Product image of Nabila (Memantine) supplied by GNH India

Nabila

Active Ingredient:
Memantine
Origin:
EU

Nabila (Memantine)

Memantine, the active ingredient in Nabila, is a NMDA receptor antagonist presented as an oral tablet for oral use. It is used to treat cognitive decline in patients with moderate to severe Alzheimer’s disease. The medication is indicated for patients diagnosed with Alzheimer’s disease who require symptomatic improvement of memory, reasoning and functional abilities.

GNH India supplies Nabila as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. Our supply chain adheres to stringent quality standards, ensuring product integrity from manufacturing to delivery.

Manufacturer / TM Owner

Exeltis Healthcare S.L

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Indications & Clinical Uses

  • Memantine is used in the management of Alzheimer’s disease, targeting the glutamatergic pathway to improve cognitive function.
  • Alzheimer’s disease (moderate to severe): improves cognition, memory and daily functioning in patients with advanced disease.
  • Alzheimer’s disease (mild to moderate) as adjunct therapy: may provide additional benefit when combined with cholinesterase inhibitors.
  • Behavioral symptoms of Alzheimer’s disease: can help reduce agitation and improve overall patient behavior.

How It Works

  • Memantine 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 prolonged glutamate activation, thereby reducing excitotoxic neuronal injury. This modulation of glutamatergic neurotransmission helps preserve neuronal function and slows the progression of cognitive decline in Alzheimer’s disease. The drug’s voltage‑dependent blocking properties allow normal synaptic activity while preventing pathological over‑stimulation.

Side Effects

Memantine may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness: sensation of light‑headedness or imbalance.
  • Headache: mild to moderate pain in the head.
  • Constipation: reduced bowel movements or hard stools.

Serious or Rare Side Effects

  • Seizures: convulsive episodes requiring immediate medical attention.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Hallucinations: visual or auditory disturbances.

Precautions & Warnings

When prescribing Memantine, clinicians should consider several precautionary measures to ensure patient safety.

  • Renal impairment: dose adjustment may be required in patients with reduced kidney function.
  • Hepatic disease: monitor liver function as metabolism may be affected.
  • Concomitant use with NMDA antagonists: avoid additive neuro‑psychiatric effects.
  • History of seizures: use with caution and monitor for seizure activity.
  • Psychiatric disorders: assess for worsening depression or psychosis.
  • Store at ambient temperature: keep in original packaging, protect from moisture and heat.

Avoid Interactions

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

Major Interactions (Avoid)

  • Amantadine: combined NMDA antagonism may increase neuro‑psychiatric side effects.
  • Ketamine: additive NMDA blockade can lead to excessive sedation or cognitive impairment.

Moderate Interactions (Monitor Closely)

  • Anticholinesterase inhibitors (e.g., donepezil): monitor for altered cognitive response.
  • Diuretics (e.g., furosemide): may increase risk of renal dysfunction.
  • CNS depressants (e.g., benzodiazepines): may enhance sedation.
  • Anticonvulsants (e.g., carbamazepine): may affect memantine plasma levels.

Frequently Asked Questions

Nabila contains memantine and is prescribed for the symptomatic treatment of cognitive decline in patients with moderate to severe Alzheimer’s disease. It helps improve memory, reasoning, and daily functional abilities by modulating glutamatergic activity in the brain.

Memantine is a non‑competitive NMDA‑receptor antagonist. It blocks excessive calcium entry through the NMDA‑associated ion channel, reducing glutamate‑induced excitotoxicity and helping preserve neuronal function, which can slow cognitive deterioration in Alzheimer’s disease.

The dosage of Nabila is determined individually by the prescribing healthcare professional based on the patient’s clinical condition, renal function, and response to therapy. No fixed regimen is provided here; the prescriber sets the appropriate dose.

Safety data for memantine during pregnancy and lactation are limited. It should only be used when the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the treating physician.

To request Nabila, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.

The primary alternative class for Alzheimer’s disease is acetylcholinesterase inhibitors such as donepezil. While those agents enhance cholinergic transmission, memantine works by reducing excitotoxic glutamate activity. Both may be used together for complementary effects, but their mechanisms and side‑effect profiles differ.

Nabila should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and excessive heat to maintain its stability and potency throughout its shelf life.

Nabila is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed unless specifically instructed by a healthcare professional.

Serious adverse reactions include seizures, severe allergic responses (such as rash, swelling, or breathing difficulty), and hallucinations. Patients should seek immediate medical attention if any of these events occur.

Nabila is contraindicated in individuals with known hypersensitivity to memantine or any of its excipients, and it should be used with caution or avoided in patients with severe renal impairment or uncontrolled psychiatric disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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