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Clinical data | |
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Trade names | Motilium, many others |
AHFS/Drugs.com | Micromedex Detailed Consumer Information |
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Routes of administration |
Oral, intramuscular, intravenous (d/c'd), rectal |
ATC code | |
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Pharmacokinetic data | |
Bioavailability | Oral: 13–17% Intramuscular: 90% |
Protein binding | ~92% |
Metabolism | Hepatic (CYP3A4/5) and intestinal (first-pass) |
Metabolites | All inactive |
Biological half-life | 7.5 hours |
Excretion |
Feces: 66% Urine: 32% Breast milk: small quantities |
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ChEMBL | |
ECHA InfoCard | 100.055.408 |
Chemical and physical data | |
Formula | C22H24ClN5O2 |
Molar mass | 425.911 g/mol |
3D model (Jmol) | |
Melting point | 242.5 °C (468.5 °F) |
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Domperidone, sold under the brand name Motilium among others, is a peripherally selective dopamine D2 receptor antagonist that was developed by Janssen Pharmaceutica and is used as an antiemetic, gastroprokinetic agent, and galactagogue. It may be administered orally or rectally, and is available in the form of tablets, orally disintegrating tablets (based on Zydis technology),suspension, and suppositories. The drug is used to relieve nausea and vomiting; to increase the transit of food through the stomach (by increasing gastrointestinal peristalsis); and to promote lactation (breast milk production) by release of prolactin.
The uses or indications of domperidone vary between nations. For instance, in Italy it is used in the treatment of gastroesophageal reflux disease and in Canada, the drug is indicated in upper gastrointestinal motility disorders and to prevent gastrointestinal symptoms associated with the use of dopamine agonist antiparkinsonian agents. In the United States, domperidone is not currently a legally marketed human drug and it is not approved for sale in the U.S. On 7 June 2004, FDA issued a public warning that distributing any domperidone-containing products is illegal. In the United Kingdom, domperidone is only indicated for the treatment of nausea and vomiting and the treatment duration is usually limited to 1 week.