y retention 6.0% the most common adverse events reported by patients receiving oxybutynin chloride 5 to 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 1 to <5% of patients using oxybutynin chloride (5 to 20 mg/day) in all studies. infections and infestations : nasopharyngitis, upper respiratory tract infection, bronchitis, cystitis, fungal infection; metabolism and nutrition disorders : fluid retention; psychiatric disorders : confusional state; nervous system disorders : dysgeusia, sinus headache; eye disorders : keratoconjunctivitis sicca, eye irritation; cardiac disorders : palpitations, sinus arrhythmia; vascular disorders : flushing; respiratory, thoracic and mediastinal disorders : nasal dryness, cough, pharyngolaryngeal pain, dry throat, sinus congestion, hoarseness, asthma, nasal congestion; gastrointestinal disorders : diarrhea, abdominal pain, loose stools, flatulence, vomiting, abdominal pain upper, dysphagia, aptyalism, eructation, tongue coated; skin and subcutaneous tissue disorders : dry skin, pruritis; musculoskeletal and connective tissue disorders : back pain, arthralgia, pain in extremity, flank pain; renal and urinary disorders : dysuria, pollakiuria; general disorders and administration site conditions : fatigue, edema peripheral, asthenia, pain, thirst, edema; investigations : blood pressure increased, blood glucose increased, blood pressure decreased; injury, poisoning, and procedural complications : fall. postmarketing surveillance because postmarketing adverse events 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. the following additional adverse events have been reported from worldwide postmarketing experience with oxybutynin chloride: psychiatric disorders : psychotic disorder, agitation, hallucinations; nervous system disorders : convulsions; eye disorders : cycloplegia, mydriasis; cardiac disorders : tachycardia; gastrointestinal disorders : decreased gastrointestinal motility; skin and subcutaneous tissue disorders : rash, decreased sweating; renal and urinary disorders : impotence; reproductive system and breast disorders : suppression of lactation.

, has pharmacological activity similar to that of oxybutynin in in vitro studies. pharmacokinetics absorption following oral administration of oxybutynin chloride oral solution, oxybutynin is rapidly absorbed achieving c max 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%). 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) parameters (units) r-oxybutynin s-oxybutynin c max (ng/ml) 3.6 (2.2) 7.8 (4.1) t max (h) 0.89 (0.34) 0.65 (0.32) auc t (ng.h/ml) 22.6 (11.3) 35.0 (17.3) auc inf (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 were 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 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 2b (for oral solution). the plasma-time concentration profiles 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 2b mean ± sd r- and s-oxybutynin and r- and s-desethyloxybutynin pharmacokinetic parameters in children aged 5 to 15 following administration of 5 mg to 22.5 mg total daily dose of oxybutynin chloride oral solution (n=12) all available data normalized to an equivalent of oxybutynin chloride oral solution 5 mg bid or tid at steady state r-oxybutynin s-oxybutynin r- desethyloxybutynin s- desethyloxybutynin c max * (ng/ml) 5.7 ± 6.2 7.3 ± 7.3 54.2 ± 34.0 27.8 ± 20.7 t max (hr) 1.0 1.0 1.0 1.0 auc** 16.3 ± 17.1 20.2 ± 20.8 209.1 ± 174.2 99.1 ± 87.5 (ng.hr/ml) *reflects c max for pooled data **auc 0- end of dosing interval 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 to 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 oral administration. the volume of distribution is 193 l after 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. image description image description