Gravol (Dimenhydrinate) Dosing for Nausea and Vomiting
For adults with nausea and vomiting, administer dimenhydrinate 50 mg intramuscularly or intravenously every 4 hours as needed, with a maximum of 100 mg every 4 hours when drowsiness is acceptable; for oral administration, use 25-50 mg three times daily. 1, 2
Adult Dosing
Parenteral Administration
- Intramuscular route: 50 mg (1 mL) injected every 4 hours as needed 1
- Intravenous route: 50 mg diluted in 10 mL of 0.9% Sodium Chloride, injected over 2 minutes, every 4 hours 1
- Higher dose option: 100 mg every 4 hours may be used when drowsiness is not objectionable or is desirable 1
- Duration of action: Approximately 4 hours of symptom control per 50 mg dose 1
Oral Administration
- Standard dose: 25-50 mg three times daily 2
- Long-acting formulation (Gravol L/A): Contains 25 mg immediate-release plus 50 mg sustained-release dimenhydrinate, providing extended coverage 3
Pediatric Dosing
Parenteral Administration
- Intramuscular route: 1.25 mg/kg body weight OR 37.5 mg/m² body surface area, administered four times daily 1
- Maximum daily dose: 300 mg per day 1
- Important contraindication: Injectable form is contraindicated in neonates due to benzyl alcohol content 1
Clinical Context and Efficacy
Comparative Effectiveness
- Dimenhydrinate demonstrates moderate antiemetic efficacy, with studies showing reduction in nausea/vomiting scores from 8.6 to 3.8 in early pregnancy 4
- When used alone for postoperative nausea and vomiting (PONV), dimenhydrinate reduced incidence to 34.5% compared to 41.3% with placebo, though this difference was not statistically significant 5
- Combination therapy is more effective: Dimenhydrinate combined with droperidol reduced PONV to 19.6% and showed synergistic effects 5
Route Selection Considerations
- Use parenteral route when: Oral administration is impractical due to active vomiting or inability to tolerate oral medications 1
- Oral long-acting formulation: Particularly useful for outpatient procedures requiring extended prophylaxis, with preoperative administration providing coverage through the postoperative period 3
Important Safety Considerations
Common Adverse Effects
- Drowsiness: Expected with therapeutic dosing; may be dose-dependent 1
- Patients should be counseled about sedation, especially when higher doses (100 mg) are used 1
Toxicity Threshold
- Pediatric patients <6 years: Refer to emergency department if ingestion ≥7.5 mg/kg 6
- Patients ≥6 years: Refer to emergency department if ingestion ≥7.5 mg/kg or 300 mg (whichever is less) 6
- Symptom onset: Monitor for 6 hours post-ingestion; if no symptoms develop by 6 hours, emergency referral is not needed 6
Administration Precautions
- Intravenous administration: Must dilute 50 mg in 10 mL normal saline and inject slowly over 2 minutes to minimize adverse reactions 1
- Inspect solution: Visually inspect for particulate matter and discoloration before administration 1
Clinical Positioning
Dimenhydrinate is FDA-indicated for prevention and treatment of nausea, vomiting, or vertigo of motion sickness 1, but is commonly used off-label for other causes of nausea. In contemporary emergency department practice, dimenhydrinate is not listed among first-line agents (which include dopaminergic antagonists like haloperidol, metoclopramide, or prochlorperazine) 7, suggesting it may be most appropriate for motion sickness or as an adjunctive agent when first-line therapies are contraindicated or unavailable.