Consumer Medicine Information
What is in this leaflet
This leaflet answers some common questions about ELIGARD. It does not contain all
the available information. It does not take the place of talking to your doctor or
All medicines have risks and benefits. Your doctor has weighed the risks of you taking
ELIGARD against the benefits they expect it will have for you.
If you have any concerns about taking this medicine, ask your doctor or pharmacist.
Keep this leaflet with the medicine.
You may need to read it again.
What ELIGARD is used for
ELIGARD is used to reduce the symptoms of advanced cancer of the prostate gland, or
to treat high-risk localised prostate cancer in combination with radiotherapy. This
medicine is similar to a hormone called gonadotrophin releasing hormone, which is
normally released from the brain.
When it is given regularly to males, this medicine works by reducing the amount of
testosterone produced. This inhibits the growth of prostate cancers which rely on
testosterone to grow.
Ask your doctor if you have any questions about why this medicine has been prescribed
Your doctor may have prescribed it for another reason.
This medicine is not addictive.
This medicine is available only with a doctor's prescription.
Before you are given ELIGARD
When you must not be given it
You must not be given ELIGARD if you have an allergy to:
any medicine containing leuprorelin
any of the ingredients listed at the end of this leaflet
any other similar medicines (such as goserelin).
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.
Do not use ELIGARD following surgical removal of your testes, as in that case ELIGARD
does not lead to further decrease in serum testosterone levels.
You must not be given this medicine if you are pregnant or plan to become pregnant
or are breastfeeding.
This medicine has not been studied in women.
If used during pregnancy, it may affect the developing baby.
This medicine must not be given to children.
Safety and effectiveness has not been established in children.
You must not be given this medicine after the expiry date printed on the pack or if
the packaging is torn or shows signs of tampering.
If it has expired or is damaged, return it to your pharmacist for disposal.
If you are not sure whether you should be given this medicine, talk to your doctor.
Before you are given it
Tell your doctor if you have allergies to any other medicines, foods, preservatives
Tell your doctor if you have nerve problems caused by bone lesions in the spine, problems
passing urine or blood in your urine.
These conditions may get worse for a short time after treatment is started. Your doctor
may prescribe another medicine when you first receive ELIGARD to reduce the likelihood
of this occurring.
Tell your doctor if you have or have had any of the following medical conditions:
cardiovascular disease, heart problems or blood vessel conditions, including heart
rhythm problems (arrhythmia), or are being treated with medicines for these conditions.
The risk of you having further heart rhythm problems may increase with ELIGARD
history of epilepsy, fits or seizures
tumour in your pituitary gland.
Talk to your doctor about the effects ELIGARD may have on fertility.
This medicine may impair fertility in men. Use of this medicine for a short time has
shown a full return to fertility after stopping the medicine. Fertility suppression
may or may not be permanent when the medicine is given for a long time.
If you have not told your doctor about any of the above, tell him/her before you start
treatment with ELIGARD.
Taking other medicines
Tell your doctor or pharmacist if you are taking any other medicines, including any
that you get without a prescription from your pharmacy, supermarket or health food
ELIGARD may interfere with some medicines used to treat heart rhythm problems, such
ELIGARD may increase the risk of heart rhythm problems when used with other medicines
which also have the same risk, such as:
methadone (used for pain relief and part of drug addiction detoxification)
moxifloxacin (an antibiotic)
antipsychotics used for serious mental illness.
ELIGARD has not been found to interact with other commonly used medicines.
Your doctor and pharmacist have more information on medicines to be careful with or
avoid while taking this medicine.
How ELIGARD is given
Follow all directions given to you by your doctor or pharmacist carefully.
They may differ from the information contained in this leaflet.
How much is given
Your doctor will decide what dose of ELIGARD you will receive.
The usual dose of ELIGARD is:
one 7.5 mg injection every month or
one 22.5 mg injection every three months or
one 30 mg injection every four months or
one 45 mg injection every six months.
How it is given
ELIGARD should only be given to you by a doctor or nurse.
The content of the two syringes in the ELIGARD kit (one containing the active ingredient
and the other containing the delivery system) will be mixed together, then injected
underneath the skin. The site of the injection should be varied from time to time.
How long it is given for
Continue treatment with your medicine for as long as your doctor tells you.
This medicine helps to control your condition, but does not cure it. It is important
that you continue to receive your medicine even if you feel well.
If you forget to have your injection
If you have missed your injection, contact your doctor or pharmacist to find out what
If you take too much (overdose)
As ELIGARD will be given to you under the supervision of your doctor, it is very unlikely
that you will receive an overdose. However, if you think that you or anyone else may
have been given too much ELIGARD, immediately telephone your doctor or the Poisons
Information Centre (telephone 13 11 26) for advice, or go to Accident and Emergency
at the nearest hospital. Do this even if there are no signs of discomfort or poisoning.
You may need urgent medical attention.
There have not been any unwanted effects seen with overdosage of ELIGARD.
While you are being given ELIGARD
Things you must do
If your condition worsens, tell your doctor.
If you are about to be started on any new medicine, remind your doctor and pharmacist
that you are being given ELIGARD.
Tell any other doctors, dentists, and pharmacists who treat you that you are being
given this medicine.
If you are about to have any blood tests, tell your doctor that you are taking this
It may interfere with the results of some tests.
Keep all of your doctor's appointments so that your progress can be checked.
Your doctor may do some blood and other tests from time to time to make sure the medicine
Things you must not do
Do not give your medicine to anyone else, even if they have the same condition as
Do not stop treatment with your medicine without checking with your doctor.
Things to be careful of
Be careful driving or operating machinery until you know how ELIGARD affects you.
This medicine may cause fatigue, dizziness and visual disturbances in some people.
If you have any of these symptoms, do not drive, operate machinery or do anything
else that could be dangerous.
Tell your doctor, nurse or pharmacist as soon as possible if you do not feel well
while you are being given ELIGARD.
This medicine helps most people with prostate cancer, but it may have unwanted side
effects in a few people. All medicines can have side effects. Sometimes they are serious,
most of the time they are not. You may need medical attention if you get some of the
Do not be alarmed by the following lists of side effects. You may not experience any
Ask your doctor, nurse or pharmacist to answer any questions you may have.
Tell your doctor, nurse or pharmacist if you notice any of the following and they
short-lived burning, stinging, pain, redness or itching at the injection site
mild bruising at the injection site
feelings of warmth or periods of excessive sweating
pain or a decrease in size of the testicles
nausea, vomiting or diarrhoea
more frequent urination
changes in your breasts.
The above list includes the more common side effects of your medicine. They are usually
Tell your doctor, nurse or pharmacist as soon as possible if you notice any of the
tingling or numbness of the hands and feet
difficulty in passing urine
blood in your urine
bone pain or fractures (this may be a sign of weakening of the bones).
The above list includes serious side effects that may require medical attention.
If any of the following happen, tell your doctor or nurse immediately or go to Accident
and Emergency at your nearest hospital:
signs of an allergic reaction, such as 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
headache and vomiting, eye problems, altered mental state, or collapse
The above list includes very serious side effects. You may need urgent medical attention
or hospitalisation. These side effects are rare.
Tell your doctor, nurse or pharmacist if you notice anything that is making you feel
Other side effects not listed above may also occur in some people.
Some of these side can only be found when your doctor does tests from time to time
to check your progress.
After being given ELIGARD
ELIGARD will be stored in the refrigerator (below 8°C) in the pharmacy.
Once ELIGARD is dispensed to you, keep it in a place where the temperature stays below
It may be stored in this manner for a period of up to 8 weeks prior to administration.
Keep this medicine in the original pack until it is time to use it.
If you take it out of the pack, it may not keep well.
Do not store ELIGARD or any other medicine in the bathroom or near a sink. Do not
leave it on a window sill or in the car.
Heat and dampness can destroy some medicines.
Keep it where children cannot reach it.
A locked cupboard at least one-and-a-half metres above the ground is a good place
to store medicines.
If your doctor tells you to stop taking this medicine or the expiry date has passed,
ask your pharmacist what to do with any medicine that is left over.
What it looks like
ELIGARD is available in a single use kit, containing a cardboard frame and two removable
sealed plastic trays. The tray containing syringe A contains a syringe filled with
the delivery system, known as the Atrigel® Delivery System, plus a long white replacement plunger rod and a desiccant pack (to
absorb moisture). The tray containing syringe B contains a syringe filled with a powder
which is the active ingredient, plus a needle and a desiccant pack (to absorb moisture).
Once the contents of syringe A and syringe B have been mixed together (prior to injection),
the colour of the resulting liquid will be:
light tan to tan for ELIGARD
colourless to pale yellow for ELIGARD 3 month, ELIGARD
4 month and ELIGARD 6 month.
The mixed solution may appear slightly grey due to tiny air bubbles. This is acceptable
and not representative of product quality.
ELIGARD comes in single packs.
ELIGARD contains leuprorelin acetate as the active ingredient. The Atrigel® delivery system consists of a biodegradable polymer, dissolved in a solvent (N-methyl-2-pyrrolidone).
Each presentation of ELIGARD contains a different mixture and volume of the polymer.
ELIGARD comes in the following strengths:
ELIGARD 1 month (7.5 mg leuprorelin acetate)
ELIGARD 3 month (22.5 mg leuprorelin acetate)
ELIGARD 4 month (30 mg leuprorelin acetate)
ELIGARD 6 month (45 mg leuprorelin acetate)
This medicine does not contain lactose, sucrose, gluten, tartrazine or any other azo
ELIGARD is supplied in Australia by:
Mundipharma Pty Limited
ABN 87 081 322 509
88 Phillip Street
SYDNEY NSW 2000
® ELIGARD and ATRIGEL are trademarks of Tolmar Therapeutics, Inc. used under licence.
This leaflet was prepared in September 2018.
ELIGARD 1 month AUST R 97449
ELIGARD 3 month AUST R 97450
ELIGARD 4 month AUST R 97451
ELIGARD 6 month AUST R 101581