Product image of Memantina Alter (Memantine Hydrochloride) supplied by GNH India

Memantina Alter

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Alter (Memantine Hydrochloride)

Memantine, the active ingredient in Memantina Alter, is an 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 adults, helping to improve cognition and daily functioning.

GNH India supplies Memantina Alter as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with consistent quality and regulatory compliance across EU markets. The company ensures reliable supply chains, appropriate documentation, and responsive customer support for global procurement.

Manufacturer / TM Owner

Alter S.A.

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Indications & Clinical Uses

  • Memantine is an NMDA receptor antagonist used in the management of neurodegenerative disorders.
  • Alzheimer’s disease (moderate to severe): improves cognition and global clinical status
  • Alzheimer’s disease (mild to moderate): may be added to cholinesterase inhibitors to support cognition
  • Alzheimer’s disease (behavioral symptoms): may help reduce agitation and aggression

How It Works

  • Memantine acts as a non‑competitive antagonist at the NMDA (N‑methyl‑D‑aspartate) receptor. By binding to the receptor-associated ion channel with moderate affinity, it blocks excessive calcium influx caused by prolonged glutamate activation, thereby reducing excitotoxic neuronal injury while preserving normal synaptic transmission essential for learning and memory.

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, manageable with dietary fiber
  • Confusion: occasional disorientation, particularly in elderly patients
  • Somnolence: mild sleepiness, may improve over time

Serious or Rare Side Effects

  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis
  • Seizures: rare but may occur, especially with high plasma levels
  • Hallucinations or psychosis: uncommon, warrant immediate medical review
  • Cardiac arrhythmias: rare cases of QT prolongation reported
  • Hepatic dysfunction: elevated liver enzymes in isolated reports

Precautions & Warnings

  • Memantine should be used with caution in specific clinical situations.
  • Renal impairment: dose adjustment may be required in patients with reduced kidney function
  • History of seizures: monitor closely for increased seizure activity
  • Concurrent NMDA antagonists: avoid co‑administration to prevent additive CNS effects
  • Cardiovascular disease: monitor blood pressure and heart rhythm during therapy
  • Pregnancy and lactation: use only if potential benefit justifies potential risk to fetus or infant
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight

Avoid Interactions

Memantine may interact with several medications; monitoring is advised.

Major Interactions (Avoid)

  • Amantadine: increased risk of neurotoxicity when combined
  • Other NMDA antagonists (e.g., ketamine): additive central nervous system depression
  • High‑dose quinidine: may raise memantine plasma concentrations

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: possible reduction in therapeutic benefit
  • Loop diuretics (e.g., furosemide): may increase memantine levels
  • CNS depressants (e.g., benzodiazepines): enhanced sedation or drowsiness

Frequently Asked Questions

Memantina Alter contains memantine, which is prescribed for the symptomatic treatment of moderate to severe Alzheimer’s disease. It helps improve cognitive function and daily living activities in adults by reducing excitotoxic neuronal damage associated with the disease.

Memantine acts as a non‑competitive antagonist of the NMDA receptor. By blocking excessive calcium influx caused by prolonged glutamate activation, it reduces excitotoxic neuronal injury while allowing normal synaptic transmission needed for learning and memory.

The appropriate dose of Memantina Alter is determined by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and response to therapy. Dosage adjustments are made individually and should follow the prescriber’s instructions.

Memantine is classified as a prescription‑only medication and should only be used during pregnancy or lactation if the potential benefit outweighs any possible risk to the fetus or infant. Decisions should be made in consultation with a qualified healthcare provider.

To request Memantina Alter, submit an enquiry on the product page at gnhindia.com indicating 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 any necessary import documentation.

Memantine belongs to the NMDA receptor antagonist class, differing from cholinesterase inhibitors such as donepezil or rivastigmine. While cholinesterase inhibitors enhance acetylcholine signaling, memantine reduces glutamate‑mediated excitotoxicity. In practice, memantine may be used alone or in combination with a cholinesterase inhibitor for additive benefit.

Memantina Alter should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the tablets from moisture, excessive heat and direct sunlight to maintain product stability throughout its shelf life.

Memantina Alter is taken orally, usually once daily, with or without food as directed by the prescriber. Swallow the tablet whole with a glass of water; do not crush or chew unless specifically instructed.

Serious adverse events, although rare, include severe skin reactions such as Stevens‑Johnson syndrome, seizures, hallucinations or psychosis, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience any of these symptoms.

Memantina Alter is contraindicated in patients with known hypersensitivity to memantine or any of its excipients. Caution is advised for individuals with severe renal impairment, uncontrolled seizures, or those taking other NMDA antagonists, unless specifically approved by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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