Product image of Levomepromazine Hydrochloride Wockhardt Uk (Levomepromazine Hydrochloride) supplied by GNH India

Levomepromazine Hydrochloride Wockhardt Uk

Active Ingredient:
Levomepromazine Hydrochloride
Origin:
EU

Levomepromazine Hydrochloride Wockhardt Uk (Levomepromazine Hydrochloride)

Levomepromazine Hydrochloride, the active ingredient in Levomepromazine Hydrochloride Wockhardt Uk, is a phenothiazine presented as an injectable solution for intramuscular, intravenous, and subcutaneous use. It is employed to manage psychotic disorders, severe agitation, nausea, vomiting, and pain in adult patients.
GNH India supplies Levomepromazine Hydrochloride Wockhardt Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Wockhardt Uk Ltd

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Indications & Clinical Uses

Levomepromazine is a phenothiazine antipsychotic used across several clinical pathways.

  • Schizophrenia: helps control psychotic symptoms such as delusions, hallucinations and thought disorder.
  • Severe agitation: calms extreme restlessness and aggressive behavior in acute settings.
  • Nausea and vomiting: reduces chemotherapy‑induced and postoperative emesis.
  • Pain management: provides analgesic benefit as part of multimodal therapy for severe pain.

How It Works

  • Levomepromazine Hydrochloride acts primarily as an antagonist at dopamine D2 receptors, reducing dopaminergic neurotransmission linked to psychosis. It also blocks histamine H1, adrenergic α1, and muscarinic receptors, contributing to its antiemetic, sedative, and analgesic properties while influencing cardiovascular and anticholinergic pathways.

Side Effects

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

Common Side Effects

  • Sedation: drowsiness or excessive sleepiness.
  • Orthostatic hypotension: dizziness upon standing.
  • Anticholinergic effects: dry mouth, blurred vision, constipation.
  • Weight gain: increased appetite leading to weight increase.
  • Extrapyramidal symptoms: mild tremor or rigidity.
  • Nausea: occasional upset stomach.

Serious or Rare Side Effects

  • Neuroleptic malignant syndrome: life‑threatening fever and muscle rigidity.
  • Severe hypotension: marked drop in blood pressure requiring medical attention.
  • Cardiac arrhythmias: irregular heart rhythms.
  • Agranulocytosis: dangerously low white blood cell count.
  • Severe extrapyramidal reactions: acute dystonia or parkinsonism.
  • Seizures: rare occurrence of convulsive episodes.

Precautions & Warnings

When prescribing Levomepromazine, clinicians should consider several safety measures.

  • Dose adjustment in elderly: start low and monitor for excessive sedation or hypotension.
  • Assess cardiovascular status: patients with pre‑existing heart disease may be prone to orthostatic drops.
  • Monitor for extrapyramidal symptoms: report any involuntary movements promptly.
  • Use caution in hepatic impairment: reduced metabolism may increase plasma levels.
  • Avoid abrupt discontinuation: taper gradually to prevent withdrawal phenomena.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of severe hypertension.
  • Anticholinergic drugs: additive anticholinergic burden may worsen dry mouth, constipation, and blurred vision.
  • Central nervous system depressants (e.g., benzodiazepines, opioids): enhanced sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • Antihypertensives: additive hypotensive effect may require dose adjustment.
  • Lithium: increased risk of neurotoxicity.
  • Other antipsychotics: heightened chance of extrapyramidal symptoms and cardiac effects.

Frequently Asked Questions

Levomepromazine Hydrochloride is prescribed for the management of schizophrenia, severe agitation, nausea and vomiting (especially related to chemotherapy or surgery), and as part of multimodal therapy for severe pain. It works across these indications by modulating dopamine, histamine, adrenergic, and muscarinic pathways.

The drug blocks dopamine D2 receptors, reducing psychotic signaling, and also antagonizes histamine H1, adrenergic α1, and muscarinic receptors. This combined activity provides antipsychotic, antiemetic, sedative, and analgesic effects, while influencing blood pressure and anticholinergic responses.

The specific dose of Levomepromazine Hydrochloride is determined by the prescribing clinician based on the patient’s condition, severity, age, and response to therapy. Healthcare professionals tailor the regimen to achieve optimal therapeutic benefit while minimizing adverse effects.

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 a qualified healthcare provider after careful assessment.

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 (including cold‑chain if needed) and import documentation.

Levomepromazine belongs to the phenothiazine class, offering a broader receptor profile than many atypical antipsychotics. It provides additional antiemetic and analgesic benefits, but it may have a higher propensity for anticholinergic and sedative side effects compared with newer agents that have more selective dopamine blockade.

Levomepromazine Hydrochloride should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain stability.

The medication is supplied as an injectable solution and can be given intramuscularly, intravenously, or subcutaneously. The route and rate of administration are determined by the prescriber according to the clinical situation and patient needs.

Serious risks include neuroleptic malignant syndrome, severe hypotension, cardiac arrhythmias, agranulocytosis, and life‑threatening extrapyramidal reactions. Patients should be monitored closely for signs of these conditions, and any concerning symptoms should prompt immediate medical evaluation.

Levomepromazine is contraindicated in patients with known hypersensitivity to phenothiazines, those taking monoamine oxidase inhibitors, and individuals with severe cardiovascular instability where hypotension could be dangerous. Caution is also advised for patients with hepatic impairment or a history of severe extrapyramidal disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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