Kemadrin 5mg Tablets
Out of date information, search another3. How to take Kemadrin
3. How to take Kemadrin
Kemadrin® 5mg Tablets
(procyclidine hydrochloride)
PACKAGE LEAFLET: INFORMATION FOR THE USER
Your medicine is available using the name Kemadrin 5mg Tablets, but will be referred to as Kemadrin throughout this leaflet.
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 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.
In this leaflet:
1. What Kemadrin is and what it is used for
2. Before you take Kemadrin
3. How to take Kemadrin
4. Possible side effects
5. How to store Kemadrin
6. Further information
1. What Kemadrin is and what it is used for
Kemadrin contains a medicine called procyclidine. This belongs to a group of medicines called anticholinergics. They stop a substance called acetylcholine working in your body. Kemadrin is used to:
■ treat and relieve the signs of Parkinson's disease such as:
■ stiff muscles, paralysis and tremor
■ problems talking, writing and walking
■ producing too much saliva and dribbling
■ sweating and uncontrolled eye movements
■ depression
■ stop side effects similar to the signs of Parkinson's disease or restlessness and unusual head and body movements caused by some medicines. Some people call these 'extrapyramidal effects'.
2. Before you take Kemadrin
Do not take Kemadrin if:
■ you are allergic (hypersensitive) to procyclidine or any of the other ingredients of Kemadrin (see Section 6: Further information)
■ you have problems passing water (urinary retention)
■ you suffer from a problem caused by too much pressure in your eye called 'closed angle glaucoma'
■ you have stomach cramps and pains or constipation.
Take special care with Kemadrin
Check with your doctor or pharmacist before taking your medicine if:
■ you are elderly. Your dose may need to be carefully monitored to prevent any side effects
■ you have an enlarged prostate gland
■ you have a mental illness and are taking Kemadrin to control the side effects of your medicines. Occasionally people who take this medicine may have a psychotic episode
■ you have kidney or liver problems.
If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before taking Kemadrin.
Kemadrin contains lactose monohydrate (a type of sugar). If you have been told by your doctor that you cannot tolerate or digest some sugars, talk to your doctor before taking this medicine.
Taking other medicines
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. This includes herbal medicines. This is because Kemadrin can affect the way some other medicines work. Also some other medicines can affect the way Kemadrin works.
In particular tell your doctor or pharmacist if you are taking any of the following:
■ medicines used to treat mental health problems (including Alzheimer's disease and dementia)
■ levodopa and amantadine, used in Parkinson's disease
■ disopyramide, quinidine and nitrate tablets (including tablets that dissolve under the tongue), used to treat heart problems
■ cisapride, domperidone and metoclopramide, used to treat sickness, indigestion and feeling sick (nausea)
■ antihistamines, used to treat hayfever and allergies
■ nefopam, used to treat pain
■ ketoconazole, used to treat fungal infections.
If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before taking Kemadrin.
Taking Kemadrin with food
You can take Kemadrin at any time of day, with or without food. Some people find they feel less sick if they take it at meal times.
Pregnancy and breast-feeding
Talk to your doctor before taking this medicine if you are pregnant, might become pregnant or are breast-feeding.
Driving and using machines
You may have blurred vision, dizziness, confusion or disorientation while taking Kemadrin. If this happens do not drive or use any tools or machines.
Always take Kemadrin exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.
■ Swallow the tablets with a drink of water.
■ The tablet may be cut or broken in half along the break-line to divide the dose in two equal halves.
To treat Parkinson's disease:
■ The usual starting dose is half a tablet three times a day.
■ This can be increased by half or 1 tablet each day, every two or three days until an effect is seen. This is known as the 'maintenance dose'. The daily maintenance dose is usually three to six tablets.
■ The maximum your doctor may decide to prescribe is 12 tablets.
■ Although the dose is usually taken three times a day, your doctor may ask you to take a fourth dose before bedtime.
To treat uncontrolled body movements (extrapyramidal symptoms) caused by taking other medicines:
Kemadrin can be used to control side effects caused by other medicines.
■ The usual starting dose is half a tablet three times a day.
■ This can be increased by half a tablet each day until an effect is seen.
■ The daily maintenance dose is usually two to six tablets.
■ Your doctor may decide to stop your Kemadrin after 3 or 4 months to see if your side effects return.
Elderly
If you are elderly, your dose may need to be carefully monitored to prevent any side effects.
Children
Kemadrin tablets are not usually recommended for use in children.
If you take more Kemadrin than you should
If you take more Kemadrin than you should, talk to a doctor or go to a hospital straight away. Take the medicine pack with you.
If you forget to take Kemadrin
Take a dose as soon as you remember it and then go on as before.
If you stop taking Kemadrin
Do not stop taking Kemadrin without talking to your doctor.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
Do not take if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking Kemadrin.
If you are taking a medicine for mental illness (called a neuroleptic) at the same time as Kemadrin:
■ you can develop uncontrolled movements of your face and tongue (tardive dyskinesia). The dose of either of your medicines may need to be adjusted.
■ unusual body movements, particularly of your hands, arms and legs which may have previously been occurring with the medicine for your mental illness can be made worse by the addition of Kemadrin.
If either of these happen, tell your doctor straight away.
Like all medicines, Kemadrin can cause side effects, although not everybody gets them. The following side effects may happen with this medicine:
Common (affects less than 1 in 10 people)
■ problems passing water (urinary retention)
■ blurred vision
■ dry mouth or constipation.
Uncommon (affects less than 1 in 100 people)
■ feeling sick (nausea) or being sick (vomiting)
■ inflamed gums (gingivitis)
■ dizziness, nervousness, feeling confused, reduced concentration or memory, hearing unexpected noises or seeing unexpected sights (hallucinations), anxiety, agitation (feeling irritable)
■ skin rash.
Rare (affects less than 1 in 1,000 people)
■ 'psychotic' symptoms occurring together such as dizziness, confusion, reduced concentration or memory, disorientation, hearing unexpected noises or seeing unexpected sights (hallucinations), anxiety, agitation (feeling irritable).
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.
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.aov.uk/vellowcard. By reporting side effects, you can help provide more information on the safety of this medicine.
■ Keep out of the sight and reach of children.
■ Do not store above 25°C.
■ Do not use Kemadrin after the expiry date which is stated on the carton or container. The expiry date refers to the last day of that month.
■ If your doctor decides to stop your treatment, take any tablets you have left back to the pharmacy.
■ If your tablets appear to be discoloured or show any other signs of deterioration, take them back to your pharmacist who will advise 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.
6. Further information
What Kemadrin contains
■ Each tablet contains 5mg procyclidine hydrochloride.
■ The other ingredients are: lactose monohydrate, povidone, magnesium stearate and sodium starch glycollate.
What Kemadrin looks like and contents of the pack
Kemadrin Tablets are white, round, biconvex tablets with break-line on both faces, debossed with KT above and 05 below the break-line on one face and plain on the reverse.
These are available in a bottle containing 100 tablets.
Manufacturer:
Kemadrin Tablets are manufactured by:
Aspen Bad Oldesloe GmbH, Industriestrasse 32-36,
23843 Bad Oldesloe, Germany.
Procured from within the EU and repackaged by: Doncaster Pharmaceuticals Group Ltd., Kirk Sandall, Doncaster, DN3 1QR.
Product Licence holder: Landmark Pharma Ltd., 7 Regents Drive, Prudhoe, Northumberland, NE42 6PX.
PL No: 21828/0349 POM
Leaflet revision 8i issue date (Ref): 22.10.14
Other formats:
If you wish to receive this leaflet in Braille, large font or audio format please contact 01302 365000 and ask for the Regulatory Department
Please be ready to give the following information:
Product name Kemadrin 5mg tablets Reference number 21828/0349
Kemadrin® is a registered trademark of Aspen Global Incorporated.
Procyclidine Hydrochloride 5mg Tablets
PACKAGE LEAFLET: INFORMATION FOR THE USER
Your medicine is available using the name Procyclidine Hydrochloride 5mg Tablets, but will be referred to as Procyclidine Hydrochloride throughout this leaflet.
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 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.
In this leaflet:
1. What Procyclidine Hydrochloride is and what it is used for
2. Before you take Procyclidine Hydrochloride
3. How to take Procyclidine Hydrochloride
4. Possible side effects
5. How to store Procyclidine Hydrochloride
6. Further information
1. What Procyclidine Hydrochloride is and what it is used for
Procyclidine Hydrochloride contains a medicine called procyclidine. This belongs to a group of medicines called anticholinergics. They stop a substance called acetylcholine working in your body. Procyclidine Hydrochloride is used to:
■ treat and relieve the signs of Parkinson's disease such as:
■ stiff muscles, paralysis and tremor
■ problems talking, writing and walking
■ producing too much saliva and dribbling
■ sweating and uncontrolled eye movements
■ depression
■ stop side effects similar to the signs of Parkinson's disease or restlessness and unusual head and body movements caused by some medicines. Some people call these 'extrapyramidal effects'.
2. Before you take Procyclidine Hydrochloride
Do not take Procyclidine Hydrochloride if:
■ you are allergic (hypersensitive) to procyclidine or any of the other ingredients of Procyclidine Hydrochloride (see Section 6: Further information)
■ you have problems passing water (urinary retention)
■ you suffer from a problem caused by too much pressure in your eye called 'closed angle glaucoma'
■ you have stomach cramps and pains or constipation.
Do not take if any of the above apply to you. If you are not sure, talk to your doctor or pharmacist before taking Procyclidine Hydrochloride.
Take special care with Procyclidine Hydrochloride
Check with your doctor or pharmacist before taking your medicine if:
■ you are elderly. Your dose may need to be carefully monitored to prevent any side effects
■ you have an enlarged prostate gland
■ you have a mental illness and are taking Procyclidine Hydrochloride to control the side effects of your medicines. Occasionally people who take this medicine may have a psychotic episode
■ you have kidney or liver problems.
If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before taking Procyclidine Hydrochloride. Procyclidine Hydrochloride contains lactose monohydrate (a type of sugar). If you have been told by your doctor that you cannot tolerate or digest some sugars, talk to your doctor before taking this medicine.
Taking other medicines
Please tell your doctor or pharmacist if you are taking or have recently taken any other medicines, including medicines obtained without a prescription. This includes herbal medicines. This is because Procyclidine Hydrochloride can affect the way some other medicines work. Also some other medicines can affect the way Procyclidine Hydrochloride works.
In particular tell your doctor or pharmacist if you are taking any of the following:
■ medicines used to treat mental health problems (including Alzheimer's disease and dementia)
■ levodopa and amantadine, used in Parkinson's disease
■ disopyramide, quinidine and nitrate tablets (including tablets that dissolve under the tongue), used to treat heart problems
■ cisapride, domperidone and metoclopramide, used to treat sickness, indigestion and feeling sick (nausea)
■ antihistamines, used to treat hayfever and allergies
■ nefopam, used to treat pain
■ ketoconazole, used to treat fungal infections.
If you are not sure if any of the above apply to you, talk to your doctor or pharmacist before taking Procyclidine Hydrochloride.
Taking Procyclidine Hydrochloride with food
You can take Procyclidine Hydrochloride at any time of day, with or without food.
Some people find they feel less sick if they take it at meal times.
Pregnancy and breast-feeding
Talk to your doctor before taking this medicine if you are pregnant, might become pregnant or are breast-feeding.
Driving and using machines
You may have blurred vision, dizziness, confusion or disorientation while taking Procyclidine Hydrochloride. If this happens do not drive or use any tools or machines.
Always take Procyclidine Hydrochloride exactly as your doctor has told you. You should check with your doctor or pharmacist if you are not sure.
■ Swallow the tablets with a drink of water.
■ The tablet may be cut or broken in half along the break-line to divide the dose in two equal halves.
To treat Parkinson's disease:
■ The usual starting dose is half a tablet three times a day.
■ This can be increased by half or 1 tablet each day, every two or three days until an effect is seen. This is known as the 'maintenance dose'. The daily maintenance dose is usually three to six tablets.
■ The maximum your doctor may decide to prescribe is 12 tablets.
■ Although the dose is usually taken three times a day, your doctor may ask you to take a fourth dose before bedtime.
To treat uncontrolled body movements (extrapyramidal symptoms) caused by taking other medicines:
Procyclidine Hydrochloride can be used to control side effects caused by other medicines.
■ The usual starting dose is half a tablet three times a day.
■ This can be increased by half a tablet each day until an effect is seen.
■ The daily maintenance dose is usually two to six tablets.
■ Your doctor may decide to stop your Procyclidine Hydrochloride after 3 or 4 months to see if your side effects return.
Elderly
If you are elderly, your dose may need to be carefully monitored to prevent any side effects.
Children
Procyclidine Hydrochloride tablets are not usually recommended for use in children.
If you take more Procyclidine Hydrochloride than you should
If you take more Procyclidine Hydrochloride than you should, talk to a doctor or go to a hospital straight away. Take the medicine pack with you.
If you forget to take Procyclidine Hydrochloride
Take a dose as soon as you remember it and then go on as before.
If you stop taking Procyclidine Hydrochloride
Do not stop taking Procyclidine Hydrochloride without talking to your doctor.
If you have any further questions on the use of this product, ask your doctor or pharmacist.
If you are taking a medicine for mental illness (called a neuroleptic) at the same time as Procyclidine Hydrochloride:
■ you can develop uncontrolled movements of your face and tongue (tardive dyskinesia). The dose of either of your medicines may need to be adjusted.
■ unusual body movements, particularly of your hands, arms and legs which may have previously been occurring with the medicine for your mental illness can be made worse by the addition of Procyclidine Hydrochloride.
If either of these happen, tell your doctor straight away.
Like all medicines, Procyclidine Hydrochloride can cause side effects, although not everybody gets them. The following side effects may happen with this medicine:
Common (affects less than 1 in 10 people)
■ problems passing water (urinary retention)
■ blurred vision
■ dry mouth or constipation.
Uncommon (affects less than 1 in 100 people)
■ feeling sick (nausea) or being sick (vomiting)
■ inflamed gums (gingivitis)
■ dizziness, nervousness, feeling confused, reduced concentration or memory, hearing unexpected noises or seeing unexpected sights (hallucinations), anxiety, agitation (feeling irritable)
■ skin rash.
Rare (affects less than 1 in 1,000 people)
■ 'psychotic' symptoms occurring together such as dizziness, confusion, reduced concentration or memory, disorientation, hearing unexpected noises or seeing unexpected sights (hallucinations), anxiety, agitation (feeling irritable).
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.
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.aov.uk/vellowcard. By reporting side effects, you can help provide more information on the safety of this medicine.
■ Keep out of the sight and reach of children.
■ Do not store above 25°C.
■ Do not use Procyclidine Hydrochloride after the expiry date which is stated on the carton or container. The expiry date refers to the last day of that month.
■ If your doctor decides to stop your treatment, take any tablets you have left back to the pharmacy.
■ If your tablets appear to be discoloured or show any other signs of deterioration, take them back to your pharmacist who will advise 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.
6. Further information
What Procyclidine Hydrochloride contains
■ Each tablet contains 5mg procyclidine hydrochloride.
■ The other ingredients are: lactose monohydrate, povidone, magnesium stearate and sodium starch glycollate.
What Procyclidine Hydrochloride looks like and contents of the pack
Procyclidine Hydrochloride Tablets are white, round, biconvex tablets with break-line on both faces, debossed with KT above and 05 below the break-line on one face and plain on the reverse.
These are available in a bottle containing 100 tablets.
Manufacturer:
Procyclidine Hydrochloride Tablets are manufactured by:
Aspen Bad Oldesloe GmbH, Industriestrasse 32-36,
23843 Bad Oldesloe, Germany.
Procured from within the EU and repackaged by:
Doncaster Pharmaceuticals Group Ltd., Kirk Sandall, Doncaster, DN3 1QR.
Product Licence holder: Landmark Pharma Ltd., 7 Regents Drive, Prudhoe, Northumberland, NE42 6PX.
PL No: 21828/0349 POM
Leaflet revision 8i issue date (Ref): 22.10.14
Other formats:
If you wish to receive this leaflet in Braille, large font or audio format please contact 01302 365000 and ask for the Regulatory Department
Please be ready to give the following information:
Product name Procyclidine Hydrochloride 5mg tablets Reference number 21828/0349
Page 2 of 2