laronidase-rch [lar-on-I-daze R.C.H.] 500 U, Concentrate for Solution for Infusion
Consumer Medicine Information
What is in this leaflet
This leaflet answers some common questions about ALDURAZYME.
It does not contain all the available information.
It does not take the place of talking to your treating physician or a trained health
All medicines have risks and benefits. Your treating physician has weighed the risks
of you or your child having ALDURAZYME against the benefits they expect it will have.
If you have any concerns about this medicine, ask your treating physician or nurse.
Keep this leaflet.
You may need to read it again.
What ALDURAZYME is used for
ALDURAZYME is used as enzyme replacement therapy in Mucopolysaccharidosis I (MPS I)
storage disorder, a disease in which the level of α-L-iduronidase is absent or lower
How it works
Patients with MPS I disease do not produce enough of their own enzyme, α-L-iduronidase.
The reduced or absent α-L-iduronidase activity in patients results in the accumulation
of substances called glycosaminoglycans (GAGs) in most cell types and tissues. ALDURAZYME
is an enzyme replacement therapy that is intended to restore a level of enzyme activity
sufficient to remove the accumulated GAGs and to prevent further accumulation.
Before you are given ALDURAZYME
When you or your child must not be given it
Do not take ALDURAZYME if you or your child have a known, severe, life-threatening
allergic reaction to any of the ingredients listed at the end of this leaflet.
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
skin rash, itching or hives
If you are not sure whether you or your child should have ALDURAZYME, talk to your
treating physician or nurse.
Before you or your child are given it
Tell your treating physician if you or your child have reacted to previous treatments
with any of the following:
life-threatening allergic reaction
Tell your treating physician if you or your child have allergies to:
any other medicines
any other substances, such as foods, preservatives or dyes
Tell your treating physician if you are pregnant or intend to become pregnant.
There is no information available regarding the use of ALDURAZYME in pregnant women.
Your treating physician will discuss the possible risks and benefits of having ALDURAZYME
Tell your treating physician if you are breast-feeding.
It is not known whether ALDURAZYME passes into breast milk. Your treating physician
will discuss the possible risks and benefits of having ALDURAZYME during breast-feeding.
Tell your treating physician if you or your child have difficulty breathing or suffer
from acute breathing problems.
Your treating physician will discuss the possible risks and benefits of treatment
Tell your treating physician if your child is under 5 years of age and has been prescribed
If your child has been prescribed ALDURAZYME, you may wish to discuss this with your
child's treating physician.
Patients with an acute illness at the time of ALDURAZYME infusion may be at greater
risk for infusion-associated reactions. Your treating physician may recommend you
receive pre-treatment to minimise your risk of an infusion-associated reaction.
Taking other medicines
Tell your treating physician or nurse if you or your child is taking any other medicines,
including any that you buy without a prescription from your pharmacy, supermarket
or health food shop.
Some medicines and ALDURAZYME may interfere with each other. No studies have been
carried out on drug interactions.
Tell your treating physician or nurse if you or your child are using medicines with
chloroquine (a medicine that is used as an antimalarial) or procaine (a medicine used
as local anaesthetic) as these medicines may be affected by ALDURAZYME, or may affect
how well it works (different amounts of these medicines may be needed or different
medicines may need to be taken). Your treating physician or nurse will advise you
and decide whether or not to give you or your child ALDURAZYME.
How ALDURAZYME is given
How much to use
The recommended dosage for ALDURAZYME is 100 U/kg (0.58 mg/kg) of body weight once
every week. ALDURAZYME will be given to you or your child directly into the vein
(intravenously) by a trained health care professional in a hospital or a clinic.
If you are given too much (overdose)
There have been no reported overdoses of ALDURAZYME.
Your treating physician is trained to work out the correct dose and to contact the
Australian Poisons Information Centre (telephone 13 11 26), or the New Zealand National
Poisons Centre (telephone 0800 POISON or 0800 764 766) in case of an overdose.
Things you or your child must do
Keep appointments with your treating physician or clinic.
It is important to have the infusion with ALDURAZYME at the appropriate times to make
sure the medicine has the best chance of providing treatment for the condition.
After having ALDURAZYME
Have any tests when your treating physician says to.
Your treating physician may recommend to perform blood tests to monitor your or your
child's body's response to ALDURAZYME to make sure that it is working, and to check
your or your child's immune reaction to ALDURAZYME's active ingredient.
Things to be careful of
Be careful driving or operating machinery until you know how ALDURAZYME affects you.
The effect of ALDURAZYME on your ability to drive a car or operate machinery has not
been studied. Make sure that you know how you react to ALDURAZYME before you drive
a car or operate machinery or do anything else that may be dangerous if you are dizzy,
light-headed, tired or drowsy.
Tell your treating physician or nurse as soon as possible if you or your child do
not feel well after having ALDURAZYME.
ALDURAZYME may have unwanted side effects. Sometimes the side effects are serious,
most of the time they are not. You or your child may need urgent medical treatment
if you experience a serious reaction.
Pre-existing upper airway obstruction may contribute to the severity of some reactions.
Ask your treating physician or nurse to answer any questions you may have.
Tell your treating physician or pharmacist if you notice any of the following and
they worry you:
local reaction around the injection site such as redness, itchiness, tenderness, pain
or discomfort, warmth, burning or stinging, swelling or the formation of hard lumps
flushing or redness of the skin
soreness, aching muscles, muscle tenderness or weakness (not caused by exercise)
If any of the following happen, tell your doctor immediately or go to Accident and
Emergency at your nearest hospital:
sudden signs of allergy such as rash, itching or hives on the skin,
swelling of the face, lips, tongue or other parts of the body,
shortness of breath, wheezing or trouble breathing
The above list includes side effects which may be very serious. You may need urgent
medical attention or hospitalisation. These side effects are very rare.
ALDURAZYME will be stored in the hospital or clinic pharmacy.
What it looks like
ALDURAZYME is a colourless to pale yellow, clear to slightly opalescent solution.
sodium chloride, sodium phosphate - monobasic monohydrate, dibasic sodium phosphate
heptahydrate, polysorbate 80 and water for injections.
In Australia this product is registered by:
Genzyme Australasia Pty Ltd.
12-24 Talavera Road
Macquarie Park, NSW 2113
Toll Free Number: 1800 818 806
In New Zealand this product is registered by:
sanofi-aventis new zealand limited
56 Cawley Street Ellerslie
Tell Free Number: 0800 283 684
AUST R 100847
ALDURAZYME® is manufactured by BioMarin Pharmaceutical Inc, USA.
ALDURAZYME® is a registered trademark of BioMarin/Genzyme LLC.
This leaflet was prepared in December 2018