Product image of Metoclopramide Sandoz (Metoclopramide Hydrochloride) supplied by GNH India

Metoclopramide Sandoz

Active Ingredient:
Metoclopramide Hydrochloride
Origin:
EU

Metoclopramide Sandoz (Metoclopramide Hydrochloride)

Metoclopramide hydrochloride, the active ingredient in Metoclopramide Sandoz, is a dopamine antagonist (antiemetic, gastroprokinetic) presented as an oral dosage form for oral use. It treats nausea, vomiting and related gastrointestinal motility disorders in adults.

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

Manufacturer / TM Owner

Sandoz

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Indications & Clinical Uses

Metoclopramide is employed to manage conditions that involve nausea, vomiting and delayed gastric emptying.

  • Nausea and vomiting: reduces the frequency and severity of episodes.
  • Post‑operative nausea and vomiting: prevents or treats nausea after surgery.
  • Gastroparesis: enhances gastric motility and alleviates related symptoms.
  • Gastro‑oesophageal reflux disease (GERD) adjunct: used alongside other agents to improve reflux control.

How It Works

  • Metoclopramide blocks dopamine D2 receptors in the chemoreceptor trigger zone and throughout the gastrointestinal tract, diminishing the neural stimulus for nausea and vomiting. By inhibiting D2 receptors it also increases acetylcholine release, promoting coordinated gastric contractions and accelerating gastric emptying. Weak antagonism of 5‑HT3 receptors adds to its antiemetic effect.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Fatigue: reduced energy and increased tiredness.
  • Restlessness: an uneasy feeling or inability to stay still.
  • Diarrhea: loose, frequent stools.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: dystonia, akathisia, or other movement disorders.
  • Tardive dyskinesia: potentially irreversible involuntary movements with long‑term use.
  • Neuroleptic malignant syndrome: rare but life‑threatening reaction with fever and muscle rigidity.
  • Hyperprolactinemia: elevated prolactin causing galactorrhea or menstrual disturbances.

Precautions & Warnings

When prescribing Metoclopramide, clinicians should consider several safety measures.

  • Assess neurological status: monitor for extrapyramidal symptoms, especially in the elderly.
  • Limit duration: avoid use beyond 12 days to reduce risk of tardive dyskinesia.
  • Use caution in renal impairment: dose adjustment may be required.
  • Avoid in patients with known hypersensitivity to metoclopramide.
  • Pregnancy and lactation: use only if benefits outweigh risks, as safety data are limited.
  • Store at ambient temperature: keep below 25 °C, protect from moisture and light, retain in original packaging.

Avoid Interactions

Metoclopramide can interact with other medicines, requiring attention to avoid adverse outcomes.

Major Interactions (Avoid)

  • Anticholinergic agents: may diminish the prokinetic effect.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase metoclopramide plasma concentrations.
  • Other dopamine antagonists (e.g., phenothiazines): additive risk of extrapyramidal symptoms.

Moderate Interactions (Monitor Closely)

  • Opioids: may enhance constipation and sedation.
  • Serotonergic agents (e.g., ondansetron): potential additive antiemetic effect but increased risk of serotonin syndrome.

Frequently Asked Questions

Metoclopramide Sandoz is prescribed to treat nausea and vomiting of various origins, to prevent post‑operative nausea and vomiting, to improve gastric emptying in gastroparesis, and as an adjunct therapy for gastro‑oesophageal reflux disease when additional pro‑kinetic support is needed.

The drug blocks dopamine D2 receptors in the chemoreceptor trigger zone and throughout the gastrointestinal tract, which reduces the neural drive for nausea and vomiting. It also enhances acetylcholine release, promoting coordinated stomach contractions and faster gastric emptying, while weakly antagonising 5‑HT3 receptors.

The dose of Metoclopramide is determined by the prescribing clinician based on the specific indication, patient age, weight, renal function and severity of symptoms. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Metoclopramide in pregnancy and lactation are limited. It should be used only when the potential benefit justifies any possible risk to the fetus or infant, and always under the guidance of a qualified healthcare professional.

To place an 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.

Metoclopramide is a dopamine antagonist, whereas agents such as ondansetron are 5‑HT3 antagonists. Metoclopramide also has pro‑kinetic activity that promotes gastric motility, a property not shared by many pure antiemetics. Choice of therapy depends on the underlying cause of nausea, patient tolerance and risk‑benefit considerations.

Metoclopramide tablets should be stored at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct light, and ensure the container is tightly closed to maintain stability.

Metoclopramide is taken orally. Swallow the tablet whole with a glass of water. It may be taken with or without food, but patients should follow any specific instructions from their prescriber regarding timing relative to meals.

Serious adverse effects include extrapyramidal symptoms such as dystonia or akathisia, tardive dyskinesia with long‑term use, neuroleptic malignant syndrome, and hyperprolactinemia leading to galactorrhea or menstrual disturbances. Patients should be monitored closely for these reactions, especially during prolonged therapy.

Metoclopramide is contraindicated in individuals with known hypersensitivity to the drug, those with pheochromocytoma, seizure disorders, severe depression, or a history of extrapyramidal reactions. It should also be avoided in patients taking other dopamine antagonists unless specifically directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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