The degree to which it contributes to the efficacy of carisoprodol is unknown. Carisoprodol is dialyzable by peritoneal and hemodialysis. Carisoprodol is metabolized in the liver and is excreted by the kidneys. One of the products of metabolism, is active as an anxiolytic.
This enzyme exhibits genetic polymorphism. Carisoprodol is metabolized in the liver via cytochrome P450 enzyme, CYP2C19. For Caucasians and Blacks, the prevalence of poor metabolizers is3-5-%. These levels are approximay 1/4 of those seen following a single 400 mg dose of meprobamate. Following a single 350 mg dose of carisoprodol, the corresponding normalized peak concentration of meprobamate, which is a metabolite of carisoprodol, was 2.08 + 0.48 mcg/mL. For example,15-20% of Asian populations may be expected to be poor metabolizers.
Carisoprodol should be used with caution in addiction prone individuals (see DRUG ABUSE AND DEPENDENCE). In postmarketing experience, cases of drug abuse, dependence and withdrawal have been reported.
Each Tablet Contains Carisoprodol 350mg.
Carisoprodol is metabolized in the liver and excreted by the kidney; to avoid its excess accumulation, caution should be exercised in administration to patients with compromised liver or kidney function.
Nausea, vomiting, hiccup, and epigastric distress.
In such cases, tracheal intubation should be considered for airway protection and respiratory support. Treatment of Overdosage : Basic life support measures should be instituted as dictated by the clinical presentation. In cases of severe CNS depression, airway protective reflexes may be compromised. Circulatory support should be administered with volume infusion and pressor agents as indicated. Gastric lavage should be considered soon after ingestion (usually within 1 hour). Induced emesis is not recommended due to the risk of CNS and respiratory depression.
In case of allergic or idiosyncratic reactions to carisoprodol, discontinue the drug and initiate appropriate symptomatic therapy, which may include epinephrine, antihistamines, and in severe cases corticosteroids.
Concomitant use of carisoprodol and meprobamate is not recommended. Since the effects of carisoprodol and alcohol or carisoprodol and other CNS depressants or psychotropic drugs may be additive, appropriate caution should be exercised with patients who take more than one of these aents simultaneously.
The efficacy and safety of carisoprodol in patients under 12 years of age has not been determined.
Seizures should be treated with a benzodiazepine IV and may be followed with phenobarbital if seizures recur.
The pharmacokinetic profile of carisoprodol in elderly patients has not been evaluated.
However, there have been cases reported with carisoprodol alone. Withdrawal symptoms including abdominal cramps, insomnia, headache, nausea, and seizure, have been reported following abrupt cessation after prolonged use. One of the metabolites of carisoprodol, meprobamate, may be habit forming (see Pharmacokinetics). In postmarketing experience, drug abuse and dependence have been reported. The majority of cases of drug abuse, dependence and withdrawal have been reported with prolonged use of carisoprodol (beyond several months of treatment) or in combination with other CNS depressant or psychotropic drugs.
Carisoprodol is present in breast milk of lactating mothers at concentrations two to four times that of maternal plasma. The safety of this drug in pregnancy or lactation has not been established. This factor should be taken into account when use of the drug is contemplated in breast-feeding patients. Therefore, use of this drug in pregnancy, in nursing mothers, or in women of childbearing potential requires that the potential benefits of the drug be weighed against the potential hazards to mother and child.
Patients should be warned that carisoprodol may have sedative properties and may impair the mental and/or physical abilities required for the performance of potentially hazardous tasks such as driving a motor vehicle or operating machinery.
Symptoms usually subside over the course of the next several hours. Symptoms reported include: extreme weakness, transient quadriplegia, dizziness, ataxia, temporary loss of vision, diplopia, mydriasis, dysarthria, agitation, euphoria, confusion, and disorientation. On very rare occasions, the first dose of carisoprodol has been followed by idiosyncratic symptoms appearing within minutes or hours. Supportive and symptomatic therapy, including hospitalization, may be necessary.
For more information on the management of overdose or unintentional ingestion, contact a Poison Control Center.
The pharmacokinetics of carisoprodol was determined in a small in vivo biostudy of 5 men and 5 women. When the dose was normalized to 350 mg, the mean peak plasma concentration (Cmax) achieved was 2.29 + 0.68 mcg/mL. Women tended to reach peak plasma concentrations earlier than men (1.45 vs. The clinical significance of these findings is unknown and they may in part be due to the small number of subjects present in the trial. 0.38 L/hour/kg). 2.5 hours) and had a faster apparent oral clearance (0.772 vs.
The onset of action is rapid and lasts four to six hours. The mode of action of carisprodol in relieving acute muscle spasm of local origin has not been clearly identified, but may be related to its sedative properties. In animals, carisoprodol has been shown to produce muscle relaxation by blocking interneuronal activity and depressing transmission of polysynaptic neurons in the spinal cord and in the descending reticular formation of the brain. Carisoprodol is a centrally acting skeletal muscle relaxant that does not directly relax skeletal muscles in man.
30 Tablets NDC CARISOPRODOL Tablets, USP Rx Only 350MG.
Store at 20° to 25°C (68° to 77°F).
CARISOPRODOL - carisoprodol tablet Apotheca, Inc.
Also observed: dizziness, vertigo, ataxia, tremor, agitation, irritability, headache, depressive reactions, syncope, seizures, and insomnia (see Idiosyncratic Reactions under WARNINGS). Drowsiness and other CNS effects may require dosage reduction.
There have been rare reports of seizures in postmarketing surveillance in temporal association with carisoprodol. These events have involved patients with and without previous medical histories of seizures and have occurred during therapeutic use, with overdose and during withdrawal from prolonged use. The role of carisoprodol in the causality of these seizures has not been established.
The mean Cmax of metabolite, meprobamate, was 2.08 + 0.48 mcg/mL, a subtherapeutic concentration when compared to a plasma concentration of a single oral meprobamate 400 mg tablet which would yield a meprobamate concentration of approximay 8.0 mcg/mL. By normalizing to a single 350 mg Carisoprodol tablet, the mean peak plasma concentration (Cmax) was 2.29 + 0.68 mcg/mL, the area under the plasma level time curve (AUC0-0) was 10.33 + 3.87 mcg/mL* hour, and the oral clearance (Cl/F) was 39.52 + 16.83 L/hour. Following a single oral dose of carisoprodol, the time to maximum concentratin (Tmax) was 1.98 + 1.16 hours and the terminal elimination half-life was 2.44 + 0.93 hours.
Occasionally, within the period of the first to fourth dose of carisoprodol allergic reactions have occurred in patients who have had no previous contact with the drug. Skin rash, erythema multiforme, pruritus, eosinophilia, and fixed drug eruption have been reported with carisoprodol with cross reaction to meprobamate. Severe reactions have been manifested by asthmatic episodes, fever, weakness, dizziness, angioneurotic edema, smarting eyes, hypotension, and anaphylactoid shock (see also Idiosyncratic Reactions under WARNINGS).
Carisoprodol should be used with caution in addiction-prone individuals, and its use should generally be limited to the acute treatment setting and not for more than 2-3 weeks.
Tachycardia, postural hypotension, and facial flushing.
The following types of treatment have been used successfully with the related drug meprobamate: activated charcoal (oral or via nasogastric tube), forced diuresis, peritoneal dialysis, and hemodialysis (carisoprodol is dialyzable). Carisoprodol is metabolized in the liver and excreted by the kidney. Carisoprodol can be measured in biological fluids by gas chromatography (Douglas, J.F. et al.: J Pharm Sci 58: 145, 1969). Observe for possible relapse due to incomplete gastric emptying and delayed absorption. Careful monitoring of urinary output is necessary and caution should be taken to avoid overhydration.
DISPENSE IN TIGHT, LIGHT-RESISTANT CONTAINER.
The following signs ans symptoms may be associated with carisoprodol overdosage: horizontal and vertical nystagmus, blurred vison, mydriasis, mild tachycardia and hypotension, respiratory depression, euphoria,, CNS stimulation, muscular incoordination, and/or rigidity, confusion, headache, hallucinations, and dystonic reactions. Shock, respiratory depression, seizures and death have also been reported rarely. Fatal accidental and non-accidental overdoses have been reported alone or in combination with alcohol or psychotropic drugs. The effects of an overdosage of carisoprodol and alcohol or other CNS depressants or psychotropic agents can be additive even ewhen one of the drugs has been taken in the usual recommended dosage. Overdosage of carisoprodol produces CNS depression, and in severe cases coma.Carisoprodol