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Carisoprodol (Soma) 350 mg
- Generic name: Carisoprodol
- Trade names: Carisoma, Soma, Somadril (Wallace), Vanadom
- Dosages: 350 mg tablets
- Pharmacologic category: Skeletal muscle relaxant
- FDA approved: April 09, 1959
- Habit forming? Possibly
- Pregnancy risk factor: C
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Medical uses
Carisoprodol is used with rest, physical therapy, and other measures
to relax muscles and relieve pain, stiffness and discomfort caused by strains,
sprains, and other muscle injuries. Muscle relaxers are for specific
muscle injury and pain and should not be used for general body aches and pains.
In clinical trial Carisoprodol was better than propoxyphene in relieving stiffness and increasing movement. It was
better than butabarbital for increasing movement and leading to general improvement. Carisoprodol was superior to diazepam
for relieving the symptoms of acute lower back pain. According to the clinical data, it was similarly effective as the centrally
acting muscle relaxant cyclobenzaprine. [3-6]
Dosage:
Carisoprodol (Soma) is most often taken therapeutically in doses of 350 mg up to 3 or 4 times per day. It is not recommended in children under 12 yr. If you need to discontinue, do it gradually.
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Pharmacological characteristics
- Elimination half-life: 3-4 hours
- Metabolism: metabolized to to its metabolites hydroxycarisoprodol, hydroxymeprobamate, and meprobamate in the liver
via cytochrome P450 enzyme, CYP2C19.
- Excretion: eliminated by both renal and non-renal routes. It is dialyzable by peritoneal and hemodialysis.
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Benefits
- Potent muscle relaxer - for many people carisoprodol is the best out of all muscle relaxers.
- Effective for muscle spasms and back pain - disrupts the spasm-pain-spasm progression, improves range of motion, and maximizes everyday functionality [1].
- Can alleviate pain and induce sleep in fibromyalgia [2].
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Concerns
- Potential for abuse and dependence. Carisoprodol itself is probably not addictive, but it is metabolized into meprobamate in the liver, which is habit forming. The majority of cases of drug abuse, dependence and withdrawal have been reported with prolonged use of carisoprodol (beyond several months) or in combination with other CNS depressants or psychotropic drugs. However, there have been cases reported with carisoprodol alone.
- Withdrawal symptoms following abrupt cessation after prolonged use.
- Possible intoxication and psychomotor impairment. Carisoprodol is pretty unsafe for drivers.
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Mechanism of action
Carisoprodol works by blocking nerve impulses (or pain sensations)
that are sent to the brain. It interrupts neuronal communication within the reticular formation and spinal cord.
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Reviews, Discussions & Forums
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References
- 1. Toth PP, Urtis J. Commonly used muscle relaxant therapies
for acute low back pain: a review of carisoprodol, cyclobenzaprine, and metaxalone. Clin Ther. 2004 Sep;26(9):1355-67.
PubMed
- 2. Vaeroy H, Abrahamsen A, Forre O, Kass E. Fibromyalgia
(fibrositis syndrome): a parallel double blind trial with carisoprodol,
paracetamol and caffeine (Somadril comp) versus placebo. Clin
Rheumatol. 1989 Jun;8(2):245-50. PubMed
- 3. Hindle T. Comparison of carisoprodol, butabarbital, and
placebo in low back syndrome. Calif Med. 1972;117:7-11.
- 4. Baratta RR. A double-blind comparative study of carisoprodol,
propoxyphene, and placebo in the management of low back syndrome.
Curr Ther Res Clin Exp. Sep 1976;20(3):233-240.
- 5. Boyles W, Glassmann J, Soyka J. Management of acute muskuloskeletal
conditions: thoracolumbar strain and sprain. A double-blind
evaluation comparing the efficacy and safety of carisoprodol
with diazepam. Today's Ther Trends. 1983;1:1-16.
- 6. Rollings H, Glassmann J, Soyka J. Management of acute musculoskeletal
conditions - thoracolumbar strain and sprain: a double-blind
evaluation comparing the efficacy and safety of carisoprodol
with cyclobenzadrine. Curr Ther Res. 1982;34(6):917-928.
Last modified: August, 2010
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Interesting facts
- Carisoprodol is a non-controlled skeletal muscle relaxant whose
active metabolite is meprobamate (Schedule IV controlled substance
in Florida, Indiana, Oregon, Oklahoma, Texas, and some other states, but not a federally Schedule IV controlled substance).
- Carisoprodol is chemically, structurally, and pharmacologically
related to meprobamate. Meprobamate is a CNS depressant, indicated
for the management of anxiety.
- In addition to the desired skeletal muscle relaxing properties, carisoprodol
produces weak anticholinergic, antipyretic and analgesic action.
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