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MUSCULO-SKELETAL SYSTEM › MUSCLE RELAXANTS › MUSCLE RELAXANTS, CENTRALLY ACTING AGENTS › Other centrally acting agents
cyclobenzaprine
M03BX08
Forms & Strengths
- Oral tablet: 5 mg
- Oral tablet: 7.5 mg
- Oral tablet: 10 mg
- Extended-release capsule (ER): 15 mg
- Extended-release capsule (ER): 30 mg
Adult Dosing
- Immediate-release: 5 mg to 10 mg orally three times daily as needed; maximum 10 mg per dose and 30 mg per day; limit use to 2 to 3 weeks.
- Extended-release (Amrix): 15 mg to 30 mg orally once daily.
Pediatric Dosing
- Children < 15 years: Safety and efficacy have not been established.
- Adolescents >= 15 years: Dosing similar to adult immediate-release (5 mg to 10 mg orally three times daily) if indicated for short-term use.
Indications
- Adjunct to rest and physical therapy for the relief of muscle spasm associated with acute, painful musculoskeletal conditions.
Mechanism of Action
- Centrally acting skeletal muscle relaxant structurally related to tricyclic antidepressants.
- Acts primarily at the brain stem to reduce tonic somatic motor activity, influencing both alpha and gamma motor neurons.
Contraindications
- Hypersensitivity to cyclobenzaprine or any component of the formulation.
- Concurrent use of monoamine oxidase (MAO) inhibitors or within 14 days of discontinuing them.
- Acute recovery phase of myocardial infarction, and patients with arrhythmias, heart block, or conduction disturbances.
- Congestive heart failure.
- Hyperthyroidism.
Adverse Reactions
- Drowsiness
- Dizziness
- Dry mouth
- Fatigue
- Headache
- Nausea
- Constipation
- Blurred vision
- Tachycardia
Drug Interactions
- MAO inhibitors: Risk of severe, potentially fatal hyperpyretic crisis, seizures, and death.
- CNS depressants (alcohol, opioids, sedatives, hypnotics, anxiolytics): Enhanced central nervous system depression and psychomotor impairment.
- Serotonergic agents (SSRIs, SNRIs, tricyclic antidepressants): Risk of serotonin syndrome.
- Tramadol: Increased risk of seizures and serotonin syndrome.
Curated Content: Needs Vetting Before Put to Clinical Use