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Dantrium 25mg Capsules

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Document: leaflet MAH BRAND_PLPI 18799-2136 change

PACKAGE LEAFLET: INFORMATION FOR THE USER


Dantrium® 25mg capsules

(dantrolene sodium)

Read all of this leaflet carefully before you start taking this medicine.

•    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. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.

•    If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

The name of your medicine is Dantrium 25mg capsules but will be referred to as Dantrium Capsules throughout this leaflet.

In this leaflet:

1.    What Dantrium Capsules are and what they are used for

2.    Before you take Dantrium Capsules

3.    How to take Dantrium Capsules

4.    Possible side effects

5.    How to store Dantrium Capsules

6.    Further information

1.    What Dantrium Capsules are and what they are used for

Dantrium Capsules contain the active substance dantrolene sodium - this is a muscle relaxant which is used to treat severe, long term muscle stiffness (spasticity) in adults.

2.    Before you take Dantrium Capsules

DO NOT take Dantrium Capsules if you:

•    are allergic to any ingredients in the product (see section 6 and end of Section 2)

•    have a known liver function impairment

•    have acute skeletal muscle spasms (your muscles go rigid suddenly)

•    need spasticity to stand up, walk or cope with daily activities.

DO NOT give Dantrium Capsules to children.

Take special care with Dantrium Capsules if you:

•    have heart or lung function impairment

•    have liver disorders or notice signs or symptoms of liver toxicity (e.g., discoloured faeces, intense itching, jaundice, anorexia, nausea, vomiting during therapy) - contact your doctor immediately

•    are elderly.

Liver function tests should be performed frequently before start and during Dantrium Capsules therapy as the risk of liver toxicity appears to be greater in

•    females

•    patients over 30 years old

•    patients taking other medication

•    females using oral oestrogen contraception.

Taking other medicines:

Please tell your doctor if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

Talk to your doctor before taking Dantrium Capsules if you are already taking:

•    Oestrogen (found in most oral contraceptive pills and hormone replacement therapy) or other drugs which might affect the liver.

•    Tranquillisers (e.g, diazepam, lorazepam or temazepam).

•    Medicines used to treat abnormal heart beat, angina or high blood pressure (e.g.products containing verapamil)

•    Products normally used to help doctors anaesthetise patients (e.g.products containing vecuronium).

Taking Dantrium Capsules with food and drink

Avoid taking alcohol with this medicine as it may make you feel dizzy or drowsy.

Pregnancy and breast-feeding

Do not take the capsules if pregnant or breastfeeding unless advised otherwise by your doctor. Ask your doctor or pharmacist for advice before taking any medicine.

Driving and using machines

Dantrium Capsules may cause drowsiness or dizziness. These symptoms may be intensified if you have consumed alcohol.

Do not take the capsules without talking to your doctor if you drive or are involved in hazardous activities.

Important information about some of the ingredients of Dantrium Capsules

Lactose - if you know you have intolerance to some sugars, speak to your doctor before taking this medicine.

Wheat starch - suitable for people with coeliac disease. Patients with wheat allergy (different from coeliac disease) should not take this medicine.

3. How to take Dantrium Capsules

Always take Dantrium Capsules exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Your doctor will want to make sure that the capsules do not affect your liver. This will mean having blood tests before you start and while you are taking them.

Adults and Elderly:

Dantrium Capsules are to be taken by mouth. Swallow the capsule with a glass of water.

The dose will vary from person to person.

•    The starting dose is usually one 25mg capsule a day.

•    If there is no improvement, your doctor may increase your dose every week until the right dose for you is reached.

•    The normal maximum dose is one 100mg capsule four times a day. It is important to take the lowest dose which works for you.

•    If there is no improvement after about 6-8 weeks, your medication will be stopped by your doctor.

Children should NOT be given Dantrium Capsules.

If you take more Dantrium Capsules than you should

Do not exceed the recommended dose. If you take too much medicine, tell your doctor immediately or go to your nearest Accident & Emergency Department (take the pack with you if possible).

If you forget to take Dantrium Capsules

If you miss a dose, do not take a double dose to make up for a forgotten capsule; continue taking your medicine as normal at the correct time.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. Possible side effects

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

You may suffer an allergic reaction, symptoms of which include rash, itching, difficulty in breathing or swelling of the face, lips, throat or tongue. If this happens to you, stop taking the capsules immediately and seek urgent medical attention.

The following side effects have also been reported:

Most common side effects

•    dizziness, drowsiness

•    weakness, tiredness

•    feeling generally unwell

•    diarrhoea - if severe diarrhoea occurs, your doctor may stop the capsules for a short while. If you start taking them again and the diarrhoea returns, Dantrium Capsules is usually stopped permanently.

Less common side effects

•    loss of appetite (anorexia)

•    seizures

•    speech or visual disturbance

•    headache

•    inflammation of the membrane around the heart, sometimes accompanied by fluid in the lungs

•    feeling sick (nausea, vomiting)

•    abdominal pain

•    liver toxicity (characterised by inflammation of the liver), problems with liver function.

•    skin rash, acne

•    fever, chills.

Rare side effects

•    confusion, nervousness

•    depression

•    difficulty sleeping (insomnia)

•    fast heart beat

•    worsening of heart problems

•    unstable blood pressure

•    difficulty in breathing

•    difficulty in swallowing

•    constipation (which may on rare occasions lead to a blockage in bowel movement)

•    sweating

•    increased urinary frequency

•    tiny crystals or traces of blood in the urine, difficulty in controlling the bladder (incontinence), being unable to pass urine easily

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.

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 Dantrium Capsules

Keep out of the sight and reach of children.

Do not store above 30°C.

Store in the original pack in order to protect from light and moisture

Do not take Dantrium Capsules after the expiry date which is stated on the carton and blister labels after ‘Exp’. The expiry date refers to the last day of that month.

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.    Further information

What Dantrium Capsules contain

-    Each capsule contains 25mg dantrolene sodium.

-    The other ingredients are: lactose monohydrate, wheat starch, talc and magnesium stearate.

-    The capsule shell of Dantrium capsules 25mg contains gelatin and colouring agents erythrosine (E127), iron oxide and titanium dioxide (E171).

What Dantrium Capsules looks like and contents of the pack

The capsules are orange and beige. The capsules are supplied in blister packs of 50 capsules.

Manufactured by: Famar L’Aigle, Zone Industrielle No.1, Route de crulai - 61300 L’Aigle, France.

OR

Merck, S.L. - Poligono Merck - 08100 Mollet Del Vellas, Barcelona, Spain.

Procured from within the EU and repackaged by the Product licence holder: B&S Healthcare Unit 4, Bradfield Road, Ruislip, Middlesex,

HA4 0NU, UK.

®

Dantrium 25mg capsules    .-.

PL 18799/2136

Leaflet date: 14.07.2016

PACKAGE LEAFLET: INFORMATION FOR THE USER

Dantrolene sodium 25mg capsules

Read all of this leaflet carefully before you start taking this medicine.

•    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. Do not pass it on to others. It may harm them, even if their symptoms are the same as yours.

•    If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

The name of your medicine is Dantrolene sodium 25mg capsules but will be referred to as Dantrolene Sodium throughout this leaflet.

In this leaflet:

1.    What Dantrolene Sodium is and what it is used for

2.    Before you take Dantrolene Sodium

3.    How to take Dantrolene Sodium

4.    Possible side effects

5.    How to store Dantrolene Sodium

6.    Further information

1.    What Dantrolene Sodium is and what it is used for

Dantrolene Sodium contains the active substance dantrolene sodium - this is a muscle relaxant which is used to treat severe, long term muscle stiffness (spasticity) in adults.

2.    Before you take Dantrolene Sodium

DO NOT take Dantrolene Sodium if you:

•    are allergic to any ingredients in the product (see section 6 and end of Section 2)

•    have a known liver function impairment

•    have acute skeletal muscle spasms (your muscles go rigid suddenly)

•    need spasticity to stand up, walk or cope with daily activities.

DO NOT give Dantrolene Sodium to children.

Take special care with Dantrolene Sodium if you:

•    have heart or lung function impairment

•    have liver disorders or notice signs or symptoms of liver toxicity (e.g., discoloured faeces, intense itching, jaundice, anorexia, nausea, vomiting during therapy) - contact your doctor immediately

•    are elderly.

Liver function tests should be performed frequently before start and during Dantrolene Sodium therapy as the risk of liver toxicity appears to be greater in

•    females

•    patients over 30 years old

•    patients taking other medication

. females using oral oestrogen contraception.

Taking other medicines:

Please tell your doctor if you are taking or have recently taken any other medicines, including medicines obtained without a prescription.

Talk to your doctor before taking Dantrolene Sodium if you are already taking:

•    Oestrogen (found in most oral contraceptive pills and hormone replacement therapy) or other drugs which might affect the liver.

•    Tranquillisers (e.g, diazepam, lorazepam or temazepam).

•    Medicines used to treat abnormal heart beat, angina or high blood pressure (e.g.products containing verapamil)

•    Products normally used to help doctors anaesthetise patients (e.g.products containing vecuronium).

Taking Dantrolene Sodium with food and drink

Avoid taking alcohol with this medicine as it may make you feel dizzy or drowsy.

Pregnancy and breast-feeding

Do not take the capsules if pregnant or breastfeeding unless advised otherwise by your doctor. Ask your doctor or pharmacist for advice before taking any medicine.

Driving and using machines

Dantrolene Sodium may cause drowsiness or dizziness. These symptoms may be intensified if you have consumed alcohol.

Do not take the capsules without talking to your doctor if you drive or are involved in hazardous activities.

Important information about some of the ingredients of Dantrolene Sodium

Lactose - if you know you have intolerance to some sugars, speak to your doctor before taking this medicine.

Wheat starch - suitable for people with coeliac disease. Patients with wheat allergy (different from coeliac disease) should not take this medicine.

3. How to take Dantrolene Sodium

Always take Dantrolene Sodium exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.

Your doctor will want to make sure that the capsules do not affect your liver. This will mean having blood tests before you start and while you are taking them.

Adults and Elderly:

Dantrolene Sodium are to be taken by mouth. Swallow the capsule with a glass of water.

The dose will vary from person to person.

•    The starting dose is usually one 25mg capsule a day.

•    If there is no improvement, your doctor may increase your dose every week until the right dose for you is reached.

•    The normal maximum dose is one 100mg capsule four times a day. It is important to take the lowest dose which works for you.

•    If there is no improvement after about 6-8 weeks, your medication will be stopped by your doctor.

Children should NOT be given Dantrolene Sodium.

If you take more Dantrolene Sodium than you should

Do not exceed the recommended dose. If you take too much medicine, tell your doctor immediately or go to your nearest Accident & Emergency Department (take the pack with you if possible).

If you forget to take Dantrolene Sodium

If you miss a dose, do not take a double dose to make up for a forgotten capsule; continue taking your medicine as normal at the correct time.

If you have any further questions on the use of this product, ask your doctor or pharmacist.

4. Possible side effects

•    sweating

•    increased urinary frequency

•    tiny crystals or traces of blood in the urine, difficulty in controlling the bladder (incontinence), being unable to pass urine easily

If any of the side effects gets serious, or if you notice any side effects not listed in this leaflet, please tell your doctor.

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 Dantrolene Sodium

Keep out of the sight and reach of children.

Do not store above 30°C.

Like all medicines, Dantrolene Sodium can cause    Store in the original package in order to protect from

side effects, although not everybody gets them.    light and moisture

You may suffer an allergic reaction, symptoms of which include rash, itching, difficulty in breathing or swelling of the face, lips, throat or tongue. If this happens to you, stop taking the capsules immediately and seek urgent medical attention.

The following side effects have also been reported: Most common side effects

•    dizziness, drowsiness

•    weakness, tiredness

•    feeling generally unwell

•    diarrhoea - if severe diarrhoea occurs, your doctor may stop the capsules for a short while. If you start taking them again and the diarrhoea returns, Dantrolene Sodium is usually stopped permanently.

Less common side effects

•    loss of appetite (anorexia)

•    seizures

•    speech or visual disturbance

•    headache

•    inflammation of the membrane around the heart, sometimes accompanied by fluid in the lungs

•    feeling sick (nausea, vomiting)

•    abdominal pain

•    liver toxicity (characterised by inflammation of the liver), problems with liver function.

•    skin rash, acne

•    fever, chills.

Rare side effects

•    confusion, nervousness

•    depression

•    difficulty sleeping (insomnia)

•    fast heart beat

•    worsening of heart problems

•    unstable blood pressure

•    difficulty in breathing

•    difficulty in swallowing

•    constipation (which may on rare occasions lead to a blockage in bowel movement)

Do not take Dantrolene Sodium after the expiry date which is stated on the carton and blister labels after ‘Exp’. The expiry date refers to the last day of that month.

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. Further information

What Dantrolene Sodium contains

-    Each capsule contains 25mg dantrolene sodium.

-    The other ingredients are: lactose monohydrate, wheat starch, talc and magnesium stearate.

-    The capsule shell of Dantrolene Sodium 25mg contains gelatin and colouring agents erythrosine (E127), iron oxide and titanium dioxide (E171).

What Dantrolene Sodium looks like and contents of the pack

The hard capsules are orange and beige. Capsule contains a deep orange powder. The capsules are supplied in blister packs of 50 capsules.

Manufactured by: Famar L’Aigle, Zone Industrielle No.1, Route de crulai - 61300 L’Aigle, France.

OR

Merck, S.L. - Poligono Merck - 08100 Mollet Del Vellas, Barcelona, Spain.

Procured from within the EU and repackaged by the Product licence holder: B&S Healthcare,

Unit 4, Bradfield Road, Ruislip, Middlesex,

HA4 0NU, UK.

Dantrolene sodium 25mg capsules PL 18799/2136

Leaflet date:14.07.2016

POM