Medine.co.uk

Letrozole 2.5m Tablets

2. What you need to know before you

take Femara

Package leaflet: Information for the user

Femara® 2.5mg Tablets

(letrozole)

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 or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

The name of your medicine is Femara 2.5mg Tablets but will be referred to as Femara throughout this leaflet.

What is in this leaflet

1.    What Femara is and what it is used for

2.    What you need to know before you take Femara

3.    Flow to take Femara

4.    Possible side effects

5.    Flow to store Femara

6.    Contents of the pack and other information

1. What Femara is and what it is used for

What Femara is and how it works

Femara contains an active substance called letrozole. It belongs to a group of medicines called aromatase inhibitors. It is a hormonal (or ‘endocrine’) breast cancer treatment. Growth of breast cancer is frequently stimulated by oestrogens which are female sex hormones. Femara reduces the amount of oestrogen by blocking an enzyme (‘aromatase’) involved in the production of oestrogens and therefore may block the growth of breast cancer that needs oestrogens to grow. As a consequence tumour cells slow or stop growing and/or spreading to other parts of the body.

What Femara is used for

Femara is used to treat breast cancer in women who have gone through menopause i.e. cessation of periods.

It is used to prevent cancer from happening again. It can be used as first treatment before breast cancer surgery in case immediate surgery is not suitable or it can be used as first treatment after breast cancer surgery or following five years treatment with tamoxifen. Femara is also used to prevent breast tumour spreading to other parts of the body in patients with advanced breast cancer.

If you have any questions about how Femara works or why this medicine has been prescribed for you, ask your doctor.

Follow all the doctor’s instructions carefully. They may differ from the general information in this leaflet.

Do not take Femara

if you are allergic to letrozole or to any of the other ingredients of this medicine (listed in section 6),

if you still have periods, i.e. if you have not yet gone through the menopause,

if you are pregnant, if you are breast-feeding.

If any of these conditions apply to you, do not take this medicine and talk to your doctor.

Warnings and precautions

Talk to your doctor or pharmacist before taking Femara

if you have a severe kidney disease, if you have a severe liver disease,

if you have a history of osteoporosis or bone fractures (see also ‘Follow-up during Femara treatment’ in section 3).

If any of these conditions apply to you, tell your doctor. Your doctor will take this into account during your treatment with Femara.

Children and adolescents (below 18 years)

Children and adolescents should not use this medicine.

People aged 65 years and over can use this medicine at the same dose as for other adults.

Other medicines and Femara

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

Pregnancy, breast-feeding and fertility

You should only take Femara when you have gone through the menopause. However, your doctor should discuss with you the use of effective contraception, as you may still have the potential to become pregnant during treatment with Femara.

You must not take Femara if you are pregnant or breast-feeding as it may harm your baby.

Driving and using machines

If you feel dizzy, tired, drowsy or generally unwell, do not drive or operate any tools or machines until you feel normal again.

Femara contains lactose

Femara contains lactose (milk sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

3. How to take Femara

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

The usual dose is one tablet of Femara to be taken once a day. Taking Femara at the same time each day will help you remember when to take your tablet.

The tablet can be taken with or without food and should be swallowed whole with a glass of water or another liquid.

How long to take Femara

Continue taking Femara every day for as long as your doctor tells you. You may need to take it for months or even years. If you have any questions about how long to keep taking Femara, talk to your doctor.

Follow-up during Femara treatment

You should only take this medicine under strict medical supervision. Your doctor will regularly monitor your condition to check whether the treatment is having the right effect.

Femara may cause thinning or wasting of your bones (osteoporosis) due to the reduction of oestrogens in your body. Your doctor may decide to measure your bone density (a way of monitoring for osteoporosis) before, during and after treatment.

If you take more Femara than you should

If you have taken too much Femara, or if someone else accidentally takes your tablets, contact a doctor or hospital for advice immediately. Show them the pack of tablets. Medical treatment may be necessary.

If you forget to take Femara

If it is almost time for your next dose (e.g. within 2 or 3 hours), skip the dose you missed and take your next dose when you are meant to.

Otherwise, take the dose as soon as your remember, and then take the next tablet as you would normally.

Do not take a double dose to make up for the one that you missed.

If you stop taking Femara

Do not stop taking Femara unless your doctor tells you to. See also the section above ‘How long to take Femara’.

4. Possible side effects

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

Most of the side effects are mild to moderate and will generally disappear after a few days to a few weeks of treatment.

Some of these side effects, such as hot flushes, hair loss or vaginal bleeding, may be due to the lack of oestrogens in your body.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

Some side effects could be serious:

Rare or uncommon side effects (i.e. they may affect between 1 to 100 in every 10,000 patients):

Weakness, paralysis or loss of feeling in any part of the body (particularly arm or leg), loss of coordination, nausea, or difficulty speaking or breathing (sign of a brain disorder, e.g. stroke).

Sudden oppressive chest pain (sign of a heart disorder).

Difficulty breathing, chest pain, fainting, rapid heart rate, bluish skin discoloration, or

Swelling and redness along a vein which is extremely tender and possibly painful when touched.

Severe fever, chills or mouth ulcers due to infections (lack of white blood cells).

Severe persistent blurred vision.

If any of the above occurs, tell your doctor straight away.

You should also inform the doctor straight away if you experience any of the following symptoms during treatment with Femara:

Swelling mainly of the face and throat (signs of allergic reaction).

Yellow skin and eyes, nausea, loss of appetite, dark-coloured urine (signs of hepatitis).

Rash, red skin, blistering of the lips, eyes or mouth, skin peeling, fever (signs of skin disorder).

Some side effects are very common. These side effects may affect more than 10 in every 100 patients.

Hot flushes

Increased level of cholesterol (hypercholesterolaem ia)

Fatigue

Increased sweating

Pain in bones and joints (arthralgia)

If any of these affects you severely, tell your doctor.

Some side effects are common. These side effects may affect between 1 to 10 in every 100 patients.

Skin rash

Headache

Dizziness

Malaise (generally feeling unwell)

Gastrointestinal disorders such as nausea, vomiting, indigestion, constipation, diarrhoea

Increase in or loss of appetite Pain in muscles

Thinning or wasting of your bones (osteoporosis), leading to bone fractures in some cases (see also ‘Follow-up during Femara treatment’ in section 3)

Swelling of arms, hands, feet, ankles (oedema)

Depression

Weight increase Hair loss

Raised blood pressure (hypertension) Abdominal pain Dry skin

Vaginal bleeding

If any of these affects you severely, tell your doctor.

Other side effects are uncommon.

These side effects may affect between 1 to 10 in every 1,000 patients.

Nervous disorders such as anxiety, nervousness, irritability, drowsiness, memory problems, somnolence, insomnia Pain or burning sensation in the hands or wrist (carpal tunnel syndrome)

Impairment of sensation, especially that of touch

Eye disorders such as blurred vision, eye irritation

Palpitations, rapid heart rate Skin disorders such as itching (urticaria) Vaginal discharge or dryness Joint stiffness (arthritis)

Breast pain Fever

Thirst, taste disorder, dry mouth Dryness of mucous membranes

Weight decrease

Urinary tract infection, increased frequency of urination

Cough

Increased level of enzymes

Side effects with frequency not known

Trigger finger, a condition in which your finger or thumb catches in a bent position.

If any of these affects you severely, tell your doctor.

Reporting 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.aov.uk/vellowcard

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

5. How to store Femara

Store the tablets in their original pack. Do not store above 30°C.

Keep out of the sight and reach of children.

Do not take your tablets after the expiry date which is stated on the box label after ‘Exp’. The expiry date refers to the last day of that month

Remember if your doctor tells you to stop taking this medicine; return any unused tablets to your pharmacist for safe disposal. Only keep this medicine if your doctor tells you to.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment

6. Contents of the pack and other information What Femara contains

They contain 2.5mg of the active ingredient, letrozole. They also contain the inactive ingredients colloidal anhydrous silica, microcrystalline cellulose, lactose, magnesium stearate, maize starch, sodium carboxymethyl starch, hydroxypropyl methylcellulose, polyethylene glycol, talc, titanium dioxide(E171) and iron oxide yellow (E172).

What Femara looks like and contents of the pack

Femara are dark yellow, round, film-coated tablets, with markings ‘FV’ on one side and ‘CG’ on reverse.

The tablets come in blister packs of 30.

Manufactured by: Novartis Pharma GmbH, Roonstrasse 25, D-90429, Nurnberg, Germany.

Procured from within the EU and repackaged by the Product Licence holder:

B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 ONU, UK.

Femara® 2.5mg Tablets

PL: 18799/1882    ,_,

I POM I

Leaflet date: 16.11.2015    -

Femara is a registered trademark of Novartis Pharmaceuticals UK Limited.

Letrozole 2.5mg Tablets

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 or pharmacist. This includes any possible side effects not listed in this leaflet. See section 4.

The name of your medicine is Letrozole 2.5mg Tablets but will be referred to as Letrozole throughout this leaflet.

What is in this leaflet

1.    What Letrozole is and what it is used for

2.    What you need to know before you take Letrozole

3.    How to take Letrozole

4.    Possible side effects

5.    How to store Letrozole

6.    Contents of the pack and other information

1. What Letrozole is and what it is used for

What Letrozole is and how it works

Letrozole contains an active substance called letrozole. It belongs to a group of medicines called aromatase inhibitors. It is a hormonal (or ‘endocrine’) breast cancer treatment. Growth of breast cancer is frequently stimulated by oestrogens which are female sex hormones. Letrozole reduces the amount of oestrogen by blocking an enzyme (‘aromatase’) involved in the production of oestrogens and therefore may block the growth of breast cancer that needs oestrogens to grow. As a consequence tumour cells slow or stop growing and/or spreading to other parts of the body.

What Letrozole is used for

Letrozole is used to treat breast cancer in women who have gone through menopause i.e. cessation of periods.

It is used to prevent cancer from happening again. It can be used as first treatment before breast cancer surgery in case immediate surgery is not suitable or it can be used as first treatment after breast cancer surgery or following five years treatment with tamoxifen. Letrozole is also used to prevent breast tumour spreading to other parts of the body in patients with advanced breast cancer.

If you have any questions about how Letrozole works or why this medicine has been prescribed for you, ask your doctor.

Follow all the doctor’s instructions carefully. They may differ from the general information in this leaflet.

Do not take Letrozole

if you are allergic to letrozole or to any of the other ingredients of this medicine (listed in section 6),

if you still have periods, i.e. if you have not yet gone through the menopause,

if you are pregnant, if you are breast-feeding.

If any of these conditions apply to you, do not take this medicine and talk to your doctor.

Warnings and precautions

Talk to your doctor or pharmacist before taking Letrozole

if you have a severe kidney disease, if you have a severe liver disease,

if you have a history of osteoporosis or bone fractures (see also ‘Follow-up during Letrozole treatment’ in section 3).

If any of these conditions apply to you, tell your doctor. Your doctor will take this into account during your treatment with Letrozole.

Children and adolescents (below 18 years)

Children and adolescents should not use this medicine.

People aged 65 years and over can use this medicine at the same dose as for other adults.

Other medicines and Letrozole

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines, including medicines obtained without a prescription.

Pregnancy, breast-feeding and fertility

You should only take Letrozole when you have gone through the menopause.

However, your doctor should discuss with you the use of effective contraception, as you may still have the potential to become pregnant during treatment with Letrozole.

You must not take Letrozole if you are pregnant or breast-feeding as it may harm your baby.

Driving and using machines

If you feel dizzy, tired, drowsy or generally unwell, do not drive or operate any tools or machines until you feel normal again.

Letrozole contains lactose

Letrozole contains lactose (milk sugar). If you have been told by your doctor that you have an intolerance to some sugars, contact your doctor before taking this medicine.

3. How to take Letrozole

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

The usual dose is one tablet of Letrozole to be taken once a day. Taking Letrozole at the same time each day will help you remember when to take your tablet.

The tablet can be taken with or without food and should be swallowed whole with a glass of water or another liquid.

How long to take Letrozole

Continue taking Letrozole every day for as long as your doctor tells you. You may need to take it for months or even years. If you have any questions about how long to keep taking Letrozole, talk to your doctor.

Follow-up during Letrozole treatment

You should only take this medicine under strict medical supervision. Your doctor will regularly monitor your condition to check whether the treatment is having the right effect.

Letrozole may cause thinning or wasting of your bones (osteoporosis) due to the reduction of oestrogens in your body. Your doctor may decide to measure your bone density (a way of monitoring for osteoporosis) before, during and after treatment.

If you take more Letrozole than you should

If you have taken too much Letrozole, or if someone else accidentally takes your tablets, contact a doctor or hospital for advice immediately. Show them the pack of tablets. Medical treatment may be necessary.

If you forget to take Letrozole

If it is almost time for your next dose (e.g. within 2 or 3 hours), skip the dose you missed and take your next dose when you are meant to.

Otherwise, take the dose as soon as your remember, and then take the next tablet as you would normally.

Do not take a double dose to make up for the one that you missed.

If you stop taking Letrozole

Do not stop taking Letrozole unless your doctor tells you to. See also the section above ‘How long to take Letrozole’.

4. Possible side effects

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

Most of the side effects are mild to moderate and will generally disappear after a few days to a few weeks of treatment.

Some of these side effects, such as hot flushes, hair loss or vaginal bleeding, may be due to the lack of oestrogens in your body.

Do not be alarmed by this list of possible side effects. You may not experience any of them.

Some side effects could be serious:

Rare or uncommon side effects (i.e. they may affect between 1 to 100 in every 10,000 patients):

Weakness, paralysis or loss of feeling in any part of the body (particularly arm or leg), loss of coordination, nausea, or difficulty speaking or breathing (sign of a brain disorder, e.g. stroke).

Sudden oppressive chest pain (sign of a heart disorder).

Difficulty breathing, chest pain, fainting, rapid heart rate, bluish skin discoloration, or

Swelling and redness along a vein which is extremely tender and possibly painful when touched.

Severe fever, chills or mouth ulcers due to infections (lack of white blood cells).

Severe persistent blurred vision.

If any of the above occurs, tell your doctor straight away.

You should also inform the doctor straight away if you experience any of the following symptoms during treatment with Letrozole:

Swelling mainly of the face and throat (signs of allergic reaction).

Yellow skin and eyes, nausea, loss of appetite, dark-coloured urine (signs of hepatitis).

Rash, red skin, blistering of the lips, eyes or mouth, skin peeling, fever (signs of skin disorder).

Some side effects are very common. These side effects may affect more than 10 in every 100 patients.

Hot flushes

Increased level of cholesterol (hypercholesterolaem ia)

Fatigue

Increased sweating

Pain in bones and joints (arthralgia)

If any of these affects you severely, tell your doctor.

Some side effects are common. These side effects may affect between 1 to 10 in every 100 patients.

Skin rash

Headache

Dizziness

Malaise (generally feeling unwell)

Gastrointestinal disorders such as nausea, vomiting, indigestion, constipation, diarrhoea

Increase in or loss of appetite Pain in muscles

Thinning or wasting of your bones (osteoporosis), leading to bone fractures in some cases (see also ‘Follow-up during Letrozole treatment’ in section 3)

Swelling of arms, hands, feet, ankles (oedema)

Depression

Weight increase Hair loss

Raised blood pressure (hypertension) Abdominal pain Dry skin

Vaginal bleeding

If any of these affects you severely, tell your doctor.

Other side effects are uncommon.

These side effects may affect between 1 to 10 in every 1,000 patients.

Nervous disorders such as anxiety, nervousness, irritability, drowsiness, memory problems, somnolence, insomnia Pain or burning sensation in the hands or wrist (carpal tunnel syndrome)

Impairment of sensation, especially that of touch

Eye disorders such as blurred vision, eye irritation

Palpitations, rapid heart rate Skin disorders such as itching (urticaria) Vaginal discharge or dryness Joint stiffness (arthritis)

Breast pain Fever

Thirst, taste disorder, dry mouth Dryness of mucous membranes

Weight decrease

Urinary tract infection, increased frequency of urination

Cough

Increased level of enzymes

Side effects with frequency not known

Trigger finger, a condition in which your finger or thumb catches in a bent position.

If any of these affects you severely, tell your doctor.

Reporting 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.aov.uk/vellowcard

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

5. How to store Letrozole

Store the tablets in their original pack. Do not store above 30°C.

Keep out of the sight and reach of children.

Do not take your tablets after the expiry date which is stated on the box label after ‘Exp’. The expiry date refers to the last day of that month

Remember if your doctor tells you to stop taking this medicine; return any unused tablets to your pharmacist for safe disposal. Only keep this medicine if your doctor tells you to.

Medicines should not be disposed of via wastewater or household waste. Ask your pharmacist how to dispose of medicines no longer required. These measures will help to protect the environment

6. Contents of the pack and other information What Letrozole contains

They contain 2.5mg of the active ingredient, letrozole. They also contain the inactive ingredients colloidal anhydrous silica, microcrystalline cellulose, lactose, magnesium stearate, maize starch, sodium carboxymethyl starch, hydroxypropyl methylcellulose, polyethylene glycol, talc, titanium dioxide(E171) and iron oxide yellow (E172).

What Letrozole looks like and contents of the pack

Letrozole are dark yellow, round, film-coated tablets, with markings ‘FV’ on one side and ‘CG’ on reverse.

The tablets come in blister packs of 30.

Manufactured by: Novartis Pharma GmbH, Roonstrasse 25, D-90429, Nurnberg, Germany.

Procured from within the EU and repackaged by the Product Licence holder:

B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 ONU, UK.

Letrozole 2.5mg Tablets

PL: 18799/1882    ,_,

I POM I

Leaflet date: 16.11.2015    -