Product image of Memantine Hydrochloride Chanelle Medical (Memantine Hydrochloride) supplied by GNH India

Memantine Hydrochloride Chanelle Medical

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Hydrochloride Chanelle Medical (Memantine Hydrochloride)

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

Manufacturer / TM Owner

Chanelle Medical Unlimited Company

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Indications & Clinical Uses

Memantine Hydrochloride is an NMDA receptor antagonist used in the management of Alzheimer’s disease and related cognitive disorders.

  • Moderate to severe Alzheimer’s disease: improves cognition, memory, and daily functioning in patients with significant disease progression.
  • Alzheimer’s disease as adjunct therapy: enhances the therapeutic effect when combined with cholinesterase inhibitors.
  • Mild to moderate Alzheimer’s disease: may support cognitive function and delay functional decline.

How It Works

  • Memantine Hydrochloride acts as a non‑competitive antagonist at the N‑methyl‑D‑aspartate (NMDA) 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 and supporting neuronal survival in the brain.

Side Effects

Memantine Hydrochloride 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.
  • Confusion: transient difficulty concentrating or disorientation.
  • Somnolence: feeling unusually sleepy or fatigued.

Serious or Rare Side Effects

  • Seizures: rare occurrence of convulsive episodes.
  • Severe allergic reactions: rash, itching, swelling, or difficulty breathing.
  • Stevens‑Johnson syndrome: rare skin blistering and mucosal involvement.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Cardiac arrhythmias: irregular heart rhythms reported in isolated cases.

Precautions & Warnings

When prescribing Memantine Hydrochloride, clinicians should consider several safety factors.

  • Renal impairment: adjust dose or monitor closely in patients with reduced kidney function.
  • Hepatic impairment: use with caution and assess liver function periodically.
  • History of seizures: evaluate risk as memantine may lower seizure threshold.
  • Concomitant NMDA antagonists: avoid combining with other agents that block NMDA receptors.
  • Pregnancy and breastfeeding: safety not established; weigh potential benefits against risks.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

Avoid Interactions

Memantine Hydrochloride can interact with several medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Amantadine: additive NMDA antagonism may increase neuropsychiatric effects.
  • Ketamine: combined NMDA blockade can enhance central nervous system depression.
  • Dextromethorphan: may potentiate dizziness and confusion.
  • High‑dose anticholinesterase inhibitors: risk of excessive cholinergic activity.
  • Strong CYP450 inhibitors: may alter memantine clearance.

Moderate Interactions (Monitor Closely)

  • Diuretics: may affect renal excretion of memantine.
  • Antihypertensives: monitor blood pressure for additive hypotensive effects.
  • Other psychotropic agents: observe for increased sedation or cognitive changes.

Frequently Asked Questions

Memantine Hydrochloride is prescribed to treat moderate to severe Alzheimer’s disease. It works by modulating glutamate activity in the brain, which helps improve cognition, memory, and daily functioning in patients with significant cognitive decline.

The drug acts as a non‑competitive antagonist of the NMDA receptor. By blocking excessive calcium influx caused by over‑activation of glutamate, it reduces excitotoxic neuronal damage and supports neuronal health, which can slow the progression of Alzheimer’s symptoms.

The specific dose and titration schedule are determined by the prescribing clinician based on the patient’s condition, renal function, and response to therapy. Patients should follow the individualized regimen provided by their healthcare professional.

Safety data for use in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

To request supply, 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.

Memantine belongs to the NMDA receptor antagonist class, whereas cholinesterase inhibitors such as donepezil act by increasing acetylcholine levels. Memantine is typically used in moderate to severe stages and can be combined with cholinesterase inhibitors for additive benefit.

Store the product at ambient temperature, preferably below 25 °C. Keep it in the original container, protect it from moisture and direct sunlight, and ensure the packaging remains sealed until use.

Memantine Hydrochloride is taken orally, usually in tablet form, with or without food as directed by the prescriber. The medication should be swallowed whole with a glass of water and not crushed or chewed unless specifically instructed.

Serious adverse events, though rare, include seizures, severe allergic reactions such as Stevens‑Johnson syndrome, hepatic dysfunction, and cardiac arrhythmias. Patients should seek immediate medical attention if they experience any of these symptoms.

Patients with known hypersensitivity to memantine or any component of the formulation should avoid the drug. Caution is also advised for individuals with severe renal impairment, uncontrolled seizures, or those taking other NMDA antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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