oxybutynin chloride

Generic Name: oxybutynin chloride
Dosage Form: Oral solution

Rx only

oxybutynin chloride Description

Each 5 mL of oxybutynin chloride syrup (oxybutynin chloride oral solution) contains 5 mg of oxybutynin chloride, USP.

Chemically, oxybutynin chloride is d,l (racemic) 4-diethylamino-2-butynyl phenylcyclohexylglycolate hydrochloride. The empirical formula of oxybutynin chloride is C22H31NO3•HCl. The structural formula appears below:

oxybutynin chloride is a white crystalline solid with a molecular weight of 393.9. It is readily soluble in water and acids, but relatively insoluble in alkalis.

oxybutynin chloride Syrup (oxybutynin chloride Oral Solution) also contains: Apple-Watermelon flavor, citric acid, FD&C Green #3, glycerin, methylparaben, purified water, sodium citrate, sorbitol solution, and sucrose.

oxybutynin chloride Syrup (oxybutynin chloride Oral Solution) is for oral administration.

Therapeutic Category: Antispasmodic, anticholinergic.

oxybutynin chloride - Clinical Pharmacology

oxybutynin chloride exerts a direct antispasmodic effect on smooth muscle and inhibits the muscarinic action of acetylcholine on smooth muscle. oxybutynin chloride exhibits only one-fifth of the anticholinergic activity of atropine on the rabbit detrusor muscle, but four to ten times the antispasmodic activity. No blocking effects occur at skeletal neuromuscular junctions or autonomic ganglia (antinicotinic effects).

oxybutynin chloride relaxes bladder smooth muscle. In patients with conditions characterized by involuntary bladder contractions, cystometric studies have demonstrated that oxybutynin chloride increases bladder (vesical) capacity, diminishes the frequency of uninhibited contractions of the detrusor muscle, and delays the initial desire to void. oxybutynin chloride thus decreases urgency and the frequency of both incontinent episodes and voluntary urination.

Antimuscarinic activity resides predominately in the R-isomer. A metabolite, desethyloxybutynin, has pharmacological activity similar to that of oxybutynin in in vitro studies.

Pharmacokinetics

Absorption

Following oral administration of oxybutynin chloride, oxybutynin is rapidly absorbed achieving Cmax within an hour, following which plasma concentration decreases with an effective half-life of approximately 2 to 3 hours. The absolute bioavailability of oxybutynin is reported to be about 6% (range 1.6 to 10.9%) for both the tablet and oral solution. Wide interindividual variation in pharmacokinetic parameters is evident following oral administration of oxybutynin.

The mean pharmacokinetic parameters for R- and S-oxybutynin are summarized in Table 1. The plasma concentration-time profiles for R- and S-oxybutynin are similar in shape; Figure 1 shows the profile for R-oxybutynin.

Table 1

Mean (SD) R- and S-Oxybutynin Pharmacokinetic Parameters Following Three doses of oxybutynin chloride 5 mg administered every 8 hours (n=23)
	R-oxybutynin	S-oxybutynin
Parameters (units)
Cmax (ng/mL)	3.6 (2.2)	7.8 (4.1)
Tmax (h)	0.89 (0.34)	0.65 (0.32)
AUCt (ng∙h/mL)	22.6 (11.3)	35.0 (17.3)
AUCinf (ng∙h/mL)	24.3 (12.3)	37.3 (18.7)

Figure 1. Mean R-oxybutynin plasma concentrations following three doses of oxybutynin chloride 5 mg administered every 8 hours for 1 day in 23 healthy adult volunteers

oxybutynin chloride steady-state pharmacokinetics was also studied in 23 pediatric patients with detrusor overactivity associated with a neurological condition (e.g., spina bifida). These pediatric patients were on oxybutynin chloride tablets (n=11) with total daily dose ranging from 7.5 mg to 15 mg (0.22 to 0.53 mg/kg) or oxybutynin chloride syrup (oxybutynin chloride oral solution) (n=12) with total daily dose ranging from 5 mg to 22.5 mg (0.26 to 0.75 mg/kg). Overall, most patients (86.9%) were taking a total daily oxybutynin chloride dose between 10 mg and 15 mg. Sparse sampling technique was used to obtain serum samples. When all available data are normalized to an equivalent of 5 mg twice daily oxybutynin chloride, the mean pharmacokinetic parameters derived for R- and S-oxybutynin and R- and S-desethyloxybutynin are summarized in Table 2a (for tablet) and Table 2b (for oral solution). The plasma-time concentration profile for R- and S-oxybutynin are similar in shape; Figure 2 shows the profile for R-oxybutynin when all available data are normalized to an equivalent of 5 mg twice daily.

Table 2a

Mean ± SD R- and S-Oxybutynin and R- and S-Desethyloxybutynin Pharmacokinetic Parameters In Children Aged 5-15 Following Administration of 7.5 mg to 15 mg Total Daily Dose of oxybutynin chloride Tablets (N=11)
All Available Data Normalized to An Equivalent of oxybutynin chloride Tablets 5 mg BID or TID at Steady State
* Reflects Cmax for pooled data † AUC0-end of dosing interval
	R-Oxybutynin	S-Oxybutynin	R-Desethyloxybutynin	S-Desethyloxybutynin
Cmax=* (ng/mL)	6.1 ± 3.2	10.1 ± 7.5	55.4 ± 17.9	28.2 ± 10.0
Tmax (hr)	1.0	1.0	2.0	2.0
AUC† (ng∙hr/mL)	19.8 ± 7.4	28.4 ± 12.7	238.8 ± 77.6	119.5 ± 50.7

Table 2b

Mean ± SD R- and S-Oxybutynin and R- and S-Desethyloxybutynin Pharmacokinetic Parameters In Children Aged 5-15 Following Administration of 5 mg to 22.5 mg Total Daily Dose of oxybutynin chloride Syrup (oxybutynin chloride Oral Solution) (N=12)
All Available Data Normalized to An Equivalent of oxybutynin chloride Syrup (oxybutynin chloride Oral Solution) 5 mg BID or TID at Steady State
* Reflects Cmax for pooled data † AUC0-end of dosing interval
	R-Oxybutynin	S-Oxybutynin	R-Desethyloxybutynin	S-Desethyloxybutynin
Cmax=* (ng/mL)	5.7 ± 6.2	7.3 ± 7.3	54.2 ± 34.0	27.8 ± 20.7
Tmax (hr)	1.0	1.0	1.0	1.0
AUC† (ng∙hr/mL)	16.3 ± 17.1	20.2 ± 20.8	209.1 ± 174.2	99.1 ± 87.5

Figure 2. Mean steady-state (±SD) R-oxybutynin plasma concentrations following administration of total daily oxybutynin chloride dose of 5 mg to 30 mg (0.21 mg/kg to 0.77 mg/kg) in children 5-15 years of age. – Plot represents all available data normalized to the equivalent of oxybutynin chloride 5 mg BID or TID at steady state

Food Effects

Data in the literature suggests that oxybutynin solution co-administered with food resulted in a slight delay in absorption and an increase in its bioavailability by 25% (n=18).1

Distribution

Plasma concentrations of oxybutynin decline biexponentially following intravenous or oral administration. The volume of distribution is 193 L after intravenous administration of 5 mg oxybutynin chloride.

Metabolism

Oxybutynin is metabolized primarily by the cytochrome P450 enzyme systems, particularly CYP3A4 found mostly in the liver and gut wall. Its metabolic products include phenylcyclohexylglycolic acid, which is pharmacologically inactive, and desethyloxybutynin, which is pharmacologically active.

Excretion

Oxybutynin is extensively metabolized by the liver, with less than 0.1% of the administered dose excreted unchanged in the urine. Also, less than 0.1% of the administered dose is excreted as the metabolite desethyloxybutynin.

Clinical Studies

oxybutynin chloride was well tolerated in patients administered the drug in controlled studies of 30 days" duration and in uncontrolled studies in which some of the patients received the drug for 2 years.

Indications and Usage for oxybutynin chloride

oxybutynin chloride syrup (oxybutynin chloride oral solution) is indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

Contraindications

oxybutynin chloride is contraindicated in patients with urinary retention, gastric retention and other severe decreased gastrointestinal motility conditions, uncontrolled narrow-angle glaucoma and in patients who are at risk for these conditions.

oxybutynin chloride is also contraindicated in patients who have demonstrated hypersensitivity to the drug substance or other components of the product.

Precautions

General

oxybutynin chloride should be used with caution in the frail elderly, in patients with hepatic or renal impairment, and in patients with myasthenia gravis.

oxybutynin chloride may aggravate the symptoms of hyperthyroidism, coronary heart disease, congestive heart failure, cardiac arrhythmias, hiatal hernia, tachycardia, hypertension, myasthenia gravis, and prostatic hypertrophy.

Urinary Retention

oxybutynin chloride should be administered with caution to patients with clinically significant bladder outflow obstruction because of the risk of urinary retention (see CONTRAINDICATIONS).

Gastrointestinal Disorders

oxybutynin chloride should be administered with caution to patients with gastrointestinal obstructive disorders because of the risk of gastric retention (see CONTRAINDICATIONS).

Administration of oxybutynin chloride to patients with ulcerative colitis may suppress intestinal motility to the point of producing a paralytic ileus and precipitate or aggravate toxic megacolon, a serious complication of the disease.

oxybutynin chloride, like other anticholinergic drugs, may decrease gastrointestinal motility and should be used with caution in patients with conditions such as ulcerative colitis, and intestinal atony.

oxybutynin chloride should be used with caution in patients who have gastroesophageal reflux and/or who are concurrently taking drugs (such as bisphosphonates) that can cause or exacerbate esophagitis.

Information for Patients

Patients should be informed that heat prostration (fever and heat stroke due to decreased sweating) can occur when anticholinergics such as oxybutynin chloride are administered in the presence of high environmental temperature.

Because anticholinergic agents such as oxybutynin may produce drowsiness (somnolence) or blurred vision, patients should be advised to exercise caution.

Patients should be informed that alcohol may enhance the drowsiness caused by anticholinergic agents such as oxybutynin.

Drug Interactions

The concomitant use of oxybutynin with other anticholinergic drugs or with other agents which produce dry mouth, constipation, somnolence (drowsiness), and/or other anticholinergic-like effects may increase the frequency and/or severity of such effects.

Anticholinergic agents may potentially alter the absorption of some concomitantly administered drugs due to anticholinergic effects on gastrointestinal motility. This may be of concern for drugs with a narrow therapeutic index.

Mean oxybutynin chloride plasma concentrations were approximately 3-4 fold higher when oxybutynin chloride was administered with ketoconazole, a potent CYP3A4 inhibitor.

Other inhibitors of the cytochrome P450 3A4 enzyme system, such as antimycotic agents (e.g., itraconazole and miconazole) or macrolide antibiotics (e.g., erythromycin and clarithromycin), may alter oxybutynin mean pharmacokinetic parameters (i.e., Cmax and AUC). The clinical relevance of such potential interactions is not known. Caution should be used when such drugs are co-administered.

Carcinogenesis, Mutagenesis, Impairment of Fertility

A 24-month study in rats at dosages of oxybutynin chloride of 20, 80, and 160 mg/kg/day showed no evidence of carcinogenicity. These doses are approximately 6, 25, and 50 times the maximum human exposure, based on surface area.

oxybutynin chloride showed no increase of mutagenic activity when tested in Schizosaccharomyces pompholiciformis, Saccharomyces cerevisiae and Salmonella typhimurium test systems.

Reproduction studies using oxybutynin chloride in the hamster, rabbit, rat, and mouse have shown no definite evidence of impaired fertility.

Pregnancy

Category B. Reproduction studies using oxybutynin chloride in the hamster, rabbit, rat, and mouse have shown no definite evidence of impaired fertility or harm to the animal fetus. The safety of oxybutynin chloride administered to women who are or who may become pregnant has not been established. Therefore, oxybutynin chloride should not be given to pregnant women unless, in the judgment of the physician, the probable clinical benefits outweigh the possible hazards.

Nursing Mothers

It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when oxybutynin chloride is administered to a nursing woman.

Pediatric Use

The safety and efficacy of oxybutynin chloride administration have been demonstrated for pediatric patients 5 years of age and older (see DOSAGE AND ADMINISTRATION).

The safety and efficacy of oxybutynin chloride tablets and oxybutynin chloride syrup (oxybutynin chloride oral solution) were studied in 30 and in 26 children, respectively, in a 24-week, open-label trial. Patients were aged 5-15 years, all had symptoms of detrusor overactivity in association with a neurological condition (e.g., spina bifida), all used clean intermittent catheterization, and all were current users of oxybutynin chloride. Study results demonstrated that the administration of oxybutynin chloride was associated with improvement in clinical and urodynamic parameters.

At total daily doses ranging from 5 mg to 15 mg, treatment with oxybutynin chloride tablets was associated with an increase from baseline in mean urine volume per catheterization from 122 mL to 145 mL, an increase from baseline in mean urine volume after morning awakening from 148 mL to 168 mL, and an increase from baseline in the mean percentage of catheterizations without a leaking episode from 43% to 61%. Urodynamic results in these patients were consistent with the clinical results. Treatment with oxybutynin chloride tablets was associated with an increase from baseline in maximum cystometric capacity from 230 mL to 279 mL, a decrease from baseline in mean detrusor pressure at maximum cystometric capacity from 36 cm H2O to 33 cm H2O, and a reduction in the percentage of patients demonstrating uninhibited detrusor contractions (of at least 15 cm H2O) from 39% to 20%.

At total daily doses ranging from 5 mg to 30 mg, treatment with oxybutynin chloride syrup (oxybutynin chloride oral solution) was associated with an increase from baseline in mean urine volume per catheterization from 113 mL to 133 mL, an increase from baseline in mean urine volume after morning awakening from 143 mL to 165 mL, and an increase from baseline in the mean percentage of catheterizations without a leaking episode from 34% to 63%. Urodynamic results were consistent with these clinical results. Treatment with oxybutynin chloride syrup (oxybutynin chloride oral solution) was associated with an increase from baseline in maximum cystometric capacity from 192 mL to 294 mL, a decrease from baseline in mean detrusor pressure at maximum cystometric capacity from 46 cm H2O to 37 cm H2O, and a reduction in the percentage of patients demonstrating uninhibited detrusor contractions (of at least 15 cm H2O) from 67% to 28%.

As there is insufficient clinical data for pediatric patients under age 5, oxybutynin chloride is not recommended for this age group.

Geriatric Use

Clinical studies of oxybutynin chloride did not include sufficient numbers of subjects age 65 and over to determine whether they respond differently from younger patients. Other reported clinical experience has not identified differences in responses between healthy elderly and younger patients; however, a lower initial starting dose of 2.5 mg given 2 or 3 times a day has been recommended for the frail elderly due to a prolongation of the elimination half-life from 2-3 hours to 5 hours.2,3,4 In general, dose selection for an elderly patient should be cautious, usually starting at the low end of the dosing range, reflecting the greater frequency of decreased hepatic, renal or cardiac function, and of concomitant disease or other drug therapy.

Adverse Reactions

The safety and efficacy of oxybutynin chloride was evaluated in a total of 199 patients in three clinical trials comparing oxybutynin chloride with oxybutynin chloride extended release tablets (see Table 3). These participants were treated with oxybutynin chloride 5-20 mg/day for up to 6 weeks. Table 3 shows the incidence of adverse events judged by investigator to be at least possibly related to treatment and reported by at least 5% of patients.

Table 3

Incidence (%) of Adverse Events Reported by > 5% of Patients Using oxybutynin chloride (5-20 mg/day)
Body System	Adverse Event	Oxybutynin   Chloride   (5 - 20   mg / day)   (n=199)
General	Abdominal pain	6.5%
	Headache	6.0%
Digestive	Dry mouth	71.4%
	Constipation	12.6%
	Nausea	10.1%
	Dyspepsia	7.0%
	Diarrhea	5.0%
Nervous	Dizziness	15.6%
	Somnolence	12.6%
Special Senses	Blurred vision	9.0%
Urogenital	Urination impaired	10.6%
	Post void residuals increase	5.0%
	Urinary tract infection	5.0%

The most common adverse events reported by patients receiving oxybutynin chloride 5-20 mg/day were the expected side effects of anticholinergic agents. The incidence of dry mouth was dose-related.

In addition, the following adverse events were reported by 2 to <5% of patients using oxybutynin chloride (5-20 mg/day) in all studies. General: asthenia, dry nasal and sinus mucous membranes; Cardiovascular: palpitation; Metabolic and Nutritional System: peripheral edema; Nervous System: insomnia, nervousness, confusion; Skin: dry skin; Special Senses: dry eyes, taste perversion.

Other adverse events that have been reported include: tachycardia, hallucinations, cycloplegia, mydriasis, impotence, suppression of lactation, vasodilatation, rash, decreased gastrointestinal motility, flatulence, urinary retention, convulsions and decreased sweating.

Overdosage

Treatment should be symptomatic and supportive. Activated charcoal as well as a cathartic may be administered.

Overdosage with oxybutynin chloride has been associated with anticholinergic effects including central nervous system excitation (e.g., restlessness, tremor, irritability, convulsions, delirium, hallucinations), flushing, fever, dehydration, cardiac arrhythmia, vomiting, and urinary retention. Other symptoms may include hypotension or hypertension, respiratory failure, paralysis, and coma.

Ingestion of 100 mg oxybutynin chloride in association with alcohol has been reported in a 13 year old boy who experienced memory loss, and a 34 year old woman who developed stupor, followed by disorientation and agitation on awakening, dilated pupils, dry skin, cardiac arrhythmia, and retention of urine. Both patients fully recovered with symptomatic treatment.

oxybutynin chloride Dosage and Administration

Adults:

The usual dose is one teaspoonful (5 mg/5 mL) of oral solution two to three times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) of oral solution four times a day. A lower starting dose of 2.5 mg two or three times a day is recommended for the frail elderly.

Pediatric patients over 5 years of age:

The usual dose is one teaspoonful (5 mg/5 mL) of oral solution two times a day. The maximum recommended dose is one teaspoonful (5 mg/5 mL) of oral solution three times a day.

How is oxybutynin chloride Supplied

oxybutynin chloride Syrup (oxybutynin chloride Oral Solution, USP 5 mg per 5 mL) is supplied in bottles of 4 fluid ounces (118 mL) and 16 fluid ounces (473 mL).

Dispense in a tight, light-resistant container as defined in the USP.

Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature].

REFERENCES

1 Yong C et al. Effect of Food on the Pharmacokinetics of Oxybutynin in normal subjects. Pharm Res. 1991;8 (Suppl.): S-320.

2 Hughes KM et al. Measurement of oxybutynin and its N-desethyl metabolite in plasma, and its application to pharmacokinetic studies in young, elderly and frail elderly volunteers. Xenobiotica. 1992; 22 (7): 859-869.

3 Ouslander J et al. Pharmacokinetics and Clinical Effects of Oxybutynin in Geriatric Patients. J. Urol. 1988; 140: 47-50.

4 Yarker Y et al. Oxybutynin: A review of its Pharmacodynamic and Pharmacokinetic Properties, and its Therapeutic Use in Detrusor Instability. Drugs & Aging. 1995; 6 (3): 243-262.

Manufactured by:
VINTAGE PHARMACEUTICALS, LLC
Huntsville, AL 35811

8180539
R2/07-R3

oxybutynin chloride (oxybutynin chloride)

PRODUCT INFO Product Code 0254-9341 Dosage Form SOLUTION Route Of Administration ORAL DEA Schedule

INGREDIENTS Name (Active Moiety) Type Strength oxybutynin chloride (oxybutynin ) Active 5 MILLIGRAM  In 5 MILLILITER Apple-Watermelon flavor Inactive   citric acid Inactive   FD&C Green #3 Inactive   glycerin Inactive   methylparaben Inactive   water Inactive   sodium citrate Inactive   sorbitol solution Inactive   sucrose Inactive

IMPRINT INFORMATION Characteristic Appearance Characteristic Appearance Color Score Shape Symbol Imprint Code Coating Size

PACKAGING # NDC Package Description Multilevel Packaging 1 0254-9341-53 118 MILLILITER In 1 BOTTLE None 2 0254-9341-58 473 MILLILITER In 1 BOTTLE None

Revised: 04/2007