Robaxin
Robaxin
Generic Name
Robaxin
Mechanism
- Central nervous system depressant that reduces polysynaptic reflex activity in the spinal cord.
- Likely enhances inhibitory gamma‑aminobutyric acid (GABA) neurotransmission and/or modulates other excitatory pathways, resulting in decreased motoneuron excitability.
- Does not act directly on skeletal muscle fibers; rather, it lowers the neural drive to muscles.
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Pharmacokinetics
- Absorption: Oral bioavailability ~90 %; peak plasma concentrations 2–4 h post‑dose.
- Distribution: Lipophilic; extensive tissue distribution.
- Metabolism: Hepatic conversion to inactive metabolites (mainly via glucuronidation).
- Excretion: Renal (≈ 60 % unchanged drug) and hepatic.
- Half‑life: 2.5–5 h (dependent on renal/hepatic function).
- Drug interactions: May potentiate CNS depression when combined with alcohol, benzodiazepines, or opioids.
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Indications
- Acute musculoskeletal spasm (e.g., low back pain, neck strain).
- Post‑operative pain from minor procedures.
- Whiplash-associated disorders and other short‑term spinal injuries.
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Contraindications
- Hypersensitivity to methocarbamol or any formulation component.
- Pregnancy (Category C; caution advised).
- Liver or renal impairment: dose adjustment or avoidance.
- Severe CNS depression (e.g., coma, severe sleep apnea).
- Caution in patients on other CNS depressants or anticholinergic drugs.
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Dosing
| Population | Typical Regimen | Notes |
| Adults | 1500 mg IV/IM × 3 days OR 1500–3000 mg/day orally divided q6‑h | Maximum 4 g/day for short courses. |
| Children (≥12 yrs) | Same as adults; monitor closely. | |
| Geriatrics, renal/hepatic impairment | Start at lower dose; adjust per serum creatinine or ALT/AST. |
• Administration: Oral tablets or IV infusion (for acute inpatient settings).
• Avoid mixing with benzodiazepines or alcohol without monitoring.
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Adverse Effects
- Common (≈ 10 %): dizziness, sedation, nausea, vomiting, anorexia, somnolence.
- Serious: severe allergic reactions (anaphylaxis), respiratory depression in high doses, hepatotoxicity (rare).
- Note: Rare reports of mild headaches, fatigue, and visual disturbances.
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Monitoring
- Baseline: CBC, CMP (ALT/AST, BUN/Cr).
- Follow‑up: Repeat CMP in > 7 days if prolonged therapy planned, monitor liver enzymes.
- Clinical: Assess for CNS depression, pain reduction, and any signs of intolerance or allergy.
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Clinical Pearls
- “First‑line in the emergency department”: Methocarbamol is FDA‑approved for acute spasms but operates slower than local anesthetics; use in mild to moderate pain before resorting to opioids.
- Drug interaction vigilance: Combining methocarbamol with benzodiazepines, opioids, or alcohol may precipitate deep sedation or respiratory depression—emphasize on discharge meds.
- Renal/hepatic dosing: A 50 % dose reduction is recommended for CrCl < 30 mL/min; no dosing recommendation exists for severe hepatic failure—use with caution.
- Pregnancy: Category C; limited data but no teratogenic findings—use only if benefits outweigh potential risks.
- Pediatric use: Not recommended under 12 yrs due to insufficient safety data; adult dosing may be extrapolated cautiously if necessary.
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• Key take-home: Methocarbamol (Robaxin) is a useful, centrally acting muscle relaxant for short‑term spasm control, but demands careful patient selection, monitoring, and awareness of additive CNS depressant effects.