Drug Guide
Methocarbamol
Classification
Therapeutic: Muscle relaxant
Pharmacological: Central muscle relaxant
FDA Approved Indications
- Relief of discomfort associated with acute, painful musculoskeletal conditions
Mechanism of Action
Methocarbamol acts centrally to produce sedative and muscle relaxant effects, likely through general depression of nerve transmission within the reticulospinal pathways in the brain.
Dosage and Administration
Adult: Typically, 1500 mg four times daily for 2-3 days, then 750 mg four times daily as needed. Tapering is not usually required.
Pediatric: Safety and efficacy not established; use in children is not generally recommended.
Geriatric: Use with caution; consider lower doses due to increased sensitivity and risk of side effects.
Renal Impairment: Adjust dosage based on severity of impairment; monitoring recommended.
Hepatic Impairment: Use with caution; no specific dosage adjustment established.
Pharmacokinetics
Absorption: Well absorbed from the gastrointestinal tract
Distribution: Distributed widely, crosses the blood-brain barrier
Metabolism: Minimal hepatic metabolism
Excretion: Primarily via the urine in unchanged form and conjugates
Half Life: Approximately 1-2 hours in healthy adults
Contraindications
- Allergy to methocarbamol or any component of the formulation.
- Severe renal impairment
Precautions
- Use with caution in patients with hepatic impairment, renal impairment, or with a history of hypersensitivity reactions.
- May cause drowsiness; caution in patients performing hazardous tasks.
- Potential for drug interactions with central nervous system depressants.
Adverse Reactions - Common
- Drowsiness (Common)
- Dizziness (Common)
- Lightheadedness (Common)
- Gastrointestinal upset (nausea, vomiting) (Less common)
Adverse Reactions - Serious
- Seizures (Rare)
- Allergic reactions (rash, angioedema, anaphylaxis) (Rare)
- Blood dyscrasias (e.g., leukopenia, anemia) (Very rare)
Drug-Drug Interactions
- CNS depressants (e.g., opioids, benzodiazepines) may increase Sedation.
- Potential additive effect with other muscle relaxants.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for effectiveness in relieving muscle spasm and pain; observe for side effects such as sedation or allergic reactions.
Diagnoses:
- Ineffective airway clearance related to CNS depression.
- Risk for injury related to dizziness or sedation.
Implementation: Administer with food or milk to minimize gastrointestinal upset. Assess for allergic reactions and sedation periodically.
Evaluation: Assess relief of muscle spasm and pain, monitor for adverse effects.
Patient/Family Teaching
- Do not operate machinery or drive until response is known.
- Avoid alcohol and other CNS depressants.
- Report excessive drowsiness, rash, or difficulty breathing.
- Take medication exactly as prescribed.
Special Considerations
Black Box Warnings: N/A
Genetic Factors: None specific.
Lab Test Interference: None reported.
Overdose Management
Signs/Symptoms: Drowsiness, vomiting, hypotension, possible coma.
Treatment: Supportive care, maintain airway and breathing, activated charcoal if ingestion is recent, seizure control if necessary, no specific antidote.
Storage and Handling
Storage: Store at room temperature, away from moisture, heat, and light.
Stability: Stable under recommended conditions.