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Dincilezan 40 mg/ ml concentrate and solvent for solution for infusion
Read all of this leaflet carefully before you are given this medicine, because it contains important
information for you.
Keep this leaflet. You may need to read it again.
If you have any further questions, ask your doctor, pharmacist or nurse.
If you get any side effects, talk to your doctor, hospital pharmacist or nurse. This includes any
possible side effects not listed in this leaflet.

In this leaflet:
What Dincilezan is and what it is used for
What you need to know before you use Dincilezan
How to use Dincilezan
Possible side effects
How to store Dincilezan
Contents of the pack and other information

1. What Dincilezan is and what it is used for
The name of this medicine is Dincilezan. Its common name is docetaxel. Docetaxel is a substance
derived from the needles of yew trees.
Docetaxel belongs to the group of anti-cancer medicines called taxoids.
Dincilezan has been prescribed by your doctor for the treatment of breast cancer, special forms of lung
cancer (non-small cell lung cancer), prostate cancer, gastric cancer or head and neck cancer:
- For the treatment of advanced breast cancer, Dincilezan could be administered either alone or in
combination with doxorubicin, or trastuzumab, or capecitabine.
- For the treatment of early breast cancer with or without lymph node involvement, Dincilezan could
be administered in combination with doxorubicin and cyclophosphamide.
- For the treatment of lung cancer, Dincilezan could be administered either alone or in combination
with cisplatin.
- For the treatment of prostate cancer, Dincilezan is administered in combination with prednisone or
- For the treatment of metastatic gastric cancer, Dincilezan is administered in combination with
cisplatin and 5-fluorouracil.
- For the treatment of head and neck cancer, Dincilezan is administered in combination with
cisplatin and 5-fluorouracil.

2. What you need to know before you use Dincilezan
You must not be given Dincilezan

you are allergic (hypersensitive) to docetaxel or any of the other ingredients of Dincilezan
the number of white blood cells is too low
you have a severe liver disease.

Warnings and precautions
Before each treatment with Dincilezan, you will have blood tests to check that you have enough blood
cells and sufficient liver function to receive Dincilezan. In case of white blood cell disturbances, you
may experience associated fever or infections.

You will be asked to take premedication consisting of an oral corticosteroid such as dexamethasone,
one day prior to Dincilezan administration and to continue for one or two days after it in order to
minimise certain undesirable effects which may occur after the infusion of Dincilezan in particular
allergic reactions and fluid retention (swelling of the hands, feet, legs or weight gain).
During treatment, you may be given other medicines to maintain the number of your blood cells.

Other medicines and Dincilezand
Please tell your doctor or hospital pharmacist if you are taking or have recently taken any other
medicines, including medicines obtained without a prescription. This is because Dincilezan or the
other medicines may not work as well as expected and you may be more likely to get a side effect.

Pregnancy, breast-feeding and fertility
Ask your doctor for advice before being given any medicine.
Dincilezan must NOT be administered if you are pregnant unless clearly indicated by your doctor.
You must not become pregnant during treatment with this medicine and must use an effective method
of contraception during therapy because Dincilezan may be harmful for the unborn baby. If pregnancy
occurs during your treatment, you must immediately inform your doctor.
You must not breast-feed while you are treated with Dincilezan.
If you are a man being treated with Dincilezan you are advised not to father a child during and up to 6
months after treatment and to seek advice on conservation of sperm prior to treatment because
docetaxel may alter male fertility.

Driving and using machines
No studies on the effects on the ability to drive and use machines have been performed.
Dincilezan concentrate and solvent for solution for infusion both contain small amounts of ethanol
(alcohol), less than 100 mg per infusion.

3. How to use Dincilezan
Dincilezan will be administered to you by a healthcare professional.
Usual dose
The dose will depend on your weight and your general condition. Your doctor will calculate your body
surface area in square meters (m²) and will determine the dose you should receive.
Method and route of administration
Dincilezan will be given by infusion into one of your veins (intravenous use). The infusion will last
approximately one hour during which you will be in the hospital.
Frequency of administration
You should usually receive your infusion once every 3 weeks.
Your doctor may change the dose and frequency of dosing depending on your blood tests, your
general condition and your response to Dincilezan. In particular, please inform your doctor in case of

diarrhoea, sores in the mouth, feeling of numbness or pins and needles, fever and give her/him results
of your blood tests. Such information will allow her/him to decide whether a dose reduction is needed.
If you have any further questions on the use of this medicine, ask your doctor or hospital pharmacist.

4. Possible side effects
Like all medicines, Dincilezan can cause side effects, although not everybody gets them.
Your doctor will discuss these with you and will explain the potential risks and benefits of your
The most commonly reported adverse reactions of Dincilezan alone are: decrease in the number of red
blood cells or white blood cells, alopecia, nausea, vomiting, sores in the mouth, diarrhoea and
The severity of adverse events of Dincilezan may be increased when Dincilezan is given in
combination with other chemotherapeutic agents.
During the infusion at the hospital the following allergic reactions may occur (may affect more than
1 in 10 people):
- flushing, skin reactions, itching
- chest tightness; difficulty in breathing
- fever or chills
- back pain
- low blood pressure.
More severe reactions may occur.
The hospital staff will monitor your condition closely during treatment. Tell them immediately if you
notice any of these effects.
Between infusions of Dincilezan the following may occur, and the frequency may vary with the
combinations of medicines that are received:
Very common (may affect more than 1 in 10 people):
- infections, decrease in the number of red (anaemia), or white blood cells (which are important in
fighting infection) and platelets
- fever: if this happens you must tell your doctor immediately
- allergic reactions as described above
- loss of appetite (anorexia)
- insomnia
- feeling of numbness or pins and needles or pain in the joints of muscles
- headache
- alteration in sense of taste
- inflammation of the eye or increased tearing of the eyes
- swelling caused by faulty lymphatic drainage
- shortness of breath
- nasal drainage; inflammation of the throat and nose; cough
- bleeding from the nose
- sores in the mouth
- stomach upsets including nausea, vomiting and diarrhoea, constipation
- abdominal pain
- indigestion
- hair loss (in most cases normal hair growth should return)
- redness and swelling of the palms of your hands or soles of your feet which may cause your skin to
peel (this may also occur on the arms, face, or body)


change in the color of your nails, which may detach
muscle aches and pains; back pain or bone pain
change or absence of menstrual period
swelling of the hands, feet, legs
tiredness; or flu-like symptoms
weight gain or loss.

Common (may affect upto 1 in 10 people):
- oral candidiasis
- dehydration
- dizziness
- hearing impaired
- decrease in blood pressure; irregular or rapid heart beat
- heart failure
- oesophagitis
- dry mouth
- difficulty or painful swallowing
- haemorrhage
- raised liver enzymes (hence the need for regular blood tests).
Uncommon (may affect upto 1 in 100 people):
- fainting
- at the injection site, skin reactions, phlebitis (inflammation of the vein) or swelling
- inflammation of the colon, small intestine; intestinal perforation
- blood clots
If you get any side effects, talk to your doctor, hospital pharmacist or nurse. This includes any side
effects not listed in this leaflet.

5. How to store Dincilezan
Keep this medicine out of the sight and reach of children.
This medicine should not be used after the expiry date shown on the carton, blister pack and vials.
Store below 25°C.
Store in the original package in order to protect from light.
The premix solution should be used immediately after preparation. However the chemical and physical
stability of the premix solution has been demonstrated for 8 hours when stored either between 2°C and
8°C or at room temperature (below 25°C).
The infusion solution should be used within 4 hours at room temperature (below 25°C).
Both, the premix solution and the infusion solution should not be stored below 2°C.

6. Contents of the pack and other information
What Dincilezan concentrate contains
- The active substance is docetaxel.
Each ml of docetaxel concentrate for solution for infusion contains 40 mg of docetaxel
One vial of concentrate contains 20 mg /0.5 ml docetaxel
One vial of concentrate contains 80 mg/2 ml docetaxel.


The other ingredients are: polysorbat 80 (E433), citric acid anhydrous (E330), ethanol absolute
and nitrogen.

What solvent vial contains
13% (w/w) ethanol 96% in water for injection.
What Dincilezan looks like and contents of the pack
The concentrate is a clear yellow to brownish-yellow, viscous solution.
The solvent is a clear, colourless solution.
Each carton contains a blister pack with one single dose vial of concentrate and one single dose vial of
Marketing Authorisation Holder and Manufacturer
Regiomedica GmbH
Teichstr. 66
79539 Lörrach
This medicinal product is authorised in the Member States of the EEA under the following
Dincilezan 40 mg/ml
Dincilezan 40 mg/ml
The Netherlands
Dincilezan 40 mg/ml
United Kingdom
Dincilezan 40 mg/ml
This leaflet was approved in 09/2012

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Source: Medicines and Healthcare Products Regulatory Agency

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.