Product image of Memaxa (Memantine Hydrochloride) supplied by GNH India

Memaxa

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memaxa (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memaxa, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is indicated for the treatment of moderate to severe Alzheimer’s disease in adults.
GNH India supplies Memaxa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Krka, D.D., Novo Mesto

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Indications & Clinical Uses

Memaxa belongs to the NMDA receptor antagonist class and is used in the management of neurodegenerative dementia.

  • Alzheimer’s disease (moderate to severe): improves cognition, daily functioning, and overall clinical status.
  • Behavioral disturbances in Alzheimer’s disease: may reduce agitation, aggression, and related symptoms.
  • Cognitive impairment associated with Alzheimer’s disease: helps maintain memory and attention functions.

How It Works

  • Memantine Hydrochloride acts as an uncompetitive antagonist at the NMDA (N‑methyl‑D‑aspartate) receptor. By binding within the ion channel when it is excessively open, it reduces calcium influx and limits excitotoxic neuronal damage, thereby stabilising synaptic transmission in brain regions affected by Alzheimer’s pathology.

Side Effects

Memaxa may cause a range of adverse reactions, most of which are mild to moderate in severity.

Common Side Effects

  • Dizziness: sensation of light‑headedness or unsteadiness.
  • Headache: mild to moderate pain in the head region.
  • Constipation: reduced bowel movements or hard stools.
  • Fatigue: feeling unusually tired or lacking energy.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Severe skin reactions: such as Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Allergic reactions: including rash, itching, swelling, or anaphylaxis.

Precautions & Warnings

Before initiating Memaxa, clinicians should consider several safety aspects.

  • Renal impairment: assess kidney function and adjust dose if necessary.
  • Hepatic impairment: monitor liver enzymes and consider dose modification.
  • Concomitant NMDA antagonists: avoid co‑administration to reduce additive CNS effects.
  • History of seizures: observe closely for increased seizure activity.
  • Pregnancy: safety not established; use only if potential benefit outweighs risk.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Memaxa can interact with other medicines; some require avoidance while others need monitoring.

Major Interactions (Avoid)

  • Amantadine: combined use may increase CNS adverse effects.
  • Dextromethorphan: may potentiate neuropsychiatric side effects.
  • High‑dose quinidine: can raise memantine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may enhance blood pressure elevation.
  • Anticholinergic agents: could diminish memantine’s cognitive benefits.
  • Carbamazepine: may reduce memantine levels, affecting efficacy.

Frequently Asked Questions

Memaxa contains memantine hydrochloride and is prescribed for the treatment of moderate to severe Alzheimer’s disease. It helps improve cognitive function, daily activities, and overall clinical status in patients with this form of dementia.

Memantine acts as an uncompetitive antagonist of the NMDA receptor. By blocking excessive calcium influx through the receptor’s ion channel, it reduces excitotoxic neuronal damage, which contributes to the cognitive decline seen in Alzheimer’s disease.

The dosage of Memaxa is determined individually by a qualified prescriber based on the patient’s clinical condition, renal function, and response to therapy. Physicians set the appropriate dose and titration schedule.

The safety of memantine during pregnancy and lactation has not been established. It should be used only if the potential benefit justifies any possible risk to the fetus or infant, and only under medical supervision.

To request Memaxa, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any required import documentation.

Memaxa belongs to the NMDA receptor antagonist class, whereas other approved agents such as donepezil, rivastigmine, and galantamine are acetylcholinesterase inhibitors. Memantine targets glutamatergic excitotoxicity, offering a complementary mechanism that may be used alone or in combination with cholinesterase inhibitors.

Memaxa should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, heat, and direct sunlight to maintain its stability and potency.

Memaxa is taken orally, usually once daily after a meal. The tablet should be swallowed whole with water and not crushed, chewed, or broken, unless otherwise instructed by a healthcare professional.

Serious risks include seizures, severe skin reactions such as Stevens‑Johnson syndrome, and allergic reactions that may lead to anaphylaxis. Patients should seek immediate medical attention if they experience any of these symptoms.

Memaxa is contraindicated in patients with known hypersensitivity to memantine or any of its excipients. It should also be avoided in individuals taking other NMDA antagonists or those with uncontrolled severe renal impairment without appropriate dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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