Methocarbamol
Administration
- Type: Muscle relaxant; FDA-approved as an adjunct for muscle spasms such as Lower back pain
- Dosage Forms: 500 mg or 750 mg tablet
- Routes of Administration: PO
- Common Trade Names: Robaxin
Adult Dosing
- 500 mg to 1500 mg PO every 8 hours
- IV and IM formulations sometimes used in post-op settings but not commonly in ED
Pediatric Dosing
- Efficacy/safety not established in pediatric population
Special Populations
Pregnancy Rating
- Unknown
- Case reports have found possible teratogenic effects (Hall 1982) [1]
Lactation risk
- Not known
Renal Dosing
- Adult: No exact adjustment noted by manufacturer, but clearance may be decreased in patients with renal impairment
- Pediatric:
Hepatic Dosing
- Adult: No exact adjustment noted by manufacturer, but clearance may be decreased in cirrhosis patients
- Pediatric:
Contraindications
- Allergy to class/drug
- Co-administration with other CNS depressants (benzos, opioids, etc)
Adverse Reactions
- Dizziness
- Confusion
- Weakness
- Bradycardia
- Falls
Pharmacology
- Onset (PO): 30 minutes
- Half-life: 1-2 hours
- Metabolism: Predominantly hepatic
- Excretion: Urinary
Mechanism of Action
- Exact mechanism unknown but theorized to be a CNS-depressant
See Also
References
- Sibrack J, Patel P, Hammer R. Methocarbamol. [Updated 2024 Sep 10]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2026 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK565868/
- ↑ Hall JG, Reed SD. Teratogens associated with congenital contractures in humans and in animals. Teratology. 1982 Apr;25(2):173-91. doi: 10.1002/tera.1420250207. PMID: 7101197.
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