Package Leaflet: Information for the User
HALAVEN 0.44 mg/ml solution for injection
eribulin
Read all of this leaflet carefully before you start using this medicine because it contains important information for you.
Contents of the pack and other information
Contents of the pack and further information
HALAVEN contains the active substance eribulin and is a cancer medicine that works by slowing down the growth and spread of cancer cells.
It is used to treat adult patients with locally advanced or metastatic breast cancer (breast cancer that has spread beyond the original tumor) when at least one other treatment has been used and is no longer effective.
It is also used to treat adult patients with advanced or metastatic liposarcoma (a type of cancer that occurs in fat tissue) when previous treatment has been used and is no longer effective.
Do not use HALAVEN:
Warnings and precautions
Tell your doctor or nurse before you start using HALAVEN
If you are affected by any of these, tell your doctor as they may want to stop your treatment or reduce your dose.
Children and adolescents
Do not give this medicine to children from 0 to 18 years old as it is not effective in them.
Other medicines and HALAVEN
Tell your doctor if you are using, have recently used, or might use any other medicines.
Pregnancy, breast-feeding, and fertility
HALAVEN may cause serious birth defects and should not be used during pregnancy unless clearly necessary after careful consideration of the risks to you and the baby. It may also cause permanent fertility problems in men in the future if they take it, and they should discuss this with their doctor before starting treatment. Women of childbearing age should use highly effective contraceptive methods during treatment with HALAVEN and for up to 7 months after the end of treatment.
HALAVEN should not be used during breast-feeding due to the potential risk to the baby.
Men with female partners of childbearing age should not get them pregnant while receiving HALAVEN. They should use effective contraceptive methods during treatment with HALAVEN and for up to 4 months after the end of treatment.
Driving and using machines
HALAVEN may cause side effects such as fatigue (very common) and dizziness (common). Do not drive or use machines if you feel tired or dizzy.
HALAVEN contains ethanol (alcohol)
This medicine contains small amounts of ethanol (alcohol), less than 100 mg per vial.
A healthcare professional will give you HALAVEN as an injection into a vein over a period of 2 to 5 minutes. The dose you receive will be based on your body surface area (expressed in square meters, or m2) calculated from your weight and height. The usual dose of HALAVEN is 1.23 mg/m2, but your doctor may adjust it based on the results of blood tests or other factors. After administration of HALAVEN, it is recommended to flush the vein with a saline solution to ensure that the full dose of HALAVEN is administered.
Frequency of administration of HALAVEN
HALAVEN is usually given on days 1 and 8 of each 21-day cycle. Your doctor will decide how many cycles of treatment you should receive. Depending on the results of blood tests, your doctor may need to delay the administration of the medicine until the blood test results return to normal. At that time, your doctor may also decide to reduce the dose you receive.
If you have any further questions on the use of this medicine, ask your doctor.
Like all medicines, this medicine can cause side effects, although not everybody gets them.
If you experience any of the following serious symptoms, stop taking HALAVEN and go to your doctor immediately:
Other side effects:
Very common side effects (may affect more than 1 in 10 people) are:
Common side effects (may affect up to 1 in 10 people) are:
Uncommon side effects (may affect up to 1 in 100 people) are:
Rare side effects (may affect up to 1 in 1,000 people) are:
Reporting of side effects
If you experience any side effects, talk to your doctor or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Spanish Medicines Surveillance System for Human Use www.notificaRAM.es. 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 carton and vial after EXP. The expiry date is the last day of the month shown.
No special storage conditions are required.
If HALAVEN is diluted for infusion, the diluted solution should be used immediately. If not used immediately, the diluted solution should be stored between 2°C and 8°C for no more than 72 hours.
If HALAVEN as an undiluted solution has been transferred to a syringe, it should be stored between 15°C and 25°C in ambient light for no more than 4 hours, or between 2°C and 8°C for no more than 24 hours.
Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help protect the environment.
Composition of HALAVEN
Appearance and pack of the product
HALAVEN is a clear and colorless aqueous solution for injection, which comes in glass vials containing 2 ml of solution. Each carton contains 1 or 6 vials.
Marketing authorisation holder
Eisai GmbH
Edmund-Rumpler-Straße 3
60549 Frankfurt am MainGermany
e-mail: [email protected]
Manufacturer
Eisai GmbH
Edmund-Rumpler-Straße 3
60549 Frankfurt am MainGermany
You can obtain further information on this medicine from the local representative of the marketing authorisation holder:
België/Belgique/Belgien Eisai SA/NV Tél/Tel: +32 (0)800 158 58 | Lietuva Ewopharma AG Tel: +370 5 248 73 50 |
| Luxembourg/Luxemburg Eisai SA/NV Tél/Tel: + 32 (0)800 158 58 (Belgique/Belgien) |
Ceská republika Eisai GesmbH organizacní složka Tel: + 420 242 485 839 | Magyarország Ewopharma Hungary Ltd. Tel.: +36 1 200 46 50 |
Danmark Eisai AB Tlf: + 46 (0) 8 501 01 600 (Sverige) | Malta Cherubino LTD Tel: +356 21343270 |
Deutschland Eisai GmbH Tel: + 49 (0) 69 66 58 50 | Nederland Eisai B.V. Tel: + 31 (0) 900 575 3340 |
Eesti Ewopharma AG Tel: +370 5 248 73 50 | Norge Eisai AB Tlf: + 46 (0) 8 501 01 600 (Sverige) |
Ελλάδα Eisai Ltd. Τηλ: + 44 (0)208 600 1400 (Ηνωμένο Βασίλειο) | Österreich Eisai GesmbH Tel: + 43 (0) 1 535 1980-0 |
España Eisai Farmacéutica, S.A. Tel: + (34) 91 455 94 55 | Polska Ewopharma AG Sp. z o.o. Tel.: +48 (22) 620 11 71 |
France Eisai SAS Tél: + (33) 1 47 67 00 05 | Portugal Eisai Farmacêutica, Unipessoal Lda Tel: + 351 214 875 540 |
Hrvatska Ewopharma d.o.o. Tel: +385 (0) 1 6646 563 | România Ewopharma AG Tel: +40 21 260 13 44 |
Ireland Eisai GmbH Tel: + 49 (0) 69 66 58 50 (Germany) | Slovenija Ewopharma d.o.o. Tel: +386 590 848 40 |
Ísland Eisai AB Sími: + 46 (0)8 501 01 600 (Svíþjóð) | Slovenská republika Eisai GesmbH organizacní složka Tel.: + 420 242 485 839 (Ceská republika) |
Italia Eisai S.r.l. Tel: + 39 02 5181401 | Suomi/Finland Eisai AB Puh/Tel: + 46 (0) 8 501 01 600 (Ruotsi) |
Κύπρος Eisai Ltd. Τηλ: +44 (0)208 600 1400 (Ηνωμένο Βασίλειο) | Sverige Eisai AB Tel: + 46 (0) 8 501 01 600 |
Latvija Ewopharma AG Tel: +371 677 04000 | United Kingdom (Northern Ireland) Eisai GmbH Tel: + 49 (0) 69 66 58 50 (Germany) |
Date of last revision of this leaflet:
Detailed information on this medicine is available on the European Medicines Agency website: http://www.ema.europa.eu.
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