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

Mentifar

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Mentifar (Memantine Hydrochloride)

Memantine, the active ingredient in Mentifar, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is indicated for the symptomatic treatment of moderate to severe Alzheimer's disease in adult patients, helping to improve cognition and daily functioning.

GNH India supplies Mentifar as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, offering consistent quality and regulatory support for global procurement.

Manufacturer / TM Owner

Rafarm Sa.

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Indications & Clinical Uses

Mentifar (memantine) is used in the management of neurodegenerative disorders, specifically targeting glutamatergic excitotoxicity in Alzheimer's disease.

  • Alzheimer's disease (moderate to severe): improves cognition and functional abilities.
  • Alzheimer's disease (mild to moderate) as adjunct to cholinesterase inhibitors: provides additional symptomatic benefit.
  • Behavioral symptoms in Alzheimer's disease: may reduce agitation and improve overall patient management.

How It Works

  • Memantine acts as a non‑competitive antagonist at the NMDA (N‑methyl‑D‑aspartate) receptor, binding to the receptor-associated ion channel with moderate affinity. By blocking excessive calcium influx caused by overstimulation of glutamate, it reduces excitotoxic neuronal damage while preserving normal synaptic transmission, thereby supporting cognitive function in Alzheimer's disease.

Side Effects

Common Side Effects

  • Dizziness: transient light‑headedness, especially after dose initiation.
  • Headache: mild to moderate intensity, often resolves with continued therapy.
  • Constipation: reduced bowel movements, may require dietary adjustment.
  • Fatigue: feeling of tiredness, usually improves over time.

Serious or Rare Side Effects

  • Seizures: increased risk, monitor patients with epilepsy.
  • Severe allergic reaction: rash, swelling, or anaphylaxis requiring immediate medical attention.
  • Hepatic dysfunction: elevated liver enzymes, monitor liver function tests.
  • Suicidal ideation: emergence of depressive thoughts, assess mental health regularly.
  • Stevens‑Johnson syndrome: rare skin reaction, discontinue if signs appear.

Precautions & Warnings

Memantine should be used with caution in patients with the following considerations:

  • Renal impairment: adjust dose or monitor renal function closely.
  • Hepatic impairment: use with caution; monitor liver enzymes.
  • History of seizures: monitor for increased seizure frequency.
  • Concurrent use with other NMDA antagonists: avoid combined therapy.
  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Memantine may interact with several medicines; awareness of the interaction level is essential.

Major Interactions (Avoid)

  • Amantadine: additive NMDA antagonism may increase toxicity.
  • Ketamine: combined NMDA antagonism may cause excessive CNS depression.
  • Other NMDA antagonists: avoid concurrent use.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): increase memantine plasma levels.
  • Strong CYP3A4 inducers (e.g., rifampicin): decrease memantine plasma levels.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: may reduce cognitive benefit of memantine.
  • Diuretics: monitor for potential hypotension or electrolyte imbalance.

Frequently Asked Questions

Mentifar contains memantine, which is prescribed for the symptomatic treatment of moderate to severe Alzheimer's disease in adult patients, helping to improve cognition and daily functioning.

Memantine acts as a non‑competitive antagonist at NMDA receptors, reducing excessive calcium influx caused by glutamate over‑activation. This limits excitotoxic neuronal damage while preserving normal synaptic activity.

The dosage of Mentifar is determined by the prescribing clinician based on the patient’s condition, renal function, and treatment response. Patients should follow the prescriber’s specific instructions.

Safety of memantine in pregnancy and lactation has not been established. Prescribers should evaluate the potential benefits against possible risks before initiating therapy in these populations.

Enquiries can be submitted on the product page at gnhindia.com with the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and import documentation.

Mentifar (memantine) is an NMDA receptor antagonist, differing from cholinesterase inhibitors such as donepezil. It is typically used in moderate to severe disease or as add‑on therapy, offering a distinct mechanism that targets glutamate‑mediated excitotoxicity.

Mentifar should be stored at ambient temperature, below 25 °C, in its original packaging, protected from moisture and direct light to maintain stability.

Mentifar is taken orally, usually as a tablet, with or without food as directed by the prescriber. Swallow the tablet whole and do not crush or chew unless instructed otherwise.

Serious risks include seizures, severe allergic reactions, hepatic dysfunction, suicidal ideation, and rare skin reactions such as Stevens‑Johnson syndrome. Patients should be monitored for these events and seek immediate medical attention if they occur.

Mentifar is contraindicated in patients with known hypersensitivity to memantine or any component of the formulation, and it should be used with caution in individuals with severe renal or hepatic impairment, uncontrolled epilepsy, or those taking other NMDA antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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