Library

Carisoprodol

Carisoprodol is a carbamate sedative-hypnotic and centrally acting muscle relaxant first approved for medical use in 1959. Developed as an improvement upon meprobamate, it functions as a prodrug that is metabolized into meprobamate in the body. Prescribed for the short-term treatment of musculoskeletal pain, it also possesses anxiolytic and hypnotic properties. Its effects are often compared to barbiturates, and it has been largely supplanted by benzodiazepines due to safety concerns. Its European Union approval was withdrawn in 2008.

Carisoprodol molecular structure
Carisoprodol molecular structure diagram from the DrugsPRO substance library.

Also known as: Soma, Rela, Myolax, Vanadom, Carisoma, Somadril, Isomeprobamate, Isopropyl meprobamate, Carisoprodolum, Carisoprodolo

Classification

  • Chemical: Medicine
  • Psychoactive: Depressant
  • Tag: 1,3-Propanediol dicarbamate
  • Tag: Anxiolytic
  • Tag: Carbamate
  • Tag: GABAergic
  • Tag: Habit-Forming
  • Tag: Muscle Relaxant
  • Tag: Sedative

Effects

  • Physical Euphoria
  • Sedation
  • Muscle Relaxation
  • Headache
  • Nausea
  • Increased Heart Rate
  • Cognitive Euphoria
  • Sociability Enhancement
  • Anxiety Suppression
  • Amnesia
  • Confusion
  • Motor Control Loss
  • Cognitive Dysphoria
  • Disinhibition
  • External Hallucination
  • Double Vision
  • Dulled Perception

Routes of Administration

Oral

Dosage

  • Heavy: 700+ mg
  • Light: 100 – 350 mg
  • Common: 350 – 500 mg
  • Strong: 500 – 700 mg
  • Threshold: 100 mg

Duration

  • Onset: 0.25-1 h
  • Peak: 1.5-2 h
  • After Effects: 1-12 h
  • Offset: 2-4 h
  • Total Duration: 4-6 h

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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Carisoprodol - DrugsPRO substansvejledning

Carisoprodol: Carisoprodol is a carbamate sedative-hypnotic and centrally acting muscle relaxant first approved for medical use in 1959. Developed as an improvement upon meprobamate, it functions as a prodrug that is metabolized into meprobamate in the body. Prescribed for the short-term treatment o

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