), the active metabolite of fesoterodine. compared with cyp2d6 extensive metabolizers not taking ketoconazole, further increases in the exposure to 5-hmt were observed in subjects who were cyp2d6 poor metabolizers taking ketoconazole [see clinical pharmacology (12.3). there is no clinically relevant effect of moderate cyp3a4 inhibitors on the pharmacokinetics of fesoterodine. following blockade of cyp3a4 by coadministration of the moderate cyp3a4 inhibitor fluconazole 200 mg twice a day for 2 days, the average (90% confidence interval) increase in c max and auc of the active metabolite of fesoterodine was approximately 19% (11% to 28%) and 27% (18% to 36%) respectively. no dosing adjustments are recommended in the presence of moderate cyp3a4 inhibitors (e.g., erythromycin, fluconazole, diltiazem, verapamil and grapefruit juice). the effect of weak cyp3a4 inhibitors (e.g. cimetidine) was not examined; it is not expected to be in excess of the effect of moderate inhibitors [ see clinical pharmacology (12.3) ]. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 7.3 cyp3a4 inducers no dosing adjustments are recommended in the presence of cyp3a4 inducers, such as rifampin and carbamazepine. following induction of cyp3a4 by coadministration of rifampin 600 mg once a day, c max and auc of the active metabolite of fesoterodine decreased by approximately 70% and 75%, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg. the terminal half-life of the active metabolite was not changed. 7.4 cyp2d6 inhibitors the interaction with cyp2d6 inhibitors was not tested clinically. in poor metabolizers for cyp2d6, representing a maximum cyp2d6 inhibition, c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively. no dosing adjustments are recommended in the presence of cyp2d6 inhibitors. 7.5 drugs metabolized by cytochrome p450 in vitro data indicate that at therapeutic concentrations, the active metabolite of fesoterodine does not have the potential to inhibit or induce cytochrome p450 enzyme systems [ see clinical pharmacology(12.3) ]. 7.6 oral contraceptives in the presence of fesoterodine, there are no clinically significant changes in the plasma concentrations of combined oral contraceptives containing ethinyl estradiol and levonorgestrel [ see clinical pharmacology (12.3) ]. 7.7 warfarin a clinical study has shown that fesoterodine 8 mg once daily has no significant effect on the pharmacokinetics or the anticoagulant activity (pt/inr) of warfarin 25 mg. standard therapeutic monitoring for warfarin should be continued [ see clinical pharmacology (12.3) ]. 7.8 drug-laboratory test interactions interactions between fesoterodine fumarate extended-release tablets and laboratory tests have not been studied.

nia gravis symptoms : use fesoterodine fumarate extended-release tablets with caution in patients with myasthenia gravis. (5.6) 5.1 angioedema angioedema of the face, lips, tongue, and/or larynx has been reported with fesoterodine. in some cases, angioedema occurred after the first dose; however, cases have been reported to occur hours after the first dose or after multiple doses. angioedema associated with upper airway swelling may be life-threatening. fesoterodine fumarate extended-release tablets are contraindicated in patients with a known or suspected hypersensitivity to fesoterodine fumarate extended-release tablets or any of its ingredients [see contraindications (4)]. if involvement of the tongue, hypopharynx, or larynx occurs, fesoterodine should be promptly discontinued and appropriate therapy and/or measures to ensure a patent airway should be promptly provided. 5.2 urinary retention in adult patients withbladder outlet obstruction the use of fesoterodine fumarate extended-release tablets, like other antimuscarinic drugs, in patients with clinically significant bladder outlet obstruction, including patients with urinary retention, may result in further urinary retention and kidney injury. the use of fesoterodine fumarate extended-release tablets are not recommended in patients with clinically significant bladder outlet obstruction, and is contraindicated in patients with urinary retention [see contraindications (4) and adverse reactions (6.1)] . 5.3 decreased gastrointestinal motility fesoterodine fumarate extended-release tablets are associated with decreased gastric motility. fesoterodine fumarate extended-release tablets are contraindicated in patients with gastric retention [see contraindications (4)]. the use of fesoterodine fumarate extended-release tablets are not recommended in patients with decreased gastrointestinal motility, such as those with severe constipation. 5.4 worsening of narrow-angle glaucoma fesoterodine fumarate extended-release tablets can worsen controlled narrow-angle glaucoma. fesoterodine fumarate extended-release tablets are contraindicated in patients with uncontrolled narrow-angle glaucoma [see contraindications (4)]. fesoterodine fumarate extended-release tablets should be used with caution in patients being treated for narrow-angle glaucoma. 5.5 central nervous system effects fesoterodine fumarate extended-release tablets are associated with anticholinergic central nervous system (cns) adverse reactions [see adverse reactions (6.1)]. a variety of cns anticholinergic effects have been reported, including headache, dizziness, and somnolence. patients should be monitored for signs of anticholinergic cns effects, particularly after beginning treatment or increasing the dose. advise patients not to drive or operate heavy machinery until they know how fesoterodine fumarate extended-release tablets affects them. if a patient experiences anticholinergic cns effects, fesoterodine fumarate extended-release tablets dose reduction or discontinuation should be considered. 5.6 worsening of myasthenia gravis symptoms fesoterodine fumarate extended-release tablets should be used with caution in patients with myasthenia gravis due to the risk of worsening of symptoms of the disease.

s with renal impairment the recommended dosage of fesoterodine fumarate extended-release tablets in adult patients with renal impairment is described in table 1 [see use in specific populations (8.6)]. for administration instructions, see dosage and administration (2.6) . table 1: fesoterodine fumarate extended-release tablets recommended dose in adult patients with renal impairment (administered orally once daily) estimated creatinine clearance 1 recommended dose clcr 30 to 89 ml/min 8 mg clcr 15 to 29 ml/min 4 mg clcr <15 ml/min 4 mg 1 calculate clcr using the cockcroft-gault formula 2.5 fesoterodine fumarate extended-release tablets dosage modifications due to strong cyp3a4 inhibitors adult patients with oab the maximum recommended dosage is fesoterodine fumarate extended-release tablet 4 mg orally once daily in adult patients taking strong cyp3a4 inhibitors [see drug interactions (7.2) and clinical pharmacology (12.3)] . for administration instructions, see dosage and administration (2.6) . 2.6 administration instructions swallow fesoterodine fumarate extended-release tablets whole with liquid. do not chew, divide, or crush. take with or without food [see clinical pharmacology (12.3)]. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information

d in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. adult overactive bladder (oab) the safety of fesoterodine fumarate extended-release tablets was evaluated in phase 2 and 3 controlled trials in a total of 2,859 patients with overactive bladder, of which 2,288 were treated with fesoterodine fumarate extended-release tablets. of this total, 782 received fesoterodine fumarate extended-release tablets 4 mg/day, and 785 received fesoterodine fumarate extended-release tablets 8 mg/day with treatment periods of 8-or 12-weeks. approximately 80% of these patients had greater than 10-weeks of exposure to fesoterodine fumarate extended-release tablets in these trials. a total of 1,964 patients participated in two 12-week, phase 3 efficacy and safety studies and subsequent open- label extension studies. in these two studies combined, 554 patients received fesoterodine fumarate extended-release tablets 4 mg/day and 566 patients received fesoterodine fumarate extended-release tablets 8 mg/day. in phase 2 and 3 placebo-controlled trials combined, the incidences of serious adverse events in patients receiving placebo, fesoterodine fumarate extended-release tablets 4 mg, and fesoterodine fumarate extended-release tablets 8 mg were 1.9%, 3.5%, and 2.9%, respectively. all serious adverse events were judged to be not related or unlikely to be related to study medication by the investigator, except for four patients receiving fesoterodine fumarate extended-release tablets who reported one serious adverse reaction each: angina, chest pain, gastroenteritis, and qt prolongation on ecg. the most commonly reported adverse event in patients treated with fesoterodine fumarate extended-release tablets was dry mouth. the incidence of dry mouth was higher in those taking 8 mg/day (35%) and in those taking 4 mg/day (19%), as compared to placebo (7%). dry mouth led to discontinuation in 0.4%, 0.4%, and 0.8% of patients receiving placebo, fesoterodine fumarate extended-release tablets 4 mg, and fesoterodine fumarate extended-release tablets 8 mg, respectively. for those patients who reported dry mouth, most had their first occurrence of the event within the first month of treatment. the second most commonly reported adverse event was constipation. the incidence of constipation was 2% in those taking placebo, 4% in those taking 4 mg/day, and 6% in those taking 8 mg/day. table 4 lists adverse events, regardless of causality, that were reported in the combined phase 3, randomized, placebo-controlled trials at an incidence greater than placebo and in 1% or more of patients treated with fesoterodine fumarate extended-release tablets 4 mg or 8 mg once daily for up to 12-weeks. t able 4: adverse events with an incidence exceeding the placebo rate and reported by ≥1% of patients from double-blind, placebo-controlled phase 3 trials of 12-weeks treatment duration system organ class/preferred term placebo n=554 % fesoterodine fumarate extended-release tablet 4 mg/day n=554 % fesoterodine fumarate extended-release tablet 8 mg/day n=566 % alt = alanine aminotransferase; ggt = gamma glutamyltransferase gastrointestinal disorders dry mouth 7.0 18.8 34.6 constipation 2.0 4.2 6.0 dyspepsia 0.5 1.6 2.3 nausea 1.3 0.7 1.9 abdominal pain upper 0.5 1.1 0.5 infections urinary tract infection 3.1 3.2 4.2 upper respiratory tract infection 2.2 2.5 1.8 eye disorders dry eyes 0 1.4 3.7 renal and urinary disorders dysuria 0.7 1.3 1.6 urinary retention 0.2 1.1 1.4 respiratory disorders cough 0.5 1.6 0.9 dry throat 0.4 0.9 2.3 general disorders edema peripheral 0.7 0.7 1.2 musculoskeletal disorders back pain 0.4 2.0 0.9 psychiatric disorders insomnia 0.5 1.3 0.4 investigations alt increased 0.9 0.5 1.2 ggt increased 0.4 0.4 1.2 skin disorders rash 0.5 0.7 1.1 patients also received fesoterodine fumarate extended-release tablets for up to three years in open-label extension phases of one phase 2 and two phase 3 controlled trials. in all open-label trials combined, 857, 701, 529, and 105 patients received fesoterodine fumarate extended-release tablets for at least 6 months, 1 year, 2 years, and 3 years, respectively. the adverse events observed during long-term, open-label studies were similar to those observed in the 12-week, placebo-controlled studies, and included dry mouth, constipation, dry eyes, dyspepsia, and abdominal pain. similar to the controlled studies, most adverse events of dry mouth and constipation were mild to moderate in intensity. serious adverse events, judged to be at least possibly related to study medication by the investigator and reported more than once during the open-label treatment period of up to 3 years, included urinary retention (3 cases), diverticulitis (3 cases), constipation (2 cases), irritable bowel syndrome (2 cases), and electrocardiogram qt corrected interval prolongation (2 cases). pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 6.2 post-marketing experience the following adverse reactions have been identified during post-approval use of fesoterodine fumarate extended-release tablet. 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. cardiac disorders: palpitations central nervous system disorders: dizziness, headache, somnolence eye disorders: blurred vision general disorders and administrative site conditions: hypersensitivity reactions, including angioedema with airway obstruction, face edema skin and subcutaneous tissue disorders: urticaria, pruritus

), the active metabolite of fesoterodine. compared with cyp2d6 extensive metabolizers not taking ketoconazole, further increases in the exposure to 5-hmt were observed in subjects who were cyp2d6 poor metabolizers taking ketoconazole [see clinical pharmacology (12.3). there is no clinically relevant effect of moderate cyp3a4 inhibitors on the pharmacokinetics of fesoterodine. following blockade of cyp3a4 by coadministration of the moderate cyp3a4 inhibitor fluconazole 200 mg twice a day for 2 days, the average (90% confidence interval) increase in c max and auc of the active metabolite of fesoterodine was approximately 19% (11% to 28%) and 27% (18% to 36%) respectively. no dosing adjustments are recommended in the presence of moderate cyp3a4 inhibitors (e.g., erythromycin, fluconazole, diltiazem, verapamil and grapefruit juice). the effect of weak cyp3a4 inhibitors (e.g. cimetidine) was not examined; it is not expected to be in excess of the effect of moderate inhibitors [ see clinical pharmacology (12.3) ]. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 7.3 cyp3a4 inducers no dosing adjustments are recommended in the presence of cyp3a4 inducers, such as rifampin and carbamazepine. following induction of cyp3a4 by coadministration of rifampin 600 mg once a day, c max and auc of the active metabolite of fesoterodine decreased by approximately 70% and 75%, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg. the terminal half-life of the active metabolite was not changed. 7.4 cyp2d6 inhibitors the interaction with cyp2d6 inhibitors was not tested clinically. in poor metabolizers for cyp2d6, representing a maximum cyp2d6 inhibition, c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively. no dosing adjustments are recommended in the presence of cyp2d6 inhibitors. 7.5 drugs metabolized by cytochrome p450 in vitro data indicate that at therapeutic concentrations, the active metabolite of fesoterodine does not have the potential to inhibit or induce cytochrome p450 enzyme systems [ see clinical pharmacology(12.3) ]. 7.6 oral contraceptives in the presence of fesoterodine, there are no clinically significant changes in the plasma concentrations of combined oral contraceptives containing ethinyl estradiol and levonorgestrel [ see clinical pharmacology (12.3) ]. 7.7 warfarin a clinical study has shown that fesoterodine 8 mg once daily has no significant effect on the pharmacokinetics or the anticoagulant activity (pt/inr) of warfarin 25 mg. standard therapeutic monitoring for warfarin should be continued [ see clinical pharmacology (12.3) ]. 7.8 drug-laboratory test interactions interactions between fesoterodine fumarate extended-release tablets and laboratory tests have not been studied.

27 times the expected exposure at the maximum recommended human dose (mrhd)of 8 mg based on auc (75 mg/kg/day, oral), increased resorptions and decreased live fetuses were observed. one fetus with cleft palate was observed at each dose (15, 45, and 75 mg/kg/day), at an incidence within the background historical range. in rabbits treated at 3 to 11 times the mrhd (27 mg/kg/day, oral), incompletely ossified sternebrae (retardation of bone development) and reduced survival were observed in fetuses. in rabbits at 9 to 11 times the mrhd (4.5 mg/kg/day, subcutaneous), maternal toxicity and incompletely ossified sternebrae were observed in fetuses (at an incidence within the background historical range). in rabbits at 3 times the mrhd (1.5 mg/kg/day, subcutaneous), decreased maternal food consumption in the absence of any fetal effects was observed. oral administration of 30 mg/kg/day fesoterodine to mice in a pre- and post-natal development study resulted in decreased body weight of the dams and delayed ear opening of the pups. no effects were noted on mating and reproduction of the f 1 dams or on the f 2 offspring. 8.2 lactation risk summary there is no information on the presence of fesoterodine in human milk, the effects on the breastfed child, or the effects on milk production. the developmental and health benefits of breastfeeding should be considered along with the mother’s clinical need for fesoterodine fumarate extended-release tablets and any potential adverse effects on the breastfed child from fesoterodine fumarate extended-release tablets or from the underlying maternal condition. 8.4 pediatric use the safety and effectiveness of fesoterodine fumarate have not been established in pediatric patients younger than 6 years of age or weighing 25 kg or less. pediatric use information is approved for pfizer inc.'s toviaz® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 8.5 geriatric use no dose adjustment is recommended for the elderly. the pharmacokinetics of fesoterodine are not significantly influenced by age. of the 1,567 patients who received fesoterodine fumarate extended-release tablets 4 mg or 8 mg orally once daily in phase 2 and 3, placebo-controlled, efficacy and safety studies for oab, 515 (33%) were 65 years of age or older, and 140 (9%) were 75 years of age or older. no overall difference in effectiveness was observed between patients younger than 65 years of age and those 65 years of age or older in these studies. however, the incidence of antimuscarinic adverse reactions, including dry mouth, constipation, dyspepsia, increase in residual urine, dizziness (8 mg only) and urinary tract infection, was higher in patients 75 years of age and older as compared to younger patients [see clinical studies (14.1) and adverse reactions (6)] . 8.6 renal impairment in adult patients with severe renal impairment (cl cr <30 ml/min), c max and auc are increased 2.0-and 2.3-fold, respectively. doses of fesoterodine fumarate extended-release tablets greater than 4 mg are not recommended in adult patients with severe renal impairment. in patients with mild or moderate renal impairment (cl cr ranging from 30 to 80 ml/min), c max and auc of the active metabolite are increased up to 1.5-and 1.8-fold, respectively, as compared to healthy subjects. no dose adjustment is recommended in patients with mild or moderate renal impairment [see clinical pharmacology (12.3) and dosage and administration (2.3)] . pediatric use information is approved for pfizer inc.'s toviaz® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. 8.7 hepatic impairment patients with severe hepatic impairment (child-pugh c) have not been studied; therefore fesoterodine fumarate extended-release tablets are not recommended for use in these patients. in patients with moderate (child-pugh b) hepatic impairment, c max and auc of the active metabolite are increased 1.4- and 2.1-fold, respectively, as compared to healthy subjects. no dose adjustment is recommended in patients with mild or moderate hepatic impairment [ see clinical pharmacology (12.3) ].

at the maximum recommended human dose (mrhd)of 8 mg based on auc (75 mg/kg/day, oral), increased resorptions and decreased live fetuses were observed. one fetus with cleft palate was observed at each dose (15, 45, and 75 mg/kg/day), at an incidence within the background historical range. in rabbits treated at 3 to 11 times the mrhd (27 mg/kg/day, oral), incompletely ossified sternebrae (retardation of bone development) and reduced survival were observed in fetuses. in rabbits at 9 to 11 times the mrhd (4.5 mg/kg/day, subcutaneous), maternal toxicity and incompletely ossified sternebrae were observed in fetuses (at an incidence within the background historical range). in rabbits at 3 times the mrhd (1.5 mg/kg/day, subcutaneous), decreased maternal food consumption in the absence of any fetal effects was observed. oral administration of 30 mg/kg/day fesoterodine to mice in a pre- and post-natal development study resulted in decreased body weight of the dams and delayed ear opening of the pups. no effects were noted on mating and reproduction of the f 1 dams or on the f 2 offspring.

rophysiology: the effect of fesoterodine 4 mg and 28 mg on the qt interval was evaluated in a double-blind, randomized, placebo- and positive-controlled (moxifloxacin 400 mg once a day) parallel trial with once-daily treatment over a period of 3 days in 261 male and female subjects aged 44 to 65 years. electrocardiographic parameters were measured over a 24-hour period at pre-dose, after the first administration, and after the third administration of study medication. fesoterodine 28 mg was chosen because this dose, when administered to cyp2d6 extensive metabolizers, results in an exposure to the active metabolite that is similar to the exposure in a cyp2d6 poor metabolizer receiving fesoterodine 8 mg together with cyp3a4 blockade. corrected qt intervals (qtc) were calculated using fridericia’s correction and a linear individual correction method. analyses of 24-hour average qtc, time-matched baseline-corrected qtc, and time-matched placebo- subtracted qtc intervals indicate that fesoterodine at doses of 4 and 28 mg/day did not prolong the qt interval. the sensitivity of the study was confirmed by positive qtc prolongation by moxifloxacin. in this study, conducted in subjects aged 44 to 65 years, fesoterodine fumarate extended-release tablets was associated with an increase in heart rate that correlates with increasing dose. when compared to placebo, the mean increase in heart rate associated with fesoterodine 4 mg/day and fesoterodine 28 mg/day was 3 beats/minute and 11 beats/minute, respectively. in the two, phase 3, placebo-controlled studies in adult in patients with overactive bladder, the mean increases in heart rate compared to placebo were 3 to 4 beats/minute in the fesoterodine 4 mg/day group and 3 to 5 beats/minute in the fesoterodine 8 mg/day group. 12.3 pharmacokinetics abs o r p tio n : after oral administration, fesoterodine is well absorbed. due to rapid and extensive hydrolysis by nonspecific esterases to its active metabolite 5-hydroxymethyl tolterodine, fesoterodine cannot be detected in plasma. bioavailability of the active metabolite is 52%. after single or multiple-dose oral administration of fesoterodine in doses from 4 mg to 28 mg, plasma concentrations of the active metabolite are proportional to the dose. maximum plasma levels are reached after approximately 5 hours. no accumulation occurs after multiple- dose administration. a summary of pharmacokinetic parameters for the active metabolite after a single dose of fesoterodine fumarate extended-release tablets 4 mg and 8 mg in extensive and poor metabolizers of cyp2d6 is provided in table 8. table 8: summary of geometric mean [cv] pharmacokinetic parameters for the active metabolite after a single dose of f esoterodine fumarate extended-release tablets 4mg and 8mg in extensive and poor cyp2d6 metabolizers fesoterodine fumarate extended-release tablets 4 mg fesoterodine fumarate extended-release tablets 8 mg parameter em (n=16) pm (n=8) em (n=16) pm (n=8) c max (ng/ml) 1.89 [43%] 3.45 [54%] 3.98 [28%] 6.90 [39%] auc 0 to tz (ng*h/ml) 21.2 [38%] 40.5 [31%] 45.3 [32%] 88.7 [36%] t m ax (h) a 5 [2 to 6] 5 [5 to 6] 5 [3 to 6] 5 [5 to 6] t ½ (h) 7.31 [27%] 7.31 [30%] 8.59 [41%] 7.66 [21%] em = extensive cyp2d6 metabolizer, pm = poor cyp2d6 metabolizer, cv = coefficient of variation; c max = maximum plasma concentration, auc 0 to tz = area under the concentration time curve from zero up to the last measurable plasma concentration, t max = time to reach c max , t ½ = terminal half-life a data presented as median (range) effec t of food: there is no clinically relevant effect of food on the pharmacokinetics of fesoterodine. in a study of the effects of food on the pharmacokinetics of fesoterodine in 16 healthy male volunteers, concomitant food intake increased the active metabolite of fesoterodine auc by approximately 19% and c max by 18% [ see dosage and administration (2.1)]. d i s t ribution : plasma protein binding of the active metabolite is low (approximately 50%) and is primarily bound to albumin and alpha-1-acid glycoprotein. the mean steady-state volume of distribution following intravenous infusion of the active metabolite is 169 l. m e t a b o li s m : after oral administration, fesoterodine is rapidly and extensively hydrolyzed to its active metabolite. the active metabolite is further metabolized in the liver to its carboxy, carboxy-n-desisopropyl, and n-desisopropyl metabolites via two major pathways involving cyp2d6 and cyp3a4. none of these metabolites contribute significantly to the antimuscarinic activity of fesoterodine. variability in cyp2d6 metabolism: a subset of individuals (approximately 7% of caucasians and approximately 2% of african americans) are poor metabolizers for cyp2d6. c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively, in cyp2d6 poor metabolizers, as compared to extensive metabolizers. excretion : hepatic metabolism and renal excretion contribute significantly to the elimination of the active metabolite. after oral administration of fesoterodine, approximately 70% of the administered dose was recovered in urine as the active metabolite (16%), carboxy metabolite (34%), carboxy-n-desisopropyl metabolite (18%), or n-desisopropyl metabolite (1%), and a smaller amount (7%) was recovered in feces. the terminal half-life of the active metabolite is approximately 4 hours following an intravenous administration. the apparent terminal half-life following oral administration is approximately 7 hours. pharmacokinetics in specific populations geriatric patients: following a single 8 mg oral dose of fesoterodine, the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in 12 elderly men (mean age 67 years) were 51.8 ± 26.1 h*ng/ml and 3.8 ± 1.7 ng/ml, respectively. in the same study, the mean (±sd) auc and c max in 12 young men (mean age 30 years) were 52.0 ± 31.5 h*ng/ml and 4.1±2.1 ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by age [ see use in specific populations (8.5) ]. gender: following a single 8 mg oral dose of fesoterodine, the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in 12 elderly men (mean age 67 years) were 51.8 ± 26.1 h*ng/ml and 3.8 ± 1.7 ng/ml, respectively. in the same study, the mean (±sd) auc and c max in 12 elderly women (mean age 68 years) were 56.0 ± 28.8 h*ng/ml and 4.6 ± 2.3ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by gender. race: the effects of caucasian or black race on the pharmacokinetics of fesoterodine were examined in a study of 12 caucasian and 12 black african young male volunteers. each subject received a single oral dose of 8 mg fesoterodine. the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in caucasian males were 73.0 ± 27.8 h*ng/ml and 6.1 ± 2.7 ng/ml, respectively. the mean (±sd) auc and c max in black males were 65.8 ± 23.2 h*ng/ml and 5.5 ± 1.9 ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by race. renal impairment: in patients with mild or moderate renal impairment (cl cr ranging from 30 to 80 ml/min), c max and auc of the active metabolite are increased up to 1.5- and 1.8-fold, respectively, as compared to healthy subjects. in patients with severe renal impairment (cl cr <30 ml/min), c max and auc are increased 2.0- and 2.3-fold, respectively [ see use in specific populations (8.6), warnings and precautions (5.7), and dosage and administration (2.3) ]. hepatic impairment: in patients with moderate (child-pugh b) hepatic impairment, c max and auc of the active metabolite are increased 1.4- and 2.1-fold, respectively, as compared to healthy subjects. subjects with severe hepatic impairment (child-pugh c) have not been studied [ see use in specific populations (8.7) ]. drug-drug interactions drugs metabolized by cytochrome p450: at therapeutic concentrations, the active metabolite of fesoterodine does not inhibit cyp1a2, 2b6, 2c8, 2c9, 2c19, 2d6, 2e1, or 3a4, or induce cyp1a2, 2b6, 2c9, 2c19, or 3a4 in vitro [ see drug interactions (7.5) ]. cyp3a4 inhibitors: following blockade of cyp3a4 by coadministration of the strong cyp3a4 inhibitor ketoconazole 200 mg twice a day for 5 days, c max and auc of the active metabolite of fesoterodine increased 2.0- and 2.3-fold, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg to cyp2d6 extensive metabolizers. in cyp2d6 poor metabolizers, c max and auc of the active metabolite of fesoterodine increased 2.1- and 2.5-fold, respectively, during coadministration of ketoconazole 200 mg twice a day for 5 days. c max and auc were 4.5- and 5.7-fold higher, respectively, in subjects who were cyp2d6 poor metabolizers and taking ketoconazole compared to subjects who were cyp2d6 extensive metabolizers and not taking ketoconazole. in a separate study coadministering fesoterodine with ketoconazole 200 mg once a day for 5 days, the c max and auc values of the active metabolite of fesoterodine were increased 2.2-fold in cyp2d6 extensive metabolizers and 1.5- and 1.9-fold, respectively, in cyp2d6 poor metabolizers. c max and auc were 3.4- and 4.2-fold higher, respectively, in subjects who were cyp2d6 poor metabolizers and taking ketoconazole compared to subjects who were cyp2d6 extensive metabolizers and not taking ketoconazole. there is no clinically relevant effect of moderate cyp3a4 inhibitors on the pharmacokinetics of fesoterodine. in a drug-drug interaction study evaluating the coadministration of the moderate cyp3a4 inhibitor fluconazole 200 mg twice a day for 2 days, a single 8 mg dose of fesoterodine was administered 1 hour following the first dose of fluconazole on day 1 of the study. the average (90% confidence interval) for the increase in c max and auc of the active metabolite of fesoterodine was approximately 19% (11% to 28%) and 27% (18% to 36%) respectively. the effect of weak cyp3a4 inhibitors (e.g. cimetidine) was not examined; it is not expected to be in excess of the effect of moderate inhibitors [ see drug interactions (7.2) , and dosage and administration (2.3) ]. cyp3a4 inducers: following induction of cyp3a4 by coadministration of rifampicin 600 mg once a day, c max and auc of the active metabolite of fesoterodine decreased by approximately 70% and 75%, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg. the terminal half-life of the active metabolite was not changed. induction of cyp3a4 may lead to reduced plasma levels. no dosing adjustments are recommended in the presence of cyp3a4 inducers [ see drug interactions (7.3) ]. cyp2d6 inhibitors: the interaction with cyp2d6 inhibitors was not studied. in poor metabolizers for cyp2d6, representing a maximum cyp2d6 inhibition, c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively [ see drug interactions (7.4) ]. oral contraceptives : thirty healthy female subjects taking an oral contraceptive containing 0.03 mg ethinyl estradiol and 0.15 mg levonorgestrel were evaluated in a 2-period cross-over study. each subject was randomized to receive concomitant administration of either placebo or fesoterodine 8 mg once daily on days 1 to 14 of hormone cycle for 2 consecutive cycles. pharmacokinetics of ethinyl estradiol and levonorgestrel were assessed on day 13 of each cycle. fesoterodine increased the auc and c max of ethinyl estradiol by 1 to 3% and decreased the auc and c max of levonorgestrel by 11 to 13% [ see drug interactions (7.6) ]. warfarin: in a cross-over study in 14 healthy male volunteers (18 to 55 years), a single oral dose of warfarin 25 mg was given either alone or on day 3 of once daily dosing for 9 days with fesoterodine 8 mg. compared to warfarin alone dosing, the c max and auc of s-warfarin were lower by ~ 4 %, while the c max and auc of r-warfarin were lower by approximately 8 % and 6% for the coadministration, suggesting absence of a significant pharmacokinetic interaction. there were no statistically significant changes in the measured pharmacodynamic parameters for anticoagulant activity of warfarin (inr max , auc inr ), with only a small decrease noted in inr max of ~ 3 % with the co­-administration relative to warfarin alone. inr versus time profiles across individual subjects in the study suggested some differences following co-administration with fesoterodine, although there was no definite trend with regard to the changes noted [ see drug interactions (7.7) ]. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information.

extensive and poor cyp2d6 metabolizers fesoterodine fumarate extended-release tablets 4 mg fesoterodine fumarate extended-release tablets 8 mg parameter em (n=16) pm (n=8) em (n=16) pm (n=8) c max (ng/ml) 1.89 [43%] 3.45 [54%] 3.98 [28%] 6.90 [39%] auc 0 to tz (ng*h/ml) 21.2 [38%] 40.5 [31%] 45.3 [32%] 88.7 [36%] t m ax (h) a 5 [2 to 6] 5 [5 to 6] 5 [3 to 6] 5 [5 to 6] t ½ (h) 7.31 [27%] 7.31 [30%] 8.59 [41%] 7.66 [21%] em = extensive cyp2d6 metabolizer, pm = poor cyp2d6 metabolizer, cv = coefficient of variation; c max = maximum plasma concentration, auc 0 to tz = area under the concentration time curve from zero up to the last measurable plasma concentration, t max = time to reach c max , t ½ = terminal half-life a data presented as median (range) effec t of food: there is no clinically relevant effect of food on the pharmacokinetics of fesoterodine. in a study of the effects of food on the pharmacokinetics of fesoterodine in 16 healthy male volunteers, concomitant food intake increased the active metabolite of fesoterodine auc by approximately 19% and c max by 18% [ see dosage and administration (2.1)]. d i s t ribution : plasma protein binding of the active metabolite is low (approximately 50%) and is primarily bound to albumin and alpha-1-acid glycoprotein. the mean steady-state volume of distribution following intravenous infusion of the active metabolite is 169 l. m e t a b o li s m : after oral administration, fesoterodine is rapidly and extensively hydrolyzed to its active metabolite. the active metabolite is further metabolized in the liver to its carboxy, carboxy-n-desisopropyl, and n-desisopropyl metabolites via two major pathways involving cyp2d6 and cyp3a4. none of these metabolites contribute significantly to the antimuscarinic activity of fesoterodine. variability in cyp2d6 metabolism: a subset of individuals (approximately 7% of caucasians and approximately 2% of african americans) are poor metabolizers for cyp2d6. c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively, in cyp2d6 poor metabolizers, as compared to extensive metabolizers. excretion : hepatic metabolism and renal excretion contribute significantly to the elimination of the active metabolite. after oral administration of fesoterodine, approximately 70% of the administered dose was recovered in urine as the active metabolite (16%), carboxy metabolite (34%), carboxy-n-desisopropyl metabolite (18%), or n-desisopropyl metabolite (1%), and a smaller amount (7%) was recovered in feces. the terminal half-life of the active metabolite is approximately 4 hours following an intravenous administration. the apparent terminal half-life following oral administration is approximately 7 hours. pharmacokinetics in specific populations geriatric patients: following a single 8 mg oral dose of fesoterodine, the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in 12 elderly men (mean age 67 years) were 51.8 ± 26.1 h*ng/ml and 3.8 ± 1.7 ng/ml, respectively. in the same study, the mean (±sd) auc and c max in 12 young men (mean age 30 years) were 52.0 ± 31.5 h*ng/ml and 4.1±2.1 ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by age [ see use in specific populations (8.5) ]. gender: following a single 8 mg oral dose of fesoterodine, the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in 12 elderly men (mean age 67 years) were 51.8 ± 26.1 h*ng/ml and 3.8 ± 1.7 ng/ml, respectively. in the same study, the mean (±sd) auc and c max in 12 elderly women (mean age 68 years) were 56.0 ± 28.8 h*ng/ml and 4.6 ± 2.3ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by gender. race: the effects of caucasian or black race on the pharmacokinetics of fesoterodine were examined in a study of 12 caucasian and 12 black african young male volunteers. each subject received a single oral dose of 8 mg fesoterodine. the mean (±sd) auc and c max for the active metabolite 5-hydroxymethyl tolterodine in caucasian males were 73.0 ± 27.8 h*ng/ml and 6.1 ± 2.7 ng/ml, respectively. the mean (±sd) auc and c max in black males were 65.8 ± 23.2 h*ng/ml and 5.5 ± 1.9 ng/ml, respectively. the pharmacokinetics of fesoterodine were not significantly influenced by race. renal impairment: in patients with mild or moderate renal impairment (cl cr ranging from 30 to 80 ml/min), c max and auc of the active metabolite are increased up to 1.5- and 1.8-fold, respectively, as compared to healthy subjects. in patients with severe renal impairment (cl cr <30 ml/min), c max and auc are increased 2.0- and 2.3-fold, respectively [ see use in specific populations (8.6), warnings and precautions (5.7), and dosage and administration (2.3) ]. hepatic impairment: in patients with moderate (child-pugh b) hepatic impairment, c max and auc of the active metabolite are increased 1.4- and 2.1-fold, respectively, as compared to healthy subjects. subjects with severe hepatic impairment (child-pugh c) have not been studied [ see use in specific populations (8.7) ]. drug-drug interactions drugs metabolized by cytochrome p450: at therapeutic concentrations, the active metabolite of fesoterodine does not inhibit cyp1a2, 2b6, 2c8, 2c9, 2c19, 2d6, 2e1, or 3a4, or induce cyp1a2, 2b6, 2c9, 2c19, or 3a4 in vitro [ see drug interactions (7.5) ]. cyp3a4 inhibitors: following blockade of cyp3a4 by coadministration of the strong cyp3a4 inhibitor ketoconazole 200 mg twice a day for 5 days, c max and auc of the active metabolite of fesoterodine increased 2.0- and 2.3-fold, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg to cyp2d6 extensive metabolizers. in cyp2d6 poor metabolizers, c max and auc of the active metabolite of fesoterodine increased 2.1- and 2.5-fold, respectively, during coadministration of ketoconazole 200 mg twice a day for 5 days. c max and auc were 4.5- and 5.7-fold higher, respectively, in subjects who were cyp2d6 poor metabolizers and taking ketoconazole compared to subjects who were cyp2d6 extensive metabolizers and not taking ketoconazole. in a separate study coadministering fesoterodine with ketoconazole 200 mg once a day for 5 days, the c max and auc values of the active metabolite of fesoterodine were increased 2.2-fold in cyp2d6 extensive metabolizers and 1.5- and 1.9-fold, respectively, in cyp2d6 poor metabolizers. c max and auc were 3.4- and 4.2-fold higher, respectively, in subjects who were cyp2d6 poor metabolizers and taking ketoconazole compared to subjects who were cyp2d6 extensive metabolizers and not taking ketoconazole. there is no clinically relevant effect of moderate cyp3a4 inhibitors on the pharmacokinetics of fesoterodine. in a drug-drug interaction study evaluating the coadministration of the moderate cyp3a4 inhibitor fluconazole 200 mg twice a day for 2 days, a single 8 mg dose of fesoterodine was administered 1 hour following the first dose of fluconazole on day 1 of the study. the average (90% confidence interval) for the increase in c max and auc of the active metabolite of fesoterodine was approximately 19% (11% to 28%) and 27% (18% to 36%) respectively. the effect of weak cyp3a4 inhibitors (e.g. cimetidine) was not examined; it is not expected to be in excess of the effect of moderate inhibitors [ see drug interactions (7.2) , and dosage and administration (2.3) ]. cyp3a4 inducers: following induction of cyp3a4 by coadministration of rifampicin 600 mg once a day, c max and auc of the active metabolite of fesoterodine decreased by approximately 70% and 75%, respectively, after oral administration of fesoterodine fumarate extended-release tablets 8 mg. the terminal half-life of the active metabolite was not changed. induction of cyp3a4 may lead to reduced plasma levels. no dosing adjustments are recommended in the presence of cyp3a4 inducers [ see drug interactions (7.3) ]. cyp2d6 inhibitors: the interaction with cyp2d6 inhibitors was not studied. in poor metabolizers for cyp2d6, representing a maximum cyp2d6 inhibition, c max and auc of the active metabolite are increased 1.7- and 2-fold, respectively [ see drug interactions (7.4) ]. oral contraceptives : thirty healthy female subjects taking an oral contraceptive containing 0.03 mg ethinyl estradiol and 0.15 mg levonorgestrel were evaluated in a 2-period cross-over study. each subject was randomized to receive concomitant administration of either placebo or fesoterodine 8 mg once daily on days 1 to 14 of hormone cycle for 2 consecutive cycles. pharmacokinetics of ethinyl estradiol and levonorgestrel were assessed on day 13 of each cycle. fesoterodine increased the auc and c max of ethinyl estradiol by 1 to 3% and decreased the auc and c max of levonorgestrel by 11 to 13% [ see drug interactions (7.6) ]. warfarin: in a cross-over study in 14 healthy male volunteers (18 to 55 years), a single oral dose of warfarin 25 mg was given either alone or on day 3 of once daily dosing for 9 days with fesoterodine 8 mg. compared to warfarin alone dosing, the c max and auc of s-warfarin were lower by ~ 4 %, while the c max and auc of r-warfarin were lower by approximately 8 % and 6% for the coadministration, suggesting absence of a significant pharmacokinetic interaction. there were no statistically significant changes in the measured pharmacodynamic parameters for anticoagulant activity of warfarin (inr max , auc inr ), with only a small decrease noted in inr max of ~ 3 % with the co­-administration relative to warfarin alone. inr versus time profiles across individual subjects in the study suggested some differences following co-administration with fesoterodine, although there was no definite trend with regard to the changes noted [ see drug interactions (7.7) ]. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information.

fetuses was observed in female mice administered fesoterodine for 2-weeks prior to mating and continuing through day 7 of gestation. the maternal no-observed-effect level (noel) and the noel for effects on reproduction and early embryonic development were both 15 mg/kg/day. at the noel, the systemic exposure, based on auc, was 0.6 to 1.5 times higher in mice than in humans at the mrhd, whereas based on peak plasma concentrations, the exposure in mice was 5 to 9 times higher.

emale mice administered fesoterodine for 2-weeks prior to mating and continuing through day 7 of gestation. the maternal no-observed-effect level (noel) and the noel for effects on reproduction and early embryonic development were both 15 mg/kg/day. at the noel, the systemic exposure, based on auc, was 0.6 to 1.5 times higher in mice than in humans at the mrhd, whereas based on peak plasma concentrations, the exposure in mice was 5 to 9 times higher.

ts 8 mg/day. the majority of patients were caucasian (91%) and female (79%) with a mean age of 58 years (range 19 to 91 years). the primary efficacy endpoints were the mean change in the number of urge urinary incontinence episodes per 24 hours and the mean change in the number of micturitions (frequency) per 24 hours. an important secondary endpoint was the mean change in the voided volume per micturition. results for the primary endpoints and for mean change in voided volume per micturition from the two 12-week clinical studies of fesoterodine fumarate extended-release tablets are reported in table 10. table 10: mean baseline and change from baseline to week 12 for urge urinary incontinence episodes, number of micturitions, and volume voided per micturition study 1 study 2 parameter placebo n=279 fesoterodine fumarate extended-release tablet 4 mg/day n=265 fesoterodine fumarate extended-release tablet 8 mg/day n=276 placebo n=266 fesoterodine fumarate extended-release tablet 4 mg/day n=267 fesoterodine fumarate extended-release tablet 8 mg/day n=267 number of urge incontinence episodes per 24 hoursa baseline 3.7 3.8 3.7 3.7 3.9 3.9 change from baseline -1.20 -2.06 -2.27 -1.00 -1.77 -2.42 p-value vs. placebo - 0.001 <0.001 - <0.003 <0.001 number of micturitions per 24 hours baseline 12.0 11.6 11.9 12.2 12.9 12.0 change from baseline -1.02 -1.74 -1.94 -1.02 -1.86 -1.94 p-value vs. placebo - <0.001 <0.001 - 0.032 <0.001 voided volume per micturition (ml) baseline 150 160 154 159 152 156 change from baseline 10 27 33 8 17 33 p-value vs. placebo - <0.001 <0.001 - 0.150 <0.001 vs. = versus a only those patients who were urge incontinent at baseline were included for the analysis of number of urge incontinence episodes per 24 hours: in study 1, the number of these patients was 211, 199, and 223 in the placebo, fesoterodine fumarate extended-release tablets 4 mg/day and fesoterodine fumarate extended-release tablets 8 mg/day groups, respectively. in study 2, the number of these patients was 205, 228, and 218, respectively. figures 1 to 4: the following figures show change from baseline over time in number of micturitions and urge urinary incontinence episodes per 24 h in the two studies. a reduction in number of urge urinary incontinence episodes per 24 hours was observed for both doses as compared to placebo as early as two weeks after starting fesoterodine fumarate extended-release tablets therapy. pediatric use information is approved for pfizer inc.'s toviaz ® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. fesoterodine-fig1.jpg fesoterodine-fig2.jpg fesoterodine-fig3.jpg fesoterodine-fig4.jpg

o engage in potentially dangerous activities until the drug’s effects on the patient have been determined. heat prostration (due to decreased sweating) can occur when fesoterodine fumarate extended-release tablets, like other antimuscarinic drugs, is used in a hot environment. alcohol patients should also be informed that alcohol may enhance the drowsiness caused by fesoterodine fumarate extended-release tablets, like other anticholinergic agents. see 17 for patient counseling information and fda-approved patient labeling. pediatric use information is approved for pfizer inc.'s toviaz® (fesoterodine fumarate) extended-release tablets. however, due to pfizer inc.'s marketing exclusivity rights, this drug product is not labeled with that pediatric information. manufactured by: alkem laboratories ltd., india. distributed by: ascend laboratories, llc parsippany, nj 07054 revised: april, 2022