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Mometasone Furoate 0.1% W/W Ointment

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Document: leaflet MAH BRAND_PLPI 18799-2183 change

Package leaflet: Information for the user

Elocon® 0.1% w/w Ointment

(mometasone furoate)

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.

The name of your medicine is Elocon 0.1% w/w Ointment but it will be referred as Elocon throughout this leaflet.

What is in this leaflet:

1.    What Elocon is and what it is used for

2.    What you need to know before you use Elocon

3.    How to use Elocon

4.    Possible side effects

5.    How to store Elocon

6.    Contents of the pack and other information

1.    What Elocon is and what it is used for

Elocon is one of a group of medicines called topical corticosteroids. It is classified as a ‘potent corticosteroid’.

These medicines are put on the surface of the skin to reduce the redness and itchiness caused by certain skin problems.

In adults and children, Elocon is used to reduce redness and itchiness caused by certain skin problems called psoriasis or dermatitis.

Psoriasis is a skin disease in which itchy, scaly, pink patches develop on the elbows, knees, scalp and other parts of the body. Dermatitis is a condition brought on by the skin reacting to outside agents e.g. detergents, causing the skin to become red and itchy.

2.    What you need to know before you use Elocon Do not use Elocon:

•    if you are allergic (hypersensitive) to mometasone furoate or any of the other ingredients in this medicine (listed in section 6) or to other similar medicines.

•    on any other skin problems as it could make them worse especially:

•    rosacea (a skin condition affecting the face)

•    acne

•    skin atrophy (thinning of the skin)

•    dermatitis around the mouth

•    genital itching

•    nappy rash

•    cold sores

•    chickenpox

•    shingles

•    warts

•    ulcerated skin

•    wounds

•    other skin infections

Ask your doctor or pharmacist if you are not sure.

Warning and precautions

Talk to your doctor, pharmacist or nurse before using Elocon:

•    if your skin becomes irritated or sensitive after using Elocon, you should stop using it and tell your doctor

Other medicines and Elocon

•    Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Elocon contains propylene glycolstearate

Elocon contains propylene glycolstearate, which can cause skin irritation.

3.    How to use Elocon

Always use Elocon exactly as your doctor or pharmacist has told you. You should check with your doctor or pharmacist if you are not sure.

Use in children

Elocon is not recommended for children under the age of 2.

How much to use

Usually for adults and children aged 2 and above, a thin layer of Elocon should be gently rubbed into the affected area of skin once a day.

Before using Elocon

You should always follow these instructions when using Elocon:

•    Do not use the ointment on your face for more than 5 days

•    Do not apply the ointment to children, on any part of their body, for more than 5 days.

•    Do not put the ointment under your child’s nappy, as this makes it easier for the active drug to pass through the skin and possibly cause some unwanted effects.

•    You should check with your doctor before covering the treated areas with a bandage or plaster. Treated areas on the face or in children should not be covered with a bandage or plaster.

•    You should not use a large amount of ointment on large areas of the body for a long time (for example every day for many weeks or months).

•    Do not use in or around your eyes, including eye-lids If you use more Elocon than you should

If you (or somebody else) accidentally swallows the ointment, it should not produce any problems. However, if you are worried, you should see your doctor.

If you use the ointment more often than you should, or on large areas of the body, it can affect some of your hormones.

In children, this may affect their growth and development.

If you have not used the cream as you were told to do and have used it too often and/or for a long time, you should tell your doctor.

If you stop using Elocon

If you have been using Elocon for a long time and your skin problem seems to have got better, you should not suddenly stop using the ointment. If you do, you may find that your skin becomes red and you may notice stinging or burning. To avoid this, you should speak to your doctor as he will gradually reduce how often you need to use the ointment until you stop treatment altogether.

4.    Possible side effects

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

A few people may find that they suffer from some of the following side effects after using Elocon:

•    allergic skin reactions

•    bacterial and secondary skin infections

•    acne

•    inflammation and/ or infection of the hair follicles

•    thinning of the skin

•    red marks with associated prickly heat

•    loss of skin colour

•    burning

•    stinging

•    itching

•    tingling

•    excessive hair growth

•    softening of the skin and stretch marks

Other side effects that may occur with topical corticosteroids are dry skin, skin irritation, dermatitis, dermatitis around the mouth, and small dilated blood vessels.

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 Elocon

Keep out of the sight and reach of children.

Do not store above 25°C.

Use within one month after opening.

Do not use Elocon after the expiry date which is stated on the carton and tube label after ‘Exp’. The expiry date refers to the last day of that month.

If the ointment becomes discolored or shows any signs of deterioration, seek the advice of your pharmacist.

Remember if your doctor tells you to stop taking this medicine, return any unused medicine 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 Elocon contains

Each gram of ointment contains 1mg mometasone furoate as the active ingredient.

Other ingredients are hexylene glycol, propylene glycol stearate, white beeswax, white soft paraffin, phosphoric acid and purified water.

What Elocon looks like and contents of the pack

Elocon is available in a sealed metal collapsible tube with white plastic screw-cap (incorporating a device to break the seal on the tube) containing a white homogenous ointment.

Elocon comes in a 30 gram tube.

Manufactured by: Schering-Plough Labo N.V., Industriepark, 30, B-2220 Heist-op-den-Berg, Belgium.

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

®

Elocon 0.1 % w/w Ointment PL 18799/2183

Leaflet date: 03.05.2016

Elocon is a registered trademark of Merck Sharp & Dohme group of companies.

Package leaflet: Information for the user

Mometasone furoate 0.1% w/w Ointment

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.

The name of your medicine is Mometasone furoate 0.1% w/w Ointment but it will be referred as Mometasone furoate throughout this leaflet.

What is in this leaflet:

1.    What Mometasone furoate is and what it is used for

2.    What you need to know before you use Mometasone furoate

3.    How to use Mometasone furoate

4.    Possible side effects

5.    How to store Mometasone furoate

6.    Contents of the pack and other information

1.    What Mometasone furoate is and what it is used for

Mometasone furoate is one of a group of medicines called topical corticosteroids. It is classified as a ‘potent corticosteroid’. These medicines are put on the surface of the skin to reduce the redness and itchiness caused by certain skin problems.

In adults and children, Mometasone furoate is used to reduce redness and itchiness caused by certain skin problems called psoriasis or dermatitis.

Psoriasis is a skin disease in which itchy, scaly, pink patches develop on the elbows, knees, scalp and other parts of the body. Dermatitis is a condition brought on by the skin reacting to outside agents e.g. detergents, causing the skin to become red and itchy.

2.    What you need to know before you use Mometasone furoate Do not use Mometasone furoate:

•    if you are allergic (hypersensitive) to mometasone furoate or any of the other ingredients in this medicine (listed in section 6) or to other similar medicines.

•    on any other skin problems as it could make them worse especially:

•    rosacea (a skin condition affecting the face)

•    acne

•    skin atrophy (thinning of the skin)

•    dermatitis around the mouth

•    genital itching

•    nappy rash

•    cold sores

•    chickenpox

•    shingles

•    warts

•    ulcerated skin

•    wounds

•    other skin infections

Ask your doctor or pharmacist if you are not sure.

Warning and precautions

Talk to your doctor, pharmacist or nurse before using Mometasone furoate:

•    if your skin becomes irritated or sensitive after using Mometasone furoate, you should stop using it and tell your doctor

Other medicines and Mometasone furoate

• Tell your doctor or pharmacist if you are using, have recently used or might use any other medicines Pregnancy, breast-feeding and fertility

If you are pregnant or breast-feeding, think you may be pregnant or are planning to have a baby, ask your doctor or pharmacist for advice before taking this medicine.

Mometasone furoate contains propylene glycolstearate

Mometasone furoate contains propylene glycolstearate, which can cause skin irritation.

3.    How to use Mometasone furoate

Always use Mometasone furoate exactly as your doctor or pharmacist has told you. You should check with your doctor or pharmacist if you are not sure.

Use in children

Mometasone furoate is not recommended for children under the age of 2.

How much to use

Usually for adults and children aged 2 and above, a thin layer of Mometasone furoate should be gently rubbed into the affected area of skin once a day.

Before using Mometasone furoate

You should always follow these instructions when using Mometasone furoate:

•    Do not use the ointment on your face for more than 5 days

• Do not apply the ointment to children, on any part of their body, for more than 5 days.

• Do not put the ointment under your child’s nappy, as this makes it easier for the active drug to pass through the skin and possibly cause some unwanted effects.

•    You should check with your doctor before covering the treated areas with a bandage or plaster. Treated areas on the face or in children should not be covered with a bandage or plaster.

•    You should not use a large amount of ointment on large areas of the body for a long time (for example every day for many weeks or months).

•    Do not use in or around your eyes, including eye-lids If you use more Mometasone furoate than you should

If you (or somebody else) accidentally swallows the ointment, it should not produce any problems. However, if you are worried, you should see your doctor.

If you use the ointment more often than you should, or on large areas of the body, it can affect some of your hormones.

In children, this may affect their growth and development.

If you have not used the cream as you were told to do and have used it too often and/or for a long time, you should tell your doctor.

If you stop using Mometasone furoate

If you have been using Mometasone furoate for a long time and your skin problem seems to have got better, you should not suddenly stop using the ointment. If you do, you may find that your skin becomes red and you may notice stinging or burning.

To avoid this, you should speak to your doctor as he will gradually reduce how often you need to use the ointment until you stop treatment altogether.

4.    Possible side effects

Like all medicines, Mometasone furoate can cause side effects, although not everybody gets them.

A few people may find that they suffer from some of the following side effects after using Mometasone furoate :

•    allergic skin reactions

•    bacterial and secondary skin infections

•    acne

•    inflammation and/ or infection of the hair follicles

•    thinning of the skin

•    red marks with associated prickly heat

•    loss of skin colour

•    burning

•    stinging

•    itching

•    tingling

•    excessive hair growth

•    softening of the skin and stretch marks

Other side effects that may occur with topical corticosteroids are dry skin, skin irritation, dermatitis, dermatitis around the mouth, and small dilated blood vessels.

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 Mometasone furoate

Keep out of the sight and reach of children.

Do not store above 25°C.

Use within one month after opening.

Do not use Mometasone furoate after the expiry date which is stated on the carton and tube label after ‘Exp’. The expiry date refers to the last day of that month.

If the ointment becomes discolored or shows any signs of deterioration, seek the advice of your pharmacist.

Remember if your doctor tells you to stop taking this medicine, return any unused medicine 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 Mometasone furoate contains

Each gram of ointment contains 1mg mometasone furoate as the active ingredient.

Other ingredients are hexylene glycol, propylene glycol stearate, white beeswax, white soft paraffin, phosphoric acid and purified water.

What Mometasone furoate looks like and contents of the pack

Mometasone furoate is available in a sealed metal collapsible tube with white plastic screw-cap incorporating a device to break the seal on the tube containing a white homogenous ointment.

Mometasone furoate comes in a 30 gram tube.

Manufactured by: Schering-Plough Labo N.V., Industriepark, 30, B-2220 Heist-op-den-Berg, Belgium.

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

Mometasone furoate 0.1% w/w Ointment PL 18799/2183    poM

Leaflet date: 03.05.2016