Product image of Metopimazine Sans Sucre,édulcoré À L’aspartam Medipha (Metopimazine) supplied by GNH India

Metopimazine Sans Sucre,édulcoré À L’aspartam Medipha

Active Ingredient:
Metopimazine
Origin:
EU

Metopimazine Sans Sucre,édulcoré À L’aspartam Medipha (Metopimazine)

Metopimazine, the active ingredient in Metopimazine Sans Sucre, édulcoré À L’aspartam Medipha, is a phenothiazine antiemetic presented as an oral tablet for systemic use. It is employed to control nausea and vomiting, including post‑operative and chemotherapy‑induced episodes, and improves overall comfort during treatment.

GNH India supplies Metopimazine Sans Sucre, édulcoré À L’aspartam Medipha as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide with a focus on quality assurance and regulatory compliance and timely delivery.

Manufacturer / TM Owner

Medipha Sante

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Indications & Clinical Uses

Metopimazine is a phenothiazine antiemetic that acts on the chemoreceptor trigger zone to reduce nausea and vomiting.

  • Nausea and vomiting: Provides symptomatic relief of acute and chronic nausea and vomiting in adult patients.
  • Post‑operative nausea: Reduces incidence and severity of nausea following surgical procedures.
  • Chemotherapy‑induced nausea: Controls nausea and vomiting associated with cytotoxic chemotherapy.

How It Works

  • Metopimazine exerts its antiemetic effect primarily by antagonizing dopamine D2 receptors in the chemoreceptor trigger zone of the medulla. By blocking dopaminergic stimulation, it diminishes the neural signals that trigger the vomiting reflex, thereby reducing nausea and vomiting associated with various stimuli. It may also exhibit weak antagonism at histamine H1 and muscarinic receptors, contributing modestly to its overall anti‑emetic profile without significant antihistaminic effects.

Side Effects

Metopimazine may cause a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Drowsiness: Feeling of sleepiness or reduced alertness.
  • Dry mouth: Reduced salivation leading to a dry oral cavity.
  • Constipation: Decreased bowel movements or difficulty passing stool.
  • Dizziness: Light‑headed sensation, especially when standing quickly.
  • Blurred vision: Temporary visual disturbance.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: Involuntary muscle movements or rigidity.
  • Neuroleptic malignant syndrome: Rare life‑threatening reaction with fever and muscle rigidity.
  • Cardiac arrhythmias: Abnormal heart rhythm, potentially serious.
  • Severe hypotension: Marked drop in blood pressure causing faintness.

Precautions & Warnings

When prescribing Metopimazine, clinicians should consider several safety precautions.

  • Assess patient history: Review for prior extrapyramidal reactions or Parkinsonian symptoms.
  • Monitor cardiovascular status: Observe for hypotension or arrhythmias, especially in patients with cardiac disease.
  • Caution in the elderly: Increased sensitivity to sedation and anticholinergic effects.
  • Avoid concurrent CNS depressants: Limit use with alcohol, opioids, or other sedatives.
  • Pregnancy and lactation: Use only if the potential benefit outweighs the risk, as safety data are limited.
  • Store at ambient temperature: Keep below 25 °C in the original packaging, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Antipsychotics: Combined dopamine antagonism may increase extrapyramidal risk.
  • QT‑prolonging agents: Additive effect on cardiac repolarization, raising arrhythmia risk.

Moderate Interactions (Monitor Closely)

  • CNS depressants: Enhanced sedation when used with alcohol, opioids, or benzodiazepines.
  • Anticholinergic drugs: May worsen dry mouth and constipation.
  • MAO inhibitors: Potential for hypertensive reactions; avoid concurrent use.
  • CYP2D6 substrates: Metopimazine may inhibit metabolism, requiring dose adjustment of affected drugs.

Frequently Asked Questions

Metopimazine Sans Sucre is an oral antiemetic indicated for the treatment of nausea and vomiting, including post‑operative nausea and chemotherapy‑induced nausea, in adult patients. It works by blocking dopamine receptors in the brain area that triggers the vomiting reflex.

Metopimazine acts as a dopamine D2 receptor antagonist in the chemoreceptor trigger zone of the medulla. By inhibiting dopaminergic stimulation, it reduces the neural signals that initiate the vomiting reflex, thereby alleviating nausea and vomiting associated with various triggers.

The dosage of Metopimazine is determined by the prescribing clinician based on the patient’s condition, severity of symptoms, and individual response. Healthcare professionals set the appropriate strength, frequency, and duration according to current clinical guidelines and the product label.

Safety data for Metopimazine in pregnancy and lactation are limited. It should be used only if the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

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.

Metopimazine belongs to the phenothiazine class, whereas many alternatives such as ondansetron are serotonin 5‑HT3 antagonists. Phenothiazines primarily block dopamine receptors, which can be advantageous for certain types of nausea, but they may have a different side‑effect profile compared with serotonergic agents.

Metopimazine Sans Sucre should be stored at ambient temperature, below 25 °C, in its original packaging. The container should be kept away from moisture and direct sunlight to maintain product stability throughout its shelf life.

Metopimazine is administered orally as a tablet. The patient should swallow the tablet whole with water, unless otherwise directed by a healthcare professional. It is typically taken with or without food, following the prescriber’s instructions.

Serious risks include extrapyramidal symptoms such as dystonia or Parkinson‑like movements, neuroleptic malignant syndrome, severe hypotension, and cardiac arrhythmias. Patients should be monitored for these reactions, and any signs of severe adverse effects require immediate medical attention.

Metopimazine is contraindicated in patients with known hypersensitivity to 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 Parkinson’s disease or significant hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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