Product image of Memantine Ohre Pharma (Memantine Hydrochloride) supplied by GNH India

Memantine Ohre Pharma

Active Ingredient:
Memantine Hydrochloride
Origin:
EU

Memantine Ohre Pharma (Memantine Hydrochloride)

Memantine Hydrochloride, the active ingredient in Memantine Ohre Pharma, 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 adults. The medication works by modulating glutamatergic neurotransmission, helping to reduce excitotoxic neuronal damage associated with disease progression.

GNH India supplies Memantine Ohre Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, clinics and research institutions worldwide, with a focus on quality assurance and regulatory compliance.

Manufacturer / TM Owner

Taw Pharma (Ireland) Ltd

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Indications & Clinical Uses

  • Memantine, an NMDA receptor antagonist, is employed in the therapeutic approach to neurodegenerative conditions, with its principal clinical application being the treatment of Alzheimer’s disease, where it targets glutamate‑mediated excitotoxicity to support neuronal function.
  • Alzheimer’s disease (moderate to severe): improves cognition, functional abilities, and global clinical status in patients with symptomatic disease.
  • Behavioral symptoms in Alzheimer’s disease: may reduce agitation, aggression, and caregiver burden.
  • Dementia due to Alzheimer’s disease: supports activities of daily living and slows functional decline.

How It Works

  • Memantine Hydrochloride acts as a non‑competitive antagonist at the NMDA‑type glutamate receptor. By binding within the receptor‑associated ion channel at moderate affinity and voltage‑dependent manner, it blocks excessive calcium influx caused by prolonged glutamate activation, thereby reducing excitotoxic neuronal injury while preserving normal synaptic transmission. This modulation helps to stabilize neuronal activity without completely inhibiting physiological glutamatergic signaling, which is essential for learning and memory processes.

Side Effects

Memantine may be associated with a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Dizziness: transient sensation of light‑headedness.
  • Headache: mild to moderate intensity.
  • Constipation: reduced bowel movements.
  • Confusion: occasional disorientation.

Serious or Rare Side Effects

  • Severe skin rash (e.g., Stevens‑Johnson syndrome): requires immediate medical attention.
  • Seizures: rare but potentially life‑threatening.
  • Hallucinations or psychosis: may occur in susceptible individuals.
  • Cardiac arrhythmia: irregular heart rhythm requiring evaluation.

Precautions & Warnings

When prescribing Memantine, clinicians should consider several safety aspects.

  • Renal impairment: assess renal function and adjust dose if necessary.
  • Hepatic impairment: use with caution and monitor liver enzymes.
  • History of seizures: monitor closely for increased seizure activity.
  • Concurrent use with other NMDA antagonists: avoid additive neurotoxicity.
  • Psychiatric disorders: observe for worsening of symptoms.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Memantine can interact with other medications, requiring careful management.

Major Interactions (Avoid)

  • Amantadine: increased risk of neurotoxicity.
  • Ketamine: additive NMDA antagonism may enhance CNS effects.
  • Other NMDA antagonists: heightened central nervous system depression.

Moderate Interactions (Monitor Closely)

  • Anticholinergics: may reduce Memantine efficacy.
  • CNS depressants (e.g., benzodiazepines, opioids): enhanced sedation and respiratory depression.
  • Diuretics (e.g., furosemide): may alter plasma concentrations of Memantine.

Frequently Asked Questions

Memantine Ohre Pharma contains memantine hydrochloride, which is prescribed for the treatment of moderate to severe Alzheimer’s disease. It helps improve cognitive function and daily living activities by reducing excitotoxic neuronal damage associated with the disease.

Memantine acts as a non‑competitive antagonist of the NMDA‑type glutamate receptor. By blocking excessive calcium influx through the receptor channel, it reduces excitotoxicity while allowing normal synaptic transmission, thereby protecting neurons from damage.

The dosage of Memantine Ohre Pharma is determined by the prescribing clinician based on the patient’s condition, age, renal function, and other clinical factors. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for memantine during pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against possible risks and discuss alternative options when treating pregnant or nursing individuals.

To order, 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 necessary import documentation.

Memantine belongs to the NMDA receptor antagonist class, differing from acetylcholinesterase inhibitors such as donepezil. While both improve symptoms, memantine targets glutamate‑mediated excitotoxicity, often used in later stages of disease or in combination therapy for broader symptom control.

Store the product at ambient temperature, below 25 °C, in the original packaging. Protect it from moisture, excessive heat and direct sunlight to maintain stability and potency.

Memantine Ohre Pharma is taken orally, usually as a tablet, with or without food. The exact administration schedule should follow the prescriber’s directions, typically once daily after a titration period.

Serious adverse events include severe skin reactions such as Stevens‑Johnson syndrome, seizures, hallucinations, and cardiac arrhythmias. Patients should seek immediate medical attention if any of these symptoms occur.

Memantine is contraindicated in patients with known hypersensitivity to memantine hydrochloride or any excipients, and 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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