Product image of Metoclopramide Crescent Pharma International (Metoclopramide Hydrochloride) supplied by GNH India

Metoclopramide Crescent Pharma International

Active Ingredient:
Metoclopramide Hydrochloride
Origin:
EU

Metoclopramide Crescent Pharma International (Metoclopramide Hydrochloride)

Metoclopramide, the active ingredient in Metoclopramide Crescent Pharma International, is a dopamine antagonist presented as an oral tablet for oral use. It is employed to relieve nausea and vomiting of various origins and to enhance gastric emptying in patients with gastroparesis.

GNH India supplies Metoclopramide Crescent Pharma International as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies, clinics and transplant centres worldwide.

Manufacturer / TM Owner

Crescent Pharma International Limited

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Indications & Clinical Uses

Metoclopramide acts on dopaminergic pathways that trigger nausea and on gastrointestinal motility, making it useful in several emetic and motility disorders.

  • Nausea and vomiting of various origins: reduces the frequency and severity of symptoms.
  • Post‑operative nausea and vomiting: helps prevent and treat nausea after surgery.
  • Chemotherapy‑induced nausea and vomiting: improves patient tolerance to anticancer regimens.
  • Gastroparesis: accelerates gastric emptying and relieves associated discomfort.
  • Gastro‑oesophageal reflux disease (GERD) adjunct: used as an add‑on to improve reflux symptoms when standard therapy is insufficient.

How It Works

  • Metoclopramide competitively antagonises dopamine D2 receptors in the chemoreceptor trigger zone and throughout the gastrointestinal tract, diminishing emetic signalling. It also blocks peripheral 5‑HT3 receptors and enhances acetylcholine release, which together promote coordinated gastric contractions and accelerate gastric emptying, thereby reducing nausea and improving gastrointestinal motility.

Side Effects

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

Common Side Effects

  • Drowsiness: feeling unusually sleepy or fatigued.
  • Restlessness or akathisia: inner sense of agitation.
  • Diarrhoea: loose or frequent stools.
  • Dry mouth: reduced salivary flow.
  • Headache: mild to moderate head pain.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: muscle rigidity, tremor, or dystonia.
  • Tardive dyskinesia: involuntary, repetitive movements with long‑term use.
  • Neuroleptic malignant syndrome: high fever, muscle rigidity, autonomic instability.
  • Severe allergic reactions: rash, swelling, or difficulty breathing.

Precautions & Warnings

Before prescribing Metoclopramide, clinicians should consider several safety aspects.

  • Renal or hepatic impairment: adjust use or monitor closely.
  • History of movement disorders: avoid or use with extreme caution.
  • Elderly patients: increased risk of CNS side effects; monitor closely.
  • Concomitant CNS depressants: may enhance drowsiness or sedation.
  • Pregnancy and breastfeeding: safety not established; weigh benefits against potential risks.
  • Store at ambient temperature: keep below 25 °C, in the original container, protected from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Monoamine oxidase inhibitors (MAOIs): risk of hypertensive crisis.
  • Antipsychotics that block dopamine: may reduce therapeutic effect.
  • CNS depressants (e.g., benzodiazepines, opioids): additive sedation.

Moderate Interactions (Monitor Closely)

  • CYP2D6 substrates (e.g., metoprolol, codeine): possible altered plasma levels.
  • Anticholinergic agents: may diminish pro‑kinetic benefit.
  • Antihistamines: could increase risk of extrapyramidal symptoms.

Frequently Asked Questions

Metoclopramide Crescent Pharma International is indicated for the treatment of nausea and vomiting of various causes, including post‑operative and chemotherapy‑induced nausea, as well as for gastroparesis and as an adjunct in gastro‑oesophageal reflux disease when standard therapy is insufficient.

Metoclopramide works by blocking dopamine D2 receptors in the chemoreceptor trigger zone, reducing the brain’s nausea signals. It also antagonises peripheral 5‑HT3 receptors and enhances acetylcholine release, which together stimulate coordinated gastric contractions and speed gastric emptying.

The appropriate dose of metoclopramide is determined by the prescribing healthcare professional based on the patient’s condition, age, renal and hepatic 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 when the potential benefit justifies any possible risk to the fetus or infant, and the decision must be made by a qualified healthcare provider.

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 and any necessary import documentation.

Metoclopramide differs from many antiemetics by combining dopamine antagonism with pro‑kinetic activity, making it useful for both nausea control and gastric motility. Other classes, such as 5‑HT3 antagonists, primarily block serotonin receptors and lack the gastric emptying benefit.

Metoclopramide Crescent Pharma International should be stored at ambient temperature, below 25 °C. Keep the tablets in the original packaging, protect them from moisture, heat and direct sunlight to maintain potency.

The medication is supplied as oral tablets and is taken by mouth with or without food, as directed by the prescriber. Swallow the tablet whole; do not crush or chew unless specifically instructed.

Serious risks include extrapyramidal symptoms such as dystonia or akathisia, tardive dyskinesia with long‑term use, and rare occurrences of neuroleptic malignant syndrome. Patients should be monitored for any abnormal movements or severe reactions and seek immediate medical attention if they occur.

Metoclopramide is contraindicated in individuals with known hypersensitivity to the drug, those with a history of seizure disorders, and patients with pheochromocytoma. Caution is also advised for patients with severe depression, Parkinson’s disease, or uncontrolled hypertension.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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