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

Levorol

Active Ingredient:
Levomepromazine Maleate
Origin:
EU

Levorol (Levomepromazine Maleate)

Levomepromazine, the active ingredient in Levorol, is a phenothiazine presented as an oral tablet for oral use. It is employed in the management of schizophrenia, severe agitation, nausea and vomiting, and as a sedative in palliative‑care settings for adult patients.

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

Manufacturer / TM Owner

Galvany Pharma Limited

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Indications & Clinical Uses

Levorol (levomepromazine) acts on dopaminergic pathways and is indicated for several psychiatric and supportive‑care conditions.

  • Schizophrenia: helps control psychotic symptoms such as delusions and hallucinations.
  • Severe agitation: calms acute behavioral disturbances when rapid sedation is required.
  • Nausea and vomiting: reduces emesis associated with chemotherapy, postoperative states, or other causes.
  • Palliative care: provides symptom control for pain, anxiety, and distress in terminal illness.

How It Works

  • Levomepromazine antagonizes dopamine D2 receptors while also blocking histamine H1, muscarinic, and alpha‑adrenergic receptors. This multi‑receptor profile reduces dopaminergic neurotransmission, produces sedation, and diminishes nausea, contributing to its antipsychotic, antiemetic, and tranquilizing effects.

Side Effects

Levomepromazine may cause a range of adverse reactions that vary in frequency and severity.

Common Side Effects

  • Drowsiness: excessive sleepiness or fatigue.
  • Dry mouth: reduced salivation leading to discomfort.
  • Constipation: slowed gastrointestinal motility.
  • Orthostatic hypotension: drop in blood pressure upon standing.
  • Blurred vision: temporary visual disturbances.
  • Weight gain: increase in body weight over time.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Severe hypotension: marked drop in blood pressure causing dizziness or fainting.
  • Cardiac arrhythmia: irregular heart rhythm, especially in patients with pre‑existing heart disease.
  • Agranulocytosis: dangerous drop in white blood cells.
  • Seizures: occurrence of convulsive episodes.
  • Tardive dyskinesia: persistent involuntary movements after prolonged use.

Precautions & Warnings

When prescribing levomepromazine, clinicians should observe several safety measures.

  • Blood pressure monitoring: check for orthostatic hypotension, especially after dose changes.
  • Cardiac assessment: evaluate for QT prolongation or existing arrhythmias.
  • Extrapyramidal vigilance: watch for signs of movement disorders.
  • Elderly caution: start low and increase slowly to reduce sedation and falls.
  • Discontinuation: avoid abrupt cessation to prevent withdrawal phenomena.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Levomepromazine can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • CNS depressants: may intensify sedation and respiratory depression.
  • Anticholinergic agents: increase risk of severe anticholinergic toxicity.
  • Antihypertensives: additive hypotensive effect.
  • Other dopamine antagonists: enhance extrapyramidal symptoms.
  • MAO inhibitors: risk of hypertensive crisis.

Moderate Interactions (Monitor Closely)

  • CYP450 inhibitors/inducers: may change levomepromazine plasma levels.
  • Alcohol: potentiates central nervous system depression.
  • Antihistamines: increase sedation.
  • SSRIs: monitor for serotonin syndrome.
  • Antiepileptics: may affect seizure threshold.

Frequently Asked Questions

Levorol contains levomepromazine, which is prescribed for schizophrenia, severe agitation, nausea and vomiting, and as a sedative in palliative‑care settings to help control pain, anxiety, and distress in adult patients.

Levomepromazine blocks dopamine D2 receptors and also antagonizes histamine H1, muscarinic, and alpha‑adrenergic receptors. This combined action reduces psychotic symptoms, produces sedation, and diminishes nausea by interfering with multiple neurotransmitter pathways.

The appropriate dose of Levorol is determined by the prescribing clinician based on the patient’s condition, age, response, and tolerability. Dosage regimens vary and should follow the prescriber’s instructions.

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

To request Levorol, 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.

Levorol (levomepromazine) is a typical phenothiazine antipsychotic, differing from atypical agents by its stronger dopamine D2 blockade and broader receptor profile. It often provides more pronounced sedation and antiemetic effects, but may carry a higher risk of extrapyramidal symptoms and anticholinergic side effects.

Levorol should be stored at room temperature, below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight, and excessive heat to maintain product stability.

Levorol is administered orally, typically as a tablet swallowed with water. The exact dosing schedule and whether it is taken with or without food should follow the prescriber’s directions.

Serious risks include neuroleptic malignant syndrome, severe hypotension, cardiac arrhythmias, agranulocytosis, seizures, and tardive dyskinesia. Patients should be monitored closely for any signs of these conditions, and treatment should be discontinued immediately if they occur.

Levorol is contraindicated in patients with known hypersensitivity to levomepromazine or other phenothiazines, those with severe cardiovascular disease prone to arrhythmias, and individuals with a history of neuroleptic malignant syndrome. Caution is also advised for patients with glaucoma, urinary retention, or severe liver impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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