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

Memantina Teva

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Teva (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantina, 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, helping to improve cognition and daily functioning.

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Memantina is a NMDA receptor antagonist used in the management of Alzheimer’s disease and its associated symptoms.

  • Moderate Alzheimer’s disease: improves cognition and daily functioning.
  • Severe Alzheimer’s disease: may help maintain basic activities of daily living.
  • Behavioral symptoms of Alzheimer’s disease: can 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, it blocks excessive calcium influx caused by overstimulation with glutamate, thereby reducing excitotoxic neuronal damage and modulating synaptic transmission involved in learning and memory.

Side Effects

Memantina may cause a range of adverse reactions, which are categorized by frequency.

Common Side Effects

  • Dizziness: mild to moderate sensation of light‑headedness.
  • Headache: transient cranial pain.
  • Constipation: reduced bowel movements.
  • Confusion: temporary disorientation.
  • Hypertension: elevated blood pressure readings.
  • Insomnia: difficulty initiating or maintaining sleep.

Serious or Rare Side Effects

  • Severe skin reactions: such as Stevens‑Johnson syndrome.
  • Seizures: new‑onset convulsive episodes.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Hepatic dysfunction: abnormal liver enzyme elevations.
  • Suicidal thoughts: emergence of depressive ideation.
  • Respiratory depression: reduced breathing effort.

Precautions & Warnings

When prescribing Memantina, several safety considerations should be observed.

  • 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 monitor neurologic status.
  • Concurrent use with other NMDA antagonists: avoid additive neurotoxicity.
  • Pregnancy and breastfeeding: safety not established; weigh potential risks and benefits.
  • Store at room temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Memantina can interact with other medicines, requiring attention to the level of interaction.

Major Interactions (Avoid)

  • Amantadine: increased risk of neurotoxicity when combined.
  • Other NMDA antagonists: additive antagonistic effect may lead to excessive inhibition.
  • Strong CYP450 inducers (e.g., carbamazepine): may lower memantine plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Anticholinergic agents: may diminish the cognitive benefits of memantine.
  • Diuretics: can increase the likelihood of hypotension.
  • Antihypertensives: monitor blood pressure for additive lowering effect.

Frequently Asked Questions

Memantina contains memantine hydrochloride and is prescribed for the treatment of moderate to severe Alzheimer’s disease. It helps improve cognitive function and may reduce behavioral symptoms such as agitation in adult patients.

Memantine acts as a non‑competitive antagonist of the NMDA receptor, blocking excessive calcium entry caused by glutamate over‑activation. This reduces excitotoxic neuronal damage and helps preserve synaptic function involved in memory and learning.

The dosage of Memantina is determined by the prescribing clinician based on the patient’s condition, renal function, and tolerance. The prescriber will set the appropriate dose and titration schedule.

Safety of memantine in pregnancy and lactation has not been fully established. Healthcare providers should evaluate the potential benefits against possible risks before prescribing to pregnant or nursing women.

To order Memantina, submit an enquiry on the product page at gnhindia.com with 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.

Memantina belongs to the NMDA receptor antagonist class, differing from acetylcholinesterase inhibitors such as donepezil. While both improve cognition, memantine targets glutamatergic excitotoxicity and is typically used in moderate to severe stages, often in combination with an acetylcholinesterase inhibitor.

Memantina should be stored at room temperature below 25 °C, kept in its original packaging, and protected from moisture and direct sunlight to maintain stability.

Memantina is taken orally, usually as a tablet, with or without food. The exact administration schedule is defined by the prescribing physician.

Serious risks include severe skin reactions, seizures, cardiac arrhythmias, hepatic dysfunction, suicidal thoughts, and respiratory depression. Patients should be monitored for any of these events and seek medical attention promptly if they occur.

Memantina is contraindicated in patients with known hypersensitivity to memantine or any component of the formulation, and it should be used with caution in 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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