


Ask a doctor about a prescription for BESREMI 250 micrograms/0.5 ml solution for injection in a prefilled pen
Package Leaflet: Information for the User
Besremi 250micrograms/0.5ml solution for injectionin a pre-filled pen
ropeginterferon alfa-2b
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack
Besremi contains the active substance ropeginterferon alfa-2b, which belongs to a class of medicines known as interferons. Your immune system produces interferons to block the growth of cancer cells.
Besremi is used as monotherapy for the treatment of polycythaemia vera in adults. Polycythaemia vera is a type of cancer in which the bone marrow produces too many red blood cells, white blood cells, and platelets (the cells that help the blood to clot).
Do not useBesremi
Warnings and precautions
Talk to your doctor before you start using Besremi:
Once you have started treatment with Besremi, talk to your doctor:
Medicines based on interferons can also cause dental and gum disorders, with the possibility of tooth loss. Additionally, dry mouth can be harmful to teeth or mouth mucosa during long-term treatment with Besremi. You should brush your teeth well twice a day and have regular dental check-ups.
It will take some time to reach your optimal individual dose of Besremi. Your doctor will decide if you need to be treated with another medicine to quickly reduce the number of cells in your blood, in order to prevent the formation of clots and bleeding.
Children and adolescents
Do not give this medicine to children or adolescents, as there is no information available on the use of Besremi in this age group.
Other medicines and Besremi
Tell your doctor or pharmacist if you are using, have recently used, or might use any other medicines.
Do not use Besremi if you are taking telbivudine (for the treatment of hepatitis B), as the combination of these medicines increases the risk of developing peripheral neuropathy (numbness, tingling, or burning sensation in the arms and legs). Tell your doctor if you are receiving treatment with telbivudine.
Particularly tell your doctor if you are taking any of the following medicines:
Pregnancy and breast-feeding
If you are pregnant or breast-feeding, think you may be pregnant, or are planning to have a baby, ask your doctor or pharmacist for advice before using this medicine.
Pregnancy
The effect of Besremi during pregnancy is unknown. The use of Besremi is not recommended during pregnancy. If you are able to become pregnant, your doctor will explain which effective contraceptive method you should use during your treatment with Besremi.
Breast-feeding
It is unknown whether Besremi passes into breast milk. Your doctor will help you decide whether to stop breast-feeding while using this medicine.
Driving and using machines
Do not drive or use machines if you feel dizzy, drowsy, or confused while using Besremi.
Besremi contains benzyl alcohol
This medicine contains 5 mg of benzyl alcohol per 0.5 ml. Benzyl alcohol may cause allergic reactions.
Talk to your doctor or pharmacist:
This is because large amounts of benzyl alcohol can accumulate in the body and cause side effects (metabolic acidosis).
Besremi contains polysorbate 80
This medicine contains 0.025 mg of polysorbate 80 in each 0.5 ml. Polysorbates can cause allergic reactions. Tell your doctor if you have any known allergies.
Besremi contains sodium
This medicine contains less than 1 mmol of sodium (23 mg) per ml; this is essentially “sodium-free”.
Follow the instructions for administration of this medicine exactly as told by your doctor or pharmacist. If you are not sure, ask your doctor or pharmacist again.
Your doctor will determine the dose you need individually for your disease. The usual starting dose of Besremi is 100 micrograms every 2 weeks. After that, your doctor will gradually increase the dose and may change it during treatment. If you have severe kidney problems, the starting dose given by your doctor will be reduced to 50 micrograms.
This medicine is given by subcutaneous injection, which means it is injected into the tissue under the skin. It must not be injected into irritated skin, red skin, skin with bruises, infected skin, or skin with scars.
If you inject this medicine yourself, you will be taught how to prepare the medicine and inject it.
Never share the pre-filled pen Besremi with anyone, even if you change the needle, in order to avoid infectious diseases.
You can find the details of the preparation and injection of Besremi in the instruction manual. Read them before you start using Besremi.
If you use more Besremi than you should
Talk to your doctor as soon as possible.
If you forget to use Besremi
The dose should be injected as soon as you remember. But if it has been more than 2 days since you missed the dose, skip it and inject the next dose when it is due. Do not inject a double dose to make up for the missed doses. If you are not sure, ask your doctor or pharmacist again.
If you stop using Besremi
Do not stop using Besremi without talking to your doctor first.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience any of the following serious side effects during your treatment with Besremi, contact your doctor immediately:
Common side effects (may affect up to 1 in 10 people):
Uncommon side effects (may affect up to 1 in 100 people):
Rare side effects (may affect up to 1 in 1,000 people):
Very rare side effects (may affect up to 1 in 10,000 people):
Frequency not known (cannot be estimated from the available data):
Other side effects
Very common side effects (may affect more than 1 in 10 people):
Common side effects (may affect up to 1 in 10 people):
Uncommon side effects (may affect up to 1 in 100 people):
Rare side effects (may affect up to 1 in 1,000 people):
Very rare side effects (may affect up to 1 in 10,000 people):
Frequency not known (cannot be estimated from the available data):
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 national reporting system listed in Appendix V. 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 label and on the carton after “EXP”. The expiry date is the last day of the month shown.
Store in a refrigerator (between 2°C and 8°C).
Do not freeze.
Keep the pre-filled pen in its outer packaging to protect it from light.
Once opened, the pre-filled pen can be stored in the refrigerator (between 2°C and 8°C) for a maximum of 30 days, if stored with the cap on and in the carton, which protects it from light.
Do not use this medicine if you notice that the pre-filled pen is damaged, if the solution is not clear, if it has particles or flakes, if it is not colorless, or if it has a different color than light yellow.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. This will help to protect the environment.
Besremi Composition
Each pre-filled pen with 0.5 ml of solution contains 250 micrograms of ropeginterferon alfa-2b expressed in protein, which corresponds to 500 micrograms/ml.
Appearance of the Product and Package Contents
Besremi is presented in a solution for injection (injection) in a pre-filled pen. Each pre-filled pen contains 0.5 ml of solution. It is marketed in packages with:
Marketing Authorization Holder and Manufacturer
AOP Orphan Pharmaceuticals GmbH
Leopold-Ungar-Platz 2
1190 Vienna
Austria
You can request more information about this medication by contacting the local representative of the marketing authorization holder:
België/Belgique/Belgien AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | Lietuva AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
| Luxembourg/Luxemburg AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Ceská republika AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | Magyarország AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Danmark AOP Orphan Pharmaceuticals GmbH (Austria) Tlf: +43 1 5037244 | Malta AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Deutschland AOP Orphan Pharmaceuticals Germany GmbH Tel: +49 89 99 740 7600 | Nederland AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Eesti AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | Norge AOP Orphan Pharmaceuticals GmbH (Austria) Tlf: +43 1 5037244 |
Ελλάδα AOP Orphan Pharmaceuticals GmbH (Αυστρία) Τηλ: +43 1 5037244 | Österreich AOP Orphan Pharmaceuticals GmbH Tel: +43 1 5037244 |
España AOP Orphan Pharmaceuticals Iberia S.L.U. Tel: +34 91 449 19 89 | Polska AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
France AOP Orphan Pharmaceuticals GmbH (Austria) Tél: +43 1 5037244 | Portugal AOP Orphan Pharmaceuticals Iberia S.L.U. Tel: +34 91 449 19 89 |
Hrvatska AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | România AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Ireland AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | Slovenija AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Ísland AOP Orphan Pharmaceuticals GmbH (Austria) Sími: +43 1 5037244 | Slovenská republika AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Italia AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 | Suomi/Finland AOP Orphan Pharmaceuticals GmbH (Austria) Puh/Tel: +43 1 5037244 |
Κύπρος AOP Orphan Pharmaceuticals GmbH (Αυστρία) Τηλ: +43 1 5037244 | Sverige AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Latvija AOP Orphan Pharmaceuticals GmbH (Austria) Tel: +43 1 5037244 |
Date of Last Revision of this Prospectus:
Other Sources of Information
Detailed information about this medication is available on the European Medicines Agency website: https://www.ema.europa.eu.
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Instructions
Read this prospectus carefully before using the pre-filled pen Besremi 250 micrograms. If you have any doubts, consult your doctor or pharmacist.
Your doctor or pharmacist will teach you how to use the pen.
The pre-filled pen Besremi 250 micrograms can be used to inject doses within the range of 50 to 250 micrograms. The same pen can be used twice, as long as the sum of the two doses does not exceed 250 micrograms. Your doctor will indicate the dose you need. Take note of the dates and doses of the injections that your doctor indicates.
If you need a dose of more than 250 micrograms, you will need to use two pre-filled pens Besremi 250 micrograms. Each one should be injected at a different point. Your doctor or pharmacist will explain how to use the two pens.
Keep the pen in the outer packaging in the refrigerator.
Remove the pen from the refrigerator 15 minutes before injection to allow it to reach room temperature.
Sit in a well-lit and quiet area to administer the injection.
To administer the injection, you will need:
The Besremi pre-filled pen is supplied with two or six needles (depending on the package size). You must always use a new needle each time you inject.
Do not use the pen if it appears damaged. If you feel that you may have damaged the pen while using it (e.g., it has fallen or has been pressed too hard), do not continue using it. Get a new one and start again.
Description of the Besremi 250 micrograms pre-filled pen

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Do not inject into areas of irritated skin, redness, bruising, infection, or scarring. |
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| Note:Put the pen cap back on. Reusing the Pen:
Disposal of the Pen and Needle:
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Discuss dosage, side effects, interactions, contraindications, and prescription renewal for BESREMI 250 micrograms/0.5 ml solution for injection in a prefilled pen – subject to medical assessment and local rules.