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Dopamine D2 antagonist antiemetic / prokinetic

Metoclopramide hydrochloride

Brand names: Maxolon

Metoclopramide hydrochloride is a dopamine antagonist with prokinetic and antiemetic properties, used for nausea and vomiting and to promote gastric emptying.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It blocks central and peripheral dopamine D2 receptors, suppressing the chemoreceptor trigger zone while enhancing gastric and upper gastrointestinal motility, with additional 5-HT3 antagonism and weak 5-HT4 agonism at higher doses.

Prescribing in practice

  • Because of the risk of extrapyramidal and other neurological effects, MHRA advice restricts metoclopramide to short-term use and to standard rather than high doses, with particular caution and dose limitation in children and young adults.
  • It is contraindicated in gastrointestinal obstruction, perforation or haemorrhage, in phaeochromocytoma, and shortly after gastrointestinal surgery, and dose reduction is needed in renal or hepatic impairment.
  • Acute dystonic reactions can occur early in treatment, and concurrent use with other dopamine antagonists increases the risk of extrapyramidal effects.

Monitoring

Monitor for extrapyramidal symptoms, tardive dyskinesia with prolonged use, and signs of neuroleptic malignant syndrome, reviewing the need for continued treatment regularly.

Counselling the patient

  • Use this medicine only for the short course your prescriber advises.
  • Stop and seek urgent help if you develop abnormal movements, muscle spasms of the face or neck, or restlessness.

Evidence & guidelines

Following a European review, the MHRA restricted metoclopramide to short-term use at standard doses to reduce the risk of neurological adverse effects.

Reference: MHRA Drug Safety Update 2014; NICE CG150; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.