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Zoladex La 10.8mg Implant

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Read all of this leaflet carefully before you start using this medicine because it contains important information for you.

-    Keep this leaflet. You may need to read it again.

-    If you have any further questions, ask your doctor, pharmacist or nurse.

-    This medicine has been prescribed for you only. Do not pass it on to others. It may harm them, even if their signs of illness are the same as yours.

-    If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. See section 4.


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|4) POSSIBLE SIDE EFFECTS|


500186/PL1 g

Zoladex® LA 10.8 mg Implant

(goserelin)

Patient Information Leaflet

The name of your medicine is Zoladex® LA 10.8 mg Implant. Throughout this leaflet it will be referred to as Zoladex® LA.

What is in this leaflet:

1)    What Zoladex® LA is and what it is used for

®

2)    What you need to know before you use Zoladex LA

3)    How to use Zoladex® LA

4)    rossible side effects

5)    How to store Zoladex® LA

6)    Contents of the pack and other information

1) WHAT ZOLADEX® LA IS AND WHAT IT IS USED FO

Zoladex LA contains a medicine called goserelin. This belongs to a group of medicines called 'LHRH analogues'.

Zoladex® LA is used to treat prostate cancer. It works by reducing the amount of 'testosterone' (a hormone) that is produced by your body. Zoladex® LA is a long-acting form of Zoladex® and it is given every 12 weeks.

2) WHAT Y

OU NEED TO KNOW BEFORE YOU USE |

ZOLADEX® L

A

Do not use Zoladex® LA:

•    if you are allergic to goserelin or any of the other ingredients of this medicine (listed in Section 6).

•    if you are a woman.

Do not have Zoladex LA if any of the above apply to you. If you are not sure, talk to your doctor, pharmacist or nurse before having Zoladex® LA.

Warnings and precautions

Talk to your doctor, pharmacist or nurse before using Zoladex® LA:

•    if you have problems passing urine (water) or problems with your back.

•    if you have diabetes.

•    if you have high blood pressure.

•    if you have any condition that affects the strength of your

bones, especially if you are a heavy drinker, a smoker, have a family history of osteoporosis (a condition that affects the    strength of your bones) or take

anticonvulsants (medicines for epilepsy or fits) or corticosteroids (steroids).

• if you have any heart or blood vessel conditions, including heart rhythm problems (arrhythmia), or are being treated with medicines for these conditions. The risk of heart rhythm problems may be increased when using Zoladex LA.

There have been reports of depression in patients taking Zoladex® which may be severe. If you are taking Zoladex® and develop depressed mood, inform your doctor.

Medicines of this type can cause a reduction in bone calcium (thinning of bones).

Children

Zoladex LA® should not be given to children.

Other medicines and Zoladex LA

Tell your doctor, pharmacist or nurse if you are taking, have recently taken or might take any other medicines. This includes medicines that you buy without a prescription and herbal medicines.

Zoladex® LA might interfere with some medicines used to treat heart rhythm problems (e.g. quinidine, procainamide, amiodarone and sotalol) or might increase the risk of heart rhythm problems when used with some other drugs (e.g. methadone (used for pain relief and part of drug addiction detoxification), moxifloxacin (an antibiotic), antipsychotics used for serious mental illnesses).

Driving and using machines

Zoladex® LA is not likely to affect you being able to drive or use any tools or machines.

3) HOW TO USE ZOLADEX® LA

The Zoladex LA 10.8 mg Implant will be injected under the skin on your stomach every 12 weeks.

This will be done by your doctor or nurse.

It is important that you keep having Zoladex® LA treatment, even if you are feeling well.

Keep having this treatment until your doctor decides that it is time for you to stop.

Your next appointment

•    You should be given a Zoladex® LA injection every 12 weeks.

•    Always remind the doctor or nurse to set up an appointment for your next injection.

•    If you are given an appointment for your next injection which is earlier or later than 12 weeks from your last injection, tell your doctor or nurse.

•    If it has been more than 12 weeks since your last injection, contact your doctor or nurse so that you can receive your injection as soon as possible.

Like all medicines, this medicine can cause side effects, although not everybody gets them.

Allergic reactions:

These are rare. The symptoms can include sudden onset of:

•    Rash, itching or hives on the skin.

•    Swelling of the face, lips or tongue or other parts of the body.

•    Shortness of breath, wheezing or trouble breathing.

If this happens to you, see a doctor straight away.

Other possible side effects:

Very common (may affect more than 1 in 10 people)

•    Hot flushes and sweating.

Occasionally these side effects may continue for some time (possibly months) after stopping Zoladex®.

•    A reduced sex drive and impotence.

Continued overleaf


If you go into hospital, tell the medical staff that you are having Zoladex® LA.


POM


Common (may affect up to 1 in 10 people)

•    Pain in your lower back or problems passing urine. If this happens, talk to your doctor.

•    Bone pain at the beginning of treatment. If this happens, talk to your doctor.

•    Thinning of your bones.

•    Rises in blood sugar levels.

•    Tingling in your fingers or toes.

• Skin rashes.

• Weight gain.

•    Pain, bruising, bleeding, redness or swelling where Zoladex® LA is injected.

•    Reduced heart function or heart attack.

•    Changes in blood pressure.

•    Swelling and tenderness of your breasts.

•    Changes in your mood (including depression).

Uncommon (may affect up to 1 in 100 people)

•    Pain in the joints.

Very rare (may affect up to 1 in 10,000 people)

•    Psychiatric problems called psychotic disorders which may include hallucinations (seeing, feeling or hearing things that are not there), disordered thoughts and personality changes. This is very rare.

•    The development of a tumour of the pituitary gland in your head or, if you already have a tumour in your pituitary gland, Zoladex® LA may make the tumour bleed or collapse. These effects are very rare. Pituitary tumours can cause severe headaches, feeling or being sick, loss of eyesight and becoming unconscious.

Not known (frequency cannot be estimated from the available data)

•    Hair loss.

•    Changes in your blood.

•    Liver problems.

•    A blood clot in your lungs causing chest pain or shortness of breath.

•    Inflammation of the lungs. The symptoms may be like pneumonia (such as feeling short of breath and coughing).

•    Changes in ECG (QT prolongation).

Do not be concerned by this list of possible side effects. You may not get any of them.

Reporting of side effects

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.

By reporting side effects you can help provide more information on the safety of this medicine.

6) CONTENTS OF THE PACK AND OTHER INFORMATION

What Zoladex LA 10.8 mg Implant contains

The active substance is goserelin.

Each Zoladex® LA 10.8 mg Implant contains 10.8 mg of goserelin.

The other ingredient is lactide/glycolide copolymer which is an inactive substance.

What Zoladex® LA 10.8 mg Implant looks like and contents of the pack

Zoladex® LA 10.8 mg Implant comes as an implant (a very small pellet) in a pre-filled syringe, ready to be used by the doctor or nurse.

Zoladex® LA 10.8 mg Implant is produced in packs of one implant (injection).

Procured from within the EU. Product Licence Holder Ginova Limited, repackager Ginova UK Limited, both of St. James' House, 8 Overcliffe, Gravesend, Kent, DA11 0HJ.

Zoladex® LA is manufactured by: AstraZeneca UK Limited, Silk Road Business Park, Macclesfield, Cheshire, SK10 2NA, UK.

Zoladex® LA 10.8 mg Implant

PL No: 18067/0207

Zoladex® and SafeSystem™ are trademarks of the AstraZeneca group.

This leaflet was last approved on 23rd February 2015.

To request a copy of this leaflet in Braille, large print or audio please call 01622 690172.

5) HOW TO STORE ZOLADEX® L


•    Your doctor may give you a prescription so that you can get your medicine from the pharmacy and give it to your doctor when you see him or her again.

•    Keep it in its original package and do not break the seal.

•    Do not store above 25°C.

•    Keep out of the sight and reach of children.

•    Do not use this medicine after the expiry date which is stated on the carton. The expiry date refers to the last day of that month.

•    Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away medicines you no longer use. These measures will help protect the environment.

500186/PL1g