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Valios 5 mg Orodispersible Tablets – patient leaflet, side effects, dosage

Last updated: · Text from the MHRA, as of · About this document

Medicine status: Prescription only (POM) Details

Medicine strength:
5 mg
Contains active substance:
ATC code:
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Patient leaflet - Valios 5 mg orodispersible tablets

1. What Valios is and what it is used for

Valios contains the active substance memantine hydrochloride. It 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 so-called N-methyl-D-aspartate (NMDA)-receptors that are involved in transmitting nerve signals important in learning and memory. Valios belongs to a group of medicines called NMDA-receptor antagonists. Valios acts on these NMDA-receptors improving the transmission of nerve signals and the memory.

Valios is used for the treatment of patients with moderate to severe Alzheimer’s disease.

2. What you need to know before you take Valios

Do not take Valios:

  • if you are allergic to memantine hydrochloride or any of

    the other ingredients of this medicine (listed in section 6).

Warnings and precautions

Talk to your doctor or pharmacist before taking Valios

  • 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 the treatment should be carefully supervised, and the clinical benefit of Valios 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

Valios is not recommended for children and adolescents under the age of 18 years.

Other medicines and Valios

Tell your doctor or pharmacist if you are taking, have recently taken or might take any other medicines.

In particular, Valios may change the effects of the following medicines and their dose may need to be adjusted by your doctor:

  • amantadine, ketamine, dextromethorphan
  • dantrolene, baclofen
  • cimetidine, ranitidine, procainamide, quinidine, quinine,

    nicotine

  • hydrochlorothiazide (or any combination with

    hydrochlorothiazide)

  • anticholinergics (substances generally used to treat

    movement disorders or intestinal cramps)

    • anticonvulsants (substances used to prevent and relieve

      seizures)

    • barbiturates (substances generally used to induce sleep)
    • dopaminergic agonists (substances such as L-dopa,

      bromocriptine)

    • neuroleptics (substances used in the treatment of mental

      disorders)

    • oral anticoagulants.

If you go into hospital, let your doctor know that you are taking Valios.

Valios 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 tubular 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.

Pregnancy

The use of memantine in pregnant women is not recommended.

Breast-feeding

Women taking Valios 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, Valios may change your reactivity, making driving or operating machinery inappropriate.

Valios contains aspartame and lactose

Aspartame contains a source of phenylalanine which may be harmful for people with phenylketonuria.

If you have been told by your doctor that you have intolerance to some sugars, contact your doctor before taking this medicinal product.

3. How to take Valios

Always take this medicine exactly as your doctor or pharmacist has told you. Check with your doctor or pharmacist if you are not sure.

The recommended dose of Valios for adults and older people is 20 mg once a day. In order to reduce the risk of side effects this dose is achieved gradually by the following daily treatment scheme.

Maintenance dose

The recommended daily dose is 20 mg (four 5 mg tablets) once a day.

For continuation of the treatment please consult your doctor.

Dosage in patients with impaired kidney function

If you have impaired 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.

Administration

Valios should be administered orally 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.

Valios orodispersible tablets break easily, so you should handle the tablets carefully. Do not handle the tablets with wet hands as the tablets may break up.

  • Hold the blister strip at the edges and separate one

    blister cell from the rest of the strip by gently tearing along the perforations around it.

  • Carefully peel off the backing.
  • Place the tablet on your tongue. The tablet will rapidly

    disintegrate and can be swallowed without water.

Duration of treatment

Continue to take Valios as long as it is of benefit to you. Your doctor should assess your treatment on a regular basis.

If you take more Valios than you should

  • In general, taking too much Valios 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 Valios, contact your

    doctor or get medical advice, as you may need medical attention.

If you forget to take Valios

  • If you find you have forgotten to take your dose of

    Valios, wait and take your next dose at the usual time.

  • 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, pharmacist or nurse.

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)

  • Drug hypersensitivity, headache, sleepiness,

    constipation, elevated liver function tests, dizziness, balance disorders, shortness of breath and high blood pressure

Uncommon (may affect up to 1 in 100 people)

  • Tiredness, fungal infections, confusion, hallucinations,

    vomiting, abnormal gait, heart failure and venous blood clotting (thrombosis/thromboembolism)

Very rare (may affect up to 1 in 10,000 people)

  • Seizures

Not known (frequency cannot be estimated from the available data)

  • Inflammation of the pancreas, inflammation of the liver

    (hepatitis) and psychotic reactions

Alzheimer’s disease has been associated with depression, suicidal ideation and suicide. These events have been reported in patients treated with memantine.

Reporting of side effects

If you get any side effects, talk to your doctor or pharmacist. This includes any possible side effects not listed in this leaflet. You can also report side effects directly via the Yellow Card Scheme, website

www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. By reporting side effects you can help provide more information on the safety of this medicine.

5. How to store Valios

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 storage conditions.

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 Valios contains

The active substance is memantine hydrochloride. Each 5 mg orodispersible tablet contains 5 mg memantine hydrochloride equivalent to 4.15 mg memantine.

The other ingredients are polacrilin, sodium hydroxide (for pH-adjustment), lactose monohydrate, cellulose, microcrystalline, mannitol (E421), croscarmellose sodium, aspartame (E951), silica, colloidal anhydrous, iron oxide red (E172), flavour peppermint [containing Maltodextrin (maize), Modified starch E1450 (waxy maize), Peppermint oil (mentha arvensis)], magnesium stearate.

What Valios looks like and contents of the pack

Valios 5 mg orodispersible tablets are presented as light pink round, flat, speckled tablets with bevelled edges, with a diameter of 7 mm and engraved with “5” on one side.

Valios orodispersible tablets are available in blister packs of 5 mg: 28 orodispersible tablets

Not all pack sizes may be marketed.

Marketing Authorisation Holder

Dr. Reddy’s Laboratories (UK) Ltd,

410 Cambridge Science Park, Milton Road, Cambridge, CB4 0PE, United Kingdom

Manufacturer

Genepharm S.A.

18th km Marathonos Ave, Pallini Attiki, 15351, Greece betapharm Arzneimittel GmbH, Kobelweg 95, 86156 Augsburg, Germany

This leaflet was last revised in 02/2023.

Week 1 (day 1-7)One 5 mg tablet once a day
Week 2 (day 8-14)Two 5 mg tablets once a day

Week 3

(day 15-21)

Three 5 mg tablets once a day
Week 4 onwardsFour 5 mg tablets once a day

07MMDROD05UK002610

DR0000000 180 mm

About this document

Source: MHRA - Medicines and Healthcare products Regulatory Agency (products.mhra.gov.uk) · Marketing authorisation: PL 08553/0694

Last revision stated in the text: February 2023 · MHRA data as of 13 October 2026

Found a mistake? Tell us on the contact page.

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

Facts about Valios 5 mg orodispersible tablets

Prescription needed? Yes, prescription-only medicine (POM)
Active substance Memantine
Strength 5 mg
Pharmaceutical form Orodispersible tablet
Light pink, round, flat, speckled tablets with beveled edges, with a diameter of 7 mm and engraved with “5” on one side.
How is it taken Oral
Excipients Polacrilin, Sodium hydroxide (for pH-adjustment) Lactose monohydrate, Cellulose, microcrystalline, Mannitol (E 421), Croscarmellose sodium, Aspartame (E 951), Silica, colloidal anhydrous, Iron oxide red (E 172), Flavor peppermint [containing Maltodextrin (maize), Modified starch E1450 (waxy maize), Peppermint oil (mentha arvensis)] Magnesium stearate
Pack sizes 28 tablet
Is it available? Listed as available (NHS Dictionary of Medicines and Devices – not a record of current supplies)
Shelf life 5 years
Storage This medicinal product does not require any special storage conditions.
Drug group (ATC) Psychoanaleptics. Other Anti-dementia drugs
  1. N Nervous system drugs
    1. N06 Psychoanaleptics
      1. N06D Anti-dementia drugs
        1. N06DX Other anti-dementia drugs
          1. N06DX01 memantine
Marketing authorisation PL 08553/0694 (first authorised 24 July 2023)
Marketing authorisation holder Dr. Reddy’s Laboratories (UK) Ltd.
Codes GTIN 5036072008076 · BNF 04110000

Sources: the MHRA product information (products.mhra.gov.uk) and the NHS Dictionary of Medicines and Devices (dm+d), release 10.2.0 of 19 October 2026, NHS Business Services Authority. Contains public sector information licensed under the Open Government Licence v3.0.