Registered Kenya · PPB

METOCLOPROMIDE INJ 10MG/2ML

METOCLOPROMIDE INJ 10MG/2ML

15138 10MG/2ML GENERIC/BIOSIMILARS

What it does

Inj is a medication used to treat various health conditions.

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Plain-language summary for general understanding - not medical advice. Always follow your pharmacist/doctor.

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Registration & product details

Registration no.
15138
Registration date
-
Expiry date
-
Status
Registered
Active ingredient
METOCLOPROMIDE INJ 10MG/2ML
Dosage form
10MG/2ML
Strength
-
Pack size
AMPOULE
Therapeutic class
GENERIC/BIOSIMILARS
Manufacturer / MAH
United Pharma
Applicant / LTR
UNITED PHARMA (K) LIMITED
Country of origin
FOREIGN
Manufacturer location
Warehouses 1,2, Universal Industrial and Logistics Park, 3 Old Mombasa Rd, Nairobi, Kenya

Source: Pharmacy and Poisons Board · fetched 2026-01-28 19:25:40 · updated 2026-08-03 03:03:54

Disclaimer: This information is sourced from Pharmacy and Poisons Board (Kenya). Always consult a qualified healthcare professional before using any medication.

About inj

Inj is a medication used to treat various health conditions.

How it works

Inj works by affecting certain processes in the body to help manage symptoms or treat conditions.

Who it's for

Inj is prescribed for patients with specific medical needs as determined by a healthcare professional.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

About metoclopromide

Metoclopramide is a medication that helps with nausea and vomiting.

What it treats

  • nausea and vomiting
  • migraine-related nausea
  • post-surgery nausea
  • nausea from chemotherapy

How it works

It works by blocking signals in the brain that cause nausea and helps the stomach empty faster.

Who it's for

It is used for people experiencing severe nausea or vomiting due to various conditions.

AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.

Clinical monograph: metoclopromide

Metoclopramide is a dopamine receptor antagonist that is primarily used as an antiemetic and prokinetic agent. It works by increasing the motility of the upper gastrointestinal tract and accelerating gastric emptying, making it effective in treating conditions such as nausea, vomiting, and gastroesophageal reflux disease (GERD). Metoclopramide is also used in the management of migraine-associated nausea and for facilitating small bowel intubation.

Indications

  • Nausea and vomiting associated with chemotherapy
  • Postoperative nausea and vomiting
  • Gastroparesis
  • Gastroesophageal reflux disease (GERD)
  • Migraine-associated nausea
  • Facilitation of small bowel intubation

Dosage

Children: Refer to the BNF for Children for paediatric dosing recommendations.

Adults: Refer to the BNF for specific dosing guidelines.

Mechanism of action

Metoclopramide antagonizes dopamine D2 receptors in the central nervous system and the gastrointestinal tract. It also enhances the action of acetylcholine on muscarinic receptors in the smooth muscle of the gastrointestinal tract, leading to increased gastric motility and accelerated gastric emptying. Additionally, it has some serotonin receptor agonist activity which contributes to its antiemetic effects.

Pharmacodynamics

The pharmacodynamic effects of metoclopramide include its ability to reduce nausea and vomiting by blocking dopamine receptors in the chemoreceptor trigger zone (CTZ) of the brain. It increases the amplitude of gastric contractions and relaxes the pyloric sphincter, promoting gastric emptying. It also exerts a modest effect on increasing esophageal peristalsis, which can alleviate symptoms of GERD.

Pharmacokinetics

Metoclopramide is well absorbed from the gastrointestinal tract, with peak plasma concentrations occurring within 1 to 2 hours after oral administration. It is primarily metabolized in the liver, with a half-life of approximately 5 to 6 hours. The drug is excreted mainly in the urine, with a significant portion being eliminated unchanged. Renal impairment can prolong the half-life and increase the risk of adverse effects.

Contra-indications

  • Pheochromocytoma
  • Gastrointestinal obstruction
  • Perforation or hemorrhage
  • Hypersensitivity to metoclopramide or any of its components
  • Concurrent use with other dopamine antagonists
  • History of tardive dyskinesia associated with metoclopramide

Adverse effects

  • Drowsiness
  • Fatigue
  • Dizziness
  • Headache
  • Nausea
  • Diarrhea
  • Extrapyramidal symptoms
  • Tardive dyskinesia
  • Neuroleptic malignant syndrome

Interactions

  • Increased sedation with central nervous system depressants
  • Anticholinergic drugs may reduce the efficacy of metoclopramide
  • May enhance the effects of other dopamine antagonists
  • Caution with drugs that increase the risk of extrapyramidal symptoms

Precautions

  • Use with caution in patients with a history of seizures
  • Avoid in patients with Parkinson's disease
  • Monitor for signs of tardive dyskinesia in long-term use
  • Caution in patients with renal impairment

Pregnancy

Metoclopramide is classified as category B. It should only be used during pregnancy if the potential benefit justifies the potential risk to the fetus.

Breast-feeding

Metoclopramide is excreted in breast milk. Use with caution; potential effects on a nursing infant should be considered.

Storage

Store at room temperature, away from moisture and heat. Keep out of reach of children.

Formulations

  • Tablets
  • Oral solution
  • Injection

AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.

This drug in other countries

The same active ingredient registered across other registries we cover - including different brands.