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Therefore, patients should be advised not to motilium drive or use machinery or engage in other activities requiring mental alertness and coordination until they have established how MOTILIUM affects them .
8 ADVERSE EFFECTS (UNDESIRABLE EFFECTS) Clinical Trial Data The safety of MOTILIUM was evaluated motilium dosage for lactation is motilium safe motilium instant 10 mg motilium for breast milk in 1221 patients with gastroparesis, or symptoms of it in 45 clinical trials included in the safety database .
All patients were ≥ 15 years old and received at least one dose of oral motilium domperidone breastfeeding buy motilium instants motilium drug interactions does motilium MOTILIUM (domperidone base) .
Slightly fewer than one-half (553/1221) of motilium patients were diabetic .
The median total daily dose was 80 mg (range 10 to 160 mg), with 230 patients motilium suspension is motilium available over the counter buy motilium without prescription receiving a dose greater than 80 mg .
Median duration of motilium exposure was 56 days (range 1 to 2248 days) .
Adverse Reactions (ARs) - reported by ≥ motilium 1% of patients treated with domperidone in these 45 clinical trials are shown in Table 1 .
Table 1: Adverse motilium Reactions Reported by ≥ 1% of Domperidone - Treated Patients in 45 Clinical Trials System/Organ Class Adverse Reaction Domperidone (n=1221) Psychiatric Disorders Libido Decreased/Loss of Libido Nervous System Disorders Gastrointestinal Disorders Skin and Subcutaneous Tissue Disorders Reproductive System and Breast Disorders Breast Enlargement/Gynaecomastia Breast Tenderness Menstruation Irregular Lactation Disorder MOTILIUM (190204) API System/Organ Class Adverse Reaction Domperidone (n=1221) General Disorders and Administration Site Conditions ARs that occurred in < 1% of Domperidone-treated patients in the 45 clinical trials (n=1221) are listed below in Table 2 .

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