Carisoprodol Facts
Depressant;
Description
Carisoprodol — Soma — is a synthetic depressant of the propanediol dicarbamate class. It is a structural relative of meprobamate, modified to deliver muscle relaxation with reduced abuse liability. It amplifies inhibitory GABA signaling in the brain — and can open GABA receptors directly without GABA present — producing sedation, anxiety relief, and muscle relaxation.[1]
Subjective effects include sedation, anxiolysis, muscle relaxation, dizziness, and psychomotor impairment. The experience is defined by a heavy, body-dominant calm that blankets motor control and thought simultaneously — more physically engulfing than benzodiazepine sedation.[2]
Carisoprodol produces rapid physical dependence, and the gap between a therapeutic and fatal blood concentration is narrow.[3] Its active metabolite meprobamate accumulates with repeated dosing and compounds both dependence and overdose risk; combining carisoprodol with opioids increases overdose risk by 84%.[4]
Dose and durationby route · individual sensitivity varies
Starts in 15 – 60 minLasts 4 – 8 hoursAfter-effects 1 – 12 hours
Body and dependence
- Acute toxicity
- High
- Chronic toxicity
- High
- Physical dependence
- High
- Psychological dependence
- High
- Withdrawal
- Life-threatening · fatal · medical supervision
- Compulsive redosing
- Moderate
Tolerance
- Builds
- Moderate
- Fully resets after
- 30 days
- Carries over to
- benzodiazepines;
barbiturates; alcohol
Effectslikely at a common dose
- Perception
- none likely · 5 possible, including Spatial disorientation, Visual acuity suppression, Vestibular distortion
- Body
- Sedation;
Motor control impairment; Muscle relaxation; Physical fatigue; +10 possible, including Dizziness, Nausea, Headache - Thinking
- Cognitive impairment;
+18 possible, including Analysis suppression, Decision impairment, Information processing suppression - Feeling
- none likely · 3 possible
- Self
- none likely · 4 possible, including Communication suppression
- Time
- none likely · 2 possible, including Temporal disorientation
Who shouldn't take it
Combinations60 recorded
Seek help immediately if
- Extreme drowsiness — can't stay awake or be roused
- Confusion, slurred speech, severe loss of coordination
- Slow, shallow, or irregular breathing
- Unconsciousness / unresponsive; limp, floppy body
- Blue lips or fingertips
- Vomiting while sedated (choking / aspiration risk)
- Cold, clammy skin; weak pulse
What to do
- Try to wake them — shout, firm sternal rub
- If unresponsive or breathing is impaired, call emergency services
- Place them in the recovery position — critical, they can choke on vomit
- Monitor breathing continuously; be ready to give rescue breaths / CPR
- Never leave them alone to "sleep it off"
- Do not give other drugs, stimulants, or more depressants
Most depressant overdoses resolve with airway protection, breathing support, and monitoring. The danger is respiratory depression and choking on vomit — sharply worse when combined with opioids or alcohol. GHB/GBL overdoses often involve sudden deep unconsciousness and may self-resolve, but airway protection is essential.
988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE
References
- [1]^Kumar M, Gonzalez LA, Dillon GH (2015) Assessment of subunit-dependent direct gating and allosteric modulatory effects of carisoprodol at GABA(A) receptors — Neuropharmacology doi:10.1016/j.neuropharm.2015.04.007
- [2]^Zacny JP, Paice JA, Coalson DW (2011) Characterizing the subjective and psychomotor effects of carisoprodol in healthy volunteers — Pharmacology Biochemistry and Behavior doi:10.1016/j.pbb.2011.08.011
- [3]^McIntyre IM, Sherrard J, Lucas J (2012) Postmortem carisoprodol and meprobamate concentrations in blood and liver: lack of significant redistribution — Journal of Analytical Toxicology doi:10.1093/jat/bks011
- [4]^Li Y, Delcher C, Wei YJ, Reisfield GM, Brown JD, Tighe P, Winterstein AG (2020) Risk of Opioid Overdose Associated With Concomitant Use of Opioids and Skeletal Muscle Relaxants: A Population-Based Cohort Study — Clinical Pharmacology and Therapeutics doi:10.1002/cpt.1807