Product image of Memantină Terapia (Memantine Hydrochloride) supplied by GNH India

Memantină Terapia

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantină Terapia (Memantine Hydrochloride)

Memantine, the active ingredient in Memantína Terapia, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is indicated for the treatment of Alzheimer’s disease in adults, where it helps to mitigate excitotoxic neuronal damage associated with disease progression.

GNH India supplies Memantína Terapia as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to European Union quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Terapia S.A.

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Indications & Clinical Uses

Memantine is an NMDA receptor antagonist used in the management of neurodegenerative conditions, particularly Alzheimer’s disease.

  • Mild Alzheimer’s disease: modest improvement in cognition and daily living activities.
  • Moderate Alzheimer’s disease: stabilization of functional decline and behavioral symptoms.
  • Severe Alzheimer’s disease: may provide modest benefit in global clinical status.
  • Very mild Alzheimer’s disease: may delay onset of functional decline.

How It Works

  • Memantine acts as a non‑competitive antagonist at the N‑methyl‑D‑aspartate (NMDA) receptor ion channel. By binding within the receptor-associated channel at moderate affinity, it reduces excessive calcium influx caused by prolonged glutamate activation. This moderation of excitatory neurotransmission limits excitotoxic neuronal injury, which is implicated in the pathophysiology of Alzheimer’s disease, thereby supporting neuronal survival and function.

Side Effects

Memantine may be associated with a range of adverse reactions, varying in frequency and severity.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Fatigue: feeling of tiredness.
  • Nausea: upset stomach.

Serious or Rare Side Effects

  • Seizures: convulsive episodes, especially in predisposed patients.
  • Severe allergic reactions: rash, angioedema, or anaphylaxis.
  • Hallucinations or psychosis: visual or auditory disturbances.
  • Cardiac arrhythmias: irregular heart rhythm, rarely reported.

Precautions & Warnings

When prescribing Memantína Terapia, clinicians should consider several safety considerations.

  • Renal impairment: dose may need adjustment in severe renal dysfunction.
  • Hepatic impairment: monitor liver function tests during therapy.
  • History of seizures: use with caution as the drug can lower seizure threshold.
  • Concomitant use with other NMDA antagonists: avoid combined therapy due to additive effects.
  • Pregnancy and lactation: safety not established; use only if potential benefit justifies risk.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantine can interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism may increase neuropsychiatric adverse events.
  • High‑dose quinidine: may raise memantine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: may reduce cognitive benefits of memantine.
  • Carbamazepine: enzyme induction can lower memantine levels.
  • Proton pump inhibitors (e.g., omeprazole): may increase memantine exposure.
  • Alcohol: excessive use may exacerbate dizziness and CNS effects.
  • CNS depressants (e.g., benzodiazepines): may enhance sedation.

Frequently Asked Questions

Memantína Terapia contains memantine, which is prescribed to treat Alzheimer’s disease. It helps to improve or stabilize cognitive function and daily activities in patients with mild to severe forms of the disease by reducing excitotoxic neuronal damage.

Memantine works as a non‑competitive antagonist of the NMDA receptor. By blocking excessive calcium influx caused by prolonged glutamate activation, it limits excitotoxic injury to neurons, a key process involved in the progression of Alzheimer’s disease.

The dosage of Memantína Terapia is determined by the prescribing clinician based on the patient’s condition, age, renal function and other factors. The prescriber will set the appropriate dose and titration schedule.

Safety data for memantine during pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

To order, 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 necessary import documentation.

The primary alternative class for Alzheimer’s disease is acetylcholinesterase inhibitors such as donepezil. While those agents enhance cholinergic transmission, memantine modulates glutamatergic activity. In practice, they are sometimes used together to target different pathways, offering complementary benefits.

Store the tablets at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture, direct sunlight and extreme heat to maintain potency throughout the shelf life.

Memantína Terapia is taken orally, usually with water. The tablet is swallowed whole and can be taken with or without food, following the dosing schedule prescribed by the healthcare professional.

Serious risks include the possibility of seizures, severe allergic reactions such as rash or angioedema, and rare cardiac arrhythmias. Patients should report any sudden neurological changes, skin reactions or irregular heartbeats to their physician promptly.

Memantína Terapia should be avoided in patients with known hypersensitivity to memantine or any tablet excipients, and used with caution in those with severe renal or hepatic impairment, uncontrolled seizures, or who are taking other NMDA antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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