Product image of Levomepromazin Neuraxpharm (Levomepromazine Maleate) supplied by GNH India

Levomepromazin Neuraxpharm

Active Ingredient:
Levomepromazine Maleate
Origin:
EU

Levomepromazin Neuraxpharm (Levomepromazine Maleate)

Levomepromazine maleate, the active ingredient in Levomepromazin Neuraxpharm, is a phenothiazine antipsychotic presented as an oral formulation for oral use. It is employed to treat schizophrenia, other psychotic disorders, severe agitation, nausea and vomiting, and to aid pain management in palliative care settings.

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

Manufacturer / TM Owner

Neuraxpharm Arzneimittel Gmbh

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Indications & Clinical Uses

Levomepromazine acts on dopaminergic and other neurotransmitter pathways to manage several psychiatric and supportive care conditions.

  • Schizophrenia: helps control delusions, hallucinations and thought disorder.
  • Psychotic disorders: reduces acute psychotic symptoms and stabilises mood.
  • Severe agitation: calms extreme restlessness and aggressive behaviour.
  • Nausea and vomiting: alleviates refractory nausea when other treatments fail.
  • Pain management in palliative care: provides analgesic and sedative effects for severe cancer‑related pain.

How It Works

  • Levomepromazine maleate exerts its therapeutic effect primarily as a dopamine D2 receptor antagonist, decreasing dopaminergic neurotransmission in the central nervous system. It also blocks histamine H1, muscarinic acetylcholine, and alpha‑adrenergic receptors, contributing to its antihistaminic, anticholinergic, and vasodilatory properties, which together modulate mood, perception, and autonomic functions.

Side Effects

Levomepromazin Neuraxpharm may cause a range of adverse reactions, some of which are more frequently observed than others.

Common Side Effects

  • Sedation: drowsiness or reduced alertness.
  • Dry mouth: decreased salivation leading to discomfort.
  • Constipation: slowed gastrointestinal motility.
  • Orthostatic hypotension: dizziness on standing due to blood pressure drop.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Tardive dyskinesia: persistent involuntary movements of the face or limbs.
  • Agranulocytosis: severe reduction in white blood cells increasing infection risk.

Precautions & Warnings

When prescribing Levomepromazin Neuraxpharm, clinicians should observe several safety measures.

  • Monitor blood pressure: watch for hypotension, especially after dose initiation.
  • Assess extrapyramidal symptoms: check for early signs of movement disorders.
  • Evaluate liver function: adjust use in hepatic impairment.
  • Use caution in elderly patients: increased sensitivity to sedation and anticholinergic effects.
  • Avoid abrupt discontinuation: taper to reduce withdrawal or rebound symptoms.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Levomepromazin Neuraxpharm can interact with other medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • CNS depressants (e.g., benzodiazepines, opioids): may enhance sedation and respiratory depression.
  • Antihypertensive agents: additive hypotensive effect.
  • Anticholinergic drugs: increase risk of severe anticholinergic toxicity.

Moderate Interactions (Monitor Closely)

  • CYP1A2 inhibitors (e.g., fluvoxamine): may raise levomepromazine plasma levels.
  • Certain antidepressants (e.g., SSRIs): potential for serotonin syndrome.
  • Lithium: may potentiate neurotoxic effects, requiring serum level monitoring.

Frequently Asked Questions

Levomepromazin Neuraxpharm is indicated for the treatment of schizophrenia and other psychotic disorders, management of severe agitation, control of refractory nausea and vomiting, and as part of pain management in palliative care, particularly for cancer‑related pain.

Levomepromazine maleate works by blocking dopamine D2 receptors, reducing dopaminergic activity in the brain. It also antagonises histamine H1, muscarinic acetylcholine, and alpha‑adrenergic receptors, which together produce antipsychotic, anti‑nausea, sedative, and analgesic effects.

The appropriate dose of Levomepromazin Neuraxpharm is determined by the prescribing clinician based on the individual patient's condition, severity, age, and response to therapy. Dosage adjustments are made according to clinical judgment and monitoring.

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

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.

Levomepromazin belongs to the phenothiazine class, offering strong dopamine antagonism along with antihistaminic and anticholinergic properties. Compared with newer atypical antipsychotics, it may have a higher incidence of sedation and anticholinergic effects but can be useful for severe agitation and palliative‑care pain where its sedative qualities are advantageous.

Store Levomepromazin Neuraxpharm at room temperature, below 25 °C, in the original packaging. Keep the product away from moisture, direct sunlight, and sources of heat to maintain its stability.

Levomepromazin Neuraxpharm is administered orally. The tablet or oral formulation should be swallowed with water, and dosing frequency is determined by the prescriber based on therapeutic response and tolerability.

Serious risks include neuroleptic malignant syndrome, tardive dyskinesia, severe hypotension, and agranulocytosis. Patients should be monitored closely for signs of these conditions, and any concerning symptoms should prompt immediate medical evaluation.

Levomepromazin Neuraxpharm should be avoided in patients with known hypersensitivity to levomepromazine or other phenothiazines, in those with severe cardiovascular disease prone to hypotension, and in individuals with a history of neuroleptic malignant syndrome or severe bone‑marrow suppression.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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