Domperidone
A dopamine antagonist used to improve gastric motility and control nausea.
What is Domperidone?
Domperidone is a peripheral dopamine D₂-receptor antagonist used as a prokinetic and antiemetic drug.
It enhances gastrointestinal motility without significant central effects.
History & Background
Domperidone was developed to provide anti-nausea benefits similar to metoclopramide but with fewer central nervous system side effects.
Chemical Structure & Properties
- IUPAC name: 5-chloro-1-[1-[3-(2-oxo-1-benzimidazolinyl)propyl]piperidin-4-yl]-1,3-dihydro-2H-benzimidazol-2-one
- Molecular formula: C₂₂H₂₄ClN₅O₂
- Molar mass: 425.91 g/mol
- Functional groups: Benzimidazolone, piperidine
Mechanism of Action
Domperidone blocks peripheral D₂ receptors, leading to:
- Increased gastric emptying
- Improved esophageal peristalsis
- Reduced nausea and vomiting
Pharmacokinetics
- Absorption: Moderate oral absorption
- Peak plasma time: 30–60 minutes
- Metabolism: Liver (CYP3A4)
- Half-life: ~7 hours
- Excretion: Feces and urine
Medical Uses
- Functional dyspepsia
- Gastroesophageal reflux disease (GERD)
- Nausea and vomiting
- Gastroparesis
Dosage Guidelines
Adults: 10 mg three times daily (before meals)
Maximum: 30 mg/day
⚠️ Avoid higher doses due to cardiac risk.
Side Effects
- Dry mouth
- Abdominal cramps
- Headache
- Increased prolactin levels
Warnings & Precautions
- Risk of QT prolongation
- Avoid in heart rhythm disorders
- Use lowest effective dose
Drug Interactions
- Macrolide antibiotics
- Azole antifungals
- Other QT-prolonging drugs
Frequently Asked Questions
Is domperidone safer than metoclopramide? – Fewer CNS effects.
Does it cause sleepiness? – Rare.
Can it be used long-term? – Short-term preferred.
Why is it restricted in some countries? – Cardiac safety concerns.
⚠️ Educational content only. Not a substitute for professional medical advice.