Carisoprodol
Pronunciation
(kar eye soe PROE dole)
U.S. Brand Names
Soma®
Synonyms
Carisoprodate; Isobamate
Generic Available
Yes
Canadian Brand Names
Soma®
Use
Skeletal muscle relaxant
Use - Dental
Treatment of muscle spasms and pain associated with acute temporomandibular joint pain
Pregnancy Risk Factor
C
Lactation
Enters breast milk (high concentrations)/not recommended
Contraindications
Hypersensitivity to carisoprodol, meprobamate or any component of the formulation; acute intermittent porphyria
Warnings/Precautions
May cause CNS depression, which may impair physical or mental abilities. Effects with other sedative drugs or ethanol may be potentiated. Use with caution in patients with hepatic/renal dysfunction. Tolerance or drug dependence may result from extended use.
Adverse Reactions
>10%: Central nervous system: Drowsiness
1% to 10%:
Cardiovascular: Tachycardia, tightness in chest, flushing of face, syncope
Central nervous system: Mental depression, allergic fever, dizziness, lightheadedness, headache, paradoxical CNS stimulation
Dermatologic: Angioedema
Gastrointestinal: Nausea, vomiting, stomach cramps
Neuromuscular & skeletal: Trembling
Ocular: Burning eyes
Respiratory: Dyspnea
Miscellaneous: Hiccups
<1%: Ataxia, rash, urticaria, erythema multiforme, aplastic anemia, leukopenia, eosinophilia, blurred vision
Overdosage/Toxicology
Symptoms of overdose include CNS depression, stupor, coma, shock, and respiratory depression. Treatment is supportive.
Drug Interactions
Substrate
of CYP2C19 (major)
Increased toxicity: Ethanol, CNS depressants, phenothiazines
CYP2C19 inhibitors: May increase the levels/effects of carisoprodol. Example inhibitors include delavirdine, fluconazole, fluvoxamine, gemfibrozil, isoniazid, omeprazole, and ticlopidine.
Ethanol/Nutrition/Herb Interactions
Ethanol: Avoid ethanol (may increase CNS depression).
Mechanism of Action
Precise mechanism is not yet clear, but many effects have been ascribed to its central depressant actions
Pharmacodynamics/Kinetics
Onset of action: ~30 minutes
Duration: 4-6 hours
Distribution: Crosses placenta; high concentrations enter breast milk
Metabolism: Hepatic
Half-life elimination: 8 hours
Excretion: Urine
Dosage
Oral: Adults: 350 mg 3-4 times/day; take last dose at bedtime; compound: 1-2 tablets 4 times/day
Monitoring Parameters
Look for relief of pain and/or muscle spasm and avoid excessive drowsiness
Patient Education
Take exactly as directed with food. Do not increase dose or discontinue without consulting prescriber. Do not use alcohol, prescriptive or OTC antidepressants, sedatives, and pain medications without consulting prescriber. You may experience drowsiness, dizziness, lightheadedness (avoid driving or engaging in tasks requiring alertness until response to drug is known); nausea, vomiting, or cramping (small, frequent meals, frequent mouth care, or sucking hard candy may help); or postural hypotension (change position slowly when rising from sitting or lying or when climbing stairs). Report excessive drowsiness or mental agitation; palpitations, rapid heartbeat, chest pain; skin rash; muscle cramping or tremors; or respiratory difficulty.
Pregnancy/breast-feeding precautions:
Inform prescriber if you are or intend to become pregnant. Breast-feeding is not recommended.
Nursing Implications
Raise bed rails; institute safety measures; assist with ambulation
Dental Health: Effects on Dental Treatment
No significant effects or complications reported
Dental Health: Vasoconstrictor/Local Anesthetic Precautions
No information available to require special precautions
Mental Health: Effects on Mental Status
Drowsiness is common; may produce depression or paradoxical CNS stimulation
Mental Health: Effects on Psychiatric Treatment
Rarely may cause leukopenia or aplastic anemia; use caution with clozapine and carbamazepine; concurrent use with psychotropics may produce additive sedation
Dosage Forms
Tablet: 350 mg
References
Adams HR, Kerzee T, and Morehead CD, "Carisoprodol-Related Death in a Child,"
J Forensic Sci
, 1975, 20:200-2.
Backer RC, Zumwalt R, McFeeley P, et al, "Carisoprodol Concentrations From Different Anatomical Sites: Three Overdose Cases,"
J Anal Toxicol
, 1990, 14(5):332-4.
Goldberg D, "Carisoprodol Toxicity,"
Milit Med
, 1969, 34:597-601.
Luehr JG, Meyerle KA, and Larson EW, "Mail-Order (Veterinary) Drug Dependence,"
JAMA
, 1990, 263(5):657.
International Brand Names
Artifar® (GR); Carisoma® (GB, IN); Carisoprodol Sintesina® (AR); Listaflex® (AR); Mio Relax® (ES); Sanoma® (DE); Soma® (CA); Somadril® (DK, NO, SE); Somflam® (IN)
|
A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org). URAC's
accreditation program
is the first of its kind, requiring compliance with 53 standards of quality and accountability, verified by independent audit. A.D.A.M. is among the first to achieve this important distinction for online health information and services. Learn more about A.D.A.M.'s
editorial process
. A.D.A.M. is also a founding member of Hi-Ethics (www.hiethics.com) and subscribes to the principles of the Health on the Net Foundation (www.hon.ch).
|
The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed medical professional should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. © 1997-2007
A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.