| 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. |