio will be administered in combination with paclitaxel, topotecan, or pegylated liposomal doxorubicin.
Aybintio is also used for the treatment of adult patients with persistent, recurrent, or metastatic cervical cancer. Aybintio will be administered in combination with paclitaxel and cisplatin or, alternatively, paclitaxel and topotecan in patients who cannot receive platinum-based therapy..
No use Aybintio
Warnings and Precautions
Consult your doctor, pharmacist, or nurse before starting to use Aybintio:
Please consult your doctor even if any of the above situations affect you or have occurred in the past.
Before starting treatment with Aybintio or during treatment with Aybintio:
You may be advised to have a dental check-up before starting treatment with Aybintio.
Children and Adolescents
Aybintio is not recommended for use in children and adolescents under 18 years old as its safety and efficacy have not been established in these patients.
Cases of osteonecrosis (death of bone tissue) in bones other than the jaw have been reported in patients under 18 years old treated with Aybintio.
Other Medications and Aybintio
Inform your doctor, pharmacist, or nurse if you are using, have used recently, or may need to use any other medication.
The combination of Aybintio with another medication called sunitinib malate (prescribed for renal and gastrointestinal cancer) may cause severe adverse effects. Consult your doctor to ensure that you do not combine these medications.
Consult your doctor if you are receiving platinum-based or taxane-based chemotherapy for metastatic breast or lung cancer. These therapies in combination with Aybintio may increase the risk of severe adverse effects.
Inform your doctor if you have recently received or are receiving radiation therapy.
Pregnancy, Breastfeeding, and Fertility
You should not use this medication if you are pregnant. Aybintio may harm the fetus, as it may slow down the formation of new blood vessels. Your doctor should advise you to use a contraceptive method during treatment with Aybintio and at least 6 months after the last dose of Aybintio.
Inform your doctor immediately if you are already pregnant, become pregnant during treatment with this medication, or intend to become pregnant.
You should not breastfeed your baby during treatment with Aybintio and at least 6 months after the last dose of Aybintio, as this medication may interfere with your baby's growth and development.
Aybintio may affect female fertility. Consult your doctor for more information.
Consult your doctor, pharmacist, or nurse before using any medication.
Driving and Operating Machines
Aybintio has not been observed to decrease your ability to drive or operate tools or machines. However, drowsiness and fainting have been reported with the use of Aybintio. If you experience symptoms that affect your vision or concentration, or your reaction time, do not drive or operate machines until the symptoms disappear.
Important Information about Some Components of Aybintio
This medication contains less than 1 mmol of sodium (23 mg) per vial, which is essentially "sodium-free".
Dosage and Administration Frequency
The dose of Aybintio required depends on your weight and the type of cancer being treated. The recommended dose is 5 mg, 7.5 mg, 10 mg, or 15 mg per kilogram of body weight. Your doctor will prescribe the most suitable dose of Aybintio for your case, and you will be treated with Aybintio once every 2 or 3 weeks. The number of infusions you receive will depend on how you respond to treatment and you should continue it until Aybintio can no longer stop tumor growth. Your doctor will discuss these aspects with you.
Form and Route of Administration
Do not shake the vial. Aybintio is a concentrate for solution for infusion. Depending on the dose prescribed, a fraction or the entire contents of the Aybintio vial will be diluted with sodium chloride solution before administration. A doctor or nurse will administer this diluted Aybintio solution as intravenous infusion (drip in your veins). The first infusion will be administered over 90 minutes. If you tolerate this infusion well, the second can be administered over 60 minutes. Subsequent infusions can be administered over 30 minutes.
Aybintio Administration Must Be Temporarily Interrupted:
Aybintio Administration Must Be Permanently Suspended If You Have:
If You Use More Aybintio Than You Should
If You Forget to Use Aybintio
If You Interrupt Treatment with Aybintio
Stopping treatment with Aybintio may suppress its effect on tumor growth.
Do not stop treatment with Aybintio unless you have consulted with your doctor.
If you have any other doubts 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.
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.
The side effects listed below have been observed when Aybintio is administered with chemotherapy. This does not necessarily mean that these side effects were strictly caused by Aybintio.
If you have an allergic reaction, consult your doctor or healthcare professional immediately. The signs may include: difficulty breathing or chest pain. You may also experience skin redness or flushing, rashes, chills, and tremors, dizziness or nausea, swelling, dizziness, tachycardia, loss of consciousness.
You must seek immediate help if you experience any of the following side effects.
Severe side effects that may bevery common(may affect more than 1 in 10 patients) include:
Severe side effects that may becommon(may affect up to 1 in 100 patients) include:
?allergic reactions (the signs may include difficulty breathing, facial redness, skin rash, low blood pressure or high blood pressure, low oxygen levels in blood, chest pain or nausea/vomiting),
Severe side effects that may berare(may affect up to 1 in 1000 patients) include:
Severe side effects of unknown frequency(cannot be estimated from available data) include:
If you experience any of these side effects mentioned, seek medical attention as soon as possible.
Side effectsvery common(may affect up to 1 in 10 patients) that were not severe are:
Side effectscommon(may affect up to 1 in 100 patients) that were not severe are:
Patients over 65 years old have a higher risk of experiencing the following:
Aybintio may also cause changes in laboratory tests that your doctor will perform. These changes may include a decrease in the number of white blood cells, particularly neutrophils (a type of white blood cell that facilitates protection against infections), presence of proteins in urine, decrease in potassium, sodium, or phosphorus in blood, increase in blood sugar, increase in alkaline phosphatase (an enzyme) in blood, decrease in hemoglobin (which is found in red blood cells and transports oxygen), which may be severe.
Pain in the mouth, teeth, and/or jaw, swelling, or sores in the mouth, numbness or heaviness of the jaw, or tooth loss. These may be signs and symptoms of jaw bone damage (osteonecrosis). Inform your doctor and dentist immediately if you experience any of them.
Pre-menopausal women (women with menstrual cycle) may notice that their periods become irregular or disappear and may experience fertility problems. If you are thinking of having children, consult your doctor before starting your treatment.
Aybintio has been developed and manufactured to treat cancer through intravenous injection. It has not been developed or manufactured for injection into the eye. Therefore, it is not authorized for use in this way. When Aybintio is injected directly into the eye (unapproved use), the following side effects may occur:
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 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 packaging and on the vial label after EXP. The expiration date is the last day of the month indicated.
Store in refrigerator (between 2°C and 8°C).
Do not freeze.
Store the vial in the outer packaging to protect it from light.
The unopened vial can be stored at temperatures not exceeding 30°C for a maximum of 35 days. The vial must be discarded if it is not used within 35 days once removed from the refrigerator, even if it has been returned to the refrigerator during this period.
The infusion solution must be administered immediately after dilution. If it is not administered immediately, the storage times and conditions in use are the responsibility of the user and are normally not more than 24 hours at between 2°C and 8°C, unless the infusion solutions have been prepared in a sterile environment. When the dilution has taken place in a sterile environment, Abyntio is stable for 45 days at between 2°C and 8°C plus an additional 72 hours at temperatures not exceeding 30°C.
Do not use Abyntio if you observe any foreign particles or discoloration before administration.
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. This will help protect the environment.
Composition of Aybintio
The active ingredient is bevacizumab.
?Each milliliter of concentrate contains 25mg of bevacizumab,
Each vial of 4ml contains 100mg of bevacizumab, corresponding to 1.4mg/ml when diluted as recommended.
Each vial of 16ml contains 400mg of bevacizumab, corresponding to 16.5mg/ml when diluted as recommended.
?The other components are trehalose dihydrate, sodium acetate trihydrate, acetic acid, polisorbate 20, and water for injection (see section2).
Appearance of the product and contents of the package
Aybintio is a concentrate for solution for infusion. The concentrate is a transparent, colorless to pale brown liquid contained in a glass vial with a rubber stopper. Each vial contains either 100mg of bevacizumab in 4ml of solution or 400mg of bevacizumab in 16ml of solution. Each package of Aybintio contains one vial.
Marketing Authorization Holder
Samsung Bioepis NL B.V.
Olof Palmestraat 10
2616 LR Delft
Netherlands
Responsible for manufacturing
Samsung Bioepis NL B.V.
Olof Palmestraat 10
2616 LR Delft
Netherlands
To obtain more information about this medicinal product, please contact the local representative of the marketing authorization holder:
Belgium/Belgique/Belgien Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands/Pays-Bas/Niederlande | Lithuania Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
? Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft ? | Luxembourg/Luxemburg Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Holland/Niederlande | |
Czech Republic Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | Hungary Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Hollandia | |
Denmark Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Holland | Malta Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Olanda | |
Germany Organon Healthcare GmbH Tel: 0800 3384 726 (+49 (0) 89 2040022 10) | Netherlands Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Estonia Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Holland | Norway Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Greece Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Greece | Austria Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Spain Organon Salud, S.L. Tel: +34 9159112 79 | Poland Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Holland | |
France Organon France Tél: + 33 (0) 1 57 77 32 00 | Portugal Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Croatia Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands Ireland Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | Romania Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands Slovenia Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Iceland Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Holland | Slovakia Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | |
Italy Organon Italia S.r.l. Tel: +39 06 90259059 | Finland/Suomi Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands/Alankomaat/Nederländerna | |
Cyprus Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Greece | Sweden Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands/Nederländerna | |
Lithuania Samsung Bioepis NL B.V. Olof Palmestraat 10, 2616 LR Delft Netherlands | United Kingdom (Northern Ireland) Organon Pharma (Ireland) Limited Tel: +353 (0)1 2998700 |
Last update of the summary of product characteristics:
Other sources of information
The detailed information on this medicinal product is available on the website of the European Medicines Agency:http://www.ema.europa.eu.
This summary of product characteristics can be found on the website of the European Medicines Agency in all languages of the European Union/European Economic Area.
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