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Memantine Hydrochloride Tablets: Uses, Side Effects and Dosage

Updated:
Facts
Status:
Prescription (Rx)
Strength:
10 mg
Active ingredient:
ATC code:

Patient Medication Information: uses, side effects, how to take - Memantine Hydrochloride Tablets

ABOUT THIS MEDICATION

What the medication is used for:

Memantine hydrochloride tablets have been prescribed to you, by a doctor to relieve symptoms of Alzheimer’s disease.

What it does:

The brain contains N-methyl-D-aspartate (NMDA) receptors that are involved in transmitting nerve signals and may be important for learning and memory. Abnormal transmission of nerve signals through NMDA-receptors in the brain may affect memory and other mental functions and contribute to symptoms of Alzheimer’s disease. Memantine hydrochloride tablet belongs to a group of medicines called NMDA-receptor antagonists. The action of memantine hydrochloride on NMDA-receptors may help normalize the transmission of nerve signals, which may help slow the decline in some of the symptoms of Alzheimer disease.

When it should not be used:

  • You should not be taking memantine hydrochloride

    tablets if you are pregnant, unless in the opinion of the doctor, the expected benefit to the patient markedly outweighs the possible hazards to the foetus.

  • You should not be taking memantine hydrochloride

    if you are breast-feeding.

    • Do not take memantine hydrochloride tablets if you are allergic to it, or to any of the other ingredients listed in this leaflet (see ‘What the nonmedicinal ingredients are’).
    • Stop taking memantine hydrochloride tablets if you experience an allergic reaction or any severe side effect.

What the medicinal ingredient is:

Memantine hydrochloride.

What the nonmedicinal ingredients are: Lactose monohydrate, microcrystalline cellulose, croscarmellose sodium, colloidal silicon dioxide, talc, magnesium stearate, hypromellose, titanium dioxide, polyethylene glycol and iron oxide black.

What dosage forms it comes in:

Light gray colored 10 mg tablets.

WARNINGS AND PRECAUTIONS

BEFORE you use memantine hydrochloride tablets talk to your doctor or pharmacist if:

  • You have/had a medical condition, including heart problems, uncontrolled hypertension (high blood pressure), history of seizures or kidney disease
  • You are taking any medications (prescription or non-prescription) or have taken any within the last 14 days.
  • You ever had an allergic reaction to any medication
  • You are pregnant or thinking of becoming pregnant, or if you are breast-feeding.
  • There are conditions which can change the speed at which the body would normally eliminate the drug over time and you should tell your doctor, as memantine hydrochloride tablets dosage may have to be adjusted if:

    • You have recently changed or intend to change your diet substantially (e.g. from normal diet to strict vegetarian diet)
    • You are suffering from renal tubulary acidosis (RTA, an excess of acid-forming substances in the blood due to renal dysfunction [kidney problems])
    • You have a urinary tract infection.
IMPORTANT: PLEASE READ

INTERACTIONS WITH THIS MEDICATION

Drugs that may interact with memantine hydrochloride tablets include:

  • NMDA-receptor antagonists (e.g. amantadine)
  • Cimetidine
  • Ranitidine
  • Procainamide
  • Quinidine
  • Quinine
  • Hydrochlorothiazide (or any combination with

    hydrochlorothiazide)

  • Anticholinergics (generally used to treat movement

    disorders or intestinal cramps)

  • L-dopa and dopaminergic agonists (drugs such as

    bromocriptine, ropinirole, pramipexole)

  • Ketamine
  • Dextromethorphan (found in cough syrup labelled

    DM)

  • Anticoagulant (blood thinner) medications taken by

    mouth

PROPER USE OF THIS MEDICATION

Usual dose:

  • It is important that you take memantine

    hydrochloride tablets exactly as your doctor has instructed.

  • Usually your doctor will prescribe 20 mg per day,

    which you will take as two separate doses of 10 mg. In order to reduce the risk of side effects this dose will be achieved gradually by the following daily treatment scheme, starting at a dose of 5 mg per day:

10 mg Tablets
AMPM
Week 1½ tabletNone
Week 2½ tablet½ tablet
Week 31 tablet½ tablet
Week 4 and beyond1 tablet1 tablet
  • Never change the dose of memantine

    hydrochloride tablets unless your doctor tells you to.

    • Swallow the tablets whole with some water.

      Do not chew tablets. Memantine hydrochloride tablets can be taken with or without food.

    • Continue to take memantine hydrochloride tablets as long as directed by your doctor and you do not experience any unacceptable side effects. Your doctor should assess your treatment on a regular basis.

Overdose:

If you have accidentally taken too much memantine hydrochloride tablets contact your regional Poison Control Centre, hospital emergency department or your doctor immediately, even if you do not feel sick. You may require medical attention. If you go to the doctor or the hospital, take the memantine hydrochloride tablets container with you.

Missed Dose:

If you miss a dose, do not worry. Do not take the missed tablet(s) – just take the next dose when it is due.

SIDE EFFECTS AND WHAT TO DO ABOUT THEM

Like all medicines, memantine hydrochloride tablets can cause side effects, although not everybody gets them. In general, these are mild to moderate. If any of the side effects become severe or if they are troublesome or persistent, talk to your doctor.

Common side effects (affects 1 to 10 users in 100) may include:

  • headache
  • sleepiness
  • constipation
  • tiredness
  • confusion
  • hallucinations (strange visions or sounds)
  • vomiting
  • loss of appetite
  • dizziness
  • sleep disturbance
  • anxiety
  • high blood pressure
  • change in frequency of urination

Uncommon side effects (affects 1 to 10 users in 1000) may include:

  • fungal infections
  • changes in vision
  • skin allergies

Your doctor will tell you whether your illness allows you to drive or operate machinery. Also, as this product may cause sleepiness or dizziness, do not drive or operate machinery under these conditions.

Alzheimer’s disease has been associated with depression, thoughts of suicide and suicide. These events have been reported in patients treated with memantine hydrochloride tablets.

If you have previously experienced epileptic seizures, there is a possibility that memantine hydrochloride tablets may increase the chances of one occurring.

SERIOUS SIDE EFFECTS, HOW OFTEN THEY HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / EffectTalk with your doctor or pharmacistStop taking drug and seek immediate emergency treatment

Only if

severe

In all cases

Un

common

Fungal infection√

Abnormal gait

[Abnormal way of

walking]

√

Heart failure [persistent chest pain, rapid heart rate, severe shortness of breath,

swelling

of legs or ankles,

increased tiredness, lack of

appetite,

confusion]

√

Venous

blood

Clotting [pain,

swelling, changes in skin color, increased warmth in one leg]

√
SERIOUS SIDE EFFECTS, HOW OFTEN THEY
HAPPEN AND WHAT TO DO ABOUT THEM
Symptom / EffectTalk with your doctor or pharmacistStop taking drug and seek immediate emergency treatment
Only if severeIn all cases
Very Rare

Seizures

[loss of

Consciousn ess with

Uncontrolla ble shaking]

√

Hepatitis/ hepatic failure

[yellow skin and eyes, nausea, loss of appetite, dark-coloured urine]

√

Inflammatio n of the pancreas

[severe upper stomach pain, often with nausea and vomiting]

√
psychotic reactions√

Serious skin reactions

[rash, red skin, blistering of the lips, eyes or mouth, skin peeling]

√

For example:

Stevens-

Johnson

Syndrome: Severe rash with blisters and peeling skin, particularly around the mouth, nose, eyes and genitals

Acute

Generalized Exanthemat ous

√

Pustulosis: Red rash

covered

with small pus-filled bumps that can spread over the

body,

sometimes with a fever

Erythema Multiforme: Rash that may blister, with spots that look

like small targets

This is not a complete list of side effects. For any unexpected effects while taking memantine hydrochloride tablets, contact your doctor or pharmacist.

If you notice any side effects not listed in this leaflet, please tell your doctor or pharmacist.

HOW TO STORE IT

  • As with all medicines, keep memantine

    hydrochloride tablets out of the reach of children.

  • Store your tablets at room temperature (15°C-

    30°C) and in a dry place.

  • If your doctor tells you to stop taking your

    medicine you should return any leftover tablets to the pharmacist, unless the doctor tells you to keep them at home.

REMEMBER: This medicine is for YOU or for someone in your care. Only a doctor can prescribe it, so never offer it to any other person, even if their symptoms seem to be the same as yours or as for the person in your care.

REPORTING SUSPECTED SIDE EFFECTS

NOTE: THIS IS NOT AN EMERGENCY NUMBER

To monitor drug safety, Health Canada through the Canada Vigilance Program collects information on serious and unexpected side effects of drugs. If you suspect you have had a serious or unexpected reaction to this drug you may notify Canada Vigilance:

By toll-free telephone: 1-866-234-2345 By toll-free fax: 1-866-678-6789

On-line: https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting.html By email: CanadaVigilance@hc-sc.gc.ca

By regular mail:

Canada Vigilance Program

Health Canada

Postal Locator 1908C

Ottawa ON K1A 0K9

NOTE: Should you require information related to the management of the side effect, please contact your health care provider before notifying Canada Vigilance. The Canada Vigilance Program does not provide medical advice.

MORE INFORMATION

For more information, please contact your doctor, pharmacist or other healthcare professional.

Canadian Importer and Distributor:

SANIS HEALTH INC.

333, Champion street

Suite 102, Dieppe

New Brunswick E1A 1P2

CANADA

Manufacturer Address:

Alembic Pharmaceuticals Limited,

Alembic Road, Vadodara

Gujarat, India.

PIN 390003

Revised on: June 12, 2018

About this document

Source: Health Canada – Drug Product Database (DPD) and product monographs · DIN (Drug Identification Number): 02425742

Revision date stated in the text: June 12, 2018

Found a mistake? Write to us via the contact page.

The information on this site does not replace the advice of a doctor or pharmacist.

Drug information for Memantine Hydrochloride Tablets

Rx or OTC
Prescription (Rx)?
DIN 02425742
Schedule(s) PRESCRIPTION
Active ingredient(s) Memantine hydrochloride 10 MG
Dosage form(s) Tablet
Route(s) of administration Oral
Drug class (WHO ATC)
  1. N Nervous system drugs
    1. N06 Psychoanaleptics
      1. N06D Anti-dementia drugs
        1. N06DX Other anti-dementia drugs
          1. N06DX01 Memantine
Company ALEMBIC PHARMACEUTICALS LIMITED
Current status Approved
Current status date June 4, 2014

Source: Health Canada – Drug Product Database (DPD) and product monographs, data as of November 1, 2026. Data from the Health Canada Drug Product Database, as published there. Not a substitute for the advice of a doctor or pharmacist.