Product image of Metoclopramide S.A.L.F. (Metoclopramide Hydrochloride Monohydrate) supplied by GNH India

Metoclopramide S.A.L.F.

Active Ingredient:
Metoclopramide Hydrochloride Monohydrate
Origin:
EU

Metoclopramide S.A.L.F. (Metoclopramide Hydrochloride Monohydrate)

Metoclopramide, the active ingredient in Metoclopramide S.A.L.F., is a dopamine antagonist presented as an injectable solution for intramuscular and intravenous use. It is employed to treat nausea, vomiting, postoperative nausea and vomiting, and gastroparesis in adult patients.
GNH India supplies Metoclopramide S.A.L.F. as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

S.A.L.F. Spa Laboratorio Farmacologico

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Indications & Clinical Uses

Metoclopramide acts on the dopaminergic pathways that trigger nausea and impair gastric motility. It is indicated for several gastrointestinal and postoperative conditions.

  • Nausea and vomiting: reduces the frequency and severity of acute episodes.
  • Postoperative nausea and vomiting: prevents and treats nausea after surgery.
  • Gastroparesis: enhances gastric emptying and alleviates related symptoms.

How It Works

  • Metoclopramide blocks dopamine D2 receptors in the chemoreceptor trigger zone, diminishing the central stimulus for nausea. It also antagonizes peripheral D2 receptors, increasing acetylcholine release, which stimulates smooth‑muscle contraction and accelerates gastrointestinal motility, thereby facilitating gastric emptying.

Side Effects

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

Common Side Effects

  • Drowsiness: mild sedation or sleepiness.
  • Fatigue: general feeling of tiredness.
  • Restlessness: inner sense of unease or agitation.
  • Diarrhea: loose stools or increased bowel movements.
  • Headache: mild to moderate cranial pain.
  • Dizziness: sensation of light‑headedness or imbalance.

Serious or Rare Side Effects

  • Extrapyramidal symptoms: involuntary muscle movements or tremor.
  • Tardive dyskinesia: persistent, potentially irreversible dyskinetic movements.
  • Neuroleptic malignant syndrome: life‑threatening hyperthermia and rigidity.
  • Severe allergic reactions: rash, swelling, or anaphylaxis.
  • Cardiac arrhythmias: irregular heart rhythm.
  • Seizures: sudden, uncontrolled electrical activity in the brain.

Precautions & Warnings

Before using Metoclopramide, clinicians should consider several safety measures.

  • Renal and hepatic function: assess and adjust use in impairment.
  • Dose minimization: employ the lowest effective dose for the shortest duration.
  • Extrapyramidal monitoring: watch for signs of muscle rigidity or abnormal movements.
  • Prolonged therapy avoidance: limit use to prevent tardive dyskinesia.
  • Hypersensitivity: discontinue if allergic reaction occurs.
  • Store at ambient temperature: keep in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • MAO inhibitors: risk of hypertensive crisis.
  • CNS depressants (e.g., benzodiazepines, opioids): enhanced sedation.
  • Anticholinergic agents: reduced pro‑kinetic effect.
  • QT‑prolonging drugs: increased risk of cardiac arrhythmia.

Moderate Interactions (Monitor Closely)

  • CYP2D6 inhibitors (e.g., fluoxetine): may raise metoclopramide levels.
  • Antipsychotics: potential additive extrapyramidal effects.
  • Alcohol: may intensify drowsiness.
  • Antihistamines: possible increase in sedation.

Frequently Asked Questions

Metoclopramide S.A.L.F. is prescribed to manage nausea and vomiting, including postoperative nausea, and to treat gastroparesis by enhancing gastric motility. It is used in adult patients when these symptoms are acute or related to delayed stomach emptying.

Metoclopramide blocks dopamine D2 receptors in the brain’s chemoreceptor trigger zone, reducing the signal that initiates nausea. It also increases acetylcholine release in the gastrointestinal tract, stimulating smooth‑muscle contraction and speeding up gastric emptying.

The appropriate dose of Metoclopramide S.A.L.F. is determined by the prescribing clinician based on the patient’s condition, age, weight, and renal or hepatic function. Dosage regimens are individualized and should follow local prescribing guidelines.

Safety data for Metoclopramide in pregnancy and lactation are limited. Clinicians should weigh potential benefits against risks and consider alternative therapies when possible. Breastfeeding mothers should consult a healthcare professional before use.

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, confirming trade or institutional credentials before providing pricing, availability, shipping details, and necessary import documentation.

Metoclopramide differs from many antiemetics by combining dopamine antagonism with pro‑kinetic activity, making it effective for both nausea control and gastric motility. Alternatives such as ondansetron act primarily on serotonin receptors and lack the pro‑kinetic effect.

Metoclopramide S.A.L.F. should be stored at ambient temperature, below 25 °C, in its original packaging to protect from moisture and light. Ensure the container is tightly sealed and keep it out of reach of children.

The product is supplied as an injectable solution for intramuscular or intravenous administration. It is typically given by a healthcare professional in a clinical setting, following aseptic technique and appropriate dilution if required.

Serious risks include extrapyramidal symptoms such as tardive dyskinesia, neuroleptic malignant syndrome, severe allergic reactions, and cardiac arrhythmias. Patients should be monitored closely for any signs of these conditions, especially with prolonged use.

Metoclopramide is contraindicated in individuals with known hypersensitivity to the drug, those with a history of extrapyramidal disorders, and patients taking MAO inhibitors. Caution is also advised in patients with severe renal or hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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