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

Memantina Stada

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Stada (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantina Stada, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is indicated for the treatment of moderate to severe Alzheimer’s disease in adult patients.

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

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Memantina Stada is a NMDA‑receptor antagonist used in the management of Alzheimer’s disease and related cognitive disorders.

  • Moderate to severe Alzheimer’s disease: improves cognition and daily functioning.
  • Mild‑to‑moderate Alzheimer’s disease (off‑label): may provide modest cognitive benefit.
  • Behavioral disturbances in Alzheimer’s disease: may reduce agitation and aggression.

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 overstimulation, thereby reducing excitotoxic neuronal injury while preserving normal synaptic transmission essential for learning and memory.

Side Effects

Memantina Stada 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.
  • Constipation: reduced bowel movements, manageable with diet.
  • Confusion: occasional disorientation.
  • Fatigue: feeling unusually tired.
  • Hypertension: modest increase in blood pressure.

Serious or Rare Side Effects

  • Stevens‑Johnson syndrome: severe skin reaction requiring immediate medical attention.
  • Seizures: rare occurrence, monitor patients with seizure history.
  • Hepatic failure: signs of liver dysfunction.
  • Cardiac arrhythmia: irregular heartbeat.
  • Suicidal thoughts: emergent psychiatric symptoms.
  • Severe allergic reaction: anaphylaxis, airway compromise.

Precautions & Warnings

Before initiating Memantina Stada, clinicians should consider several safety factors.

  • Renal impairment: dose adjustment may be required.
  • History of seizures: monitor closely for breakthrough events.
  • Cardiovascular disease: observe blood pressure and heart rate.
  • Concurrent use with other NMDA antagonists: avoid combined therapy.
  • Pregnancy: safety unknown; use only if benefits outweigh risks.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantina Stada can interact with other medicines, influencing efficacy or safety.

Major Interactions (Avoid)

  • Amantadine: additive NMDA antagonism may increase neurotoxicity.
  • Other NMDA antagonists (e.g., ketamine): combined effect can lead to excessive blockade.
  • Strong CYP450 inhibitors (e.g., ketoconazole): may raise memantine plasma levels.

Moderate Interactions (Monitor Closely)

  • Diuretics: may potentiate hypotensive effects.
  • Antihypertensive agents: additive blood‑pressure lowering.
  • Anticholinergic drugs: may diminish cognitive benefit of memantine.

Frequently Asked Questions

Memantina Stada contains memantine hydrochloride, which is prescribed for the symptomatic treatment of moderate to severe Alzheimer’s disease. It helps improve cognition, memory, and daily functional abilities in adults diagnosed with this form of dementia.

Memantine acts as a non‑competitive antagonist at NMDA receptors. By blocking excessive calcium entry caused by overstimulation, it reduces excitotoxic neuronal damage while allowing normal synaptic activity, supporting cognitive function in Alzheimer’s patients.

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

The safety of memantine during pregnancy and lactation has not been established. It should be used only if the potential benefit justifies any 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 symptoms, memantine is typically used in moderate to severe stages and may be combined with an acetylcholinesterase inhibitor for additive benefit.

Memantina Stada should be stored at room temperature, below 25 °C, in its original packaging. Keep the product away from moisture, direct sunlight, and excessive heat to maintain stability.

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

Serious risks include rare but severe skin reactions such as Stevens‑Johnson syndrome, seizures, hepatic dysfunction, cardiac arrhythmias, and emergent psychiatric symptoms like suicidal thoughts. Patients should seek immediate medical attention if any of these occur.

Memantina Stada is contraindicated in patients with known hypersensitivity to memantine or any excipients, and it should be avoided in individuals taking other NMDA antagonists or those with uncontrolled severe renal impairment without dose adjustment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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