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    Motilium (Domperidone) is used to treat nausea and vomiting caused by other medications used to treat Parkinson’s disease. This medication increases the movements of the stomach and bowel. We currently have the brand from Turkey manufactured by Janssen-Cilag. The generic comes from Canada (by various manufacturers including Apotex and Teva), India (also called Vomistop), and UK (such as Medreich PLC). You should follow the instructions of the doctor who prescribed Motilium to you. Directions and dosage information can also be found on the pack or leaflet inside the pack. You should swallow Motilium whole with a glass of water. Motilium should be stored at room temperature away from direct sunlight and heat. Domperidone may be associated with a small increased risk of serious ventricular arrhythmias or sudden cardiac death. A higher risk was observed in patients: • older than 60 years of age; • using daily doses greater than 30 mg; • having predisposing factors for QT prolongation including concomitant use of QT-prolonging drugs or CYP 3A4 inhibitors. clonidine oral Motilium is a brand-name version of the drug domperidone. Domperidone is approved in some countries, including Canada, to treat gastrointestinal conditions. It is approved in the United Kingdom for use in the relief of nausea and vomiting. Domperidone is known to increase lactation in breastfeeding women, but it’s not approved for this use in any country. You may be able to purchase Domperidone from verified online pharmacies below if you have a valid prescription from your provider. are regulated for safety and efficacy by pharmaceutical/pharmacy regulatory authorities in other countries. Depending on the condition for which you seek treatment, the pharmacy may decline to dispense this product to you. Food and Drug Administration (FDA) and therefore not available for sale in the United States. Please check with the online pharmacy before ordering your medication. However, the FDA has created a program for people to obtain Domperidone internationally through an expanded access investigational new drug application.

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