elop, discontinue treatment until parameters of calcium metabolism have normalized. the incidence of hypercalcemia and hypercalciuria following taclonex topical suspension treatment of more than 8 weeks has not been evaluated [see clinical pharmacology (12.2) ]. 5.2 effects on endocrine system hypothalamic-pituitary-adrenal axis suppression taclonex topical suspension can cause reversible hypothalamic-pituitary-adrenal (hpa) axis suppression with the potential for clinical glucocorticosteroid insufficiency. this may occur during treatment or upon withdrawal of treatment. factors that predispose a patient to hpa axis suppression include the use of high-potency steroids, large treatment surface areas, prolonged use, use of occlusive dressings, altered skin barrier, liver failure, and young age. evaluation for hpa axis suppression may be done by using the adrenocorticotropic hormone (acth) stimulation test. if hpa axis suppression is documented, gradually withdraw taclonex topical suspension, reduce the frequency of application, or substitute with a less potent corticosteroid. the following trials evaluated the effects of taclonex topical suspension on hpa axis suppression: in a trial evaluating the effects of taclonex topical suspension and taclonex ointment on the hpa axis, 32 adult subjects applied both taclonex topical suspension on the scalp and taclonex ointment on the body. adrenal suppression was identified in 5 of 32 subjects (16%) after 4 weeks of treatment and in 2 of 11 subjects (18%) who continued treatment for 8 weeks. in another trial, 36 adult subjects applied taclonex topical suspension on the body and scalp and 7 subjects applied taclonex topical suspension on the body. adrenal suppression occurred in 3 out of 43 subjects (7%) after 4 weeks of treatment and in none of the 36 subjects who continued treatment for 8 weeks [ see clinical pharmacology (12.2) ]. in two trials, the effects of taclonex topical suspension on the hpa axis were evaluated in 31 and 30 pediatric subjects aged 12 to 17 years old who applied taclonex topical suspension on the scalp and the scalp/body, respectively. adrenal suppression occurred in 1 of 30 evaluable subjects (3%) after 4 weeks of treatment (scalp) and 5 of 31 evaluable subjects (16%) after up to 8 weeks of treatment (scalp and body) [see use in specific populations (8.4) and clinical pharmacology (12.2) ]. cushing's syndrome and hyperglycemia cushing's syndrome and hyperglycemia may occur due to the systemic effects of the topical corticosteroid. these complications are rare and generally occur after prolonged exposure to excessively large doses, especially of high-potency topical corticosteroids. additional considerations for endocrine adverse reactions pediatric patients may be more susceptible to systemic toxicity due to their larger skin surface to body mass ratios [see use in specific populations (8.4) and clinical pharmacology (12.2) ]. use of more than one corticosteroid-containing product at the same time may increase the total systemic corticosteroid exposure. 5.3 allergic contact dermatitis with topical corticosteroids allergic contact dermatitis to a topical corticosteroid is usually diagnosed by observing a failure to heal rather than a clinical exacerbation. such an observation should be corroborated with appropriate diagnostic patch testing. 5.4 allergic contact dermatitis with topical calcipotriene allergic contact dermatitis has been observed with use of topical calcipotriene. such an observation should be corroborated with appropriate diagnostic patch testing. 5.5 ophthalmic adverse reactions use of topical corticosteroids, including taclonex ® topical suspension, may increase the risk of posterior subcapsular cataracts and glaucoma. cataracts and glaucoma have been reported with the postmarketing use of topical corticosteroid products [see adverse reactions (6.2) ]. avoid contact of taclonex topical suspension with eyes. taclonex topical suspension may cause eye irritation. advise patients to report any visual symptoms and consider referral to an ophthalmologist for evaluation.

se. shake bottle before use. ( 2 ) apply taclonex topical suspension to affected areas on the scalp and body once daily for up to 8 weeks. discontinue therapy when control is achieved. ( 2 ) patients age 12 to 17 years should not use more than 60 grams per week.( 2 ) adult patients should not use more than 100 grams per week. ( 2 ) do not use with occlusive dressings unless directed by a healthcare provider. ( 2 ) avoid use on the face, groin, or axillae, or if skin atrophy is present at the treatment site. ( 2 ) not for oral, ophthalmic, or intravaginal use. ( 2 )

ted with taclonex topical suspension and at a rate higher than in subjects treated with vehicle are presented in table 1. table 1. number and percentage of subjects with adverse reactions in scalp psoriasis trials (events reported by ≥1% of subjects and for which a relationship is possible) taclonex topical suspension betamethasone dipropionate in vehicle calcipotriene in vehicle vehicle n=1,953 n=1,214 n=979 n=173 event # of subjects (%) folliculitis 16 (1%) 12 (1%) 5 (1%) 0 (0%) burning sensation of skin 13 (1%) 10 (1%) 29 (3%) 0 (0%) other less common adverse reactions (<1% but >0.1%) were, in decreasing order of incidence: acne, exacerbation of psoriasis, eye irritation, and pustular rash. in a 52-week trial, adverse reactions that were reported by >1% of subjects treated with taclonex topical suspension were pruritus (3.6%), psoriasis (2.4%), erythema (2.1%), skin irritation (1.4%), and folliculitis (1.2%). clinical trials conducted in subjects 18 years and older with psoriasis of the body in randomized, multicenter, vehicle- and/or active controlled clinical trials in adult subjects with plaque psoriasis on non-scalp areas, 824 subjects applied taclonex topical suspension once daily for 8 weeks [see clinical studies (14) ]. the median weekly dose was 22.6 grams. there were no adverse reactions that occurred in ≥1% of subjects treated with taclonex topical suspension and at a rate higher than in subjects treated with vehicle. other less common adverse reactions (<1% but >0.1%) were, in decreasing order of incidence: rash and folliculitis. clinical trials conducted in subjects 12 to 17 years with psoriasis of the scalp in two uncontrolled clinical trials, 109 subjects aged 12 to 17 years with plaque psoriasis of the scalp applied taclonex ® topical suspension once daily for up to 8 weeks. the median weekly dose was 40 grams. adverse reactions included acne, acneiform dermatitis and application site pruritus (0.9% each) [see use in specific populations (8.4) and clinical pharmacology (12.2) ] . clinical trial conducted in subjects 12 to 17 years with psoriasis of the scalp and body in an uncontrolled clinical trial, 107 subjects aged 12 to 17 years with plaque psoriasis of the scalp and body applied taclonex topical suspension once daily for up to 8 weeks. the median weekly dose was 26.6 grams. adverse reactions were folliculitis, acne, and erythema (0.9% each) [see use in specific populations (8.4) and clinical pharmacology (12.2) ] . 6.2 postmarketing experience because adverse 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. postmarketing reports for local adverse reactions to topical corticosteroids included atrophy, striae, telangiectasias, itching, dryness, hypopigmentation, perioral dermatitis, secondary infection, and miliaria. ophthalmic adverse reactions of cataracts, glaucoma, increased intraocular pressure, and central serous chorioretinopathy have been reported during use of topical corticosteroids, including topical betamethasone products.

sis resulted in an increased incidence of minor skeletal abnormalities, including enlarged fontanelles and extra ribs ( see data ). oral administration of calcipotriene to pregnant rabbits during the period of organogenesis had no apparent effects on embryo-fetal development. subcutaneous administration of betamethasone dipropionate to pregnant rats and rabbits during the period of organogenesis resulted in fetal toxicity, including fetal deaths, reduced fetal weight, and fetal malformations (cleft palate and crooked or short tail) ( see data ). the available data do not allow the calculation of relevant comparisons between the systemic exposures of calcipotriene and betamethasone dipropionate observed in animal studies to the systemic exposures that would be expected in humans after topical use of taclonex topical suspension. the estimated background risk of major birth defects and miscarriage of 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 defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. data human data available observational studies in pregnant women did not identify a drug-associated risk of major birth defects, preterm delivery, or fetal mortality with the use of topical corticosteroids of any potency. however, when the dispensed amount of potent or super potent topical corticosteroids exceeded 300 grams during the entire pregnancy, maternal use was associated with an increased risk of low birth weight in infants. animal data embryo-fetal development studies with calcipotriene were performed by the oral route in rats and rabbits. pregnant rats received dosages of 0, 6, 18, or 54 mcg/kg/day (0, 36, 108, and 324 mcg/m 2 /day, respectively) on days 6-15 of gestation (the period of organogenesis). there were no apparent effects on maternal survival, behavior, or body weight gain, no effects on litter parameters, and no effects on the incidence of major malformations in fetuses. fetuses from dams dosed at 54 mcg/kg/day exhibited a significantly increased incidence of minor skeletal abnormalities, including enlarged fontanelles and extra ribs. pregnant rabbits were dosed daily with calcipotriene at exposures of 0, 4, 12, or 36 mcg/kg/day (0, 48, 144, and 432 mcg/m 2 /day, respectively) on days 6-18 of gestation (the period of organogenesis). mean maternal body weight gain was reduced in animals dosed at 12 or 36 mcg/kg/day. the incidence of fetal deaths was increased in the group dosed at 36 mcg/kg/day; reduced fetal weight was also observed in this group. the incidence of major malformations among fetuses was not affected. an increase in the incidence of minor skeletal abnormalities, including incomplete ossification of sternebrae, pubic bones, and forelimb phalanges, was observed in the group dosed at 36 mcg/kg/day. embryo-fetal development studies with betamethasone dipropionate were performed via subcutaneous injection in mice and rabbits. pregnant mice were administered doses of 0, 156, 625, or 2500 mcg/kg/day (0, 468, 1875, and 7500 mcg/m 2 /day, respectively) on days 7 through 13 of gestation (the period of organogenesis). betamethasone dipropionate induced fetal toxicity, including fetal deaths, reduced fetal weight, malformations (increased incidence of the cleft palate and crooked or short tail), and minor skeletal abnormalities (delayed ossification of vertebra and sternebrae). fetal toxicity was observed at the lowest exposure that was evaluated (156 mcg/kg/day). pregnant rabbits were injected subcutaneously at dosages of 0, 0.625, 2.5, and 10 mcg/kg/day (0, 7.5, 30, and 120 mcg/m 2 /day, respectively) on days 6 through 18 of gestation (the period of organogenesis). betamethasone dipropionate induced fetal toxicity, including fetal deaths, reduced fetal weight, external malformations (including malformed ears, cleft palate, umbilical hernia, kinked tail, club foot, and club hand), and skeletal malformations (including absence of phalanges of the first digit and cranial dysplasia) at dosages of 2.5 mcg/kg/day and above. calcipotriene was evaluated for effects on peri- and post-natal development when orally administered to pregnant rats at dosages of 0, 6, 18 or 54 mcg/kg/day (0, 36, 108, and 324 mcg/m 2 /day, respectively) from gestation day 15 through day 20 postpartum. no remarkable effects were observed on any parameter, including survival, behavior, body weight, litter parameters, or the ability to nurse or rear pups. betamethasone dipropionate was evaluated for effects on peri- and post-natal development when orally administered to pregnant rats at dosages of 0, 100, 300, and 1000 mcg/kg/day (0, 600, 1800, and 6000 mcg/m 2 /day, respectively) from gestation day 6 through day 20 postpartum. mean maternal body weight was significantly reduced on gestation day 20 in animals dosed at 300 and 1000 mcg/kg/day. the mean duration of gestation was slightly, but statistically significantly, increased at 100, 300, and 1000 mcg/kg/day. the mean percentage of pups that survived to day 4 was reduced in relation to dosage. on lactation day 5, the percentage of pups with a reflex to right themselves when placed on their back was significantly reduced at 1000 mcg/kg/day. no effects on the ability of pups to learn were observed, and the ability of the offspring of treated rats to reproduce was not affected. 8.2 lactation risk summary there is no information regarding the presence of topically administered calcipotriene and betamethasone dipropionate in human milk, the effects on the breastfed infant, or the effects on milk production. concentrations of calcipotriene in plasma are low after topical administration, and therefore, concentrations in human milk are likely to be low [ see clinical pharmacology (12.3) ]. it is not known whether topical administration of large amounts of betamethasone dipropionate could result in sufficient systemic absorption to produce detectable quantities in human milk (see clinical considerations ). the developmental and health benefits of breastfeeding should be considered along with the mother's clinical need for taclonex ® topical suspension and any potential adverse effects on the breastfed child from taclonex topical suspension or from the underlying maternal condition. clinical considerations to minimize potential exposure to the breastfed infant via breast milk, use taclonex topical suspension on the smallest area of skin and for the shortest duration possible while breastfeeding. advise breastfeeding women not to apply taclonex topical suspension directly to the nipple and areola to avoid direct infant exposure [see use in specific populations (8.4) ] . 8.4 pediatric use the safety and effectiveness of taclonex topical suspension for the treatment of plaque psoriasis of the scalp and body have been established in pediatric patients age 12 to 17 years. the use of taclonex topical suspension for this indication is supported by evidence from adequate and well-controlled trials in adults and from three uncontrolled trials in pediatric subjects that enrolled 109 adolescents with moderate psoriasis of the scalp and 107 adolescents with psoriasis of the scalp and body. after 4 weeks of once daily treatment with taclonex topical suspension, hpa axis suppression was observed in 3% of adolescents with psoriasis of the scalp and 16% of adolescents with psoriasis of the scalp and body. calcium metabolism was evaluated in 107 adolescents with psoriasis of the scalp and body treated with taclonex topical suspension and no cases of hypercalcemia or clinically relevant changes in urinary calcium were reported [see warnings and precautions (5.2) , adverse reactions (6.1) , and clinical pharmacology (12.2) ]. because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of systemic toxicity when treated with topical corticosteroids. pediatric patients are, therefore, also at greater risk of hpa axis suppression and adrenal insufficiency with the use of topical corticosteroids including taclonex ® topical suspension [see clinical pharmacology (12.2) ]. rare systemic toxicities such as cushing's syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients, especially those with prolonged exposure to large doses of high potency topical corticosteroids. local adverse reactions including striae have also been reported with use of topical corticosteroids in pediatric patients. the safety and effectiveness of taclonex topical suspension in pediatric patients less than 12 years of age have not been established. 8.5 geriatric use clinical studies of taclonex topical suspension in plaque psoriasis on non-scalp areas included 124 subjects who were 65 years of age or older, and 36 were 75 years of age or older. clinical studies of taclonex topical suspension in subjects with psoriasis of the scalp included 334 subjects who were 65 years or older and 84 subjects who were 75 years or older. no overall differences in safety or effectiveness of taclonex topical suspension were observed between these subjects and younger subjects, and other reported clinical experience has not identified any differences in responses between the elderly and younger subjects, but greater sensitivity of some older individuals cannot be ruled out.

ncidence of minor skeletal abnormalities, including enlarged fontanelles and extra ribs ( see data ). oral administration of calcipotriene to pregnant rabbits during the period of organogenesis had no apparent effects on embryo-fetal development. subcutaneous administration of betamethasone dipropionate to pregnant rats and rabbits during the period of organogenesis resulted in fetal toxicity, including fetal deaths, reduced fetal weight, and fetal malformations (cleft palate and crooked or short tail) ( see data ). the available data do not allow the calculation of relevant comparisons between the systemic exposures of calcipotriene and betamethasone dipropionate observed in animal studies to the systemic exposures that would be expected in humans after topical use of taclonex topical suspension. the estimated background risk of major birth defects and miscarriage of 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 defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. data human data available observational studies in pregnant women did not identify a drug-associated risk of major birth defects, preterm delivery, or fetal mortality with the use of topical corticosteroids of any potency. however, when the dispensed amount of potent or super potent topical corticosteroids exceeded 300 grams during the entire pregnancy, maternal use was associated with an increased risk of low birth weight in infants. animal data embryo-fetal development studies with calcipotriene were performed by the oral route in rats and rabbits. pregnant rats received dosages of 0, 6, 18, or 54 mcg/kg/day (0, 36, 108, and 324 mcg/m 2 /day, respectively) on days 6-15 of gestation (the period of organogenesis). there were no apparent effects on maternal survival, behavior, or body weight gain, no effects on litter parameters, and no effects on the incidence of major malformations in fetuses. fetuses from dams dosed at 54 mcg/kg/day exhibited a significantly increased incidence of minor skeletal abnormalities, including enlarged fontanelles and extra ribs. pregnant rabbits were dosed daily with calcipotriene at exposures of 0, 4, 12, or 36 mcg/kg/day (0, 48, 144, and 432 mcg/m 2 /day, respectively) on days 6-18 of gestation (the period of organogenesis). mean maternal body weight gain was reduced in animals dosed at 12 or 36 mcg/kg/day. the incidence of fetal deaths was increased in the group dosed at 36 mcg/kg/day; reduced fetal weight was also observed in this group. the incidence of major malformations among fetuses was not affected. an increase in the incidence of minor skeletal abnormalities, including incomplete ossification of sternebrae, pubic bones, and forelimb phalanges, was observed in the group dosed at 36 mcg/kg/day. embryo-fetal development studies with betamethasone dipropionate were performed via subcutaneous injection in mice and rabbits. pregnant mice were administered doses of 0, 156, 625, or 2500 mcg/kg/day (0, 468, 1875, and 7500 mcg/m 2 /day, respectively) on days 7 through 13 of gestation (the period of organogenesis). betamethasone dipropionate induced fetal toxicity, including fetal deaths, reduced fetal weight, malformations (increased incidence of the cleft palate and crooked or short tail), and minor skeletal abnormalities (delayed ossification of vertebra and sternebrae). fetal toxicity was observed at the lowest exposure that was evaluated (156 mcg/kg/day). pregnant rabbits were injected subcutaneously at dosages of 0, 0.625, 2.5, and 10 mcg/kg/day (0, 7.5, 30, and 120 mcg/m 2 /day, respectively) on days 6 through 18 of gestation (the period of organogenesis). betamethasone dipropionate induced fetal toxicity, including fetal deaths, reduced fetal weight, external malformations (including malformed ears, cleft palate, umbilical hernia, kinked tail, club foot, and club hand), and skeletal malformations (including absence of phalanges of the first digit and cranial dysplasia) at dosages of 2.5 mcg/kg/day and above. calcipotriene was evaluated for effects on peri- and post-natal development when orally administered to pregnant rats at dosages of 0, 6, 18 or 54 mcg/kg/day (0, 36, 108, and 324 mcg/m 2 /day, respectively) from gestation day 15 through day 20 postpartum. no remarkable effects were observed on any parameter, including survival, behavior, body weight, litter parameters, or the ability to nurse or rear pups. betamethasone dipropionate was evaluated for effects on peri- and post-natal development when orally administered to pregnant rats at dosages of 0, 100, 300, and 1000 mcg/kg/day (0, 600, 1800, and 6000 mcg/m 2 /day, respectively) from gestation day 6 through day 20 postpartum. mean maternal body weight was significantly reduced on gestation day 20 in animals dosed at 300 and 1000 mcg/kg/day. the mean duration of gestation was slightly, but statistically significantly, increased at 100, 300, and 1000 mcg/kg/day. the mean percentage of pups that survived to day 4 was reduced in relation to dosage. on lactation day 5, the percentage of pups with a reflex to right themselves when placed on their back was significantly reduced at 1000 mcg/kg/day. no effects on the ability of pups to learn were observed, and the ability of the offspring of treated rats to reproduce was not affected.

erse reactions (6.1) , and clinical pharmacology (12.2) ]. because of a higher ratio of skin surface area to body mass, pediatric patients are at a greater risk than adults of systemic toxicity when treated with topical corticosteroids. pediatric patients are, therefore, also at greater risk of hpa axis suppression and adrenal insufficiency with the use of topical corticosteroids including taclonex ® topical suspension [see clinical pharmacology (12.2) ]. rare systemic toxicities such as cushing's syndrome, linear growth retardation, delayed weight gain, and intracranial hypertension have been reported in pediatric patients, especially those with prolonged exposure to large doses of high potency topical corticosteroids. local adverse reactions including striae have also been reported with use of topical corticosteroids in pediatric patients. the safety and effectiveness of taclonex topical suspension in pediatric patients less than 12 years of age have not been established.

he scalp in combination with taclonex ointment on the body for 4 to 8 weeks. adrenal suppression was observed in 5 of 32 subjects (16%) after 4 weeks of treatment and in 2 of 11 subjects (18%) who continued treatment for 8 weeks. in trial b, hpa axis suppression was evaluated in adult subjects (n=43) with extensive psoriasis involving 15-30% of the body surface area (including the scalp). treatment consisted of once daily application of taclonex topical suspension to the body (including the scalp in 36 out of 43 subjects) for 4 to 8 weeks. adrenal suppression was observed in 3 out of 43 subjects (7%) after 4 weeks of treatment and in none of the 36 subjects (0%) who continued treatment for 8 weeks. in trial c, hpa axis suppression was evaluated in pediatric subjects 12 to 17 years (n=30) with plaque psoriasis of the scalp involving at least 20% of the scalp area. treatment consisted of once daily application of taclonex topical suspension to the affected area on the scalp for up to 8 weeks. adrenal suppression was observed in 1 of 30 evaluable subjects (3%) after 4 weeks of treatment and in no subjects (0%) who continued treatment for 8 weeks [see use in specific populations (8.4) ] . in trial d, hpa axis suppression was evaluated in a subset of pediatric subjects aged 12 to 17 years (n=31) with plaque psoriasis of the scalp and body involving 10% to 29% of the body surface area. adrenal suppression was observed in 5 of 31 subjects (16%): 3 subjects after 4 weeks of treatment, 1 subject after 8 weeks of treatment, and 1 subject after both 4 and 8 weeks of treatment [see use in specific populations (8.4) ] . effects on calcium metabolism the effect on calcium metabolism was evaluated following the application of taclonex topical suspension (these trials are described above). in trial a, elevated urinary calcium levels outside the normal range were observed in two subjects (one at 4 weeks and one at 8 weeks). in trial b, there was no change in mean serum or urinary calcium levels. elevated urinary calcium levels outside the normal range were observed in two subjects (one at 4 weeks and one at 8 weeks). in trial c (n=109), including 31 subjects with at least 20% scalp involvement and 78 subjects with at least 10% scalp involvement, no cases of hypercalcemia and no clinically relevant changes in urinary calcium were reported. in trial d (n=107), no cases of hypercalcemia and no clinically relevant changes in urinary calcium were reported. 12.3 pharmacokinetics absorption the systemic effect of taclonex topical suspension in psoriasis was investigated in trials a, b, and d [see clinical pharmacology (12.2) ]. in trial a, the serum levels of calcipotriene and betamethasone dipropionate and their major metabolites were measured after 4 and 8 weeks of once daily application of taclonex ® topical suspension on the scalp in combination with taclonex ointment on the body. calcipotriene and betamethasone dipropionate were below the lower limit of quantification in all serum samples of the 34 subjects evaluated. however, one major metabolite of calcipotriene (mc1080) was quantifiable in 10 of 34 (29%) subjects at week 4 and in 5 of 12 (42%) subjects at week 8. the major metabolite of betamethasone dipropionate, betamethasone 17-propionate (b17p) was also quantifiable in 19 of 34 (56%) subjects at week 4 and 7 of 12 (58%) subjects at week 8. the serum concentrations for mc1080 ranged from 20-75 pg/ml. the clinical significance of this finding is unknown. in trial b, the plasma levels of calcipotriene and betamethasone dipropionate and their major metabolites were measured after 4 weeks of once daily application of taclonex topical suspension. calcipotriene and its metabolite mc1080 were below the lower limit of quantification in all plasma samples. betamethasone dipropionate was quantifiable in 4 of 43 (9) subjects. the metabolite of betamethasone dipropionate (b17p) was quantifiable in 16 of 43 (37%) subjects. the plasma concentrations of betamethasone dipropionate ranged from 30.9-63.5 pg/ml and that of its metabolite betamethasone 17-propionate ranged from 30.5-257 pg/ml. the clinical significance of this finding is unknown. in trial d, the plasma levels of calcipotriene and betamethasone dipropionate and their major metabolites were measured after 4 weeks of once daily application of taclonex topical suspension. calcipotriene and its metabolite mc1080 were below the lower limit of quantification in all plasma samples. betamethasone dipropionate was quantifiable in 4 of 32 (13%) subjects. the metabolite of betamethasone dipropionate (b17p) was quantifiable in 5 of 32 (16%) subjects. the plasma concentrations of betamethasone dipropionate ranged from 41.4-104 pg/ml and that of its metabolite betamethasone 17-propionate ranged from 30.1-126 pg/ml. the clinical significance of this finding is unknown. elimination metabolism calcipotriene: calcipotriene metabolism following systemic uptake is rapid and occurs in the liver. the primary metabolites of calcipotriene are less potent than the parent compound. calcipotriene is metabolized to mc1046 (the α,β-unsaturated ketone analog of calcipotriene), which is metabolized further to mc1080 (a saturated ketone analog). mc1080 is the major metabolite in plasma. mc1080 is slowly metabolized to calcitroic acid. betamethasone dipropionate : betamethasone dipropionate is metabolized to betamethasone 17-propionate and betamethasone, including the 6β-hydroxy derivatives of those compounds by hydrolysis. betamethasone 17-propionate (b17p) is the primary metabolite.

of this finding is unknown. in trial b, the plasma levels of calcipotriene and betamethasone dipropionate and their major metabolites were measured after 4 weeks of once daily application of taclonex topical suspension. calcipotriene and its metabolite mc1080 were below the lower limit of quantification in all plasma samples. betamethasone dipropionate was quantifiable in 4 of 43 (9) subjects. the metabolite of betamethasone dipropionate (b17p) was quantifiable in 16 of 43 (37%) subjects. the plasma concentrations of betamethasone dipropionate ranged from 30.9-63.5 pg/ml and that of its metabolite betamethasone 17-propionate ranged from 30.5-257 pg/ml. the clinical significance of this finding is unknown. in trial d, the plasma levels of calcipotriene and betamethasone dipropionate and their major metabolites were measured after 4 weeks of once daily application of taclonex topical suspension. calcipotriene and its metabolite mc1080 were below the lower limit of quantification in all plasma samples. betamethasone dipropionate was quantifiable in 4 of 32 (13%) subjects. the metabolite of betamethasone dipropionate (b17p) was quantifiable in 5 of 32 (16%) subjects. the plasma concentrations of betamethasone dipropionate ranged from 41.4-104 pg/ml and that of its metabolite betamethasone 17-propionate ranged from 30.1-126 pg/ml. the clinical significance of this finding is unknown. elimination metabolism calcipotriene: calcipotriene metabolism following systemic uptake is rapid and occurs in the liver. the primary metabolites of calcipotriene are less potent than the parent compound. calcipotriene is metabolized to mc1046 (the α,β-unsaturated ketone analog of calcipotriene), which is metabolized further to mc1080 (a saturated ketone analog). mc1080 is the major metabolite in plasma. mc1080 is slowly metabolized to calcitroic acid. betamethasone dipropionate : betamethasone dipropionate is metabolized to betamethasone 17-propionate and betamethasone, including the 6β-hydroxy derivatives of those compounds by hydrolysis. betamethasone 17-propionate (b17p) is the primary metabolite.

o patients is unknown. when betamethasone dipropionate was applied topically to cd-1 mice for up to 24 months at dosages approximating 1.3, 4.2, and 8.5 mcg/kg/day in females, and 1.3, 4.2, and 12.9 mcg/kg/day in males (up to 26 mcg/m 2 /day and 39 mcg/m 2 /day, in females and males, respectively), no significant changes in tumor incidence were observed when compared to control. when betamethasone dipropionate was administered via oral gavage to male and female sprague dawley rats for up to 24 months at dosages of 20, 60, and 200 mcg/kg/day (120, 360, and 1200 mcg/m 2 /day, respectively), no significant changes in tumor incidence were observed when compared to control. calcipotriene did not elicit any genotoxic effects in the ames mutagenicity assay, the mouse lymphoma tk locus assay, the human lymphocyte chromosome aberration test, or the mouse micronucleus test. betamethasone dipropionate did not elicit any genotoxic effects in the ames mutagenicity assay, the mouse lymphoma tk locus assay, or in the rat micronucleus test. studies in rats with oral doses of up to 54 mcg/kg/day (324 mcg/m 2 /day) of calcipotriene indicated no impairment of fertility or general reproductive performance. studies in male rats at oral doses of up to 200 mcg/kg/day (1200 mcg/m 2 /day), and in female rats at oral doses of up to 1000 mcg/kg/day (6000 mcg/m 2 /day), of betamethasone dipropionate indicated no impairment of fertility.

n betamethasone dipropionate was applied topically to cd-1 mice for up to 24 months at dosages approximating 1.3, 4.2, and 8.5 mcg/kg/day in females, and 1.3, 4.2, and 12.9 mcg/kg/day in males (up to 26 mcg/m 2 /day and 39 mcg/m 2 /day, in females and males, respectively), no significant changes in tumor incidence were observed when compared to control. when betamethasone dipropionate was administered via oral gavage to male and female sprague dawley rats for up to 24 months at dosages of 20, 60, and 200 mcg/kg/day (120, 360, and 1200 mcg/m 2 /day, respectively), no significant changes in tumor incidence were observed when compared to control. calcipotriene did not elicit any genotoxic effects in the ames mutagenicity assay, the mouse lymphoma tk locus assay, the human lymphocyte chromosome aberration test, or the mouse micronucleus test. betamethasone dipropionate did not elicit any genotoxic effects in the ames mutagenicity assay, the mouse lymphoma tk locus assay, or in the rat micronucleus test. studies in rats with oral doses of up to 54 mcg/kg/day (324 mcg/m 2 /day) of calcipotriene indicated no impairment of fertility or general reproductive performance. studies in male rats at oral doses of up to 200 mcg/kg/day (1200 mcg/m 2 /day), and in female rats at oral doses of up to 1000 mcg/kg/day (6000 mcg/m 2 /day), of betamethasone dipropionate indicated no impairment of fertility.

rity. "clear" was defined as no evidence of redness, thickness or scaling. "almost clear" was defined as an overall clinical picture of lesions with the presence of minimal erythema. table 2 contains the response rates in each of these 2 trials. table 2. percentage of subjects with clear or almost clear disease according to the investigator's global assessment of disease severity in trials on the scalp taclonex topical suspension betamethasone dipropionate in vehicle calcipotriene in vehicle vehicle trial one (n=494) (n=531) (n=256) (n=126) week 2 55.5% 46.1% 18.4% 9.5% week 8 70.0% 63.1% 36.7% 19.8% trial two (n=512) (n=517) (n=251) - week 2 47.1% 36.4% 12.7% - week 8 67.2% 59.6% 41.0% - clinical trials conducted in subjects 18 years and older with psoriasis of the body one multicenter, randomized, double-blind trial was conducted in subjects with mild to moderate plaque psoriasis on non-scalp areas, excluding face, axillae, and groin. in this trial, 1152 subjects were randomized to 1 of 4 treatment groups: taclonex topical suspension, betamethasone dipropionate in the same vehicle, calcipotriene in the same vehicle, or the vehicle alone. seventy eight percent (78%) of subjects had disease of moderate severity at baseline. subjects were treated once daily for 8 weeks. efficacy was assessed at week 4 and week 8 as the proportion of subjects who were "clear" or "almost clear" according to the investigator's global assessment of disease severity. subjects with mild disease at baseline were required to be "clear" to be considered a success. table 3 contains the response rates in this trial. table 3. percentage of subjects with clear or almost clear disease according to the investigator's global assessment of disease severity subjects with mild disease at baseline were required to be "clear" to be considered a success. in trial on the body taclonex topical suspension betamethasone dipropionate in vehicle calcipotriene in vehicle vehicle (n=482) (n=479) (n=96) (n=95) week 4 13.3% 12.5% 5.2% 2.1% week 8 29.0% 21.5% 14.6% 6.3%

the treatment area with a bandage or other covering unless directed by the healthcare provider. instruct patients to shake bottle prior to using taclonex topical suspension and to wash hands after application. local reactions and skin atrophy advise patients that local reactions and skin atrophy are more likely to occur with occlusive use, prolonged use or use of higher potency corticosteroids. hypercalcemia and hypercalciuria advise patients that hypercalcemia and hypercalciuria have been observed with the use of taclonex topical suspension [see warnings and precautions (5.1) ]. hpa axis suppression, cushing's syndrome, and hyperglycemia advise patients that taclonex topical suspension can cause hpa axis suppression, cushing's syndrome, and/or hyperglycemia [see warnings and precautions (5.2) ]. ophthalmic adverse reactions advise patients to avoid contact of taclonex topical suspension with eyes and to report any visual symptoms [see warnings and precautions (5.5) ]. possible avoidance of other products containing calcipotriene or a corticosteroid instruct patients not to use other products containing calcipotriene or a corticosteroid with taclonex topical suspension without first talking to the healthcare provider. pregnancy and lactation advise pregnant women that taclonex topical suspension may increase the potential risk of having a low birth weight infant and to use taclonex topical suspension on the smallest area of skin and for the shortest duration possible [see use in specific populations (8.1) ]. advise breastfeeding women not to apply taclonex topical suspension directly to the nipple and areola to avoid direct infant exposure [see use in specific populations (8.2) ] .

suspension, tell your healthcare provider about all of your medical conditions, including if you: have a calcium metabolism disorder. have thinning skin (atrophy) at the treatment site. are pregnant or plan to become pregnant. it is not known if taclonex topical suspension will harm your unborn baby. taclonex topical suspension may increase your chance of having a low birth weight baby. if you use taclonex topical suspension during pregnancy, use taclonex topical suspension on the smallest area of the skin and for the shortest time needed. are breastfeeding or plan to breastfeed. it is not known if taclonex topical suspension passes into your breast milk. breastfeeding women should use taclonex topical suspension on the smallest area of the skin and for the shortest time needed. do not apply taclonex topical suspension directly to the nipple and areola to avoid contact with your baby. tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. how should i use taclonex topical suspension? see the " instructions for use " for detailed information about the right way to use taclonex topical suspension. use taclonex topical suspension exactly as your healthcare provider tells you to use it. your healthcare provider should tell you how much taclonex topical suspension to use and where to use it. apply taclonex topical suspension to affected areas on the scalp and body 1 time a day for up to 8 weeks. you should stop treatment when your plaque psoriasis is under control, unless your healthcare provider gives you other instructions. if you are 12 to 17 years of age, you should not use more than 60 grams of taclonex topical suspension in 1 week . if you are 18 years of age or older, you should not use more than 100 grams of taclonex topical suspension in 1 week . do not use taclonex topical suspension longer than prescribed. using too much taclonex topical suspension, or using it too often, or for too long can increase your risk for having serious side effects. do not apply taclonex topical suspension to the scalp in the 12 hours before or after any chemical treatments to your hair. since hair treatments may involve strong chemicals, talk with your healthcare provider first. do not use taclonex topical suspension in the mouth, eyes, or vagina. do not use taclonex topical suspension on your face, groin, or armpits, or if you have thinning of your skin (atrophy) at the treatment site. if you accidentally get taclonex topical suspension on your face or in your eyes, wash the area with water right away. wash your hands after applying taclonex topical suspension. do not take a bath or shower or wash your hair right after applying taclonex topical suspension as the medicine will not work as well to treat your psoriasis. do not bandage or cover the treated skin area, unless instructed by your healthcare provider. what are the possible side effects of taclonex ® topical suspension? taclonex topical suspension may cause serious side effects, including: too much calcium in your blood or urine. your healthcare provider may tell you to stop or temporarily stop treatment with taclonex topical suspension if you have too much calcium in your blood or urine. taclonex topical suspension can pass through your skin. too much taclonex topical suspension passing through your skin can cause your adrenal glands to stop working properly. your healthcare provider may do blood tests to check for adrenal gland problems. cushing's syndrome , a condition that happens when your body is exposed to large amounts of the hormone cortisol. high blood sugar (hyperglycemia). skin problems. tell your healthcare provider if you have any skin problems, including: thinning of your skin burning inflammation itching irritation dryness changes in skin color redness infection raised bumps on your skin eye problems. using taclonex topical suspension may increase your chance of getting cataracts and glaucoma. do not get taclonex topical suspension in your eyes because it may cause eye irritation. tell your healthcare provider if you have blurred vision or other vision problems during treatment with taclonex topical suspension. the most common side effects of taclonex topical suspension include inflamed hair pores (folliculitis) and skin burning. call your doctor for medical advice about side effects. you may report side effects to fda at 1-800-fda-1088. how should i store taclonex topical suspension? store taclonex topical suspension at room temperature between 68°f to 77°f (20°c to 25°c). do not refrigerate taclonex topical suspension. keep the bottle in the carton when not in use. throw away (discard) unused taclonex topical suspension 6 months after it has been opened. keep taclonex topical suspension and all medicines out of reach of children. general information about taclonex topical suspension. medicines are sometimes prescribed for purposes other than those listed in a patient information leaflet. do not use taclonex topical suspension for a condition for which it was not prescribed. do not give taclonex topical suspension to other people, even if they have the same symptoms you have. it may harm them. you can ask your pharmacist or healthcare provider for information about taclonex topical suspension that is written for health professionals. what are the ingredients in taclonex topical suspension? active ingredients: calcipotriene and betamethasone dipropionate. inactive ingredients: hydrogenated castor oil, polyoxypropylene stearyl ether, all- rac -alpha-tocopherol, butylhydroxytoluene and mineral oil. manufactured by: leo laboratories ltd., 285 cashel road, dublin 12, ireland distributed by: leo pharma inc., madison, nj 07940, usa for more information, go to www.taclonex.com or call 1-877-494-4536.