Megace 160mg Tablets
Ref: 1406/270516/1/F
Megace 160mg Tablets
(megestrol acetate)
Patient Information Leaflet
Read all of this leaflet carefully before you start taking 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 or pharmacist.
- 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.
Your medicine is known as Megace 160mg Tablets but will be referred to as Megace tablets throughout the leaflet.
What is in this leaflet:
^ What Megace tablets are and what they are used for What you need to know before you take Megace tablets fa How to take Megace tablets ^ Possible side effects ^ How to store Megace tablets
Contents of the pack and other information
^ What Megace tablets are and what they are used for
The name of your medicine is Megace Tablets. Megace tablets contain the active ingredient megestrol acetate. Megestrol acetate belongs to a group of medicines called progestogens and is used to treat certain types of cancer known as hormone-dependent cancer, which include cancer of the breast.
3 What you need to know before you take Megace tablets
Do not take Megace tablets if you:
* are allergic to megestrol acetate or any of the other ingredients of this medicine (listed in section 6).
Warnings and precautions
Tell your doctor if you:
* have severe liver problems
* currently suffer from, or have a history of suffering from blood clots (thrombophlebitis)
* have diabetes, as Megace tablets can increase your blood sugar levels
If you are over 65 years of age your doctor may want to monitor your kidney function from time to time, as this can sometimes decrease with age.
Other medicines and Megace tablets
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
Pregnancy and breast-feeding
Do not take Megace tablets if you are pregnant, think you may be pregnant, or if you are breast-feeding.
Driving and using machines
Megace tablets do not usually affect your ability to drive.
Megace tablets contains lactose
If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.
^ How to take Megace tablets
Always take Megace tablets exactly as your doctor has told you. You should check with your doctor if you are not sure.
The usual dosage is 160 mg megestrol acetate per day.
Tablets should be swallowed with a glass of water.
This medicine is not recommended for children.
Megace tablets should be taken for at least two months to see if they are effective. Some patients take them for many years.
Do not stop taking them, unless advised to do so by your doctor.
If you take more Megace tablets than you should
If you take more Megace than you should, go to your nearest hospital emergency department or contact your doctor immediately.
Take the empty container and any remaining medicine with you.
If you forget to take Megace tablets
If you miss a dose, do not worry. If you remember within a few hours of the missed dose take it as soon as possible, but if it is almost time for your next dose then skip the forgotten one and continue as before. Do not take a double dose to make up for the one you missed.
3 Possible side effects
As with all medicines, Megace can cause side effects although not everybody gets them.
If you notice any of the following, stop taking Megace and contact your doctor immediately:
* swelling of the face, lips, or tongue
* skin rash
* difficulty breathing
As these may be signs of an allergic reaction
Megace ® 160mg Tablets
(megestrol acetate)
Patient Information Leaflet (continued)
Other side effects which may occur with Megace tablets are:
Very Common (affects more than 1 in 10 people)
* increase in appetite and weight gain (not associated with water retention)
* shortness of breath
* hot flushes, reddening of the face and neck
* high blood pressure
* increased blood sugar levels
* rounded face, sometimes called 'moon' face
* constipation
* swelling of a vein due to a blood clot
* blood clot in the lungs
Signs of a blood clot can include loss of co-ordination, slurred speech, pains in your groin, pains or numbness in your arm or leg (especially in calf of leg), shortness of breath, weakness, headache, and fainting. If you experience any of these signs tell your doctor immediately.
Common (affects between 1 in 10 to 1 in 100 people)
* temporary increase in the signs and symptoms of your disease.
* changes in mood
* numbness, pain or tingling in fingers or thumb
* heart attack
* hair loss
* diarrhoea
* tiredness
* feeling weak
* impotence
* passing wind
* needing to urinate more often
* feeling sick and being sick
* changes in vaginal bleeding (breakthrough bleeding, spotting)
* build up of fluid which causes swelling (mainly in the ankles)
* pain
* rash, including hives or nettle rash (Urticaria)
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.
[5 How to store your medicine
* KEEP OUT OF THE SIGHT AND REACH OF CHILDREN
* Do not store above 25°C.
* Store in the original package in order to protect from moisture.
* Do not take this medicine after the expiry date which is printed on the blister or carton label. If your doctor tells you to stop taking the medicine, take any remaining medicine back to the pharmacist for safe disposal. Only keep this medicine if your doctor tells you to.
* If your medicine becomes discoloured or shows any other signs of deterioration, ask your pharmacist who will advise you what to do.
* Medicines should not be disposed of via waste water or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment.
[6 Further information
What Megace tablets contain:
Each Megace tablet contains 160 mg of the active ingredient megestrol acetate. The other ingredients are: colloidal anhydrous silica, lactose monohydrate, magnesium stearate, microcrystalline cellulose, povidone K30 and sodium starch glycolate.
What Megace tablets look like and contents of the pack
Megace tablets are off-white, oval shaped, biconvex tablets with a break line
on one side and engraved ‘160' on the other side.
Each pack contains blisters of 30 Tablets.
Manufacturer and Licence Holder
This medicine is manufactured by Andersonbrecon (UK) Limited, Hereford, U.K., and is procured from within the EU and repackaged by the Product Licence Holder: Lexon (UK) Limited, Unit 18, Oxleasow Road, East Moons Moat, Redditch, Worcestershire, B98 0RE.
If you have any questions or are not sure about anything, ask your doctor or pharmacist. They will have additional information about this medicine and will be able to advise you.
|POM PL 15184/1406 Megace 160mg Tablets
Megace is a registered trademark of Bristol-Myers Squibb Company.
Revision date: 27/05/16