Vanadom

DESCRIPTION

Vanadom (carisoprodol) tablets are available as 350 mg round, white tablets.

Carisoprodol is a white, crystalline powder, having a mild, characteristic odor and a bitter taste. It is slightly solublein water; freely soluble in alcohol, inchloroform, and in acetone; and its solubility is practically independent of pH. Carisoprodol is present as a racemic mixture.

Chemically, carisoprodol is (±)-2-Methyl-2-propyl-1,3-propanediol carbamate isopropylcarbamate and the molecular formula is C¹²H²⁴N²O⁴, with a molecular weight of 260.33. The structural formula is:

Other ingredients in the Vanadom drug product include hydroxypropyl methylcellulose, lactose monohydrate, microcrystalline cellulose, sodium starch glycolate, stearic acid and talc.

INDICATIONS

Vanadom is indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults.

Limitation Of Use

Vanadom should only be used for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use has not been established and because acute, painful musculoskeletal conditions are generally of short duration. [seeDOSAGE AND ADMINISTRATION].

DOSAGE AND ADMINISTRATION

The recommended dose of Vanadom is 350 mg three times a day and at bedtime. The recommended maximum duration of Vanadom use is up to two or three weeks.

HOW SUPPLIED

Dosage Forms And Strengths

350 mg Tablets: round, convex, white tablets, inscribed with 111 on one side and “O” on the other side.

Storage And Handling

350 mg Tablets: round, convex, white tablets, inscribed with 111 on one side and “O” on the other side; available in bottles of 100 (NDC69036-920-35).

Storage

Store at controlled room temperature 20° - 25°C (68° - 77°F).

Manufactured by: Oxford Pharmaceuticals, LLC Birmingham, AL 35211. Revised: Mar 2020

SIDE EFFECTS

Clinical Studies Experience

Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect rates observed in practice.

The data described below are based on 1387 patients pooled from two double blind, randomized, multicenter, placebo controlled, one-week trials in adult patients with acute, mechanical, lower back pain [seeClinical Studies]. In these studies, patients were treated with 250 mg of carisoprodol, 350 mg of carisoprodol, or placebo three times a day and at bedtime for seven days. The mean age was about 41 years old with 54% females and 46% males and 74 % Caucasian, 16 % Black, 9% Asian, and 2% other.

There were no deaths and there were no serious adverse reactions in these two trials. In these two studies, 2.7%, 2%, and 5.4%, of patients treated with placebo, 250 mg of carisoprodol, and 350 mg of carisoprodol, respectively, discontinued due to adverse events; and 0.5%, 0.5%, and 1.8% of patients treated with placebo, 250 mg of carisoprodol, and 350 mg of carisoprodol, respectively, discontinued due to central nervous system adverse reactions.

Table 1 displays adverse reactions reported with frequencies greater than 2% and more frequently than placebo in patients treated with carisoprodol in the two trials described above.

Table 1. Patients with Adverse Reactions in Controlled Studies

Adverse Reaction	Placebo (n=560) n(%)	Carisoprodol 250 mg (n=548) n (%)	Carisoprodol 350 mg (n=279) n (%)
Drowsiness	31 (6)	73 (13)	47 (17)
Dizziness	11 (2)	43 (8)	19 (7)
Headache	11 (2)	26 (5)	9 (3)

Post-Marketing Experience

The following events have been reported during postapproval use of Vanadom. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Cardiovascular:Tachycardia, postural hypotension, and facial flushing [seeOVERDOSE].

Central Nervous System:Drowsiness, dizziness, vertigo, ataxia, tremor, agitation, irritability, headache, depressive reactions,syncope, insomnia, and seizures [seeOVERDOSE].

Gastrointestinal:Nausea, vomiting, and epigastric discomfort.

Hematologic:Leukopenia, pancytopenia

DRUG INTERACTIONS

CNS Depressants

The sedative effects of Vanadom and other CNS depressants (e.g., alcohol, benzodiazepines, opioids, tricyclic antidepressants) may be additive. Therefore, caution should be exercised with patients who take more than one of these CNS depressants simultaneously. Concomitant use of Vanadom and meprobamate, a metabolite of Vanadom, is not recommended [see警告AND PRECAUTIONS].

CYP2C19 Inhibitors And Inducers

Carisoprodol is metabolized in the liver by CYP2C19 to form meprobamate [seeCLINICAL PHARMACOLOGY]. Co-administration of CYP2C19 inhibitors, such as omeprazole or fluvoxamine, with Vanadom could result in increased exposure of carisoprodol and decreased exposure of meprobamate. Co-administration of CYP2C19 inducers, such as rifampin or St. John’s Wort, with Vanadom could result in decreased exposure of carisoprodol and increased exposure of meprobamate. Low dose aspirin also showed an induction effect on CYP2C19. The full pharmacological impact of these potential alterations of exposures in terms of either efficacy or safety of Vanadom is unknown.

Drug Abuse And Dependence

Controlled Substance

Vanadom contains carisoprodol, a Schedule IV controlled substance. Carisoprodol has been subject to abuse, misuse, and criminal diversion for nontherapeutic use [see警告AND PRECAUTIONS].

Abuse

Abuse of carisoprodol poses a risk of overdosage which may lead to death, CNS and respiratory depression, hypotension, seizures and other disorders [see警告AND PRECAUTIONSandOVERDOSE]. Patients at high risk of Vanadom abuse may include those with prolonged use of carisoprodol, with a history of drug abuse, or those who use Vanadom in combination with other abused drugs.

Prescription drug abuse is the intentional non-therapeutic use of a drug, even once, for its rewarding psychological effects. Drug addiction, which develops after repeated drug abuse, is characterized by a strong desire to take a drug despite harmful consequences, difficulty in controlling its use, giving a higher priority to drug use than to obligations, increased tolerance, and sometimes physical withdrawal. Drug abuse and drug addiction are separate and distinct from physical dependence and tolerance (for example, abuse or addiction may not be accompanied by tolerance or physical dependence) [seeDrug Abuse And Dependence].

Dependence

Tolerance is when a patient’s reaction to a specific dosage and concentration is progressively reduced in the absence of disease progression, requiring an increase in the dosage to maintain the same. Physical dependence is characterized by withdrawal symptoms after abrupt discontinuation or a significant dose reduction of a drug. Both tolerance and physical dependence have been reported with the prolonged use of Vanadom. Reported withdrawal symptoms with Vanadom include insomnia, vomiting, abdominal cramps, headache, tremors, muscle twitching, anxiety, ataxia, hallucinations, and psychosis. Instruct patients taking large doses of Vanadom or those taking the drug for a prolonged time to not abruptly stop Vanadom [see警告AND PRECAUTIONS].

警告

Included as part of the"PRECAUTIONS"Section

PRECAUTIONS

Sedation

Vanadom has sedative properties (in the low back pain trials, 13% to 17% of patients who received Vanadom experienced sedation compared to 6% of patients who received placebo) [seeADVERSE REACTIONS] 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. There have been post-marketing reports of motor vehicle accidents associated with the use of Vanadom.

Since the sedative effects of Vanadom and other CNS depressants (e.g., alcohol, benzodiazepines, opioids, tricyclic antidepressants) may be additive, appropriate caution should be exercised with patients who take more than one of these CNS depressants simultaneously.

Abuse, Dependence, And Withdrawal

Carisoprodol, the active ingredient in Vanadom, has been subject to abuse, dependence, and withdrawal, misuse and criminal diversion. [seeDrug Abuse And Dependence].

Abuse of Vanadom poses a risk of overdosage which may lead to death, CNS and respiratory depression, hypotension, seizures and other disorders [seeOVERDOSE].

Post-marketing experience cases of carisoprodol abuse and dependence have been reported in patients with prolonged use and a history of drug abuse. Although most of these patients took other drugs of abuse, some patients solely abused carisoprodol. Withdrawal symptoms have been reported following abrupt cessation of Vanadom after prolonged use.

Reported withdrawal symptoms included insomnia, vomiting, abdominal cramps, headache, tremors, muscle twitching, ataxia, hallucinations, and psychosis. One of carisoprodol’s metabolites, meprobamate (a controlled substance), may also cause dependence [seeCLINICAL PHARMACOLOGY].

To reduce the risk of Vanadom abuse assess the risk of abuse prior to prescribing. After prescribing, limit the length of treatment to three weeks for the relief of acute musculoskeletal discomfort, keep careful prescription records, monitor for signs of abuse and overdose, and educate patients and their families about abuse and on proper storage and disposal.

Seizures

已经有上市后癫痫的报告in patients who received Vanadom. Most of these cases have occurred in the setting of multiple drug overdoses (including drugs of abuse, illegal drugs, and alcohol) [seeOVERDOSE].

Nonclinical Toxicology

Carcinogenesis, Mutagenesis, Impairment Of Fertility

Carcinogenesis

Long term studies in animals have not been performed to evaluate the carcinogenic potential of carisoprodol.

Mutagenesis

Carisoprodol was not formally evaluated for genotoxicity. In published studies, carisoprodol was mutagenic in thein vitromouse lymphoma cell assay in the absence of metabolizing enzymes, but was not mutagenic in the presence of metabolizing enzymes. Carisoprodol was clastogenic in thein vitrochromosomal aberration assay using Chinese hamster ovary cells with or without the presence of metabolizing enzymes. Other types of genotoxic tests resulted in negative findings. Carisoprodol was not mutagenic in the Ames reverse mutation assay usingS.typhimuriumstrains with or without metabolizing enzymes, and was not clastogenic in anin vivomouse micronucleus assay of circulating blood cells.

Impairment Of Fertility

Carisoprodol was not formally evaluated for effects on fertility. A published reproductive study in which female mice received carisoprodol orally at doses of 300, 750, or 1200 mg/kg/day (approximately 1, 2.6, and 4.1 times the MRHD of 1400 mg per day [350 mg QID] based on body surface area [BSA] comparison) from 1-week prior to mating, to 27-weeks post-mating found no alteration in fertility although an alteration in reproductive cycles characterized by a greater time spent in estrus was observed at a carisoprodol dose of 1200 mg/kg/day. In a 13-week toxicology study that did not determine fertility, mouse testes weight and sperm motility were reduced at a dose of 1200 mg/kg/day (maternal doses equivalent to 4.2-times the MRHD based on BSA comparison). In both studies, the no effect level was 750 mg/kg/day, corresponding to approximately 2.6-times the MRHD based on a BSA comparison. The significance of these findings for human fertility is not known.

Use In Specific Populations

Pregnancy

Risk Summary

Data over many decades of carisoprodol use in pregnancy have not identified a drug-associated risk of major birth defects, miscarriage, or other adverse maternal or fetal outcomes. Data on meprobamate, the primary metabolite of carisoprodol, also do not show a consistent association between maternal use of meprobamate and an increased risk of major birth defects (seeData).

In a published animal reproduction study, pregnant mice administered carisoprodol orally at 2.6- and 4.1-times the maximum recommended human dose ([MRHD] of 1400 mg per day [350 mg QID] based on body surface area [BSA] comparison) from gestation through weaning resulted in reduced fetal weights, postnatal weight gain, and postnatal survival (seeData).

估计背景的风险主要defec诞生ts and miscarriage for the indicated population is unknown. All pregnancies have a background risk of birth defect, loss, or other adverse outcomes. In the U.S. general population, the estimated background risk of major birth defectsand miscarriage in clinically recognized pregnancies is 2 to 4% and 15 to 20%, respectively.

Data

Human Data

回顾性病例对照和正ort studies of meprobamate use during the first trimester of pregnancy have not consistently identified an increased risk or pattern of major birth defects. For children exposed to meprobamate in-utero, one study found no adverse effect on mental or motor development or IQ scores.

Animal Data

Embryofetal development studies in animals have not been completed.

In a published pre- and post-natal development animal study, pregnant mice administered carisoprodol orally at 300, 750, or 1200 mg/kg/day (approximately 1-, 2.6-, and 4.1-times the MRHD based on BSA comparison) from 7-days prior to gestation through birth and from lactation through weaning resulted in reduced fetal weights, postnatal weight gain, and postnatal survival at 2.6- and 4.1-times the MRHD.

Lactation

Risk Summary

Data from published literature report that carisoprodol and its metabolite, meprobamate, are present in breastmilk. There are no data on the effect of carisoprodol on milk production. There is one report of sedation in an infant who was breastfed by a mother taking carisoprodol (seeClinical Considerations). Because there have been no consistent reports of adverse events in breastfed infants over decades of use, the developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for Vanadom and any potential adverse effects on the breastfed infant from Vanadom or from the underlying maternal condition.

Clinical Considerations

Infants exposed to Vanadom through breast milk should be monitored for sedation.

Pediatric Use

The efficacy, safety, and pharmacokinetics of Vanadom in pediatric patients less than 16 years of age have not been established.

Geriatric Use

The efficacy, safety, and pharmacokinetics of Vanadom in patients over 65 years old have not been established.

Renal Impairment

的安全性和药物动力学Vanadom patients with renal impairment have not been evaluated. Since Vanadom is excreted by the kidney, caution should be exercised if Vanadom is administered to patients with impaired renal function. Carisoprodol is dialyzable by hemodialysis and peritoneal dialysis.

Hepatic Impairment

的安全性和药物动力学Vanadom patients with hepatic impairment have not been evaluated. Since Vanadom is metabolized in the liver, caution should be exercised if Vanadom is administered to patients with impaired hepatic function.

Patients With Reduced CYP2C19 Activity

有更高的患者减少CYP2C19活动exposure to carisoprodol. Therefore, caution should be exercised in administration of Vanadom to these patients. [seeCLINICAL PHARMACOLOGY].

OVERDOSE

Clinical Presentation

Overdosage of Vanadom commonly produces CNS depression. Death, coma, respiratory depression, hypotension, seizures, delirium, hallucinations, dystonic reactions, nystagmus, blurred vision, mydriasis, euphoria, muscular incoordination, rigidity, and/or headache have been reported with Vanadom overdosage. Serotonin syndrome has been reported with carisoprodol intoxication. Many of the carisoprodol overdoses have occurred in the setting of multiple drug overdoses (including drugs of abuse, illegal drugs, and alcohol). The effects of an overdose of carisoprodol and other CNS depressants (e.g., alcohol, benzodiazepines, opioids, tricyclic antidepressants) can be additive even when one of the drugs has been taken in the recommended dosage. Fatal accidental and non-accidental overdoses of Vanadom have been reported alone or in combination with CNS depressants.

Treatment Of Overdosage

Basic life support measures should be instituted as dictated by the clinical presentation of the Vanadom overdose. Vomiting should not be induced because of the risk of CNS and respiratory depression, and subsequent aspiration. Circulatory support should be administered with volume infusion and vasopressor agents if needed. Seizures should be treated with intravenous benzodiazepines and the reoccurrence of seizures may be treated with phenobarbital. Incases of severe CNS depression, airway protective reflexes may be compromised and tracheal intubation should be considered for airway protection and respiratory support.

去污的情况下严重的毒性,ctivated charcoal should be considered in a hospital setting in patients with large overdoses who present early and are not demonstrating CNS depression and can protect their airway.

For more information on the management of an overdose of Vanadom,contact a Poison Control Center.

CONTRAINDICATIONS

Vanadom is contraindicated in patients with a history of acute intermittent porphyria or a hypersensitivity reaction to a carbamate such as meprobamate.

CLINICAL PHARMACOLOGY

Mechanism Of Action

The mechanism of action of carisoprodol in relieving discomfort associated with acute painful musculoskeletal conditions has not been clearly identified.

In animal studies, muscle relaxation induced by carisoprodol is associated with altered interneuronal activity in the spinal cord and in the descending reticular formation of the brain.

Pharmacodynamics

Carisoprodol is a centrally acting skeletal muscle relaxant that does not directly relax skeletal muscles.

A metabolite of carisoprodol, meprobamate, has anxiolytic and sedative properties. The degree to which these properties of meprobamate contribute to the safety and efficacy of Vanadom is unknown.

Pharmacokinetics

Absorption

The pharmacokinetics of carisoprodol and its metabolite meprobamate were studied in a crossover study of 24 healthy subjects (12 male and 12 female) who received single doses of 250 mg and 350 mg carisoprodol (see Table 2). The exposure of carisoprodol and meprobamate was dose proportional between the 250 mg and 350 mg doses. The Cmax of meprobamate was 2.5 ± 0.5 μg/mL (mean ± SD) after administration of a single 350 mg dose of carisoprodol, which is approximately 30% of the Cmax of meprobamate (approximately 8 μg/mL) after administration of a single 400 mg dose of meprobamate.

Table 2. Pharmacokinetic Parameters of Carisoprodol and Meprobamate (Mean ± SD,n=24)

	250 mg Carisoprodol	350 mg Carisoprodol
Carisoprodol
Cmax (μg/mL)	1.2 ± 0.5	1.8 ± 1.0
AUCinf (μg*hr/mL)	4.5 ± 3.1	7.0 ± 5.0
Tmax (hr)	1.5 ± 0.8	1.7 ± 0.8
T1/2(hr)	1.7 ± 0.5	2.0 ± 0.5
Meprobamate
Cmax (μg/mL)	1.8 ± 0.3	2.5 ± 0.5
AUCinf (μg*hr/mL)	32 ± 6.2	46 ± 9.0
Tmax (hr)	3.6 ± 1.7	4.5 ± 1.9
T1/2(hr)	9.7 ± 1.7	9.6 ± 1.5

Absolute bioavailability of carisoprodol has not been determined. The mean time to peak plasma concentrations (Tmax) of carisoprodol was approximately 1.5 to 2 hours.

Food Effect

Co-administration of a high-fat meal with Vanadom (350 mg tablet) had no effect on the pharmacokinetics of carisoprodol. Therefore, Vanadom may be administered with or without food.

Elimination

Metabolism

The major pathway of carisoprodolmetabolismis via the liver by cytochrome enzyme CYP2C19 to form meprobamate. This enzyme exhibits geneticpolymorphism(see Patients with Reduced CYP2C19 Activity below).

Excretion

Carisoprodol is eliminated by both renal and non-renal routes with a terminal elimination half-life of approximately 2 hours. The half-life of meprobamate is approximately 10 hours.

Specific Populations

Sex

Exposure of carisoprodol is higher in female than in male subjects (approximately 30-50% on a weight adjusted basis). Overall exposure of meprobamate is comparable between female and male subjects.

Patients With Reduced CYP2C19 Activity

Vanadom should be used with caution in patients with reduced CYP2C19 activity. Published studies indicate that patients who are poor CYP2C19 metabolizers have a 4-fold increase in exposure to carisoprodol, and concomitant 50% reduced exposure to meprobamate compared to normal CYP2C19 metabolizers. Theprevalenceof poor metabolizers in Caucasians and African Americans is approximately 3-5% and in Asians is approximately 15-20%.

Clinical Studies

The safety and efficacy of carisoprodol for the relief of acute,idiopathicmechanicallow back painwas evaluated in two, 7-day, double blind, randomized, multicenter, placebo controlled, U.S. trials (Studies 1 and 2). Patients had to be 18 to 65 years old and had to have acuteback pain(≤ 3 days of duration) to be included in the trials. Patients with chronic back pain; at increased risk for vertebralfracture(e.g., history ofosteoporosis); with a history of spinalpathology(e.g., herniatednucleuspulposus,spondylolisthesisorspinal stenosis); with inflammatory back pain, or with evidence of a neurologic deficit were excluded from participation. Concomitant use of analgesics (e.g.,acetaminophen, NSAIDs, tramadol,opioidagonists), other muscle relaxants,botulinum toxin, sedatives (e.g., barbiturates,benzodiazepines, promethazine hydrochloride), and anti-epileptic drugs was prohibited.

In Study 1, patients were randomized to one of three treatment groups (i.e., carisoprodol 250 mg, carisoprodol 350 mg, or placebo) and in Study 2 patients were randomized to two treatment groups (i.e., carisoprodol 250 mg or placebo). In both studies, patients received study medication three times a day and at bedtime for seven days.

The primary endpoints were the relief from starting backache and the global impression of change, as reported by patients, on Study Day 3. Both endpoints were scored on a 5-point rating scale from 0 (worst outcome) to 4 (best outcome) in both studies. The primary statistical comparison was between the carisoprodol 250 mg and placebo groups in both studies.

The proportion of patients who used concomitant acetaminophen, NSAIDs, tramadol, opioid agonists, other muscle relaxants, and benzodiazepines was similar in the treatment groups.

The results for the primary efficacy evaluations in the acute, low back pain studies are presented in Table 3.

Table 3. Results of the Primary Efficacy Endpoints^ain Studies 1 and 2

Study	Parameter	Placebo	Carisoprodol 250 mg	Carisoprodol 350 mg
1	Number of Patients	n=269	n=264	n=273
	Relief from Starting Backache, Mean(SE)b	1.4 (0.1)	1.8 (0.1)	1.8 (0.1)
	Difference between Carisoprodol and Placebo, Mean (SE)b(95% CI)		0.4 (0.2, 0.5)	0.4 (0.2, 0.6)
	Global Impression of Change, Mean (SE)b	1.9 (0.1)	2.2 (0.1)	2.2 (0.1)
	Difference between Carisoprodol andPlacebo, Mean (SE)b(95% CI)		0.2 (0.1, 0.4)	0.3 (0.1, 0.4)
2	Number of Patients	n=278	n=269
	Relief from Starting Backache, Mean(SE)b	1.1 (0.1)	1.8 (0.1)
	Difference between Carisoprodol and Placebo, Mean (SE)b(95% CI)		0.7 (0.5, 0.9)
	Global Impression of Change, Mean (SE)b	1.7 (0.1)	2.2 (0.1)
	Difference between Carisoprodol andPlacebo, Mean (SE)b(95% CI)		0.5 (0.4, 0.7)
a.The primary efficacy endpoints (Relief from Starting Backache and Global Impression of Change) were assessed by the patients on Study Day 3. These endpoints were scored on a 5-point rating scale from 0 (worst outcome) to 4 (best outcome). b.Mean is the least squared mean and SE is the standard error of the mean. The ANOVA model was used for the primary statistical comparison between the Carisoprodol 250 mg and placebo groups.

Patients treated with carisoprodol experienced improvement in function as measured by the Roland-Morris Disability Questionnaire (RMDQ) score on Days 3 and 7.

PATIENT INFORMATION

Patients should be advised to contact their physician if they experience any adverse reactions to Vanadom.

Sedation

Advise patients that Vanadom may cause drowsiness and/or dizziness, and has been associated with motor vehicle accidents. Patients should be advised to avoid taking Vanadom before engaging in potentially hazardous activities such as driving a motor vehicle or operating machinery [see警告AND PRECAUTIONS].

Avoidance Of Alcohol And Other CNS Depressants

Advise patients to avoid alcoholic beverages while taking Vanadom and to check with their doctor before taking other CNS depressants such as benzodiazepines, opioids,tricyclic antidepressants, sedatingantihistamines, or others edatives [see警告AND PRECAUTIONS].

Vanadom Should Only Be Used For Short-Term Treatment

Advise patients that treatment with Vanadom should be limited to acute use (up to two or three weeks) for the relief of acute, musculoskeletal discomfort. In the post-marketing experience with Vanadom, cases of dependence, withdrawal, and abuse have been reported with prolonged use. If the musculoskeletal symptoms still persist, patients should contact their healthcare provider for further evaluation.

Lactation

Advise nursing mothers using Vanadom to monitor neonates for signs of sedation [seeUse In Specific Populations].