Medine.co.uk

Zafirlukast 20mg Film-Coated Tablets

Package leaflet: Information for the user

Accolate® 20mg film-coated tablets

(zafirlukast)

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 Accolate' 20mg film-coated tablets but will be referred to as Accolate throughout this leaflet.

What is in this leaflet:

1.    What Accolate is and what it is used for

2.    What you need to know before you take Accolate

3.    How to take Accolate

4.    Possible side effects

5.    How to store Accolate

6.    Contents of the pack and other information

1. What Accolate is and what it is used for

Accolate contains a medicine called zafirlukast. This belongs to a group of medicines called ‘leukotriene antagonists'. This means that it reduces the effects of ‘leukotrienes'. These are natural substances in the lung that cause asthma.

•    Accolate is used to control the symptoms of your asthma.

•    It is also used to prevent your asthma from getting worse.

Do not take Accolate to treat sudden (acute) asthma attacks. Your doctor will provide you with other medicines to treat sudden attacks.

2. What you need to know before you take Accolate

Do not take Accolate if:

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

•    If you have ever had problems with your liver.

•    If you have had problems with your liver that were caused by taking Accolate.

Do not take Accolate if any of the above applies to you. If you are not sure, talk to your doctor or pharmacist before taking this medicine.

Warnings and precautions

Talk to your doctor or pharmacist before taking Accolate:

•    If you are a smoker. This could affect the amount of Accolate that you need to take.

•    If you have kidney problems.

If you are not sure if the above apply to you, talk to your doctor or pharmacist before taking Accolate.

If you go into hospital let the medical staff know that you are taking Accolate.

Children

Accolate should not be given to children under the age of 12 years.

Other medicines and Accolate

Tell your doctor or pharmacist 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. This is because Accolate can affect the way some medicines work and some medicines can have an effect on Accolate.

In particular, tell your doctor or pharmacist if you are taking any of the following medicines:

•    Theophylline (used to treat asthma).

•    Erythromycin (an antibiotic).

•    Terfenadine (used to treat hayfever).

•    Warfarin (used to thin the blood).

•    Aspirin (if you are taking it frequently as a painkiller).

•    Fluconazole (used to treat fungal infections).

Pregnancy and breast-feeding

•    If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor will decide whether you can take Accolate during this time.

•    Do not take Accolate if you are breast-feeding.

Driving and using machines

Accolate is not likely to affect you being able to drive or use any tools or machines.

Accolate contains lactose

Accolate contains lactose, which is a type of sugar. If you have been told by your doctor that you cannot tolerate or digest some sugars (have an intolerance to some sugars), talk to your doctor before taking this medicine.

3. How to take Accolate

Always take this medicine exactly as your doctor has told you. Read the label on the container to remind you what the doctor said. Check with your doctor or pharmacist if you are not sure.

If you have been taking other medicines for asthma, do not stop taking them unless your doctor tells you that you can.

Taking this medicine

•    Take Accolate every day as prescribed by your doctor.

•    The recommended dose is one 20mg tablet taken twice a day. This is usually one tablet at the start of the morning and one tablet last thing at night.

•    Try to take your medicine at the same times each day.

•    Swallow each tablet whole with a drink of water.

•    Do not take your tablets with a meal.

•    Continue to take Accolate even when your asthma is not causing you any problems.

•    Do not stop taking your tablets when you are feeling well, unless your doctor tells you to.

If your asthma gets worse while you are taking Accolate, follow the advice that your doctor has given you for treating sudden (acute) asthma attacks and see your doctor as soon as possible.

If you take more Accolate than you should

If you take more Accolate than prescribed by your doctor, ask your doctor or pharmacist for advice.

If you forget to take Accolate

•    If you forget to take a dose, take it as soon as you remember. However, if it is nearly time for the next dose, skip the missed dose.

•    Do not take a double dose (two doses at the same time) to make up for a forgotten dose.

4. Possible side effects

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

Allergic reactions (uncommon, may affect up to 1 in 100 people)

The signs include:

•    Skin rash and itching.

•    Swelling around your lips, face, tongue and throat.

If any of these happen, stop taking Accolate and tell your doctor straight away.

Liver problems

Accolate may affect your liver. These liver effects range from non-serious increases in liver enzymes (common, may affect up to 1 in 10 people) detected by blood tests to serious conditions such as liver failure (very rare, may affect up to 1 in 10,000 people). A very small number of people have died from liver failure.

Your doctor may ask you to have blood tests before and during treatment with Accolate to check whether there are any problems with your liver.

The signs of liver problems include:

•    Yellowing of your skin or the whites of your eyes (jaundice).

•    Pain on the right side of your stomach and just below your ribs.

•    Loss of appetite.

•    Feeling itchy.

•    Feeling tired, having no energy or feeling like you have flu.

•    Feeling as though you are going to be sick or actually being sick.

If any of these happen, stop taking Accolate and tell your doctor straight away.

Infection (very common, may affect more than 1 in 10 people.)

The signs include:

•    A high temperature (fever) that does not go away.

•    Frequent sore throats.

If any of these happen, tell your doctor.

Bleeding problems (rare, may affect up to 1 in 1,000 people)

The signs include:

•    Bleeding disorders, including heavy menstrual periods.

•    Low platelet count (symptoms include bleeding or bruising more easily than normal).

If any of these happen, tell your doctor.

Unusual conditions

Unusual conditions called ‘Churg-Strauss syndrome' and ‘eosinophilic pneumonia' have been seen in a very small number of people taking Accolate for asthma. The signs include a combination of the following:

•    Sinusitis. This can cause a feeling of fullness in the nose, cheeks and behind your eyes.

•    Feeling like you have flu.

•    Feeling more and more breathless.

•    Pain in the area of your stomach or gut.

•    Skin rash.

•    A feeling of ‘pins and needles' or numbness of your arms or legs.

If you notice more than one of these signs, tell your doctor straight away.

Other possible side effects: Common (may affect up to 1 in 10 people)

•    Stomach and gut problems, such as feeling or being sick, diarrhoea or stomach pain.

These effects are usually mild.

•    Headache. This is usually mild.

•    Pain in the muscles.

Uncommon (may affect up to 1 in 100 people)

•    Swelling.

•    Difficulty sleeping.

•    Pain in the joints.

•    Feeling of discomfort or generally feeling unwell.

Rare (may affect up to 1 in 1,000 people)

•    Blisters

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

•    Marked decrease in the number of circulating white blood cells.

Not known (frequency cannot be estimated)

•    Reduced feeling in the skin/tingling feeling such as ‘pins and needles’.

•    Feeling dizzy.

•    Nightmares

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.

• 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 Accolate contains:

The active ingredient in Accolate is zafirlukast.

Each film-coated tablet contains 20mg zafirlukast.

The other ingredients are croscarmellose sodium, lactose monohydrate, microcrystalline cellulose, povidone, magnesium stearate, hypromellose and titanium dioxide (E171).

What Accolate looks like and contents of the pack

Accolate is white, round, biconvex, film-coated tablets intagliated with 'Accolate 20' on one side and plain on the reverse.

Accolate is available as calendar blister packs of 56 tablets.

Manufactured by: AstraZeneca UK Limited, Silk Road Business Park, Macclesfield, UK.

Procured from within the EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.

Accolate® 20mg film-coated tablets; PL 18799/2938

I POM

Leaflet date: 02.08.2016

5. How to store Accolate

•    Keep out of the sight and reach of children.

•    Do not store above 30°C.

•    Store in the original package.

•    Do not take the tablets after the expiry date which is stated on the carton and blister label after ‘Exp'. The expiry date refers to the last day of the month.

•    If the tablets become discoloured or show any signs of deterioration, seek the advice of your pharmacist.

Package leaflet: Information for the user

Zafirlukast 20mg film-coated 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 Zafirlukast 20mg film-coated tablets but will be referred to as Zafirlukast throughout this leaflet.

What is in this leaflet:

1.    What Zafirlukast is and what it is used for

2.    What you need to know before you take Zafirlukast

3.    How to take Zafirlukast

4.    Possible side effects

5.    How to store Zafirlukast

6.    Contents of the pack and other information

1. What Zafirlukast is and what it is used for

Zafirlukast tablet contains a medicine called zafirlukast. This belongs to a group of medicines called ‘leukotriene antagonists'. This means that it reduces the effects of ‘leukotrienes'.

These are natural substances in the lung that cause asthma.

•    Zafirlukast is used to control the symptoms of your asthma.

•    It is also used to prevent your asthma from getting worse.

Do not take Zafirlukast to treat sudden (acute) asthma attacks. Your doctor will provide you with other medicines to treat sudden attacks.

2. What you need to know before you take Zafirlukast

Do not take Zafirlukast if:

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

•    If you have ever had problems with your liver.

•    If you have had problems with your liver that were caused by taking Zafirlukast.

Do not take Zafirlukast if any of the above applies to you. If you are not sure, talk to your doctor or pharmacist before taking this medicine.

Warnings and precautions

Talk to your doctor or pharmacist before taking Zafirlukast:

•    If you are a smoker. This could affect the amount of Zafirlukast that you need to take.

•    If you have kidney problems.

If you are not sure if the above apply to you, talk to your doctor or pharmacist before taking Zafirlukast.

If you go into hospital let the medical staff know that you are taking Zafirlukast.

Children

Zafirlukast should not be given to children under the age of 12 years.

Other medicines and Zafirlukast

Tell your doctor or pharmacist 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. This is because Zafirlukast can affect the way some medicines work and some medicines can have an effect on Zafirlukast.

In particular, tell your doctor or pharmacist if you are taking any of the following medicines:

•    Theophylline (used to treat asthma).

•    Erythromycin (an antibiotic).

•    Terfenadine (used to treat hayfever).

•    Warfarin (used to thin the blood).

•    Aspirin (if you are taking it frequently as a painkiller).

•    Fluconazole (used to treat fungal infections).

Pregnancy and breast-feeding

•    If you are pregnant, think you may be pregnant or are planning to have a baby, ask your doctor for advice before taking this medicine. Your doctor will decide whether you can take Zafirlukast during this time.

•    Do not take Zafirlukast if you are breast-feeding.

Driving and using machines

Zafirlukast is not likely to affect you being able to drive or use any tools or machines.

Zafirlukast contains lactose

Zafirlukast contains lactose, which is a type of sugar. If you have been told by your doctor that you cannot tolerate or digest some sugars (have an intolerance to some sugars), talk to your doctor before taking this medicine.

3. How to take Zafirlukast

Always take this medicine exactly as your doctor has told you. Read the label on the container to remind you what the doctor said. Check with your doctor or pharmacist if you are not sure.

If you have been taking other medicines for asthma, do not stop taking them unless your doctor tells you that you can.

Taking this medicine

•    Take Zafirlukast every day as prescribed by your doctor.

•    The recommended dose is one 20mg tablet taken twice a day. This is usually one tablet at the start of the morning and one tablet last thing at night.

•    Try to take your medicine at the same times each day.

•    Swallow each tablet whole with a drink of water.

•    Do not take your tablets with a meal.

•    Continue to take Zafirlukast even when your asthma is not causing you any problems.

•    Do not stop taking your tablets when you are feeling well, unless your doctor tells you to.

If your asthma gets worse while you are taking Zafirlukast, follow the advice that your doctor has given you for treating sudden (acute) asthma attacks and see your doctor as soon as possible.

If you take more Zafirlukast than you should

If you take more Zafirlukast than prescribed by your doctor, ask your doctor or pharmacist for advice.

If you forget to take Zafirlukast

•    If you forget to take a dose, take it as soon as you remember. However, if it is nearly time for the next dose, skip the missed dose.

•    Do not take a double dose (two doses at the same time) to make up for a forgotten dose.

4. Possible side effects

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

Allergic reactions (uncommon, may affect up to 1 in 100 people)

The signs include:

•    Skin rash and itching.

•    Swelling around your lips, face, tongue and throat.

If any of these happen, stop taking Zafirlukast and tell your doctor straight away.

Liver problems

Zafirlukast may affect your liver. These liver effects range from nonserious increases in liver enzymes (common, may affect up to 1 in 10 people) detected by blood tests to serious conditions such as liver failure (very rare, may affect up to 1 in 10,000 people). A very small number of people have died from liver failure.

Your doctor may ask you to have blood tests before and during treatment with Zafirlukast to check whether there are any problems with your liver.

The signs of liver problems include:

•    Yellowing of your skin or the whites of your eyes (jaundice).

•    Pain on the right side of your stomach and just below your ribs.

•    Loss of appetite.

•    Feeling itchy.

•    Feeling tired, having no energy or feeling like you have flu.

•    Feeling as though you are going to be sick or actually being sick.

If any of these happen, stop taking Zafirlukast and tell your doctor straight away.

Infection (very common, may affect more than 1 in 10 people.)

The signs include:

•    A high temperature (fever) that does not go away.

•    Frequent sore throats.

If any of these happen, tell your doctor.

Bleeding problems (rare, may affect up to 1 in 1,000 people)

The signs include:

•    Bleeding disorders, including heavy menstrual periods.

•    Low platelet count (symptoms include bleeding or bruising more easily than normal).

If any of these happen, tell your doctor.

Unusual conditions

Unusual conditions called ‘Churg-Strauss syndrome' and ‘eosinophilic pneumonia' have been seen in a very small number of people taking Zafirlukast for asthma. The signs include a combination of the following:

•    Sinusitis. This can cause a feeling of fullness in the nose, cheeks and behind your eyes.

•    Feeling like you have flu.

•    Feeling more and more breathless.

•    Pain in the area of your stomach or gut.

•    Skin rash.

•    A feeling of ‘pins and needles’ or numbness of your arms or legs.

If you notice more than one of these signs, tell your doctor straight away.

Other possible side effects: Common (may affect up to 1 in 10 people)

•    Stomach and gut problems, such as feeling or being sick, diarrhoea or stomach pain.

These effects are usually mild.

•    Headache. This is usually mild.

•    Pain in the muscles.

Uncommon (may affect up to 1 in 100 people)

•    Swelling.

•    Difficulty sleeping.

•    Pain in the joints.

•    Feeling of discomfort or generally feeling unwell.

Rare (may affect up to 1 in 1,000 people)

•    Blisters

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

•    Marked decrease in the number of circulating white blood cells.

Not known (frequency cannot be estimated)

•    Reduced feeling in the skin/tingling feeling such as ‘pins and needles’.

•    Feeling dizzy.

•    Nightmares.

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.

• 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 Zafirlukast contains:

The active ingredient in Zafirlukast is zafirlukast.

Each film-coated tablet contains 20mg zafirlukast.

The other ingredients are croscarmellose sodium, lactose monohydrate, microcrystalline cellulose, povidone, magnesium stearate, hypromellose and titanium dioxide (E171).

What Zafirlukast looks like and contents of the pack

Zafirlukast is white, round, biconvex, film-coated tablets intagliated with 'Accolate 20' on one side and plain on the reverse.

Zafirlukast is available as calendar blister packs of 56 tablets.

Manufactured by: AstraZeneca UK Limited, Silk Road Business Park, Macclesfield, UK.

Procured from within the EU and repackaged by the Product Licence holder: B&S Healthcare, Unit 4, Bradfield Road, Ruislip, Middlesex, HA4 0NU, UK.

Zafirlukast 20mg film-coated tablets;

PL 18799/2938

I POM

Leaflet date: 02.08.2016

5. How to store Zafirlukast

•    Keep out of the sight and reach of children.

•    Do not store above 30°C.

•    Store in the original package.

•    Do not take the tablets after the expiry date which is stated on the carton and blister label after ‘Exp'. The expiry date refers to the last day of the month.

•    If the tablets become discoloured or show any signs of deterioration, seek the advice of your pharmacist.