Product image of Memantinhydrochlorid Stada (Memantine Hydrochloride) supplied by GNH India

Memantinhydrochlorid Stada

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantinhydrochlorid Stada (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantinhydrochlorid Stada, is a NMDA receptor antagonist presented as an oral dosage form for oral use. It is indicated for the treatment of moderate to severe Alzheimer’s disease in adults.

GNH India supplies Memantinhydrochlorid Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stadapharm Gmbh

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Indications & Clinical Uses

Memantine Hydrochloride acts on the glutamatergic pathway and is used in dementia management.

  • Alzheimer’s disease (moderate to severe): helps maintain cognitive function and daily living activities.
  • Alzheimer’s disease (mild to moderate) as add‑on therapy: provides additional symptomatic benefit when combined with cholinesterase inhibitors.
  • Dementia associated with Parkinson’s disease (off‑label): may improve cognition and motor function.

How It Works

  • Memantine Hydrochloride is a non‑competitive antagonist of 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 chronic glutamate stimulation, thereby reducing excitotoxic neuronal injury while preserving normal synaptic transmission.

Side Effects

Memantine is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Fatigue: feeling of tiredness or lack of energy.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Hallucinations or psychosis: visual or auditory disturbances.
  • Suicidal thoughts: emergence of depressive ideation.

Precautions & Warnings

When prescribing Memantinhydrochlorid Stada, 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.
  • History of seizures: use with caution and observe for increased seizure activity.
  • Concomitant NMDA antagonists: avoid combined use to reduce risk of additive CNS effects.
  • Pregnancy: safety not established; weigh potential benefits against risks.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantine may interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Amantadine: combined use can increase CNS side effects.
  • Ketamine: additive NMDA antagonism may enhance neurotoxicity.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): may raise memantine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • NSAIDs: may increase risk of peripheral edema.
  • Diuretics: monitor electrolyte balance and blood pressure.
  • Anticholinergic agents: can exacerbate confusion or cognitive decline.

Frequently Asked Questions

Memantinhydrochlorid Stada contains memantine hydrochloride, which is prescribed to treat moderate to severe Alzheimer’s disease. It helps improve cognition, memory, and daily functioning by reducing excitotoxic neuronal damage associated with the disease.

Memantine hydrochloride acts as a non‑competitive antagonist at the NMDA receptor. By blocking excessive calcium entry through the receptor’s ion channel, it limits glutamate‑induced excitotoxicity while preserving normal synaptic activity, thereby protecting neurons.

The dosage of Memantinhydrochlorid Stada is determined by the prescribing physician based on the patient’s clinical condition, renal function, and response to therapy. The prescriber sets the appropriate dose and titration schedule.

Safety data for memantine in pregnancy and lactation are limited. The product 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 professional.

To place an 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 necessary import documentation.

Memantine belongs to the NMDA receptor antagonist class, whereas cholinesterase inhibitors (e.g., donepezil) increase acetylcholine levels. Memantine is typically used in moderate to severe stages and may be combined with a cholinesterase inhibitor for additive benefit, offering a different mechanism of action.

Store the product at room temperature, below 25 °C, in its original packaging. Protect it from moisture, excessive heat and direct sunlight to maintain stability and potency throughout its shelf life.

Memantinhydrochlorid Stada is taken orally, usually once daily after a gradual titration period. The tablet should be swallowed whole with water and not crushed or chewed unless otherwise directed by a healthcare professional.

Serious risks include seizures, severe allergic reactions, hallucinations or psychotic symptoms, and suicidal thoughts. Patients should be monitored closely for any new or worsening neuropsychiatric symptoms, and medical attention should be sought immediately if they occur.

Memantinhydrochlorid Stada is contraindicated in patients with known hypersensitivity to memantine or any excipients in the formulation. Caution is advised for individuals with severe renal impairment, uncontrolled epilepsy, or those taking other NMDA antagonists.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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