Carisoprodal, Urine

Drug List
Amphetamine
Carisoprodal, Urine
Cocaine
Codeine
Hydrocodone
Hydromorphone
Methadone, Serum
Methadone, Urine
Methamphetamine
Methaqualone
Morphine
Oxycodone
Oxymorphone
Pentobarbital
Phenobarbital
Secobarbital

NAME OF DRUG:  CARRISOPRODAL (SOMA)
PHYSICAL CHARACTERISTICS:  Carisoprodal is a white crystalline powder and is available by prescription in tablet form.
DOSAGE/OCCURRENCE/USAGE:  Carisoprodal is a carbamate derivative used primarily as a muscle relaxant. It is administered orally in doses of 200-350 mg. In certain preparations it is found in combination with such drugs as phenacetin, caffeine and codeine.
BLOOD CONCENTRATIONS VS. DOSAGE:  No information has appeared relating to blood or plasma concentrations of carisoprodal after ingestion of therapeutic amounts.
URINE EXCRETION RATE:  Carisoprodal is known to be metabolized to meprobamate and hydroxymeprobamate. Less than 1% of a single 350 mg oral dose is excreted unchanged in the 24 hour urine, with meprobamate accounting for 4.7% of the dose. Meprobamate and the hydroxylated metabolites may be partially excreted as conjugates.
METABOLITES:  Meprobamate, Hydroxymeprobamate.
TOXICITY:  Overdosage with carisoprodal has resulted in several isolated instances of drug intoxication. One stuporous patient was found to have a blood concentration of 31 mg/L using a specific gas chromatographic method. By means of a similar procedure, serum concentrations of 36 and 15 mg/L, respectively, were found for carisoprodal and its active metabolite, meprobamate, 4.5 hours after the ingestion of 3500 mg by a 5 year old child; at the same time urine concentrations of 24 and 166 mg/L were observed for the two drugs. The patient remained comatose until his death approximately 40 hours after ingestion. Two adults who ingested 8.4 and 9.5 g of carisoprodal and survived were observed to develop maximal serum carbamate concentrations of 37-38 mg/L, as measured by a nonspecific method. A fatality due solely to the ingestion of carisoprodal was found to have concentrations of 110 mg/L in the blood and 165 mg/L in the urine by gas chromatography.
REFERENCES:  Baselt RC.  Disposition of Toxic Drugs and Chemicals in Man, Second Edition. Davis, Calif.: Biomedical Publications, 1982.

Clarke EGC.  Isolation and Identification of Drugs. London: The Pharmaceutical Press, 1969.
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