Centrally Acting Skeletal Muscle Relaxant
Pregnancy: Avoid — limited safety data; insufficient human evidence; animal studies show no teratogenicity
Methocarbamol
Brand names: Robaxin, Robaxisal
Adult dose
Dose: 1.5 g four times daily for first 48–72 hours; then 750 mg–1.5 g four times daily
Route: Oral
Frequency: Four times daily
Max: 6 g/day (first 48–72 hours); 4.5 g/day maintenance
Short-term use only (typically 5–7 days); IV available for severe spasm at 1–3 g IV at maximum 300 mg/min; take with food to reduce GI upset
Paediatric dose
Route: N/A
Frequency: N/A
Max: Not recommended under 16 years
IV formulation used in tetanus management under specialist supervision
Dose adjustments
Renal
IV formulation: avoid if eGFR <30 (polyethylene glycol vehicle potentially nephrotoxic); oral form: use with caution
Hepatic
Use with caution in hepatic impairment — reduced metabolism; no specific dose recommendation
Clinical pearls
- Mechanism: centrally acting CNS depressant with no direct peripheral neuromuscular effect — likely depresses polysynaptic pathways in spinal cord and brain; reduces muscle spasm without causing flaccid paralysis
- Acute musculoskeletal back pain: Cochrane 2003 review supports short-term (5–7 day) muscle relaxant use (including methocarbamol) as adjuncts to NSAIDs and physiotherapy for acute low back pain; not recommended beyond 2 weeks
- Urine discolouration: methocarbamol metabolites excreted as dark brown or black pigment — warn patients proactively; harmless but alarming if unexpected; no organ toxicity associated
- Tetanus (IV): methocarbamol IV adjunctively used for tetanic muscle spasm — historical indication that distinguishes it from other oral muscle relaxants; specialist use only
- Preferred over diazepam for short-term spasm in non-anxious patients: no dependence potential, no controlled drug status, no euphoria — safer for acute prescribing in orthopaedic settings; NICE CG88 supports short-term muscle relaxant use for acute back pain
Contraindications
- Renal impairment (IV formulation — PEG vehicle)
- Myasthenia gravis (potential worsening)
- Hypersensitivity to carbamate derivatives
Side effects
- Sedation
- Dizziness
- Nausea
- Urine discolouration (dark brown or black — harmless)
- Headache
- Blurred vision
- Hypotension (IV)
Interactions
- CNS depressants — additive sedation
- Alcohol — enhanced CNS depression
- Pyridostigmine — may antagonise cholinergic effect in myasthenia
Monitoring
- Sedation level
- Functional improvement in spasm
- Hepatic function if prolonged use
- Renal function if IV formulation used
Reference: BNFc; BNF 90; SPC Robaxin; Cochrane Review (Muscle relaxants for acute low back pain, 2003); NICE CG88 (Low Back Pain); Toth and Urtis, Am J Phys Med Rehabil 2004. Verify against your local formulary and the latest BNF before prescribing.
Related
Curated clinical cross-links plus same-class fallbacks.
Pathways
- Hip Fracture Management · NICE CG124 / BOA 2020
- Distal Radius Fracture · BOA / NICE
- Ankle Fracture Management · BOA / Lauge-Hansen classification
- Metastatic Spinal Cord Compression · NICE CG75 2020
- Open Fracture Management · BOA/BAPRAS 2017
- OrthoPath: Upper Limb ED Triage · OrthoPath ED Tool — ReviseMRCEM.com