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 other treatments have been used and are no longer effective.
Do not use HALAVEN:
Warnings and precautions
Talk to your doctor or nurse before 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 under 18 years old as it is not effective in this age group.
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 considering all the risks to you and your baby. It may also cause permanent fertility problems in men if taken, 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 7 months after finishing treatment.
Do not use HALAVEN during breast-feeding due to the possible 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 4 months after finishing 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 qualified 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, although your doctor may adjust it based on blood test results 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 blood test results, your doctor may need to delay administration of the medicine until blood test results return to normal. At that time, your doctor may also decide to reduce the dose you are given.
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 see a doctor immediately:
Other side effects:
Very common side effects (affects more than 1 in 10 people) are:
Common side effects (affects up to 1 in 10 people) are:
Uncommon side effects (affects up to 1 in 100 people) are:
Rare side effects (affects up to 1 in 1000 people) are:
Reporting of side effects
If you experience any side effects, talk to your doctor or nurse, even if they are 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.
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 protect the environment.
Composition of HALAVEN
Appearance and packaging
HALAVEN is a clear and colorless aqueous solution for injection, 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 Main Germany
e-mail: medinfo_de@eisai.net
Manufacturer
Eisai GmbH
Edmund-Rumpler-Straße 3
60549 Frankfurt am Main Germany
You can obtain further information on this medicine from the local representative of the marketing authorisation holder:
Belgium/Belgique/Belgien Eisai SA/NV Tel: +32 (0)800 158 58 | Lithuania Ewopharma AG Tel: +370 5 248 73 50 |
Luxembourg/Luxemburg Eisai SA/NV Tel: + 32 (0)800 158 58 (Belgium/Belgien) | |
Czech Republic Eisai GesmbH organisational unit Tel: + 420 242 485 839 | Hungary Ewopharma Hungary Ltd. Tel.: +36 1 200 46 50 |
Denmark Eisai AB Tel: + 46 (0) 8 501 01 600 (Sweden) | Malta Cherubino LTD Tel: +356 21343270 |
Germany Eisai GmbH Tel: + 49 (0) 69 66 58 50 | Netherlands Eisai B.V. Tel: + 31 (0) 900 575 3340 |
Estonia Ewopharma AG Tel: +370 5 248 73 50 | Norway Eisai AB Tel: + 46 (0) 8 501 01 600 (Sweden) |
Greece Eisai Ltd. Tel: + 44 (0)208 600 1400 (United Kingdom) | Austria Eisai GesmbH Tel: + 43 (0) 1 535 1980-0 |
Spain Eisai Farmacéutica, S.A. Tel: + (34) 91 455 94 55 | Poland Ewopharma AG Sp. z o.o. Tel.: +48 (22) 620 11 71 |
France Eisai SAS Tel: + (33) 1 47 67 00 05 | Portugal Eisai Farmacêutica, Unipessoal Lda Tel: + 351 214 875 540 |
Croatia Ewopharma d.o.o. Tel: +385 (0) 1 6646 563 | Romania Ewopharma AG Tel: +40 21 260 13 44 |
Ireland Eisai GmbH Tel: + 49 (0) 69 66 58 50 (Germany) | Slovenia Ewopharma d.o.o. Tel: +386 590 848 40 |
Iceland Eisai AB Tel: + 46 (0)8 501 01 600 (Sweden) | Slovak Republic Eisai GesmbH organisational unit Tel.: + 420 242 485 839 (Czech Republic) |
Italy Eisai S.r.l. Tel: + 39 02 5181401 | Finland Eisai AB Tel: + 46 (0) 8 501 01 600 (Sweden) |
Cyprus Eisai Ltd. Tel: +44 (0)208 600 1400 (United Kingdom) | Sweden Eisai AB Tel: + 46 (0) 8 501 01 600 |
Latvia 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.