MEMANTINE HYDROCHLORIDE COLONIS 20 MG SOLUBLE TABLETS
Memantine hydrochloride Colonis 20 mg soluble tablets
Read all of this leaflet carefully before you start taking this medicine because it contains important information
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.
What is in this leaflet
What Memantine soluble tablets are and what they are used for
What you need to know before you take Memantine soluble tablets
How to take Memantine soluble tablets
How to store Memantine soluble tablets
Contents of the pack and other information
1. What Memantine soluble tablets are and what they are used for
Memantine soluble tablets contain the active substance memantine hydrochloride which belongs to a group of
medicines known as anti-dementia medicines.
Memory loss in Alzheimer’s disease is due to a disturbance of message signals in the brain. The brain contains socalled N-methyl-D-aspartate (NMDA)-receptors that are involved in transmitting nerve signals important in learning
and memory. Memantine soluble tablets belong to a group of medicines called NMDA-receptor antagonists.
Memantine soluble tablets act on these NMDA-receptors improving the transmission of nerve signals and the
Memantine soluble tablets are used for the treatment of patients with moderate to severe Alzheimer’s disease.
2. What you need to know before you take Memantine soluble tablets
Do not take Memantine soluble tablets
- if you are allergic to memantine hydrochloride or any of the other ingredients of this medicine (listed in section 6).
Warning and precautions
Talk to your doctor or pharmacist before taking Memantine soluble tablets:
if you have a history of epileptic seizures
if you have recently experienced a myocardial infarction (heart attack), or if you are suffering from congestive
heart failure or from an uncontrolled hypertension (high blood pressure).
In these situations your treatment should be carefully supervised, and the clinical benefit of this medicine reassessed
by your doctor on a regular basis.
If you suffer from renal impairment (kidney problems), your doctor should closely monitor your kidney function and
if necessary adapt the memantine doses accordingly.
The use of medicinal products called amantadine (for the treatment of Parkinson’s disease), ketamine (a substance
generally used as an anaesthetic), dextromethorphan (generally used to treat cough) and other NMDA-antagonists at
the same time should be avoided.
Children and adolescents
Memantine soluble tablets are not recommended for children and adolescents under the age of 18 years.
Other medicines and Memantine soluble tablets
Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.
In particular, Memantine soluble tablets may change the effects of the following medicines and their dose may need
to be adjusted by your doctor:
- amantadine (substance used in the treatment of Parkinson’s disease)
- ketamine (an anaesthetic)
-dextromethorphan (substance used to treat coughs)
- dantrolene (substance used as a muscle relaxant)
- baclofen (substance used to relieve muscle spasms occurring in various illnesses such as cerebral palsy and multiple
- cimetidine, ranitidine (substances used in the treatment of indigestion, heartburn and gastric ulcers)
- procainamide, quinidine (substances used to treat irregular heartbeats)
- quinine (substance used to treat night time leg cramps)
- nicotine (substance used to help you stop smoking)
- hydrochlorothiazide (or any combination with hydrochlorothiazide – a diuretic used in the treatment of water
retention and high blood pressure)
- anticholinergics (substances generally used to treat movement disorders or intestinal cramps)
- anticonvulsants (substances used to prevent and relieve epilepsy seizures)
- barbiturates (substances generally used to induce sleep)
- dopaminergic agonists (such as L-dopa and bromocriptine which are used in Parkinson’s disease to stimulate your
- neuroleptics (substances used in the treatment of mental health disorders)
- oral anticoagulants (such as warfarin used to thin the blood)
If you go into hospital, let your doctor know that you are taking Memantine soluble tablets.
Memantine soluble tablets with food and drink
You should inform your doctor if you have recently changed or intend to change your diet substantially (e.g. from
normal diet to strict vegetarian diet) or if you are suffering from states of renal tubulary acidosis (RTA, an excess of
acid-forming substances in the blood due to renal dysfunction (poor kidney function)) or severe infections of the
urinary tract (structure that carries urine), as your doctor may need to adjust the dose of your medicine.
Pregnancy and breast-feeding
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.
The use of this medicine in pregnant women is not recommended.
Women taking this medicine should not breast-feed.
Driving and using machines
Your doctor will tell you whether your illness allows you to drive and to use machines safely. Also, this medicine
may change your reactivity, making driving or operating machinery inappropriate.
3. How to take Memantine soluble tablets
Always take Memantine soluble tablets exactly as your doctor has told you. Check with your doctor or pharmacist if
you are not sure.
The recommended dose of Memantine soluble tablets for adults and older people is 20 mg once a day.
In order to reduce the risk of side effects the maintenance dose is achieved by upward titration of 5 mg per week over
the first 3 weeks by the use of the treatment initiation pack.
week 4 and
One 5 mg tablet
One 10 mg tablet
One 15 mg tablet
One 20 mg tablet
The usual starting dose is one 5 mg tablet once a day for the first week. This is increased to one 10 mg tablet once a
day in the second week and to one 15 mg tablet once a day in the third week. From the fourth week on, the usual dose
is 20 mg once a day (two tablets of 10 mg or 1 tablet of 20 mg).
Dosage in patients with impaired kidney function
If you have impaired (poor) kidney function, your doctor will decide upon a dose that suits your condition. In this
case, monitoring of your kidney function should be performed by your doctor at specified intervals.
Method of administration
This medicine should be administered orally (by mouth) once a day.
To benefit from your medicine you should take it regularly every day at the same time of the day.
The tablets can be taken with or without food.
The tablets are best taken dissolved in a glass of water, however, they can also be taken whole, with a drink of
Dissolve the tablet, that your doctor has told you to take, in a glass of water, and then drink all of it
Do not leave your drink where someone else may drink it as your medicine could harm them.
Duration of treatment
Continue to take this medicine as long as it is of benefit to you. Your doctor should assess your treatment on a regular
If you take more Memantine soluble tablets than you should
- In general, taking more Memantine soluble tablets than you have been prescribed should not result in any harm to
you. You may experience increased symptoms as described in section 4. “Possible side effects”.
- If you take a large overdose of Memantine soluble tablets, contact your doctor or get medical advice, as you may
need medical attention.
If you forget to take Memantine soluble tablets
- If you find you have forgotten to take your dose of Memantine soluble tablets, wait and take your next dose at the
- Do not take a double dose to make up for a forgotten dose.
If you have any further questions on the use of this medicine, ask your doctor or pharmacist.
4. Possible side-effects
Like all medicines, this medicine can cause side effects, although not everybody gets them.
In general, the observed side effects are mild to moderate.
Common (may affect up to 1 in 10 people):
Elevated liver function test results.
Dizziness, problems with your balance.
Shortness of breath.
High blood pressure.
Uncommon (may affect up to 1 in 100 people):
Being sick (vomiting).
Blood clots in your veins (thrombosis/thromboembolism).
Very Rare (may affect up to 1 in 10,000 people):
Not known (frequency cannot be estimated from the available data):
Inflammation of the pancreas.
Inflammation of the liver (hepatitis).
Alzheimer’s disease has been associated with depression, suicidal thoughts and suicide. These problems have been
experienced by patients being treated with this medicine.
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:
By reporting side effects you can help provide more information on the safety of this medicine.
5. How to store Memantine soluble tablets
Keep this medicine out of the sight and reach of children.
Do not use this medicine after the expiry date which is stated on the carton and the blister after EXP. The expiry date
refers to the last day of that month.
This medicinal product does not require any special temperature storage conditions.
Store in the original package in order to protect from moisture.
Do not throw away any medicines via wastewater or household waste. Ask your pharmacist how to throw away
medicines you no longer use. These measures will help protect the environment.
6. Contents of the pack and other information
What Memantine soluble tablets contain
- The active substance is memantine hydrochloride. Each soluble tablet contains 20 mg memantine hydrochloride
equivalent to 16.62 mg memantine.
- The other ingredients are:
Disodium Hydrogen Citrate
Citric Acid Anhydrous
Macrogol 6000 (PEG 6000)
Briliant Blue FCF (E 133)
What Memantine soluble tablets look like and contents of the pack
Memantine hydrochloride soluble tablets 20 mg are blue-coloured round, flat tablets, of diameter 11.0 mm ± 0.2
mm,packed in PA/Al/PVC/Al blisters. Each blister contains 7 tablets. The colour of the blister is blue.
Pack size of 28 tablets i.e. four blisters of 7 tablets.
Marketing Authorisation Holder
Colonis Pharma Limited,
8 Church Road
Royal Tunbridge Wells, Kent
Thesi Pousi-Xatzi, Agiou Louka, Paiania, Attiki, TK 19002, Greece.
Marketed and Distributed By
Quantum Pharmaceutical Limited
Hobson Industrial Estate
This leaflet was last revised in October 2015
Source: Medicines and Healthcare Products Regulatory Agency
Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.