Motilium 1 Mg/Ml Oral Suspension
Out of date information, search anotherS1525 LEAFLET Motilium 20150206
PATIENT INFORMATION LEAFLET MOTILIUM® 1 mg/ml ORAL SUSPENSION (domperidone)
▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See the end of section 4 for how to report side effects.
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 get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
• Your doctor may have given you this medicine before from another company. It may have looked slightly different. However, either brand will have the same effect.
In this leaflet:
1. What Motilium is and what it is used for
2. What you need to know before you take Motilium
3. How to take Motilium
4. Possible side effects
5. How to store Motilium
6. Contents of the pack and other information
1. WHAT MOTILIUM IS AND WHAT IT IS USED FOR
The name of your medicine is Motilium 1mg/ml Oral Suspension (called Motilium in this leaflet). The active ingredient in this medicine is called domperidone. This belongs to a group of medicines called ‘dopamine antagonists'.
This medicine is used in adults and in children to treat nausea (feeling sick) and vomiting (being sick).
2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE MOTILIUM
Do not take Motilium if:
• You are allergic (hypersensitive) to Motilium or any of the other ingredients of Motilium 1mg/ml Oral Suspension (listed in section 6: Contents of the pack and other information). Signs of an allergic reaction include: a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue.
• You have a tumour of the pituitary gland (prolactinoma).
• You have a blockage or tear in your intestines.
• You have black, tarry bowel motions (stools) or notice blood in your bowel motions. This could be a sign of bleeding in the stomach or intestines.
• You have a moderate or severe liver disease.
• Your ECG (electrocardiogram) shows a heart problem called “prolonged QT corrected interval”.
• You have or had a problem where your heart cannot pump the blood round your body as well as it should (condition called heart failure).
• You have a problem that gives you a low level of potassium or magnesium, or a high level of potassium in your blood.
• You are taking certain medicines (see “Other medicines and Motilium”)
Do not take Motilium if any of the above applies to you. If you are
not sure, talk to your doctor or pharmacist before taking Motilium.
Warnings and precautions
Before taking this medicine contact your doctor if:
• You suffer from liver problems (liver function impairment or failure) (see “Do not take Motilium if”)
• You suffer from kidney problems (kidney function impairment or failure). It is advisable to ask your doctor for advice in case of prolonged treatment as you may need to take a lower dose or take this medicine less often, and your doctor may want to examine you regularly.
If you are not sure if any of the above apply to you, talk to your
doctor or pharmacist before taking Motilium.
Do this even if they have applied in the past.
Motilium may be associated with an increased risk of heart rhythm disorder and cardiac arrest. This risk may be more likely in those over 60 years old or taking doses higher than 30mg per day. The risk also increases when Motilium is given together with some drugs. Tell your doctor or pharmacist if you are taking drugs to treat infection (fungal infections or bacterial infection) and/or if you have heart problems or AIDS/HIV (see “Other medicines and Motilium).
Motilium should be used at the lowest effective dose in adults and children.
While taking Motilium, contact your doctor if you experience heart rhythm disorders such as palpitations, trouble breathing, loss of consciousness. Treatment with Motilium should be stopped.
Other medicines and Motilium:
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines. This includes medicines you can buy without a prescription, including herbal medicines. This is because Motilium can affect the way some other medicines work. Also, some medicines can affect the way Motilium works.
Do not take Motilium Oral Suspension if you are taking medicine to treat:
• Fungal infections such as azole anti-fungals, specifically oral ketoconazole, fluconazole or voriconazole.
• Bacterial infections, specifically erythromycin, clarithromycin, telithromycin, moxifloxacin, pentamidine (these are antibiotics)
• Heart problems or high blood pressure (e.g., amiodarone, dronedarone, quinidine, disopyramide, dofetilide, sotalol, diltiazem, verapamil)
• Psychoses (e.g., haloperidol, pimozide, sertindole)
• Depression (e.g., citalopram, escitalopram)
• Gastro-intestinal disorders (e.g., cisapride, dolasetron, prucalopride)
• Allergy (e.g., mequitazine, mizolastine)
• Malaria (in particular halofantrine)
• AIDS/HIV (protease inhibitors)
• Cancer (e.g., toremifene, vandetanib, vincamine)
Tell your doctor or pharmacist if you are taking drugs to treat infection, heart problems or AIDS/HIV.
Tell your doctor if you are taking antacids or other medicines that reduce stomach acid (such as cimetidine or sodium bicarbonate). These medicines can be taken if you are also taking Motilium but they should not be taken at the same time as they may affect how well Motilium works. Medicines that reduce stomach acid should be taken after a meal.
It is important to ask your doctor or pharmacist if Motilium Oral Suspension is safe for you when you are taking any other medicines, including medicines obtained without prescription.
Taking Motilium with food and drink
It is recommended to take Motilium before meals as when taken after meals the absorption of the medicine is slightly delayed.
Pregnancy and breast-feeding
Talk to your doctor or pharmacist before taking Motilium if:
• You are pregnant, might become pregnant or think you may be pregnant.
• You are breast-feeding. It is best not to take Motilium if you are breast-feeding.
Small amounts of Motilium have been detected in breast-milk. Motilium may cause unwanted side effects affecting the heart in a breast-fed baby. Motilium should be used during breast feeding only if your physician considers this clearly necessary. Ask your doctor for advice before taking this medicine.
Driving and using machines:
Motilium does not affect your ability to drive or use machines.
Important information about some of the ingredients of Motilium Oral Suspension:
This medicine contains sorbitol. If you have been told that you cannot digest or tolerate some sugars, talk to your doctor before taking Motilium.
This medicine also contains methylhydroxybenzoate (E218) and propylhydroxybenzoate (E216). These substances may cause allergic reactions (possibly delayed), and exceptionally, bronchospasm.
3. HOW TO TAKE MOTILIUM
Follow these instructions closely unless your doctor has advised you otherwise. You should check with your doctor or pharmacist if you are not sure.
Duration of treatment
Your doctor will decide how long you will need to take this medicine.
Symptoms usually resolve with 3-4 days of taking this medicine. Do not take Motilium Oral Suspension for longer than 7 days without consulting your doctor.
• Take this medicine by mouth.
• Adults and adolescents: take your medicine using the plastic measuring cup provided with Motilium Oral Suspension. This cup is marked in ml (millilitres) to help you measure out the correct amount of this medicine.
• Children weighing under 35kg: should be given Motilium Oral Suspension using a suitably graduated oral syringe. Your doctor or pharmacist will supply you with this syringe. If you are not supplied with an oral syringe please speak to your doctor or pharmacist.
• Take your medicine 15 to 30 minutes before a meal.
The usual dose is:
• Adults and adolescents 12 years of age and older with a body weight of 35 kg or more
The usual dose is 10 ml taken up to three times per day, if possible before meals. Do not take more than 30 ml per day.
• Children and adolescents from birth to a body weight of less than 35kg
Your doctor will work out the dose. This will depend on the weight of your child. Give the dose maximum 3 times a day, if possible before meals/feeding. Do not give more than 3 times in a 24 hour time period.
People with kidney problems
Your doctor may tell you to take a lower dose or to take the
medicine less often.
If you take more Motilium than you should:
• If you have used or taken too much Motilium Oral Suspension, contact your doctor, pharmacist or the poisons unit at your nearest hospital casualty department immediately in particular if a child has taken too much. Take the carton and bottle containing any remaining medicine with you. This is so the doctors know what you have taken. In the event of overdose, symptomatic treatment could be implemented. An ECG monitoring could be undertaken, because of the possibility of a heart problem called prolonged QT interval.
• The signs of taking more than you should include feeling sleepy, confused, uncontrolled movements (especially in children) which include unusual eye movements, unusual movements of the tongue or abnormal posture (such as a twisted neck).
If you forget to take Motilium:
• If you forget to take Motilium, take it as soon as you remember.
• However if it is almost time for the next dose, wait until that is due and then continue as normal.
• Do not take a double dose to make up for a forgotten dose.
• Disorders of the cardiovascular system: heart rhythm disorders (rapid or irregular heart beat) have been reported; if this happens, you should stop the treatment immediately. Motilium may be associated with an increased risk of heart rhythm disorder and cardiac arrest. This risk may be more likely in those over 60 years old or taking doses higher than 30 mg per day. Motilium should be used at the lowest effective dose in adults and children.
• Feeling agitated or irritable
• Feeling more nervous than usual
• Abnormal eye movements
• Inability to urinate
• Breast enlargement in men
• In women, menstrual periods may be irregular or stop
• A blood test shows changes in the way your liver is working.
Some patients who have used Motilium for conditions and dosages requiring longer term medical supervision have experienced the following unwanted effects:
Restlessness; swollen or enlarged breasts, unusual discharge from breasts, irregular menstrual periods in women, difficulty breastfeeding, depression, hypersensitivity.
Side effects such as feeling drowsy, nervous, agitated or irritable or having a fit are more likely to happen in children.
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 MOTILIUM
• KEEP OUT OF THE SIGHT AND REACH OF CHILDREN.
• Do not use Motilium after the expiry date stated on the pack.
• Do not store above 30°C.
• If the medicine becomes discoloured or shows any other signs of deterioration, you should seek the advice of your pharmacist who will tell you what to do.
• 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.
4. POSSIBLE SIDE EFFECTS
6. CONTENTS OF THE PACK AND OTHER INFORMATION
Like all medicines, Motilium can have side effects, although not
everybody gets them.
Stop taking Motilium and see your doctor or go to a hospital
straightaway if:
• You get swelling of the hands, feet, ankles, face, lips or throat which may cause difficulty in swallowing or breathing. You could also notice an itchy, lumpy rash (hives) or nettle rash (urticaria). This may mean you are having an allergic reaction to Motilium.
• You notice any uncontrolled movements. These include irregular eye movements, unusual movements of the tongue, and abnormal posture such as a twisted neck, trembling and muscle stiffness. This is more likely to happen in children.
These symptoms should stop once you stop taking Motilium.
• You have a very fast or unusual heartbeat. This could be a sign of a life-threatening heart problem.
• You have a fit (seizure)
Other side effects include:
Common (affects less than 1 in 10 people)
• Dry mouth
Uncommon (affects less than 1 in 100 people)
• Lowering of sexual drive (libido) in men.
• Feeling anxious
• Feeling drowsy
• Headaches
• Diarrhoea
• Itchy skin. You may also have a rash
• Unusual production of breast milk in men and women
• Painful or tender breasts
• A general feeling of weakness
What Motilium contains
• Each millilitre of suspension contains 1 mg of domperidone as the active ingredient.
• The other ingredients are: sorbitol (E420) , microcrystalline cellulose (E460), carmellose sodium (E466), methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), sodium saccharin (E954), polysorbate 20 (E432), sodium hydroxide and purified water.
What Motilium looks like and contents of the pack
White suspension in a white plastic bottle with a child resistant cap
and a 20 ml and 4 ml measuring cup.
Motilium comes in a 200ml plastic bottle.
Product Licence holder
Procured from within the EU and repackaged by the Product Licence holder: S&M Medical Ltd, Chemilines House, Alperton Lane, Wembley, HA0 1DX.
Manufacturer
This product is manufactured by Laboratorios Dr. Esteve, S.A., C/Sant Marti, s/n. Pol. Industrial La Roca, 08107 Martorelles (Barcelona) Spain.
|POM| PL No: 19488/1525
Leaflet revision date: 06 February 2015
Motilium is a registered trademark Johnson & Johnson.
S1525 LEAFLET Motilium 20150206
S1525 LEAFLET Domperidone 20150206
PATIENT INFORMATION LEAFLET DOMPERIDONE 1mg/ml ORAL SUSPENSION
▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See the end of section 4 for how to report side effects.
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 get serious, or if you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.
• Your doctor may have given you this medicine before from another company. It may have looked slightly different. However, either brand will have the same effect.
In this leaflet:
1. What Domperidone is and what it is used for
2. What you need to know before you take Domperidone
3. How to take Domperidone
4. Possible side effects
5. How to store Domperidone
6. Contents of the pack and other information
1. WHAT DOMPERIDONE IS AND WHAT IT IS USED FOR
The name of your medicine is Domperidone 1mg/ml Oral Suspension (called Domperidone in this leaflet). The active ingredient in this medicine is called domperidone. This belongs to a group of medicines called ‘dopamine antagonists'.
This medicine is used in adults and in children to treat nausea (feeling sick) and vomiting (being sick).
2. WHAT YOU NEED TO KNOW BEFORE YOU TAKE DOMPERIDONE
Do not take Domperidone if:
• You are allergic (hypersensitive) to Domperidone or any of the other ingredients of Domperidone 1mg/ml Oral Suspension (listed in section 6: Contents of the pack and other information). Signs of an allergic reaction include: a rash, swallowing or breathing problems, swelling of your lips, face, throat or tongue.
• You have a tumour of the pituitary gland (prolactinoma).
• You have a blockage or tear in your intestines.
• You have black, tarry bowel motions (stools) or notice blood in your bowel motions. This could be a sign of bleeding in the stomach or intestines.
• You have a moderate or severe liver disease.
• Your ECG (electrocardiogram) shows a heart problem called “prolonged QT corrected interval”.
• You have or had a problem where your heart cannot pump the blood round your body as well as it should (condition called heart failure).
• You have a problem that gives you a low level of potassium or magnesium, or a high level of potassium in your blood.
• You are taking certain medicines (see “Other medicines and Domperidone”)
Do not take Domperidone if any of the above applies to you. If you
are not sure, talk to your doctor or pharmacist before taking
Domperidone.
Warnings and precautions
Before taking this medicine contact your doctor if:
• You suffer from liver problems (liver function impairment or failure) (see “Do not take Domperidone if)
• You suffer from kidney problems (kidney function impairment or failure). It is advisable to ask your doctor for advice in case of prolonged treatment as you may need to take a lower dose or take this medicine less often, and your doctor may want to examine you regularly.
If you are not sure if any of the above apply to you, talk to your
doctor or pharmacist before taking Domperidone.
Do this even if they have applied in the past.
Domperidone may be associated with an increased risk of heart rhythm disorder and cardiac arrest. This risk may be more likely in those over 60 years old or taking doses higher than 30mg per day. The risk also increases when Domperidone is given together with some drugs. Tell your doctor or pharmacist if you are taking drugs to treat infection (fungal infections or bacterial infection) and/or if you have heart problems or AIDS/HIV (see “Other medicines and Domperidone).
Domperidone should be used at the lowest effective dose in adults and children.
While taking Domperidone, contact your doctor if you experience heart rhythm disorders such as palpitations, trouble breathing, loss of consciousness. Treatment with Domperidone should be stopped. Other medicines and Domperidone:
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines. This includes medicines you can buy without a prescription, including herbal medicines. This is because Domperidone can affect the way some other medicines work. Also, some medicines can affect the way Domperidone works.
Do not take Domperidone Oral Suspension if you are taking medicine to treat:
• Fungal infections such as azole anti-fungals, specifically oral ketoconazole, fluconazole or voriconazole.
• Bacterial infections, specifically erythromycin, clarithromycin, telithromycin, moxifloxacin, pentamidine (these are antibiotics)
• Heart problems or high blood pressure (e.g., amiodarone, dronedarone, quinidine, disopyramide, dofetilide, sotalol, diltiazem, verapamil)
• Psychoses (e.g., haloperidol, pimozide, sertindole)
• Depression (e.g., citalopram, escitalopram)
• Gastro-intestinal disorders (e.g., cisapride, dolasetron, prucalopride)
• Allergy (e.g., mequitazine, mizolastine)
• Malaria (in particular halofantrine)
• AIDS/HIV (protease inhibitors)
• Cancer (e.g., toremifene, vandetanib, vincamine)
Tell your doctor or pharmacist if you are taking drugs to treat infection, heart problems or AIDS/HIV.
Tell your doctor if you are taking antacids or other medicines that reduce stomach acid (such as cimetidine or sodium bicarbonate). These medicines can be taken if you are also taking Domperidone but they should not be taken at the same time as they may affect how well Domperidone works. Medicines that reduce stomach acid should be taken after a meal.
It is important to ask your doctor or pharmacist if Domperidone Oral Suspension is safe for you when you are taking any other medicines, including medicines obtained without prescription. Taking Domperidone with food and drink
It is recommended to take Domperidone before meals as when taken after meals the absorption of the medicine is slightly delayed. Pregnancy and breast-feeding
Talk to your doctor or pharmacist before taking Domperidone if:
• You are pregnant, might become pregnant or think you may be pregnant.
• You are breast-feeding. It is best not to take Domperidone if you are breast-feeding.
Small amounts of Domperidone have been detected in breast-milk. Domperidone may cause unwanted side effects affecting the heart in a breast-fed baby. Domperidone should be used during breast feeding only if your physician considers this clearly necessary. Ask your doctor for advice before taking this medicine.
Driving and using machines:
Domperidone does not affect your ability to drive or use machines. Important information about some of the ingredients of Domperidone Oral Suspension:
This medicine contains sorbitol. If you have been told that you cannot digest or tolerate some sugars, talk to your doctor before taking domperidone.
This medicine also contains methylhydroxybenzoate (E218) and propylhydroxybenzoate (E216). These substances may cause allergic reactions (possibly delayed), and exceptionally, bronchospasm.
3. HOW TO TAKE DOMPERIDONE
Follow these instructions closely unless your doctor has advised you otherwise. You should check with your doctor or pharmacist if you are not sure.
Duration of treatment
Your doctor will decide how long you will need to take this medicine.
Symptoms usually resolve with 3-4 days of taking this medicine. Do not take Domperidone Oral Suspension for longer than 7 days without consulting your doctor.
• Take this medicine by mouth.
• Adults and adolescents: take your medicine using the plastic measuring cup provided with Domperidone Oral Suspension. This cup is marked in ml (millilitres) to help you measure out the correct amount of this medicine.
• Children weighing under 35kg: should be given Domperidone Oral Suspension using a suitably graduated oral syringe. Your doctor or pharmacist will supply you with this syringe. If you are not supplied with an oral syringe please speak to your doctor or pharmacist.
• Take your medicine 15 to 30 minutes before a meal.
The usual dose is:
• Adults and adolescents 12 years of age and older with a body weight of 35 kg or more
The usual dose is 10 ml taken up to three times per day, if possible before meals. Do not take more than 30 ml per day.
• Children and adolescents from birth to a body weight of less than 35kg
Your doctor will work out the dose. This will depend on the weight of your child. Give the dose maximum 3 times a day, if possible before meals/feeding. Do not give more than 3 times in a 24 hour time period.
People with kidney problems
Your doctor may tell you to take a lower dose or to take the
medicine less often.
If you take more Domperidone than you should:
• If you have used or taken too much Domperidone Oral Suspension, contact your doctor, pharmacist or the poisons unit at your nearest hospital casualty department immediately in particular if a child has taken too much. Take the carton and bottle containing any remaining medicine with you. This is so the doctors know what you have taken. In the event of overdose, symptomatic treatment could be implemented. An ECG monitoring could be undertaken, because of the possibility of a heart problem called prolonged QT interval.
• The signs of taking more than you should include feeling sleepy, confused, uncontrolled movements (especially in children) which include unusual eye movements, unusual movements of the tongue or abnormal posture (such as a twisted neck).
If you forget to take Domperidone:
• If you forget to take Domperidone, take it as soon as you remember.
• However if it is almost time for the next dose, wait until that is due and then continue as normal.
• Do not take a double dose to make up for a forgotten dose.
• Disorders of the cardiovascular system: heart rhythm disorders (rapid or irregular heart beat) have been reported; if this happens, you should stop the treatment immediately. Domperidone may be associated with an increased risk of heart rhythm disorder and cardiac arrest. This risk may be more likely in those over 60 years old or taking doses higher than 30 mg per day. Domperidone should be used at the lowest effective dose in adults and children.
• Feeling agitated or irritable
• Feeling more nervous than usual
• Abnormal eye movements
• Inability to urinate
• Breast enlargement in men
• In women, menstrual periods may be irregular or stop
• A blood test shows changes in the way your liver is working.
Some patients who have used Domperidone for conditions and dosages requiring longer term medical supervision have experienced the following unwanted effects:
Restlessness; swollen or enlarged breasts, unusual discharge from breasts, irregular menstrual periods in women, difficulty breastfeeding, depression, hypersensitivity.
Side effects such as feeling drowsy, nervous, agitated or irritable or having a fit are more likely to happen in children.
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 DOMPERIDONE
• KEEP OUT OF THE SIGHT AND REACH OF CHILDREN.
• Do not use Domperidone after the expiry date stated on the pack.
• Do not store above 30°C.
• If the medicine becomes discoloured or shows any other signs of deterioration, you should seek the advice of your pharmacist who will tell you what to do.
• 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.
4. POSSIBLE SIDE EFFECTS
6. CONTENTS OF THE PACK AND OTHER INFORMATION
Like all medicines, Domperidone can have side effects, although
not everybody gets them.
Stop taking Domperidone and see your doctor or go to a
hospital straightaway if:
• You get swelling of the hands, feet, ankles, face, lips or throat which may cause difficulty in swallowing or breathing. You could also notice an itchy, lumpy rash (hives) or nettle rash (urticaria). This may mean you are having an allergic reaction to Domperidone.
• You notice any uncontrolled movements. These include irregular eye movements, unusual movements of the tongue, and abnormal posture such as a twisted neck, trembling and muscle stiffness. This is more likely to happen in children.
These symptoms should stop once you stop taking Domperidone.
• You have a very fast or unusual heartbeat. This could be a sign of a life-threatening heart problem.
• You have a fit (seizure)
Other side effects include:
Common (affects less than 1 in 10 people)
• Dry mouth
Uncommon (affects less than 1 in 100 people)
• Lowering of sexual drive (libido) in men.
• Feeling anxious
• Feeling drowsy
• Headaches
• Diarrhoea
• Itchy skin. You may also have a rash
• Unusual production of breast milk in men and women
• Painful or tender breasts
• A general feeling of weakness
What Domperidone contains
• Each millilitre of suspension contains 1 mg of domperidone as the active ingredient.
• The other ingredients are: sorbitol (E420) , microcrystalline cellulose (E460), carmellose sodium (E466), methyl parahydroxybenzoate (E218), propyl parahydroxybenzoate (E216), sodium saccharin (E954), polysorbate 20 (E432), sodium hydroxide and purified water.
What Domperidone looks like and contents of the pack
White suspension in a white plastic bottle with a child resistant cap and a 20 ml and 4 ml measuring cup.
Domperidone comes in a 200ml plastic bottle.
Product Licence holder
Procured from within the EU and repackaged by the Product Licence holder: S&M Medical Ltd, Chemilines House, Alperton Lane, Wembley, HA0 1DX.
Manufacturer
This product is manufactured by Laboratorios Dr. Esteve, S.A., C/Sant Marti, s/n. Pol. Industrial La Roca, 08107 Martorelles (Barcelona) Spain.
|POM| PL No: 19488/1525
Leaflet revision date: 06 February 2015
S1525 LEAFLET Domperidone 20150206