contains the active ingredient granisetron hydrochloride
Consumer Medicine Information
What is in this leaflet
This leaflet answers some common questions about KYTRIL tablets. It does not contain
all the available information. It does not take the place of talking to your doctor
All medicines have risks and benefits. Your doctor has weighed the risks of you taking
KYTRIL 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 KYTRIL is used for
KYTRIL contains the active ingredient granisetron.
It belongs to a group of medicines called anti-emetics.
KYTRIL is used to stop you feeling sick (nauseous) or being sick (vomiting). It is
especially useful when you need to have medical treatment that may cause you to feel
or be sick, for example, chemotherapy.
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.
It is available only with a doctor's prescription.
Before you take KYTRIL
When you must not take it
Do not take KYTRIL if you have an allergy to:
any medicine containing granisetron
any of the ingredients listed at the end of this leaflet.
Some of the symptoms of an allergic reaction may include shortness of breath, wheezing
or breathing difficulty; swelling of the face, lips, tongue or other parts of the
body; rash, itching or hives on the skin.
Do not take KYTRIL 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 start taking this medicine, talk to your doctor.
Before you start to take it
Tell your doctor if:
you have allergies to any other medicines, foods, preservatives or dyes.
you have had an allergic reaction with other medicines used to prevent or treat nausea
and vomiting, such as ondansetron and tropisetron. You may have an allergic reaction
to KYTRIL as well.
you have severe constipation.
you are pregnant or plan to become pregnant or are breast-feeding.
Your doctor can discuss with you the risks and benefits of taking KYTRIL if you are
pregnant or breast-feeding.
you have used KYTRIL before, and you became unwell.
You may need to be given another medicine instead.
you have a heart condition related to changes in the rhythm or rate of your heart
you are intolerant to lactose or galactose or your body does not absorb glucose or
If you have not told your doctor about any of the above, tell him/her before you start
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
Some medicines and KYTRIL may interfere with each other. These include:
phenobarbitone, a medicine used to treat epilepsy.
Phenobarbitone may be affected by KYTRIL or may affect how well KYTRIL works. You
may need different amounts of your medicine, or you may need to take a different medicine.
medicines that can affect the serotonin levels in your body. These may include: some
antibiotics, medicines used to treat depression, medicines that treat or prevent pain,
some medicines to treat Parkinson's disease, medicines to treat obesity; and medicines
used to treat attention hyperactivity disorder.
Your doctor and pharmacist have more information on medicines to be careful with or
avoid while taking KYTRIL.
How to take KYTRIL
Follow all directions given to you by your doctor or pharmacist carefully.
They may differ from the information contained in this leaflet.
How much to take
Your doctor or pharmacist will tell you how many KYTRIL tablets to take each day.
For the prevention of nausea and vomiting associated with chemotherapy, the usual
adult dose is one 2 mg tablet once a day, taken within 1 hour before the start of
chemotherapy, and then daily for up to one week following chemotherapy.
For the prevention of nausea and vomiting associated with radiotherapy, the usual
adult dose of KYTRIL is one 2 mg tablet taken within 1 hour before the start of radiotherapy.
How to take it
Swallow the tablets whole with a full glass of water. Do not crush or chew the tablets.
When to take it
Take your medicine at about the same time each day.
Taking it at the same time each day will have the best effect. It will also help you
remember when to take it.
It does not matter if you take this medicine before or after food.
How long to take it
Continue taking KYTRIL tablets for as long as your doctor tells you.
Your doctor will tell you when your treatment should be stopped.
If you forget to take it
If it is almost time for your next dose, skip the dose you missed and take your next
dose when you are meant to.
Otherwise, take it as soon as you remember, and then go back to taking your medicine
as you would normally.
Do not take a double dose to make up for the dose that you missed.
This may increase the chance of you getting an unwanted side effect.
If you are not sure what to do, ask your doctor or pharmacist.
If you have trouble remembering to take your medicine, ask your pharmacist for some
If you take too much (overdose)
If you think that you or anyone else may have taken too much KYTRIL, 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.
Keep telephone numbers for these places handy.
If you are not sure what to do, contact your doctor or pharmacist.
While you are taking KYTRIL
Things you must do
If you are about to start a new medicine, remind your doctor and pharmacist that you
are taking KYTRIL.
Tell any other doctors, dentists, and pharmacists who treat you that you are taking
Tell your doctor immediately if you become pregnant while taking this medicine.
Tell your doctor if, for any reason, you have not taken your medicine exactly as prescribed.
Otherwise, your doctor may think that it was not effective and change your treatment
Tell your doctor if you feel the tablets are not helping your condition.
Keep all of your doctor's appointments so that your progress can be checked.
Things you must not do
Do not take KYTRIL to treat any other complaints unless your doctor tells you to.
Do not give your medicine to anyone else, even if they have the same condition as
Do not stop taking your medicine or lower the dose without checking with your doctor.
Do not take any other medicines whether they require a prescription or not without
first telling your doctor.
Things to be careful of
Be careful driving or operating machinery until you know how KYTRIL affects you.
Be careful when drinking alcohol while you are taking KYTRIL.
Your doctor may suggest that you avoid alcohol or reduce the amount of alcohol you
drink while you are taking KYTRIL.
If you drink alcohol, dizziness or light-headedness may be worse.
Tell your doctor or pharmacist as soon as possible if you do not feel well while you
are taking KYTRIL.
This medicine helps most people with nausea and vomiting, 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 side effects.
Do not be alarmed by the following lists of side effects. You may not experience any
Ask your doctor or pharmacist to answer any questions you may have.
Tell your doctor or pharmacist if you notice any of the following and they worry you:
unusual tiredness or weakness
dizziness or light headedness
difficulty in sleeping
The above list includes the more common side effects of your medicine.
If any of the following happen, tell your doctor immediately or go to Accident and
Emergency at your nearest hospital:
changes in your heart beat
severe dizziness or fainting
symptoms of serotonin syndrome such as fever, sweating, fast heartbeat, agitation
or confusion and loss of muscle coordination, which may lead to loss of consciousness
symptoms 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.
The above list includes very serious side effects. You may need urgent medical attention
or hospitalisation. These side effects are rare.
Tell your doctor or pharmacist if you notice anything that is making you feel unwell.
Other side effects not listed above may also occur in some people.
After using KYTRIL
Keep your tablets in the pack until it is time to take them.
If you take the tablets out of the pack they may not keep well.
Keep your tablets in a cool dry place where the temperature stays below 30°C.
Do not store KYTRIL tablets, or any other medicine, in a bathroom or near a sink.
Do not leave KYTRIL tablets in the car or on window sills.
Heat and dampness can destroy some medicines.
Keep KYTRIL tablets where children cannot reach them.
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 KYTRIL looks like
KYTRIL 2 mg tablets are triangular, and white, with "K2" engraved on one side.
KYTRIL 2 mg tablets come in a:
pack containing 1 tablet; or
pack containing 5 tablets
KYTRIL is also available as an injection that is given by a healthcare professional.
Each 2 mg KYTRIL tablet contains 2 mg of granisetron.
sodium starch glycollate
This medicine does not contain sucrose, gluten, tartrazine or any other azo dyes.
Atnahs Pharma Australia Pty Ltd
10 Shelley Street,
SYDNEY, NSW, 2000, Australia
KYTRIL is supplied by:
Clinect Pty Ltd
120 - 132 Atlantic Drive
Keysborough VIC 3173
Customer enquiries: 1 800 899 005
Please check with your pharmacist for the latest Consumer Medicine Information.
Australian Registration Number (AUST R)
2 mg tablet: 60872.
This leaflet was prepared on 15 September 2017