cetuximab (rmc)
CONSUMER MEDICINE INFORMATION
NOTICE: This Consumer Medicine Information (CMI) is intended for persons living in Australia. This page contains answers to some common questions about . It does not contain all the information that is known about . It does not take the place of talking to your doctor or pharmacist. All medicines have risks and benefits. Your doctor has weighed the risk of you using this medicine against the benefits he/she expects it will have for you. If you have any concerns about using this medicine, ask your doctor or pharmacist. Bookmark or print this page, you may need to read it again.
What ERBITUX is used for
ERBITUX is used to treat certain cancers that have a protein on their cell surface called EGFR (epidermal growth factor receptor). When a growth factor called EGF attaches to EGFR it turns on signals within the cell causing it to grow and divide to form more cells. In many human tumours, there is an over-activation of these receptors, which leads to increased uncontrolled growth of cancer cells and development into a tumour.
How ERBITUX works
The active substance in ERBITUX is cetuximab. It belongs to a group of medicines called monoclonal antibodies. Monoclonal antibodies are proteins that specifically recognise and attach to other unique proteins. ERBITUX attaches to the EGFR more tightly than EGF and thereby interferes with growth of cancer cells.
What ERBITUX does
ERBITUX is used to treat metastatic colorectal cancer (cancer of the colon or large intestine and rectum that has spread to other parts of the body). It may be used alone or in combination with certain types of medicines called chemotherapy to treat metastatic colon cancer.
Before you are prescribed ERBITUX, your doctor will test your cancer cells to see if they contain either the normal (wild-type) or mutant form of a gene called K-RAS. ERBITUX is used to treat patients who express a normal K-RAS gene. Patients who express a mutation in their K-RAS gene or for whom the K-RAS status is not known should not be treated with ERBITUX.
ERBITUX is used to treat locally advanced head and neck cancer, in combination with radiation therapy. It is also used to treat head and neck cancer that has reoccurred or spread to other parts of the body in combination with certain types of chemotherapy.
Ask your doctor if you have any questions about why ERBITUX has been prescribed for you.
Your doctor may have prescribed it for another use.
ERBITUX is available only with a doctor's prescription.
There is no evidence that ERBITUX is addictive.
Use in Children
ERBITUX is not recommended for use in children under the age of 18 years, as its safety and effectiveness have not been established in this age group.
Before starting treatment with ERBITUX
When you must not have it
Do not have ERBITUX if you experience severe hypersensitivity (allergic) reactions to cetuximab.
Some of the symptoms of an allergic reaction may include:
shortness of breath
wheezing or difficulty breathing
swelling of the face, lips, tongue or other parts of the body
rash, itching or hives on the skin.
If you have had an allergic reaction to ERBITUX, your doctor will decide whether or not you can receive it again. This will depend on the severity of your reaction.
Do not have ERBITUX if you are allergic to any of the ingredients listed at the end of this leaflet.
If you receive ERBITUX in combination with chemotherapy medicines, ask your doctor or pharmacist for their Consumer Medicine Information.
Do not have ERBITUX if the expiry date printed on the pack has passed.
The nurse or hospital pharmacist will check the expiry date before giving ERBITUX to you.
Do not have ERBITUX if the packaging is torn or shows signs of tampering.
The nurse will check this for you.
Check with your doctor or pharmacist if you are not sure about any of the above.
Before you start treatment with ERBITUX
Before receiving the first dose, you should be given anti-allergy medicines (an antihistamine and a corticosteroid) to minimise the chances of an allergic reaction. Pre-treatment with an antihistamine and a corticosteroid is also recommended for the following weekly doses.
Tell your doctor if you are pregnant or plan to become pregnant.
ERBITUX is not recommended for use during pregnancy. Make sure you maintain adequate contraception during treatment and for two months after your last dose.
Tell your doctor if you are breastfeeding or wish to breastfeed during this time.
You should not breastfeed during treatment and for 2 months after your last dose.
If it is necessary for you to have ERBITUX, your doctor will discuss the risks and benefits of having it if you are pregnant or breastfeeding.
Tell your doctor if you have, or have had, any medical conditions, especially the following:
abnormal blood test results
liver problems
kidney problems
This is because ERBITUX has been tested only in patients with adequate liver and kidney function, and in those without blood disorders.
heart problems
lung problems
eye problems.
Your doctor may want to take special care if you have any of the above conditions.
Tell your doctor if you have allergies to any other medicines, foods, preservatives or dyes.
If you have not told your doctor about any of the above, tell him/her before you start receiving ERBITUX.
Taking other medicines
Tell your doctor if you are taking any other medicines, including any that you buy without a prescription from a pharmacy, supermarket, herbal or health food shop.
Your doctor and pharmacist have more information on medicines to be careful with or to avoid while using ERBITUX.
If your doctor is giving you other medicines, such as chemotherapy, with ERBITUX, he/she will discuss with you the benefits and risks involved.
ERBITUX must not be mixed with any other injections.
A separate infusion line must be used to give you any other injection.
How to use ERBITUX
How much to use
Your doctor will calculate the correct dose of ERBITUX for you because it depends on your body surface area (a measurement based on your height and weight).
The first dose is 400 mg per square metre of body surface area and the injection is given over a period of approximately 2 hours.
The following weekly doses of 250 mg per square metre are infused over a period of approximately 1 hour.
How to use ERBITUX
A doctor experienced in the use of medicines for cancer will supervise your treatment with ERBITUX. Trained nurses will administer ERBITUX to you.
ERBITUX is usually given once a week by intravenous infusion (slow injection into a vein).
ERBITUX may be administered either diluted or undiluted. Your doctor will determine the correct dose and dilution for you. If you are being treated with a chemotherapy medicine in combination with ERBITUX, the chemotherapy medicine can only be started 1 hour after the end of the ERBITUX infusion.
How long to use ERBITUX for
Your doctor will decide how long you will receive ERBITUX based on your response to the medicine and the type of cancer you have.
If you miss a dose
If you miss a dose, talk to your doctor or nurse and arrange another visit as soon as possible.
While you are being treated with ERBITUX
Things you must do
Keep all appointments with your doctor and always discuss anything that worries you during or after treatment with ERBITUX.
Before starting any new medicine, remind your doctor or pharmacist that you are receiving ERBITUX.
Tell all the doctors, dentists and pharmacists who are treating you that you are receiving ERBITUX.
If you become pregnant while you are treated with ERBITUX, tell your doctor immediately.
Things you must not do
Do not stop going to your visits for treatment with ERBITUX without checking with your doctor.
Your condition may worsen if you stop receiving ERBITUX.
Things to be careful of
Be careful driving or operating machinery until you know how ERBITUX affects you.
Treatment-related symptoms can affect your concentration and ability to react.
If this happens, do not drive, operate machinery or do anything else that could be dangerous.
Side effects
Tell your doctor or nurse as soon as possible if you do not feel well while you are having ERBITUX.
All medicines, including ERBITUX, can have unwanted side effects. Sometimes they are serious, most of the time they are not.
Most of the side effects occur during or soon after ERBITUX therapy. However, some may occur after this period.
Do not be alarmed by this list of possible side effects.
You may not experience any of them.
Infusion-related side effects
Tell your doctor or nurse if you experience any of the following symptoms, during or after treatment with ERBITUX:
fever
chills
shortness of breath
dizziness.
Mild to moderate infusion-related reactions may occur in more than 1 in 10 people who are being treated with ERBITUX. To recognise early signs of these side effects, you will be monitored closely while you are receiving each infusion and for at least 1 hour afterwards.
Your doctor may consider reducing the infusion rate of ERBITUX in order to manage these symptoms.
Sometimes these side effects may occur up to several hours later.
If you experience them any time after receiving ERBITUX, contact your doctor or nurse.
Tell your doctor or nurse immediately if you experience any of the following side effects:
asthma-like symptoms such as severe breathing difficulties with wheezing, hoarseness, and difficulty speaking
a rapidly developing lumpy rash
chest pain
leg pain
feeling dizzy or faint.
These side effects can be life-threatening and need immediate medical attention. Treatment with ERBITUX may have to be stopped.
Skin reactions
Tell your doctor if you notice any of the following symptoms of skin reaction and they worry you:
acne-like skin rash
itchy, dry, scaling skin
excessive growth of hair on your body
nail problems.
Skin reactions are very common. More than 8 in 10 people receiving ERBITUX may experience skin reactions.
Most of these side effects develop within the first three weeks of treatment. They usually disappear over time after the end of ERBITUX therapy.
Tell your doctor or nurse immediately if you experience severe blistering or peeling of the skin.
These can be symptoms of a very rare (may affect less than 1 in 10,000 people) but severe skin reaction which may have serious consequences and can be life-threatening.
Tell your doctor if you notice any other extensive skin rash.
Limit your exposure to sunlight by wearing a hat, protective clothing and sunscreen when you go outside.
Depending on how severe your skin reaction is and how often it occurs, your doctor may:
stop ERBITUX for up to 2 weeks before giving you the next dose,
administer a lower dose, or
stop treatment altogether.
Other side effects
Tell your doctor, pharmacist or nurse if you notice any of the following:
red, watery eye(s) which can be accompanied by pain and blurring of your vision, eye sore, severe dry eye(s) or crusty eyelids
weakness, fatigue, loss of appetite, anorexia, vomiting or nausea (feeling sick). These symptoms may be due to low levels of magnesium, calcium or other electrolytes in the blood. Your doctor may do blood tests to check.
abdominal pain or diarrhoea
sore, red or dry mouth, which may be accompanied by a nose bleed
signs of frequent infections such as fever, tiredness, chills, sore throat or mouth ulcers
headache
unusual infections of your skin
leg swelling or pain (signs of a blood clot)
chest pain or tightness
sudden-onset fever, severe headache, vomiting, stiff neck and sensitivity to light.
Tell your doctor immediately if you experience sudden or worsened breathing difficulties, especially if you also experience cough or fever.
These can be symptoms of lung inflammation, which is rare (may affect 1 to 10 in 10,000 people) but can be life-threatening. Your treatment with ERBITUX may have to be interrupted or stopped altogether.
Ask your doctor to answer any questions you may have.
Tell your doctor if you notice anything else that is making you feel unwell.
Other side effects not listed above may also occur in some patients.
Side effects in combination with chemotherapy or radiation therapy
If you receive ERBITUX in combination with chemotherapy medicines or radiation therapy, you may also experience some side effects from the chemotherapy medicine or the radiation therapy or from the combination of ERBITUX with these treatments.
Tell your doctor immediately if you experience:
signs of frequent infections such as fever, tiredness, chills, sore throat or mouth ulcers.
If you receive ERBITUX in combination with chemotherapy including platinum, it is more likely that you may experience the above symptoms and infectious complications which can include life-threatening conditions.
chest pain
redness and swelling of the palms of the hands or the soles of the feet which may cause the skin to peel.
If you receive ERBITUX in combination with chemotherapy containing fluoropyrimidines, it is more likely that you may experience some of the above symptoms.
Tell your doctor or nurse if you experience:
sore, red or dry mouth, which may be accompanied by a nose bleed
severe flaking or peeling or the skin
difficulty swallowing
If you receive ERBITUX in combination with radiation therapy, you may experience some of the above symptoms.
Tell your doctor if you experience any other side effects not listed in this leaflet.
After being treated with ERBITUX
Storage
ERBITUX 5 mg/mL must be kept in a refrigerator at 2° to 8°C, but it must not be frozen.
Each vial is intended for single use only. When the needed amount of solution has been withdrawn from the vial, any remaining solution must be discarded.
Product description
What it looks like
ERBITUX 5 mg/mL is a clear, colourless solution. It is supplied in 20 mL or 100 mL colourless glass vials with a rubber stopper and aluminium seal. Each pack contains 1 vial.
Ingredients
The active ingredient in ERBITUX 5 mg/mL is cetuximab. Each 20 mL vial contains 100 mg cetuximab and each 100 mL vial contains 500 mg cetuximab.
The solution also contains the following inactive ingredients:
glycine
polysorbate 80
citric acid monohydrate
sodium chloride
water for injections
sodium hydroxide.
ERBITUX solution does not contain any preservative.
Supplier
ERBITUX 5 mg/mL is supplied in Australia by:
Merck Serono Australia Pty Ltd
3-4/25 Frenchs Forest Road East
Frenchs Forest NSW 2086
ERBITUX is supplied in New Zealand by:
Healthcare Logistics
58 Richard Pearse Drive
Airport Oaks
Auckland
For enquiries about ERBITUX please call Merck Serono Australia Medical Information on 1800-MED-INF (1800-633-463) or from New Zealand call +61 2 8977 4100.
Australian registration numbers:
AUST R 132393, 132396
Date of preparation
This leaflet was prepared in
October 2011.
® Registered trademark
A007-1011
