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

Memantina Flas Combix

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantina Flas Combix (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantina Flas Combix, is a NMDA receptor antagonist presented as an oral formulation for oral use. It is indicated for the treatment of moderate to severe Alzheimer’s disease in adults.
GNH India supplies Memantina Flas Combix as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Laboratorios Combix, S.L.U.

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Indications & Clinical Uses

  • Memantina Flas Combix is a NMDA receptor antagonist used in the management of Alzheimer’s disease.
  • Alzheimer’s disease (moderate to severe): improves cognition and functional abilities in patients with moderate to severe disease.

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 glutamate over‑activation, thereby reducing excitotoxic neuronal injury that contributes to cognitive decline in Alzheimer’s disease.

Side Effects

Memantina Flas Combix may be associated with several adverse reactions.

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, typically reversible.
  • Hypertension: modest increase in blood pressure in some patients.
  • Somnolence: mild sleepiness, may improve over time.

Serious or Rare Side Effects

  • Seizures: rare occurrence, requires immediate medical attention.
  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Hallucinations or psychosis: uncommon but serious neuropsychiatric events.
  • Cardiac arrhythmias: irregular heart rhythms in susceptible individuals.
  • Suicidal thoughts: rare but necessitates prompt evaluation.
  • Stevens‑Johnson syndrome: severe skin reaction, requires discontinuation.

Precautions & Warnings

  • When prescribing Memantina Flas Combix, clinicians should consider several safety aspects.
  • Renal impairment: adjust dose or monitor renal function closely.
  • Hepatic impairment: use with caution and monitor liver enzymes.
  • History of seizures: monitor for increased seizure activity.
  • Concomitant NMDA agonists: avoid combined use to prevent antagonistic effects.
  • Pregnancy and lactation: safety not established; weigh benefits against potential risks.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Memantina Flas Combix can interact with other medicines, requiring careful management.

Major Interactions (Avoid)

  • Amantadine: additive neurotoxic risk, may exacerbate CNS side effects.
  • Other NMDA antagonists: combined effect can increase toxicity.
  • Strong CYP450 inhibitors (e.g., ketoconazole): may raise memantine plasma levels.

Moderate Interactions (Monitor Closely)

  • Anticholinesterase inhibitors (e.g., donepezil): may reduce overall efficacy.
  • Diuretics: potential for increased hypotension.
  • Antihypertensive agents: monitor blood pressure for additive lowering effect.

Frequently Asked Questions

Memantina Flas Combix contains memantine hydrochloride and is prescribed for the symptomatic treatment of moderate to severe Alzheimer’s disease. It helps improve cognition, daily functioning, and overall quality of life in patients with this form of dementia.

Memantine acts as a non‑competitive antagonist at NMDA receptors, blocking excessive calcium entry caused by glutamate over‑activation. This reduces excitotoxic neuronal damage, which is thought to contribute to the cognitive decline seen in Alzheimer’s disease.

The dosage of Memantina Flas Combix is individualized by the prescribing clinician based on the patient’s condition, renal function, and tolerability. Patients should follow the specific dosing instructions provided by their healthcare professional.

Safety data for memantine in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under close medical supervision.

To request Memantina Flas Combix, 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 cholinesterase inhibitors such as donepezil. While cholinesterase inhibitors increase acetylcholine levels, memantine reduces glutamate‑mediated excitotoxicity. Both classes may be used together for additive benefit, but they act via distinct mechanisms.

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

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

Serious risks include seizures, severe allergic reactions such as anaphylaxis, hallucinations or psychosis, cardiac arrhythmias, and rare skin conditions like Stevens‑Johnson syndrome. Patients should seek immediate medical attention if any of these symptoms occur.

Memantina Flas Combix is contraindicated in patients with known hypersensitivity to memantine or any of its excipients. Caution is advised for individuals with severe renal impairment, uncontrolled hypertension, or a history of seizures, and it should be avoided in pregnancy unless clearly justified.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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