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

Metoclopramide Accord

Active Ingredient:
Metoclopramide Hydrochloride Anhydrous
Origin:
EU

Metoclopramide Accord (Metoclopramide Hydrochloride Anhydrous)

Metoclopramide, the active ingredient in Metoclopramide Accord, is a dopamine D2 receptor antagonist and gastroprokinetic presented as an oral dosage form for oral use. It is employed to alleviate nausea and vomiting, including that associated with chemotherapy, and to improve gastric motility in conditions such as gastroparesis and gastro‑oesophageal reflux disease.

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

Manufacturer / TM Owner

Accord Healthcare B.V.

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Indications & Clinical Uses

Metoclopramide is used to treat disorders of the gastrointestinal tract and nausea pathways.

  • Nausea and vomiting (including chemotherapy‑induced): reduces the frequency and severity of nausea and vomiting episodes.
  • Gastroparesis: enhances gastric emptying and relieves associated symptoms such as early satiety and bloating.
  • Gastro‑oesophageal reflux disease (GERD): improves lower esophageal sphincter tone and decreases reflux episodes.
  • Post‑operative nausea and vomiting: prevents nausea and vomiting following surgical procedures.

How It Works

  • Metoclopramide exerts its effect by selectively antagonizing dopamine D2 receptors in the chemoreceptor trigger zone and throughout the gastrointestinal tract, which diminishes the emetic signal. Concurrently, it stimulates 5‑HT4 receptors, enhancing acetylcholine release and promoting coordinated gastrointestinal motility. The combined dopaminergic blockade and serotonergic agonism accelerate gastric emptying and increase lower esophageal sphincter pressure, thereby reducing nausea and reflux.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling of sleepiness or reduced alertness.
  • Fatigue: general lack of energy.
  • Restlessness: inner sense of agitation or inability to stay still.
  • Dry mouth: reduced salivation causing throat discomfort.

Serious or Rare Side Effects

  • Extrapyramidal reactions: involuntary muscle movements or dystonia.
  • Tardive dyskinesia: persistent, potentially irreversible facial or limb movements.
  • Neuroleptic malignant syndrome: life‑threatening reaction with fever and muscle rigidity.
  • Severe depression or suicidal thoughts: marked mood changes requiring immediate medical attention.

Precautions & Warnings

Before prescribing Metoclopramide, clinicians should evaluate several safety considerations.

  • Assess renal function: dose adjustment may be needed in impaired clearance.
  • Monitor for extrapyramidal symptoms: watch for muscle rigidity, tremor or abnormal movements.
  • Avoid in patients with known hypersensitivity: discontinue if allergic reactions occur.
  • Use caution in the elderly: increased susceptibility to central nervous system effects.
  • Review concomitant CNS‑active drugs: potential additive sedation or movement disorders.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Metoclopramide can interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid)

  • Antipsychotics (e.g., haloperidol): may counteract each other's effects and increase movement disorders.
  • MAO inhibitors: risk of hypertensive crisis and serotonin syndrome.
  • CYP2D6 inhibitors (e.g., quinidine): increase metoclopramide plasma levels.

Moderate Interactions (Monitor Closely)

  • Opioids: additive central nervous system depression and reduced gastrointestinal motility.
  • SSRIs or SNRIs: heightened risk of serotonin syndrome.

Frequently Asked Questions

Metoclopramide Accord is indicated for the relief of nausea and vomiting, including that caused by chemotherapy, for the management of gastroparesis, for the treatment of gastro‑oesophageal reflux disease, and for the prevention of post‑operative nausea and vomiting. It works by enhancing gastrointestinal motility and blocking central emetic signals.

Metoclopramide reduces nausea by blocking dopamine D2 receptors in the chemoreceptor trigger zone of the brain, which diminishes the emetic signal. At the same time it stimulates serotonin 5‑HT4 receptors in the gut, increasing acetylcholine release and promoting coordinated muscle contractions that speed gastric emptying.

The dose of Metoclopramide Accord is individualized by the prescribing healthcare professional based on the specific indication, patient age, renal function, and overall clinical condition. No fixed dosing regimen is provided here; the prescriber will set the appropriate strength and frequency.

Safety data for metoclopramide in pregnancy and lactation are limited. The drug should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant. Women who are pregnant, planning pregnancy, or breastfeeding should discuss risks with their healthcare provider.

To order Metoclopramide Accord, 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 (including any cold‑chain requirements) and the necessary import documentation.

Metoclopramide differs from agents like ondansetron in its mechanism; it blocks dopamine receptors and stimulates 5‑HT4 receptors, whereas ondansetron is a selective 5‑HT3 antagonist. Metoclopramide also promotes gastric motility, which can be advantageous in gastroparesis, while ondansetron does not have pro‑kinetic activity. Choice of therapy depends on the clinical scenario and patient tolerance.

Metoclopramide Accord should be stored at room temperature, 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 Accord is administered orally. The tablet (or other oral dosage form) is taken with or without food as directed by the prescriber. Patients should follow the exact dosing schedule provided on the prescription label.

The most serious risks include extrapyramidal reactions such as acute dystonia, tardive dyskinesia which may be irreversible, neuroleptic malignant syndrome, severe depression or suicidal ideation, and rare cases of anaphylaxis. Prompt medical attention is required if any of these symptoms appear.

Metoclopramide Accord should be avoided in individuals with known hypersensitivity to metoclopramide or any component of the formulation, in patients with a history of severe extrapyramidal disorders, and in those taking contraindicated medications such as MAO inhibitors. Caution is also advised for patients with significant renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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