Product image of Nozinan (Levomepromazine Maleate) supplied by GNH India

Nozinan

Active Ingredient:
Levomepromazine Maleate
Origin:
EU

Nozinan (Levomepromazine Maleate)

Levomepromazine, the active ingredient in Nozinan, is a phenothiazine presented as a 25 mg tablet for oral use. It is employed in the management of severe agitation, psychotic disorders, and palliative care symptom control in adult patients.

GNH India supplies Nozinan as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Neuraxpharm France

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Indications & Clinical Uses

Levomepromazine is a broad‑spectrum antipsychotic that acts on multiple neurotransmitter pathways, particularly dopamine and serotonin receptors.

  • Severe agitation and psychosis: helps calm acute episodes in adult psychiatric patients.
  • Nausea and vomiting in palliative care: reduces refractory symptoms when other anti‑emetics fail.
  • Painful muscle spasm and terminal delirium: provides sedation and comfort in end‑of‑life settings.

How It Works

  • Levomepromazine blocks dopamine D2 receptors and antagonises several serotonin (5‑HT2), histamine (H1) and muscarinic receptors. This broad receptor blockade reduces dopaminergic neurotransmission, producing antipsychotic, anti‑emetic and sedative effects, while also influencing pain pathways and autonomic tone.

Side Effects

Levomepromazine may cause a range of adverse reactions, from mild to potentially life‑threatening.

Common Side Effects

  • Drowsiness: increased sleepiness or fatigue.
  • Dry mouth: reduced salivation causing discomfort.
  • Orthostatic hypotension: light‑headedness on standing.
  • Constipation: slowed gastrointestinal motility.
  • Blurred vision: temporary visual disturbances.
  • Weight gain: increased appetite and body weight.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: muscle rigidity, tremor or akathisia.
  • Neuroleptic malignant syndrome: high fever, rigidity and autonomic instability.
  • Severe hypotension: sudden drop in blood pressure.
  • Cardiac arrhythmias: irregular heart rhythm, especially QT prolongation.
  • Agranulocytosis: markedly reduced white‑blood‑cell count.
  • Hepatotoxicity: liver enzyme elevation or injury.

Precautions & Warnings

Before initiating Levomepromazine therapy, clinicians should assess patient‑specific risk factors and monitor for adverse events.

  • Cardiovascular assessment: evaluate for pre‑existing hypotension or cardiac disease.
  • Metabolic screening: check liver and renal function prior to treatment.
  • CNS monitoring: observe for excessive sedation or extrapyramidal signs.
  • Drug‑interaction review: avoid concurrent use with other strong dopamine antagonists.
  • Pregnancy and lactation: weigh benefits against potential fetal or neonatal risks.
  • Store at below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Levomepromazine interacts with several drug classes; careful review is essential to minimise adverse outcomes.

Major Interactions (Avoid)

  • Other antipsychotics: additive dopamine blockade increasing extrapyramidal risk.
  • QT‑prolonging agents: combined effect may precipitate serious arrhythmias.
  • CNS depressants (e.g., benzodiazepines, opioids): heightened sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: may amplify orthostatic hypotension.
  • Anticholinergic drugs: increase risk of severe dry mouth and constipation.
  • CYP2D6 inhibitors: can raise levomepromazine plasma levels, requiring dose adjustment.

Frequently Asked Questions

Nozinan, whose active ingredient is levomepromazine, is prescribed for severe agitation and psychosis, refractory nausea and vomiting in palliative care, and for sedation of terminal delirium or painful muscle spasm in end‑of‑life settings. It is used in adult patients when other therapies are insufficient.

Levomepromazine blocks dopamine D2 receptors and antagonises serotonin, histamine and muscarinic receptors. This broad receptor blockade reduces dopaminergic signalling, providing antipsychotic, anti‑emetic and sedative effects while also influencing pain pathways and autonomic tone.

The dose of Nozinan is individualized by the prescribing clinician based on the patient’s condition, severity, age, renal and hepatic function, and response to therapy. Physicians determine the appropriate strength and frequency according to clinical guidelines.

Levomepromazine is classified as a pregnancy‑category C drug in many regions, indicating that risk cannot be ruled out. It should only be used when the potential benefit justifies the potential fetal risk, and it is generally not recommended during breastfeeding because it may pass into milk.

To request Nozinan, 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.

Compared with typical antipsychotics such as haloperidol, levomepromazine has a broader receptor profile, offering stronger anti‑emetic and sedative properties but also a higher likelihood of anticholinergic side effects and orthostatic hypotension. Choice of therapy depends on the clinical situation and tolerability.

Nozinan tablets should be stored at temperatures below 25 °C, in the original packaging, protected from moisture and light. Do not store in areas with high humidity or direct sunlight to maintain product stability.

Nozinan is supplied as oral tablets that are swallowed whole with water. In some clinical settings, tablets may be crushed and mixed with a small amount of liquid for patients who have difficulty swallowing, but this should be done only under medical supervision.

The most serious risks include extrapyramidal symptoms, neuroleptic malignant syndrome, severe hypotension, cardiac arrhythmias (especially QT prolongation), agranulocytosis and significant liver injury. Prompt recognition and medical intervention are essential if these events occur.

Levomepromazine is contraindicated in patients with known hypersensitivity to phenothiazines, those with a history of malignant hyperthermia, and individuals taking other strong dopamine antagonists where additive effects could be dangerous. Caution is also advised for patients with severe cardiac disease, uncontrolled epilepsy or significant hepatic impairment.

Medically reviewed by

Dr. Shweta Ashok More

M.Pharm (Quality Assurance), Ph.D. (Medicinal Chemistry), GNH India Pharmaceuticals Limited · Reviewed 30 Sep 2026

Published by GNH India Pharmaceuticals Limited · Last updated

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