Metoclopramide Dosage
The standard adult dose of metoclopramide is 10 mg administered orally or intravenously three to four times daily, with a maximum daily dose of 30 mg and treatment duration limited to 5 days to minimize the risk of extrapyramidal disorders. 1, 2
Adult Dosing by Indication
Nausea and Vomiting (General)
- 10 mg orally or IV three to four times daily is the standard dose 1, 3
- For refractory cases, can be titrated up to a maximum of 3-4 administrations daily 1
- Maximum daily dose: 30 mg/day 1
- Duration: Limited to 5 days to reduce neurological side effects 4, 1
Diabetic Gastroparesis
- 10 mg administered 30 minutes before meals and at bedtime (four times daily) 1, 2
- If severe symptoms are present, initiate therapy with IV/IM metoclopramide 10 mg slowly over 1-2 minutes 2
- May require up to 10 days of parenteral therapy before transitioning to oral administration 2
Chemotherapy-Induced Nausea and Vomiting (CINV)
- For highly emetogenic chemotherapy (cisplatin, dacarbazine): 2 mg/kg IV 2
- For less emetogenic regimens: 1 mg/kg IV 2
- Administer slowly over at least 15 minutes, 30 minutes before chemotherapy 2
- Repeat every 2 hours for two doses, then every 3 hours for three doses 2
Postoperative Nausea and Vomiting
Hiccups
Pediatric Dosing
General Considerations
- For children >14 years: 10 mg (adult dosing) 2
- For children 6-14 years: 2.5-5 mg 2
- For children <6 years: 0.1 mg/kg 2
Chemotherapy-Induced Nausea and Vomiting in Children
- Doses of 2 mg/kg or higher are associated with increased risk of extrapyramidal reactions (15%) and akathisia (33%) 6
- Doses less than 2 mg/kg have minimal toxicity 6
- Concomitant diphenhydramine should be administered to reduce extrapyramidal reactions 6
- Children receiving two consecutive days of metoclopramide have higher frequency of extrapyramidal symptoms 6
Special Populations
Renal Impairment
- For creatinine clearance <40 mL/min: Initiate at approximately one-half the recommended dosage 2
- Adjust dose based on clinical efficacy and safety 2
Hepatic Impairment
- Metoclopramide undergoes minimal hepatic metabolism 2
- Safe use has been described in patients with advanced liver disease and normal renal function 2
Elderly Patients
- Patients >59 years may require dose reduction (based on streptomycin dosing principles for age-related considerations) 4
- Increased caution warranted due to higher risk of adverse effects 5
Critical Safety Considerations
Maximum Dose and Duration Restrictions
- Absolute maximum: 30 mg/day 1
- Maximum duration: 5 days 4, 1
- These restrictions were implemented by the European Medicines Agency to minimize risk of extrapyramidal disorders and tardive dyskinesia 4, 1
Extrapyramidal Symptoms Management
- If acute dystonic reactions occur: Inject 50 mg diphenhydramine IM immediately 2
- Symptoms usually subside rapidly with diphenhydramine 2
- Extrapyramidal symptoms occur in approximately 9% of pediatric patients 7
Contraindications and Precautions
- Avoid in patients with seizure disorders or pheochromocytoma 1
- Use with caution in GI bleeding or obstruction 1
- Repeated doses can potentially prolong QT interval and precipitate torsades de pointes 5
- Caution in patients with impaired renal or hepatic function, elderly, and those with CNS depression 5
Administration Routes
Intravenous Administration
- For doses >10 mg, dilute in 50 mL of parenteral solution 2
- Preferred solution: Normal saline (can be stored frozen for up to 4 weeks) 2
- Administer slowly over 1-2 minutes for standard doses 2
- For CINV: Infuse over at least 15 minutes 2
Oral Administration
Intramuscular Administration
Common Pitfalls to Avoid
- Do not exceed 30 mg/day or 5 days duration - this significantly increases risk of tardive dyskinesia and extrapyramidal disorders 4, 1
- Do not use as first-line therapy - reserve for debilitating cases after other remedies have been tried 8
- Do not ignore early neurological symptoms - even low-dose, short-term use (30 mg total over 3 days) can cause severe, long-lasting adverse effects lasting up to 13 months 8
- Do not assume dose-responsiveness - there is no evidence of dose-responsiveness for anti-nausea effects with standard dosing regimens 9
- Do not use intermediate doses (0.4 mg/kg) expecting better efficacy - studies show no difference in effectiveness compared to standard 10 mg dosing 10