Contains the active ingredient zoledronic acid (as monohydrate)
Consumer Medicine Information
NOTICE: This Consumer Medicine Information (CMI) is intended for persons
living in Australia. This page contains answers to some common
. 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 this medicine is used for
The name of your medicine is APO-Zoledronic Acid 4mg/5mL or APO-Zoledronic Acid 4mg/100mL. It contains the active ingredient
zoledronic acid (as monohydrate).
It is used to:
lower the amount of calcium in the blood when it becomes too high, as may happen in some forms of cancer.
Some cancers can speed up normal changes in bone so that the amount of calcium released from the bones into the blood is increased.
It is also used to:
slow down the spread of cancers in bone, helping to prevent changes to the bones that may cause them to weaken.
It is used in people with advanced cancer of the bone marrow (called multiple myeloma) and other advanced cancers that have
spread to the bone. This medicine is used in addition to other standard cancer treatments.
Ask your doctor if you have any questions about why this medicine has been prescribed for you. Your doctor may have prescribed
this medicine for another reason.
This medicine is available only with a doctor's prescription.
How it works
Zoledronic acid belongs to a group of medicines called bisphosphonates, which strongly bind to bone. These medicines slow
down the rate of bone change and help to restore the amount of calcium in the blood to normal.
There is no evidence that this medicine is addictive.
Use in children
This medicine should not be used in children. The safety and effectiveness in children have not been established.
Before you take this medicine
When you must not take it
Do not take this medicine if:
You are pregnant.
Zoledronic acid may affect your developing baby if you take it during pregnancy.
You are breastfeeding.
Zoledronic acid may pass into human breast milk.
You are hypersensitive to or have had an allergic reaction to, zoledronic acid, any of the ingredients listed at the end of
this leaflet or any other bisphosphonates such as alendronate or risedronate.
If you are not sure whether you are allergic to other bisphosphonate medicines, talk to your doctor.
Symptoms of an allergic reaction may include cough, shortness of breath, wheezing or difficulty breathing; swelling of the
face, lips, tongue, throat or other parts of the body, rash, itching or hives on the skin; fainting or hayfever-like symptoms
If you think you are having an allergic reaction, do not take any more of the medicine and contact your doctor immediately
or go to the Accident and Emergency department at the nearest hospital.
The expiry date (EXP) printed on the pack has passed.
The packaging is torn, shows signs of tampering or it does not look quite right.
Before you start to take it
Before you start taking this medicine, tell your doctor if:
You have been treated with or are being treated with:
other medicines which contain zoledronic acid
other bisphosphonate medicines
diuretic therapy (commonly called 'fluid tablets').
You have allergies to:
any other medicines
any other substances, such as foods, preservatives or dyes.
You have or have had any medical conditions, especially the following:
kidney or liver problems
asthma and you are allergic to aspirin
surgery on your thyroid
pain in the teeth, gums or jaw, swelling or numbness of the jaw or a 'heavy jaw feeling' or loosening of a tooth.
You are currently receiving or are planning to receive dental treatment.
It is advisable to have a dental check-up before starting zoledronic acid. Tell your dentist you may be receiving zoledronic
A dental condition called jaw osteonecrosis has been reported in some patients being treated with zoledronic acid or other
drugs in the same class as zoledronic acid. You may need to have dental treatment completed before starting it.
You are planning to have surgery or an anaesthetic.
You are taking or are planning to take any other medicines, this includes vitamins and supplements that are available from
your pharmacy, supermarket or health food shop.
Some medicines may interact with zoledronic acid. These include:
medicines that may affect your kidneys, such as fluid tablets
aminoglycoside medicines, used to treat severe infections. The combination of aminoglycoside and bisphosphonate medicines
may cause the level of calcium in the blood to become too low anti-angiogenic medicines as part of your cancer treatment.
The combination of these medicines and bisphosphonate medicines may increase the risk of bone damage in the jaw (osteonecrosis)
any other medicine containing zoledronic acid, or other bisphosphonates such as risedronate, alendronate
thalidomide, a medicine used in clinical trials to treat multiple myeloma
loop diuretics, medicines used to treat high blood pressure or oedema.
If you are taking any of these you may need a different dose or you may need to take different medicines.
Other medicines not listed above may also interact with zoledronic acid.
How this medicine is given
Zoledronic acid is given as a no less than 20 minute infusion into a vein. You may also be given an infusion of fluids to
ensure that you do not become dehydrated.
You will have a blood test before each dose of zoledronic acid to make sure the medicine is not affecting your kidneys.
How much you will be given
Your doctor will tell you how much of this medicine you will be given. This will depend on your condition and whether you
are taking any other medicines.
To lower the amount of calcium in the blood, the usual dose of zoledronic acid is 4 mg, given as a single infusion.
To treat cancer in the bone, the usual dose is 4 mg, given as an infusion every 3 to 4 weeks.
Your doctor may give you a lower dose if you have a mild kidney problem. Your doctor may also prescribe a daily calcium supplement
and a multiple vitamin containing Vitamin D.
Make sure you drink enough fluids before and after the treatment with this medicine as directed by your doctor.
If you have too much (overdose)
If you think that you or anyone else may have had too much of this medicine, immediately telephone your doctor or the Poisons
Information Centre (Tel: 13 11 26 in Australia) for advice. Alternatively go to the Accident and Emergency Department at your
Do this even if there are no signs of discomfort or poisoning. You may need urgent medical attention. Symptoms of an overdose
unusual light headedness, dizziness or faintness
numbness or tingling sensation
These symptoms may mean the level of calcium in your blood has fallen too far.
While you are being given this medicine
Things you must do
Tell your doctor that you are taking this medicine if:
you have any dental symptoms including pain or unusual feeling in your teeth of gums, or any dental infections
you are about to be started on any new medicine
you are pregnant or are planning to become pregnant
you are breastfeeding or are planning to breastfeed
you are about to have any blood tests
you are going to have surgery or an anaesthetic or are going into hospital.
Go to your doctor regularly for a blood test to make sure the treatment is working. Regular blood tests can also help detect
side effects before they become serious.
Tell any other doctors, dentists and pharmacists who are treating you that you take this medicine.
Things to be careful of
Be careful when driving or operating machinery until you know how this medicine affects you. If you are returning home immediately
after the infusion, arrange to have someone else drive.
Many cancer medicines can cause 'dry mouth' which can lead to decay and other dental problems. Keep your mouth moist by drinking
Practice good dental hygiene. Your routine dental hygiene should include:
brushing your teeth and tongue after every meal and at bedtime
gentle flossing once a day to remove plaque
avoiding use of mouthwash that contains alcohol.
Use a mirror to check your teeth and gums regularly for any changes such as sores or bleeding gums. If you notice any problems,
tell your doctor and dentist immediately.
Possible side effects
Tell your doctor as soon as possible if you do not feel well while you are taking zoledronic acid or if you have any questions
Do not be alarmed by the following lists of side effects. You may not experience any of them. All medicines can have side
effects. Sometimes they are serious but most of the time they are not.
Tell your doctor if you notice any of the following:
short-lasting fever, sometimes with flu-like symptoms: such as chills; tiredness; fatigue; weakness; aches and pains, and
joint pain and swelling
redness, swelling or pain where the needle for the infusion was inserted
upset stomach, abdominal pain, loss of appetite
nausea (feeling sick) or vomiting
dry or sore mouth
constipation or diarrhoea
swollen aching joints or muscles, pain in the bones
swelling of fingers or lower legs due to fluid build up
anxiety, confusion, difficulty sleeping
headache, facial pain
irritated eyes, blurred vision, eye pain, sensitivity to light, runny, itchy or swollen eyes
changes in taste sensation
slow heart beat
irregular heart beat
difficulty breathing with wheezing or coughing.
If you experience any of the following, stop taking your medicine and contact your doctor immediately or go to the Accident
and Emergency department at your nearest hospital.
These may be serious side effects. You may need urgent medical attention or hospitalisation:
signs that the level of calcium in your blood may have fallen too far, such as unusual light headedness, dizziness or faintness,
numbness or tingling sensation, muscle cramps, convulsions or spasms.
constant "flu-like" symptoms (chills, fever, sore throat, sores in mouth, swollen glands, tiredness or lack of energy) that
could be a sign of blood problems
passing less urine than normal, blood in the urine
pain in the mouth, teeth or jaw, swelling or sores inside the mouth, numbness or a "heavy jaw feeling" or loosening of a tooth.
These symptoms could be a sign of a jaw-bone problem known as jaw osteonecrosis.
Patients taking zoledronic acid may be at risk of unusual fracture of the thigh bone. Contact your doctor if you experience
pain, weakness or discomfort in your thigh, hip or groin as this may be an early sign of a possible fracture of the thigh
Tell your doctor if you notice anything else that is making you feel unwell.
Other side effects not listed above may occur in some patients.
If you think you are having an allergic reaction to zoledronic acid, do not take any more of this medicine and tell your doctor
immediately or go to the Accident and Emergency department at your nearest hospital.
Symptoms of an allergic reaction may include some or all of the following:
cough, 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
Storage and disposal
It is unlikely that you will have to store zoledronic acid at home.
If you have to store it:
Keep your medicine in its original packaging until it is time to take it.
If you take your medicine out of its original packaging it may not keep well.
Keep your medicine in a cool dry place where the temperature will stay below 25°C.
Do not store your medicine, 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 this medicine 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 they have passed their expiry date, your pharmacist can dispose of
the remaining medicine safely.
What APO-Zoledronic Acid 4mg/5mL looks like
This medicine is packaged in plastic vials containing a clear, colourless, sterile solution.
Packs of 1, 4 or 10 vials
* Not all strengths, pack types and/or pack sizes may be available.
What APO-Zoledronic Acid 4 mg/100 mL looks like
This medicine is packaged in glass vials containing a clear, colourless, sterile solution.
Packs of 1, 4 or 5 vials
* Not all strengths, pack types and/or pack sizes may be available.
Each vial contains 4.264 mg of zoledronic acid (as monohydrate), equivalent to 4 mg of zoledronic acid in 5 mL, or 100 mL
of solution, as the active ingredient.
It also contains the following inactive ingredients:
water for injections.
This medicine is gluten-free, lactose-free, sucrose-free, tartrazine-free and free of other azo dyes.
Australian Registration Numbers
APO-Zoledronic Acid 4mg/5mL concentrated injection (packs of 1, 4 or 10 vials): AUST R 190337
APO-Zoledronic Acid 4mg/100mL injection solution for infusion (packs of 1, 4 or 5 vials): AUST R 205927.
Apotex Pty Ltd
16 Giffnock Avenue
Macquarie Park NSW 2113
APO and APOTEX are the registered trade marks of Apotex Inc.
This leaflet was last updated in: