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

Memantinhydrochlorid Puren

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantinhydrochlorid Puren (Memantine Hydrochloride)

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

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

Manufacturer / TM Owner

Puren Pharma Gmbh & Co. Kg

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Indications & Clinical Uses

Memantine Hydrochloride acts on the glutamatergic pathway to modulate neuronal excitotoxicity in neurodegenerative disease.

  • Alzheimer’s disease: improves cognition, daily functioning and behavioral symptoms in patients with moderate to severe disease.

How It Works

  • Memantine Hydrochloride binds to the NMDA (N‑methyl‑D‑aspartate) receptor at a site distinct from the glutamate binding site, acting as a non‑competitive antagonist. By blocking excessive calcium influx during pathological activation, it reduces excitotoxic neuronal injury while preserving normal synaptic transmission, thereby slowing disease‑related neurodegeneration.

Side Effects

Memantine Hydrochloride may cause a range of adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Dizziness: transient light‑headedness, especially at treatment initiation.
  • Headache: mild to moderate intensity, often resolves with continued therapy.
  • Constipation: reduced bowel movements, manageable with diet.
  • Confusion: occasional disorientation, usually improves over time.
  • Fatigue: feeling unusually tired or weak.
  • Hypertension: modest increase in blood pressure.

Serious or Rare Side Effects

  • Seizures: rare but may occur, requiring immediate medical attention.
  • Cardiac arrhythmia: irregular heart rhythm, potentially life‑threatening.
  • Severe allergic reaction: rash, swelling, or anaphylaxis.
  • Hepatic failure: signs of liver dysfunction such as jaundice.
  • Suicidal ideation: emergence of thoughts of self‑harm.
  • Psychosis: new or worsening hallucinations or delusions.

Precautions & Warnings

Before prescribing Memantinhydrochlorid Puren, clinicians should consider several safety factors.

  • Renal impairment: adjust dose or monitor serum levels in patients with reduced kidney function.
  • Hepatic impairment: use with caution in patients with liver disease.
  • History of seizures: evaluate risk and monitor closely.
  • Elderly patients: start at low dose and titrate slowly.
  • Concomitant NMDA antagonists: avoid combined use due to additive effects.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Amantadine: additive NMDA antagonism may increase neurotoxicity.
  • Ketamine: combined NMDA blockade can lead to excessive CNS depression.
  • Other NMDA antagonists: heightened risk of adverse neurological effects.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: may reduce cognitive benefit of memantine.
  • CNS depressants (e.g., benzodiazepines): monitor for increased sedation.
  • Diuretics: may raise serum memantine concentrations; adjust dose if needed.

Frequently Asked Questions

Memantinhydrochlorid Puren contains memantine hydrochloride, which is prescribed to treat moderate to severe Alzheimer’s disease. It works by reducing excitotoxic neuronal damage, helping to preserve cognitive function and daily living abilities in affected patients.

Memantine hydrochloride is a non‑competitive antagonist of the NMDA receptor. By blocking excessive calcium influx during pathological glutamate activation, it limits excitotoxic neuronal injury while allowing normal synaptic transmission, thereby slowing disease progression.

The appropriate dose of memantine is determined by the prescribing clinician based on the patient’s condition, renal function, and tolerability. Dosage regimens may vary, and the prescriber will adjust the amount to achieve the best therapeutic outcome.

The safety of memantine hydrochloride in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies the potential 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 any necessary import documentation.

Memantine belongs to the NMDA receptor antagonist class, differing from acetylcholinesterase inhibitors such as donepezil. While both improve cognition, memantine is typically used in moderate to severe stages and may be combined with an acetylcholinesterase inhibitor for additive benefit.

Store the product at room temperature, below 25 °C, in its original packaging. Protect it from moisture and direct sunlight to maintain stability. No refrigeration is required for this oral formulation.

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

Serious adverse events include seizures, cardiac arrhythmias, severe allergic reactions, hepatic failure, and emergence of suicidal thoughts or psychosis. Patients should be monitored closely for any of these symptoms and seek immediate medical attention if they occur.

Memantine is contraindicated in patients with known hypersensitivity to memantine hydrochloride 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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