Product image of Metoclopramide Accord-Uk (Metoclopramide Hydrochloride) supplied by GNH India

Metoclopramide Accord-Uk

Active Ingredient:
Metoclopramide Hydrochloride
Origin:
EU

Metoclopramide Accord-Uk (Metoclopramide Hydrochloride)

Metoclopramide, the active ingredient in Metoclopramide Accord-Uk, is a dopamine antagonist (antiemetic) presented as an oral dosage form for systemic use. It is employed to relieve nausea and vomiting, improve gastric emptying in gastroparesis, and aid in the management of gastro‑oesophageal reflux disease and chemotherapy‑induced nausea.

GNH India supplies Metoclopramide Accord-Uk as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Accord-Uk Limited

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Indications & Clinical Uses

  • Metoclopramide is used to treat conditions affecting the gastrointestinal tract and nausea pathways.
  • Nausea and vomiting: reduces the frequency and severity of acute and delayed episodes.
  • Gastroparesis: accelerates gastric emptying and improves digestive symptoms.
  • Gastro‑oesophageal reflux disease (GERD): enhances lower esophageal sphincter tone to reduce reflux.
  • Chemotherapy‑induced nausea: prevents and controls nausea associated with anticancer treatment.

How It Works

  • Metoclopramide acts as a selective dopamine D2 receptor antagonist, blocking dopamine‑mediated inhibition of gastrointestinal motility. By antagonizing D2 receptors in the chemoreceptor trigger zone, it provides antiemetic effects. The drug also stimulates acetylcholine release in the gut, enhancing gastric emptying, and increases lower esophageal sphincter tone. Additionally, it exhibits modest 5‑HT3 receptor antagonism, contributing to its anti‑nausea activity.

Side Effects

Metoclopramide may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Drowsiness
  • Fatigue
  • Diarrhea
  • Headache

Serious or Rare Side Effects

  • Tardive dyskinesia (involuntary movements)
  • Neuroleptic malignant syndrome (fever, muscle rigidity)
  • Severe allergic reactions (anaphylaxis)

Precautions & Warnings

  • When prescribing Metoclopramide, clinicians should consider several safety measures.
  • Assess renal function: adjust use in patients with severe renal impairment.
  • Avoid in patients with known extrapyramidal disorders: risk of worsening symptoms.
  • Use caution in the elderly: increased susceptibility to central nervous system effects.
  • Monitor for depression or suicidal ideation: discontinue if severe mood changes occur.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Metoclopramide can interact with other medicines, requiring careful assessment.

Major Interactions (Avoid)

  • Antipsychotics (e.g., phenothiazines, haloperidol): may reduce antiemetic efficacy and increase extrapyramidal risk.
  • MAO inhibitors: can potentiate central nervous system effects.
  • CNS depressants (e.g., opioids, benzodiazepines): increase sedation and respiratory depression.

Moderate Interactions (Monitor Closely)

  • Serotonergic agents (e.g., SSRIs, SNRIs): may increase risk of serotonin syndrome.
  • Opioid analgesics: may enhance gastrointestinal side effects.

Frequently Asked Questions

Metoclopramide Accord-Uk is prescribed to manage nausea and vomiting of various origins, to treat gastroparesis by enhancing gastric emptying, to support gastro‑oesophageal reflux disease through increased lower esophageal sphincter tone, and to prevent nausea associated with chemotherapy.

Metoclopramide works by blocking dopamine D2 receptors in the chemoreceptor trigger zone, which reduces the stimulus for nausea. It also stimulates acetylcholine release in the gastrointestinal tract, promoting faster gastric emptying and strengthening the lower esophageal sphincter, while modestly antagonising 5‑HT3 receptors.

The appropriate dose of Metoclopramide Accord-Uk is determined by the prescribing healthcare professional based on the patient’s condition, age, renal function and other clinical factors. Dosage regimens are individualized and should follow the prescriber’s instructions.

Safety data for Metoclopramide 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 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 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.

Metoclopramide differs from many antiemetics by combining dopamine antagonism with pro‑kinetic activity, which can be advantageous for patients with delayed gastric emptying. Other classes, such as 5‑HT3 antagonists, focus solely on nausea pathways and lack the gastrointestinal motility benefits.

Metoclopramide Accord-Uk 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 its stability.

The medication is taken orally, usually with or without food, as directed by the prescriber. Patients should swallow the tablet whole with a glass of water and follow any specific timing instructions provided by their healthcare professional.

Serious risks include the development of tardive dyskinesia, a potentially irreversible movement disorder, neuroleptic malignant syndrome, severe allergic reactions such as anaphylaxis, and significant depression or suicidal thoughts. Prompt medical attention is required if any of these occur.

Metoclopramide should be avoided in patients with known hypersensitivity to the drug, those with a history of extrapyramidal disorders, severe renal impairment without dose adjustment, and individuals taking interacting medications that are contraindicated. A healthcare professional should assess suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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