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

Metoclopramide Ennogen Ip

Active Ingredient:
Metoclopramide Hydrochloride Anhydrous
Origin:
EU

Metoclopramide Ennogen Ip (Metoclopramide Hydrochloride Anhydrous)

Metoclopramide, the active ingredient in Metoclopramide Ennogen Ip, is a dopamine antagonist presented as an intravenous solution for IV use. It is employed to treat nausea, vomiting, gastroparesis, and migraine‑associated nausea in adult patients.

GNH India supplies Metoclopramide Ennogen Ip as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory documentation for import.

Manufacturer / TM Owner

Ennogen Ip Limited

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Indications & Clinical Uses

Metoclopramide acts on dopaminergic and serotonergic pathways to control emesis and improve gastric motility.

  • Nausea and vomiting: reduces frequency and severity of acute and chemotherapy‑induced episodes.
  • Gastroparesis: enhances gastric emptying and alleviates related symptoms.
  • Migraine‑associated nausea: mitigates nausea accompanying migraine attacks.

How It Works

  • Metoclopramide blocks dopamine D2 receptors in the chemoreceptor trigger zone, diminishing the central vomiting stimulus. It also stimulates 5‑HT4 receptors in the gastrointestinal tract, promoting acetylcholine release and increasing smooth‑muscle contractility, which accelerates gastric emptying. The combined antagonism and agonism improve both anti‑emetic control and gastro‑prokinetic activity.

Side Effects

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

Common Side Effects

  • Drowsiness: mild sedation or fatigue.
  • Restlessness: feeling of inner tension or agitation.
  • Diarrhea: loose stools.
  • Headache: mild to moderate pain.
  • Extrapyramidal symptoms: transient muscle stiffness or tremor.

Serious or Rare Side Effects

  • Tardive dyskinesia: irreversible involuntary movements with prolonged use.
  • Neuroleptic malignant syndrome: high fever, rigidity, autonomic instability.
  • Seizures: rare convulsive episodes.
  • Severe allergic reaction: rash, swelling, anaphylaxis.

Precautions & Warnings

When prescribing Metoclopramide, clinicians should consider several safety measures.

  • Renal impairment: adjust dose or monitor closely in patients with reduced kidney function.
  • History of movement disorders: avoid or use with caution in patients with Parkinson’s disease or dystonia.
  • Elderly patients: increased risk of extrapyramidal effects; monitor closely.
  • Concomitant CNS depressants: may enhance sedation; observe for additive effects.
  • Store below 25°C: keep in the original container, protect from light and moisture.

Avoid Interactions

Metoclopramide can alter the activity of other medicines, requiring attention to potential interactions.

Major Interactions (Avoid)

  • Anticholinergic agents: may reduce pro‑kinetic effect; avoid concurrent use.
  • CYP2D6 inhibitors (e.g., fluoxetine, paroxetine): increase metoclopramide plasma levels; avoid.
  • Other dopamine antagonists (e.g., haloperidol): additive risk of extrapyramidal symptoms; avoid.

Moderate Interactions (Monitor Closely)

  • Opioids: may enhance nausea; monitor response.
  • MAO inhibitors: risk of hypertensive crisis; use with caution.
  • Antihistamines: may increase sedation; observe patient.

Frequently Asked Questions

Metoclopramide Ennogen Ip is an intravenous dopamine antagonist used to treat acute and chemotherapy‑induced nausea and vomiting, to improve gastric emptying in gastroparesis, and to relieve nausea that accompanies migraine attacks.

The drug blocks dopamine D2 receptors in the chemoreceptor trigger zone, reducing the central stimulus for vomiting, and activates 5‑HT4 receptors in the gut, which enhances acetylcholine release and promotes gastrointestinal motility.

The specific dose and infusion rate are determined by the prescribing clinician based on the patient’s condition, age, renal function and treatment setting. No fixed regimen is provided here.

Safety data for Metoclopramide in pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and under medical supervision.

Enquiries are submitted via the product page on gnhindia.com, where you specify 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 required import documentation.

Compared with ondansetron, which is a selective 5‑HT3 antagonist, Metoclopramide adds a pro‑kinetic effect by stimulating 5‑HT4 receptors. Unlike domperidone, it crosses the blood‑brain barrier, providing stronger anti‑emetic activity but also a higher risk of central nervous system side effects.

Store the intravenous solution below 25 °C in its original packaging, protected from light and moisture. Do not freeze. Inspect the vial for particulate matter before use and discard any solution that appears discolored or contaminated.

The product is supplied as a sterile intravenous solution. It is administered by slow IV injection or infusion, typically diluted in compatible fluids, under the supervision of qualified healthcare personnel.

Serious adverse events include tardive dyskinesia, which may be irreversible after prolonged therapy, neuroleptic malignant syndrome, and severe allergic reactions such as anaphylaxis. Prompt recognition and discontinuation are essential if these occur.

Patients with known hypersensitivity to metoclopramide or any component of the formulation, those with pheochromocytoma, seizure disorders, or severe depression should avoid the drug. Caution is also advised in individuals with Parkinson’s disease or other movement disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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