Package Leaflet: Information for the Patient
Vinorelbina Accord 20 mg Soft Capsule EFG
Read all of this leaflet carefully before you start taking this medicine because it contains important information for you.
Contents of the pack
This medicinal product contains the active substance vinorelbine, and belongs to a family of medicines called vinca alkaloids, used to treat cancer.
Vinorelbina Accord is used to treat certain types of lung and breast cancer in patients over 18 years of age.
Do not take Vinorelbina Accord
Warnings and precautions
Tell your doctor or pharmacist before taking vinorelbine if:
Before and during your treatment with vinorelbine, blood cell counts are performed to check that it is safe for you to receive the treatment. If the results of this test are not satisfactory, your treatment may be delayed and more reviews will be performed until these values return to normal.
Children and adolescents
This medicine is not recommended for use in children under 18 years of age.
Other medicines and Vinorelbina Accord
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Your doctor should pay special attention if you are taking the following medicines:
The combination of vinorelbine with other medicines with known bone marrow toxicity (affecting white and red blood cells and platelets) may also worsen some side effects.
Pregnancy, breast-feeding and fertility
If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine, as there are potential risks to the baby. You should not take this medicine if you are pregnant. You should not breast-feed if you are taking vinorelbine.
Women of childbearing age must use effective contraceptive methods (birth control) during treatment and up to 7 months after treatment.
Men treated with vinorelbine are advised not to father a child during and up to 3 months after the last capsule. You should discuss sperm banking with your doctor before starting treatment with vinorelbine, as male fertility may be altered.
Driving and using machines
No studies on the effects on the ability to drive and use machines have been performed. However, as with all cases, you should not drive if you feel unwell or if your doctor has advised you not to drive.
Vinorelbina Accord contains sorbitol, ethanol and sodium
Vinorelbina Accord 20 mg contains 8.03 mg of sorbitol (as partially dehydrated liquid sorbitol) per soft capsule.
This medicine contains 2.89 mg of alcohol in each soft capsule. The amount in each soft capsule is equivalent to less than 1 ml of beer or 1 ml of wine.
The small amount of alcohol in this medicine does not produce any noticeable effect.
This medicine contains less than 1 mmol of sodium (23 mg) per capsule; i.e., it is essentially “sodium-free”.
Before and during your treatment with vinorelbine, your doctor will check your blood cell count to determine when you will receive your treatment and what dose is suitable for you. Your doctor will tell you the number and dose of capsules you should take. This will depend on your body surface area, which your doctor will calculate from your weight and height. The usual weekly dose, taken in a single dose, is 60 mg/m2 of body surface area for the first three doses. After the third dose, your doctor will decide if the dose should be increased to 80 mg/m2 of body surface area. In any case, your doctor may adjust the dose of vinorelbine.
If you are receiving the capsules with another medicine to treat your cancer/disease, your doctor will decide what dose is suitable for you.
The total dose should never exceed 160 mg per week. Never take this medicine more than once a week. |
Follow exactly the administration instructions of this medicine given by your doctor or pharmacist. In case of doubt, consult your doctor or pharmacist again.
Before opening the blisters that contain vinorelbine, make sure that there are no damaged capsules because the liquid inside is irritating and can be harmful if it comes into contact with your skin, eyes or mucous membranes. If this happens, wash the affected area immediatelyand thoroughly with water.
Do not take any damaged capsules; return them to your doctor or pharmacist. |
Taking the soft capsules of vinorelbine:
If you take anti-nausea and vomiting medicines
This medicine may cause vomiting, (see section "4. Possible side effects"). If your doctor has prescribed an anti-nausea medicine, always take it exactly as indicated.
Take vinorelbine during a light meal; this will help reduce the feeling of nausea.
If you take more Vinorelbina Accord than you should
If you have taken more capsules than prescribed by your doctor, consult your doctor immediately.
Your body may sometimes react with intense symptoms. Some of these symptoms may appear as signs of an infection (such as fever, chills, cough, joint pain). You may also suffer from intense constipation. You should contact your doctor immediately if you experience any of these severe symptoms.
In case of overdose or accidental ingestion, consult your doctor or pharmacist immediately or call the Toxicology Information Service. Telephone 91 562 04 20, indicating the medicine and the amount ingested.
If you forget to take Vinorelbina Accord
Do not take a double dose to make up for forgotten doses. Contact your doctor, who will indicate if you should modify the dose you have to take.
If you stop taking Vinorelbina Accord
Your doctor will decide when you should stop your treatment. However, if you wish to stop your treatment beforehand, you should consult your doctor so that they can assess other treatment options.
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.
Contact your doctor immediatelyif you experience any of the following symptoms:
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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):
Frequency not known: frequency cannot be estimated from the available data
Reporting of side effects
If you experience 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 through the national reporting system: 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 blister and carton after CAD or EXP. The expiry date is the last day of the month shown.
Store in a refrigerator (between 2°C and 8°C).
Medicines should not be disposed of via wastewater or household waste. For safety reasons, return any unused medicine to your doctor or pharmacist. This will help protect the environment.
Composition of Vinorelbina Accord
The active substance is vinorelbine. Each soft capsule contains 20 mg of vinorelbine (as tartrate).
The other ingredients are:
The solution contains: macrogol, glycerol, anhydrous ethanol and purified water.
The capsule shell contains: gelatin, glycerol, partially dehydrated liquid sorbitol (E 420), titanium dioxide (E 171) and yellow iron oxide (E 172).
Printing ink: shellac (E 904), black iron oxide (E 172), ammonium hydroxide (E 527) and propylene glycol (E 1520).
Appearance of Vinorelbina Accord and contents of the pack
Soft gelatin capsules, oval in shape (9.3 mm x 6.7 mm), opaque light brown in color, free of surface defects, with “JJ1” printed in black, containing a clear and colorless liquid.
Vinorelbina Accord is available in blisters of 1, 2, 3 or 4 soft capsules.
Not all pack sizes may be marketed.
Marketing Authorisation Holder
Accord Healthcare S.L.U.
World Trade Center
Moll de Barcelona, s/n, Edifici Est, 6ª planta,
08039, Barcelona. Spain.
Manufacturer
Accord Healthcare Polska Sp. z o.o.
Ul. Lutomierska 50, 95-200,
Pabianice, Poland
or
Accord Healthcare B.V.
Winthontlaan 200, 3526 KV
Utrecht, Netherlands
or
Laboratori Fundació Dau
C/ C, 12-14 Pol.
Ind. Zona Franca,
Barcelona, 08040, Spain
or
Pharmadox Healthcare Ltd
KW20A Kordin Industrial Park
Paola, Malta
or
Accord Healthcare single member S.A.
64th Km National Road Athens,
Lamia, Schimatari,
32009, Greece
Date of last revision of this leaflet:December 2024.
Detailed information on this medicine is available on the website of the Spanish Agency for Medicines and Health Products (AEMPS) http://www.aemps.gob.es//