PEDIATRIC USE SECTION.

8.4 Pediatric Use. Pimecrolimus cream, 1% is not indicated for use in children less than years of age.The long-term safety and effects of pimecrolimus cream, 1% on the developing immune system are unknown.Three Phase pediatric trials were conducted involving 1,114 subjects to 17 years of age. Two trials were 6-week randomized vehicle-controlled trials with 20-week open-label phase and one was vehicle-controlled (up to year) safety trial with the option for sequential topical corticosteroid use. Of these subjects 542 (49%) were to years of age. In the short-term trials, 11% of pimecrolimus subjects did not complete these trials and 1.5% of pimecrolimus subjects discontinued due to adverse events. In the one-year trial, 32% of pimecrolimus subjects did not complete this trial and 3% of pimecrolimus subjects discontinued due to adverse events. Most discontinuations were due to unsatisfactory therapeutic effect.The most common local adverse event in the short-term trials of pimecrolimus cream, 1% in pediatric subjects ages to 17 was application site burning (10% vs. 13% vehicle); the incidence in the long-term trial was 9% pimecrolimus vs. 7% vehicle [see Adverse Reactions (6.1)]. Adverse events that were more frequent (greater than 5%) in subjects treated with pimecrolimus cream, 1% compared to vehicle were headache (14% vs. 9%) in the short-term trial. Nasopharyngitis (26% vs. 21%), influenza (13% vs. 4%), pharyngitis (8% vs. 3%), viral infection (7% vs. 1%), pyrexia (13% vs. 5%), cough (16% vs. 11%), and headache (25% vs. 16%) were increased over vehicle in the 1-year safety trial [see Adverse Reactions (6.1)]. In 843 subjects ages to 17 years treated with pimecrolimus cream, 1%, (0.8%) developed eczema herpeticum (5 on pimecrolimus cream, 1% alone and on pimecrolimus cream, 1% used in sequence with corticosteroids). In 211 subjects on vehicle alone, there were no cases of eczema herpeticum. The majority of adverse events were mild to moderate in severity. Two Phase trials were conducted involving 436 infants age months-23 months. One 6-week randomized vehicle-controlled trial with 20-week open-label phase and one safety trial, up to one year, were conducted. In the 6-week trial, 11% of pimecrolimus and 48% of vehicle subjects did not complete this trial; no subject in either group discontinued due to adverse events. Infants on pimecrolimus cream, 1% had an increased incidence of some adverse events compared to vehicle. In the 6-week vehicle-controlled trial these adverse events included pyrexia (32% vs. 13% vehicle), URI (24% vs. 14%), nasopharyngitis (15% vs. 8%), gastroenteritis (7% vs. 3%), otitis media (4% vs. 0%), and diarrhea (8% vs. 0%). In the open-label phase of the trial, for infants who switched to pimecrolimus cream, 1% from vehicle, the incidence of the above-cited adverse events approached or equaled the incidence of those subjects who remained on pimecrolimus cream, 1%. In the month safety data, 16% of pimecrolimus and 35% of vehicle subjects discontinued early and 1.5% of pimecrolimus and 0% of vehicle subjects discontinued due to adverse events. Infants on pimecrolimus cream, 1% had greater incidence of some adverse events as compared to vehicle. These included pyrexia (30% vs. 20%), URI (21% vs. 17%), cough (15% vs. 9%), hypersensitivity (8% vs. 2%), teething (27% vs. 22%), vomiting (9% vs. 4%), rhinitis (13% vs. 9%), viral rash (4% vs. 0%), rhinorrhea (4% vs. 0%), and wheezing (4% vs. 0%).The systemic exposure to pimecrolimus from pimecrolimus cream, 1% was investigated in 28 pediatric subjects with atopic dermatitis (20% to 80% BSA involvement) between the ages of months to 14 yrs. Following twice daily application for three weeks, blood concentrations of pimecrolimus were less than ng/mL with 60% (96/161) of the blood samples having blood concentration below the limit of quantification (0.5 ng/mL). However, more children (23 children out of the total 28 children investigated) had at least one detectable blood level as compared to the adults (12 adults out of the total 52 adults investigated) over 3-week treatment period. Due to the erratic nature of the blood levels observed, no correlation could be made between amount of cream, degree of BSA involvement, and blood concentrations. In general, the blood concentrations measured in adult atopic dermatitis subjects were comparable to those seen in the pediatric population.In second group of 30 pediatric subjects aged to 23 months with 10% to 92% BSA involvement, following twice daily application for three weeks, blood concentrations of pimecrolimus were less than 2.6 ng/mL with 65% (75/116) of the blood samples having blood concentration below 0.5ng/mL, and 27% (31/116) below the limit of quantification (0.1 ng/mL) for these trials.Overall, higher proportion of detectable blood levels was seen in the pediatric subject population as compared to adult population. This increase in the absolute number of positive blood levels may be due to the larger surface area to body mass ratio seen in these younger subjects. In addition, higher incidence of upper respiratory symptoms/infections was also seen relative to the older age group in the PK trials. At this time, causal relationship between these findings and pimecrolimus use cannot be ruled out.

ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The most commonly reported adverse reactions (greater than or equal to 1%) were application site burning, headache, nasopharyngitis, cough, influenza, pyrexia and viral infection. 6.1) To report SUSPECTED ADVERSE REACTIONS, contact Teva Pharmaceuticals USA, Inc. at 1-888-838-2872 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch. 6.1 Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.No phototoxicity and no photoallergenicity were detected in clinical trials with 24 and 33 normal volunteers, respectively. In human dermal safety trials, pimecrolimus cream, 1% did not induce contact sensitization or cumulative irritation.In one-year safety trial in pediatric subjects age to 17 years old involving sequential use of pimecrolimus cream, 1% and topical corticosteroid, 43% of pimecrolimus cream, 1% treated subjects and 68% of vehicle-treated subjects used corticosteroids during the trial. Corticosteroids were used for more than days by 34% of pimecrolimus cream, 1% treated subjects and 54% of vehicle-treated subjects. An increased incidence of impetigo, skin infection, superinfection (infected atopic dermatitis), rhinitis, and urticaria were found in the subjects that had used pimecrolimus cream, 1% and topical corticosteroid sequentially as compared to pimecrolimus cream, 1% alone.In randomized, double-blind vehicle-controlled pediatric trials and one active-controlled adult trial, 843 and 328 subjects respectively, were treated with pimecrolimus cream, 1%. In these clinical trials, 48 (4%) of the 1,171 pimecrolimus treated subjects and 13 (3%) of 408 vehicle-treated subjects discontinued therapy due to adverse events. Discontinuations for AEs were primarily due to application site reactions, and cutaneous infections. The most common application site reaction was application site burning, which occurred in 8% to 26% of subjects treated with pimecrolimus cream, 1%.Table depicts the incidence of adverse events pooled across the identically designed 6-week trials with their open label extensions and the 1-year safety trial for pediatric subjects ages to 17. Data from the adult active-controlled trial is also included in Table 1. Adverse events are listed regardless of relationship to trial drug.Table 1. Treatment Emergent Adverse Events (>=1%) in Pimecrolimus Cream Treatment Groups e di t i Subj c s e di t i Subj c s e di t i Subj c s Adu t c i e e i le -C nt o lle O e n- La e V h c le -C nt o lle C m ara to ( wee s) 2 w ee s) 1 e ar ( y ar) Pimecrolimus Cream Vehicle Pimecrolimus Cream Pimecrolimus Cream Vehicle Pimecrolimus Cream (N=267) (N=136) (N=335) (N=272) (N=75) (N=328) (%) (%) (%) (%) (%) (%) At least AE 182 (68.2%) 97 (71.3%) 240 (72.0%) 230 (84.6%) 56 (74.7%) 256 (78.0%) n e ti n a d nf s a io s Upper Respiratory Tract Infection NOS 38 (14.2%) 18 (13.2%) 65 (19.4%) 13 (4.8%) (8.0%) 14 (4.3%) Nasopharyngitis 27 (10.1%) 10 (7.4%) 32 (19.6%) 72 (26.5%) 16 (21.3%) 25 (7.6%) Skin Infection NOS (3.0%) (5.1%) 18 (5.4%) (2.2%) (4.0%) 21 (6.4%) Influenza (3.0%) (0.7%) 22 (6.6%) 36 (13.2%) (4.0%) 32 (9.8%) Ear Infection NOS (2.2%) (1.5%) 19 (5.7%) (3.3%) (1.3%) (0.6%) Otitis Media (2.2%) (0.7%) 10 (3.0%) (2.9%) (5.3%) (0.6%) Impetigo (1.9%) (2.2%) 12 (3.6%) 11 (4.0%) (5.3%) (2.4%) Bacterial Infection (1.5%) (2.2%) (1.2%) (1.1%) 6 (1.8%) Folliculitis (1.1%) (0.7%) (0.9%) (2.2%) (4.0%) 20 (6.1%) Sinusitis (1.1%) (0.7%) 11 (3.3%) (2.2%) (1.3%) (0.6%) Pneumonia NOS (1.1%) (0.7%) (1.5%) 1 (1.3%) (0.3%) Pharyngitis NOS (0.7%) (1.5%) (0.9%) 22 (8.1%) (2.7%) (0.9%) Pharyngitis Streptococcal (0.7%) (1.5%) 10 (3.0%) <1% Molluscum Contagiosum (0.7%) 4 (1.2%) (1.8%) 0 Staphylococcal Infection (0.4%) (3.7%) (2.1%) <1% (0.9%) Bronchitis NOS (0.4%) (2.2%) (1.2%) 29 (10.7%) (8.0%) (2.4%) Herpes Simplex (0.4%) 4 (1.2%) (3.3%) (2.7%) 13 (4.0%) Tonsillitis NOS (0.4%) 3 (0.9%) 17 (6.3%) 2 (0.6%) Viral Infection NOS (0.7%) (0.7%) (0.3%) 18 (6.6%) (1.3%) Gastroenteritis NOS 3 (2.2%) (0.6%) 20 (7.4%) (2.7%) (1.8%) Chickenpox (0.7%) 3 (0.9%) (2.9%) (4.0%) (0.3%) Skin Papilloma (0.4%) 2 (0.6%) (3.3%) <1% Tonsillitis Acute NOS 0 7 (2.6%) 0 Upper Respiratory Tract Infection Viral NOS (0.4%) 3 (0.9%) (1.5%) 1 (0.3%) Herpes Simplex Dermatitis 0 (0.3%) (1.5%) 2 (0.6%) Bronchitis Acute NOS 0 4 (1.5%) 0 Eye Infection NOS 0 3 (1.1%) <1% (0.3%) General Disorders and Administration Site Conditions Application Site Burning 28 (10.4%) 17 (12.5%) (1.5%) 23 (8.5%) (6.7%) 85 (25.9%) Pyrexia 20 (7.5%) 12 (8.8%) 41 (12.2%) 34 (12.5%) (5.3%) (1.2%) Application Site Reaction NOS (3.0%) (5.1%) (2.1%) (3.3%) (2.7%) 48 (14.6%) Application Site Irritation (3.0%) (5.9%) (0.9%) (0.4%) (4.0%) 21 (6.4%) Influenza Like Illness (0.4%) 2 (0.6%) (1.8%) (2.7%) (1.8%) Application Site Erythema (0.4%) 0 (2.2%) 7 (2.1%) Application Site Pruritus (1.1%) (1.5%) (0.6%) (1.8%) 18 (5.5%) Respiratory, Thoracic and Mediastinal Disorders Cough 31 (11.6%) 11 (8.1%) 31 (9.3%) 43 (15.8%) (10.7%) (2.4%) Nasal Congestion (2.6%) (1.5%) (1.8%) (1.5%) (1.3%) (0.6%) Rhinorrhea (1.9%) (0.7%) (0.9%) (0.4%) (1.3%) Asthma Aggravated (1.5%) (2.2%) 13 (3.9%) (1.1%) (1.3%) Sinus Congestion (1.1%) (0.7%) (0.6%) <1% <1% (0.9%) Rhinitis (0.4%) 5 (1.5%) 12 (4.4%) (6.7%) (2.1%) Wheezing (0.4%) (0.7%) (1.2%) (0.7%) <1% Asthma NOS (0.7%) (0.7%) 11 (3.3%) 10 (3.7%) (2.7%) (2.4%) Epistaxis 1 (0.7%) 9 (3.3%) (1.3%) (0.3%) Dyspnea NOS 0 5 (1.8%) (1.3%) (0.6%) a t oi nt s i na D s r ers Abdominal Pain Upper 11 (4.1%) (4.4%) 10 (3.0%) 15 (5.5%) (6.7%) (0.3%) Sore Throat (3.4%) (3.7%) 15 (5.4%) 22 (8.1%) (5.3%) 12 (3.7%) Vomiting NOS (3.0%) (4.4%) 14 (4.2%) 18 (6.6%) (8.0%) (0.6%) Diarrhea NOS (1.1%) (0.7%) (0.6%) 21 (7.7%) (5.3%) (2.1%) Nausea (0.4%) (2.2%) (1.2%) 11 (4.0%) (6.7%) (1.8%) Abdominal Pain NOS (0.4%) (0.7%) (1.5%) 12 (4.4%) (4.0%) (0.3%) Toothache (0.4%) (0.7%) (0.6%) (2.6%) (1.3%) (0.6%) Constipation (0.4%) 2 (0.6%) 10 (3.7%) <1% Loose Stools 1 (0.7%) (1.2%) <1% <1% R p ro u t v S s e a d r a st Di or e rs Dysmenorrhea (1.1%) 5 (1.5%) (1.1%) (1.3%) (1.2%) y D s or ers Conjunctivitis NEC (0.7%) (0.7%) (2.1%) (2.2%) (4.0%) 10 (3.0%) k n Sub ut n o s Ti ss e i or er Urticaria (1.1%) 1 (0.3%) (0.4%) <1% (0.9%) Acne NOS 1 (0.7%) (0.3%) (1.5%) <1% (1.8%) mm un S s e D s or ers Hypersensitivity NOS 11 (4.1%) (4.4%) 16 (4.8%) 14 (5.1%) (1.3%) 11 (3.4%) nju y n P oi o i g Accident NOS (1.1%) (0.7%) (0.3%) <1% (1.3%) Laceration (0.7%) (0.7%) (1.5%) <1% <1% Mu c ul s ele ta , o nn c i e Ti ss e n Bo e i or ers Back Pain (0.4%) (1.5%) (0.3%) <1% 6 (1.8%) Arthralgias 0 (0.3%) (1.1%) (1.3%) (1.5%) a a d a yri nt D s r e s Earache (0.7%) (0.7%) 8 (2.9%) (2.7%) N er o s y t m i or ers Headache 37 (13.9%) 12 (8.8%) 38 (11.3%) 69 (25.4%) 12 (16.0%) 23 (7.0%) Ages to 17 yearsTwo cases of septic arthritis have been reported in infants less than one year of age in clinical trials conducted with pimecrolimus cream, 1% (n 2,443). Causality has not been established.. 6.2 Postmarketing Experience. The following adverse reactions have been identified during post-approval use of pimecrolimus cream, 1%. Because these reactions are reported voluntarily from population of uncertain size, it is not always possible to reliably estimate their frequency or establish causal relationship to drug exposure.General: Anaphylactic reactions, ocular irritation after application of the cream to the eye lids or near the eyes, angioneurotic edema, facial edema, skin flushing associated with alcohol use, skin discoloration. Hematology/Oncology: Lymphomas, basal cell carcinoma, malignant melanoma, squamous cell carcinoma.

CARCINOGENESIS & MUTAGENESIS & IMPAIRMENT OF FERTILITY SECTION.

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility. In 2-year rat dermal carcinogenicity study using pimecrolimus cream, 1%, statistically significant increase in the incidence of follicular cell adenoma of the thyroid was noted in low, mid and high dose male animals compared to vehicle and saline control male animals. Follicular cell adenoma of the thyroid was noted in the dermal rat carcinogenicity study at the lowest dose of mg/kg/day [0.2% pimecrolimus cream; 1.5X the Maximum Recommended Human Dose (MRHD) based on AUC comparisons]. No increase in the incidence of follicular cell adenoma of the thyroid was noted in the oral carcinogenicity study in male rats up to 10 mg/kg/day (66X MRHD based on AUC comparisons). However, oral studies may not reflect continuous exposure or the same metabolic profile as by the dermal route. In mouse dermal carcinogenicity study using pimecrolimus in an ethanolic solution, no increase in incidence of neoplasms was observed in the skin or other organs up to the highest dose of mg/kg/day (0.32% pimecrolimus in ethanol) 27X MRHD based on AUC comparisons. However, lymphoproliferative changes (including lymphoma) were noted in 13 week repeat dose dermal toxicity study conducted in mice using pimecrolimus in an ethanolic solution at dose of 25 mg/kg/day (47X MRHD based on AUC comparisons). No lymphoproliferative changes were noted in this study at dose of 10 mg/kg/day (17X MRHD based on AUC comparison). However, the latency time to lymphoma formation was shortened to weeks after dermal administration of pimecrolimus dissolved in ethanol at dose of 100 mg/kg/day (179-217X MRHD based on AUC comparisons).In mouse oral (gavage) carcinogenicity study, statistically significant increase in the incidence of lymphoma was noted in high dose male and female animals compared to vehicle control male and female animals. Lymphomas were noted in the oral mouse carcinogenicity study at dose of 45 mg/kg/day (258-340X MRHD based on AUC comparisons). No drug-related tumors were noted in the mouse oral carcinogenicity study at dose of 15 mg/kg/day (60-133X MRHD based on AUC comparisons).In an oral (gavage) rat carcinogenicity study, statistically significant increase in the incidence of benign thymoma was noted in 10 mg/kg/day pimecrolimus treated male and female animals compared to vehicle control treated male and female animals. In addition, significant increase in the incidence of benign thymoma was noted in another oral (gavage) rat carcinogenicity study in mg/kg/day pimecrolimus treated male animals compared to vehicle control treated male animals. No drug-related tumors were noted in the rat oral carcinogenicity study at dose of mg/kg/day male animals (1.1X MRHD based on AUC comparisons) and at dose of mg/kg/day for female animals (21X MRHD based on AUC comparisons).In 52-week dermal photo-carcinogenicity study, the median time to onset of skin tumor formation was decreased in hairless mice following chronic topical dosing with concurrent exposure to UV radiation (40 weeks of treatment followed by 12 weeks of observation) with the pimecrolimus cream, 1% vehicle alone. No additional effect on tumor development beyond the vehicle effect was noted with the addition of the active ingredient, pimecrolimus, to the vehicle cream.A 39-week oral monkey toxicology study was conducted with pimecrolimus doses of 15 mg/kg/day, 45 mg/kg/day and 120 mg/kg/day. dose dependent increase in expression of immunosuppressive-related lymphoproliferative disorder (IRLD) associated with lymphocryptovirus (a monkey strain of virus related to human Epstein Barr virus) was observed. IRLD in monkeys mirrors what has been noted in human transplant patients after chronic systemic immunosuppressive therapy, post transplantation lymphoproliferative disease (PTLD), after treatment with chronic systemic immunosuppressive therapy. Both IRLD and PTLD can progress to lymphoma, which is dependent on the dose and duration of systemic immunosuppressive therapy. dose dependent increase in opportunistic infections (a signal of systemic immunosuppression) was also noted in this monkey study. no observed adverse effect level (NOAEL) for IRLD and opportunistic infections was not established in this study. IRLD occurred at the lowest dose of 15 mg/kg/day for 39 weeks [31X the Maximum Recommended Human Dose (MRHD) of pimecrolimus cream, 1% based on AUC comparisons] in this study. partial recovery from IRLD was noted upon cessation of dosing in this study. battery of in vitro genotoxicity tests, including Ames assay, mouse lymphoma L5178Y assay, and chromosome aberration test in V79 Chinese hamster cells and an in vivo mouse micronucleus test revealed no evidence for mutagenic or clastogenic potential for the drug. An oral fertility and embryofetal developmental study in rats revealed estrus cycle disturbances, post-implantation loss and reduction in litter size at the 45 mg/kg/day dose (38X MRHD based on AUC comparisons). No effect on fertility in female rats was noted at 10 mg/kg/day (12X MRHD based on AUC comparisons). No effect on fertility in male rats was noted at 45 mg/kg/day (23X MRHD based on AUC comparisons), which was the highest dose tested in this study.A second oral fertility and embryofetal developmental study in rats revealed reduced testicular and epididymal weights, reduced testicular sperm counts and motile sperm for males and estrus cycle disturbances, decreased corpora lutea, decreased implantations and viable fetuses for females at 45 mg/kg/day dose (123X MRHD for males and 192X MRHD for females based on AUC comparisons). No effect on fertility in female rats was noted at 10 mg/kg/day (5X MRHD based on AUC comparisons). No effect on fertility in male rats was noted at mg/kg/day (0.7X MRHD based on AUC comparisons).

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. The mechanism of action of pimecrolimus in atopic dermatitis is not known. While the following have been observed, the clinical significance of these observations in atopic dermatitis is not known. It has been demonstrated that pimecrolimus binds with high affinity to macrophilin-12 (FKBP-12) and inhibits the calcium-dependent phosphatase, calcineurin. As consequence, it inhibits cell activation by blocking the transcription of early cytokines. In particular, pimecrolimus inhibits at nanomolar concentrations Interleukin-2 and interferon gamma (Th1-type) and Interleukin-4 and Interleukin-10 (Th2-type) cytokine synthesis in human T-cells. In addition, pimecrolimus prevents the release of inflammatory cytokines and mediators from mast cells in vitro after stimulation by antigen/IgE. 12.3 Pharmacokinetics. AbsorptionIn adult subjects (n=52) being treated for atopic dermatitis [13% to 62% Body Surface Area (BSA) involvement] for periods up to year, maximum pimecrolimus concentration of 1.4 ng/mL was observed among those subjects with detectable blood levels. In the majority of samples in adult (91%; 1,244/1,362) subjects, blood concentrations of pimecrolimus were below 0.5 ng/mL. Data on blood levels of pimecrolimus measured in pediatric subjects are described in Use in Specific Populations (8.4).DistributionLaboratory in vitro plasma protein binding studies using equilibrium gel filtration have shown that 99.5% of pimecrolimus in plasma is bound to proteins over the pimecrolimus concentration range of ng/mL to 100 ng/mL tested. The major fraction of pimecrolimus in plasma appears to be bound to various lipoproteins. As with other topical calcineurin inhibitors, it is not known whether pimecrolimus is absorbed into cutaneous lymphatic vessels or in regional lymph nodes. MetabolismFollowing the administration of single oral radiolabeled dose of pimecrolimus numerous circulating Odemethylation metabolites were seen. Studies with human liver microsomes indicate that pimecrolimus is metabolized in vitro by the CYP3A sub-family of metabolizing enzymes. No evidence of skin mediated drug metabolism was identified in vivo using the minipig or in vitro using stripped human skin. EliminationBased on the results of the aforementioned radiolabeled study, following single oral dose of pimecrolimus ~81% of the administered radioactivity was recovered, primarily in the feces (78.4%) as metabolites. Less than 1% of the radioactivity found in the feces was due to unchanged pimecrolimus.

CLINICAL STUDIES SECTION.

6.1 Clinical Trials Experience. Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice.No phototoxicity and no photoallergenicity were detected in clinical trials with 24 and 33 normal volunteers, respectively. In human dermal safety trials, pimecrolimus cream, 1% did not induce contact sensitization or cumulative irritation.In one-year safety trial in pediatric subjects age to 17 years old involving sequential use of pimecrolimus cream, 1% and topical corticosteroid, 43% of pimecrolimus cream, 1% treated subjects and 68% of vehicle-treated subjects used corticosteroids during the trial. Corticosteroids were used for more than days by 34% of pimecrolimus cream, 1% treated subjects and 54% of vehicle-treated subjects. An increased incidence of impetigo, skin infection, superinfection (infected atopic dermatitis), rhinitis, and urticaria were found in the subjects that had used pimecrolimus cream, 1% and topical corticosteroid sequentially as compared to pimecrolimus cream, 1% alone.In randomized, double-blind vehicle-controlled pediatric trials and one active-controlled adult trial, 843 and 328 subjects respectively, were treated with pimecrolimus cream, 1%. In these clinical trials, 48 (4%) of the 1,171 pimecrolimus treated subjects and 13 (3%) of 408 vehicle-treated subjects discontinued therapy due to adverse events. Discontinuations for AEs were primarily due to application site reactions, and cutaneous infections. The most common application site reaction was application site burning, which occurred in 8% to 26% of subjects treated with pimecrolimus cream, 1%.Table depicts the incidence of adverse events pooled across the identically designed 6-week trials with their open label extensions and the 1-year safety trial for pediatric subjects ages to 17. Data from the adult active-controlled trial is also included in Table 1. Adverse events are listed regardless of relationship to trial drug.Table 1. Treatment Emergent Adverse Events (>=1%) in Pimecrolimus Cream Treatment Groups e di t i Subj c s e di t i Subj c s e di t i Subj c s Adu t c i e e i le -C nt o lle O e n- La e V h c le -C nt o lle C m ara to ( wee s) 2 w ee s) 1 e ar ( y ar) Pimecrolimus Cream Vehicle Pimecrolimus Cream Pimecrolimus Cream Vehicle Pimecrolimus Cream (N=267) (N=136) (N=335) (N=272) (N=75) (N=328) (%) (%) (%) (%) (%) (%) At least AE 182 (68.2%) 97 (71.3%) 240 (72.0%) 230 (84.6%) 56 (74.7%) 256 (78.0%) n e ti n a d nf s a io s Upper Respiratory Tract Infection NOS 38 (14.2%) 18 (13.2%) 65 (19.4%) 13 (4.8%) (8.0%) 14 (4.3%) Nasopharyngitis 27 (10.1%) 10 (7.4%) 32 (19.6%) 72 (26.5%) 16 (21.3%) 25 (7.6%) Skin Infection NOS (3.0%) (5.1%) 18 (5.4%) (2.2%) (4.0%) 21 (6.4%) Influenza (3.0%) (0.7%) 22 (6.6%) 36 (13.2%) (4.0%) 32 (9.8%) Ear Infection NOS (2.2%) (1.5%) 19 (5.7%) (3.3%) (1.3%) (0.6%) Otitis Media (2.2%) (0.7%) 10 (3.0%) (2.9%) (5.3%) (0.6%) Impetigo (1.9%) (2.2%) 12 (3.6%) 11 (4.0%) (5.3%) (2.4%) Bacterial Infection (1.5%) (2.2%) (1.2%) (1.1%) 6 (1.8%) Folliculitis (1.1%) (0.7%) (0.9%) (2.2%) (4.0%) 20 (6.1%) Sinusitis (1.1%) (0.7%) 11 (3.3%) (2.2%) (1.3%) (0.6%) Pneumonia NOS (1.1%) (0.7%) (1.5%) 1 (1.3%) (0.3%) Pharyngitis NOS (0.7%) (1.5%) (0.9%) 22 (8.1%) (2.7%) (0.9%) Pharyngitis Streptococcal (0.7%) (1.5%) 10 (3.0%) <1% Molluscum Contagiosum (0.7%) 4 (1.2%) (1.8%) 0 Staphylococcal Infection (0.4%) (3.7%) (2.1%) <1% (0.9%) Bronchitis NOS (0.4%) (2.2%) (1.2%) 29 (10.7%) (8.0%) (2.4%) Herpes Simplex (0.4%) 4 (1.2%) (3.3%) (2.7%) 13 (4.0%) Tonsillitis NOS (0.4%) 3 (0.9%) 17 (6.3%) 2 (0.6%) Viral Infection NOS (0.7%) (0.7%) (0.3%) 18 (6.6%) (1.3%) Gastroenteritis NOS 3 (2.2%) (0.6%) 20 (7.4%) (2.7%) (1.8%) Chickenpox (0.7%) 3 (0.9%) (2.9%) (4.0%) (0.3%) Skin Papilloma (0.4%) 2 (0.6%) (3.3%) <1% Tonsillitis Acute NOS 0 7 (2.6%) 0 Upper Respiratory Tract Infection Viral NOS (0.4%) 3 (0.9%) (1.5%) 1 (0.3%) Herpes Simplex Dermatitis 0 (0.3%) (1.5%) 2 (0.6%) Bronchitis Acute NOS 0 4 (1.5%) 0 Eye Infection NOS 0 3 (1.1%) <1% (0.3%) General Disorders and Administration Site Conditions Application Site Burning 28 (10.4%) 17 (12.5%) (1.5%) 23 (8.5%) (6.7%) 85 (25.9%) Pyrexia 20 (7.5%) 12 (8.8%) 41 (12.2%) 34 (12.5%) (5.3%) (1.2%) Application Site Reaction NOS (3.0%) (5.1%) (2.1%) (3.3%) (2.7%) 48 (14.6%) Application Site Irritation (3.0%) (5.9%) (0.9%) (0.4%) (4.0%) 21 (6.4%) Influenza Like Illness (0.4%) 2 (0.6%) (1.8%) (2.7%) (1.8%) Application Site Erythema (0.4%) 0 (2.2%) 7 (2.1%) Application Site Pruritus (1.1%) (1.5%) (0.6%) (1.8%) 18 (5.5%) Respiratory, Thoracic and Mediastinal Disorders Cough 31 (11.6%) 11 (8.1%) 31 (9.3%) 43 (15.8%) (10.7%) (2.4%) Nasal Congestion (2.6%) (1.5%) (1.8%) (1.5%) (1.3%) (0.6%) Rhinorrhea (1.9%) (0.7%) (0.9%) (0.4%) (1.3%) Asthma Aggravated (1.5%) (2.2%) 13 (3.9%) (1.1%) (1.3%) Sinus Congestion (1.1%) (0.7%) (0.6%) <1% <1% (0.9%) Rhinitis (0.4%) 5 (1.5%) 12 (4.4%) (6.7%) (2.1%) Wheezing (0.4%) (0.7%) (1.2%) (0.7%) <1% Asthma NOS (0.7%) (0.7%) 11 (3.3%) 10 (3.7%) (2.7%) (2.4%) Epistaxis 1 (0.7%) 9 (3.3%) (1.3%) (0.3%) Dyspnea NOS 0 5 (1.8%) (1.3%) (0.6%) a t oi nt s i na D s r ers Abdominal Pain Upper 11 (4.1%) (4.4%) 10 (3.0%) 15 (5.5%) (6.7%) (0.3%) Sore Throat (3.4%) (3.7%) 15 (5.4%) 22 (8.1%) (5.3%) 12 (3.7%) Vomiting NOS (3.0%) (4.4%) 14 (4.2%) 18 (6.6%) (8.0%) (0.6%) Diarrhea NOS (1.1%) (0.7%) (0.6%) 21 (7.7%) (5.3%) (2.1%) Nausea (0.4%) (2.2%) (1.2%) 11 (4.0%) (6.7%) (1.8%) Abdominal Pain NOS (0.4%) (0.7%) (1.5%) 12 (4.4%) (4.0%) (0.3%) Toothache (0.4%) (0.7%) (0.6%) (2.6%) (1.3%) (0.6%) Constipation (0.4%) 2 (0.6%) 10 (3.7%) <1% Loose Stools 1 (0.7%) (1.2%) <1% <1% R p ro u t v S s e a d r a st Di or e rs Dysmenorrhea (1.1%) 5 (1.5%) (1.1%) (1.3%) (1.2%) y D s or ers Conjunctivitis NEC (0.7%) (0.7%) (2.1%) (2.2%) (4.0%) 10 (3.0%) k n Sub ut n o s Ti ss e i or er Urticaria (1.1%) 1 (0.3%) (0.4%) <1% (0.9%) Acne NOS 1 (0.7%) (0.3%) (1.5%) <1% (1.8%) mm un S s e D s or ers Hypersensitivity NOS 11 (4.1%) (4.4%) 16 (4.8%) 14 (5.1%) (1.3%) 11 (3.4%) nju y n P oi o i g Accident NOS (1.1%) (0.7%) (0.3%) <1% (1.3%) Laceration (0.7%) (0.7%) (1.5%) <1% <1% Mu c ul s ele ta , o nn c i e Ti ss e n Bo e i or ers Back Pain (0.4%) (1.5%) (0.3%) <1% 6 (1.8%) Arthralgias 0 (0.3%) (1.1%) (1.3%) (1.5%) a a d a yri nt D s r e s Earache (0.7%) (0.7%) 8 (2.9%) (2.7%) N er o s y t m i or ers Headache 37 (13.9%) 12 (8.8%) 38 (11.3%) 69 (25.4%) 12 (16.0%) 23 (7.0%) Ages to 17 yearsTwo cases of septic arthritis have been reported in infants less than one year of age in clinical trials conducted with pimecrolimus cream, 1% (n 2,443). Causality has not been established.

INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. See FDA-approved patient labeling Medication Guide) Patients using pimecrolimus cream, 1% should receive the following information and instructions:Pimecrolimus cream, 1% may cause serious side effects. It is not known if pimecrolimus cream, 1% is safe to use for long period of time. very small number of people who have used pimecrolimus cream, 1% have had cancer (for example, skin or lymphoma). However, link with pimecrolimus cream, 1% use has not been shown. Because of this concern: patient should not use pimecrolimus cream, 1% continuously for long time. Pimecrolimus cream, 1% should be used only on areas of skin that have eczema. Pimecrolimus cream, 1% is not for use on child under years old. patient should not use sun lamps, tanning beds, or get treatment with ultraviolet light therapy during treatment with pimecrolimus cream, 1%. patient should limit sun exposure during treatment with pimecrolimus cream, 1% even when the medicine is not on the skin. If patient needs to be outdoors after applying pimecrolimus cream, 1%, the patient should wear loose fitting clothing that protects the treated area from the sun. The physician should advise the patient about other types of protection from the sun. patient should not cover the skin being treated with bandages, dressings or wraps. patient can wear normal clothing. Pimecrolimus cream, 1% is for use on the skin only. Do not get pimecrolimus cream, 1% in your eyes, nose, mouth, vagina, or rectum (mucous membranes). If you get pimecrolimus cream, 1% in any of these areas, burning or irritation can happen. Wipe off any pimecrolimus cream, 1% from the affected area and then rinse the area well with cold water. Pimecrolimus cream, 1% is for external use only. patient should use pimecrolimus cream, 1% for short periods, and if needed, treatment may be repeated with breaks in between. Wash hands before using pimecrolimus cream, 1%. When applying pimecrolimus cream, 1% after bath or shower, the skin should be dry. Apply thin layer of pimecrolimus cream, 1% only to the affected skin areas, twice day, as directed by the physician. Use the smallest amount of pimecrolimus cream, 1% needed to control the signs and symptoms of eczema. patient should not bathe, shower or swim right after applying pimecrolimus cream, 1%. This could wash off the cream. patient can use moisturizers with pimecrolimus cream, 1%. They should be sure to check with the physician first about the products that are right for them. Because the skin of patients with eczema can be very dry, it is important they keep up good skin care practices. If patient uses moisturizers, he or she should apply them after pimecrolimus cream, 1%.Repackaged and Distributed By:Remedy Repack, Inc.625 Kolter Dr. Suite Indiana, PA 1-724-465-8762. Pimecrolimus cream, 1% may cause serious side effects. It is not known if pimecrolimus cream, 1% is safe to use for long period of time. very small number of people who have used pimecrolimus cream, 1% have had cancer (for example, skin or lymphoma). However, link with pimecrolimus cream, 1% use has not been shown. Because of this concern: A patient should not use pimecrolimus cream, 1% continuously for long time. Pimecrolimus cream, 1% should be used only on areas of skin that have eczema. Pimecrolimus cream, 1% is not for use on child under years old. A patient should not use sun lamps, tanning beds, or get treatment with ultraviolet light therapy during treatment with pimecrolimus cream, 1%. A patient should limit sun exposure during treatment with pimecrolimus cream, 1% even when the medicine is not on the skin. If patient needs to be outdoors after applying pimecrolimus cream, 1%, the patient should wear loose fitting clothing that protects the treated area from the sun. The physician should advise the patient about other types of protection from the sun. A patient should not cover the skin being treated with bandages, dressings or wraps. patient can wear normal clothing. Pimecrolimus cream, 1% is for use on the skin only. Do not get pimecrolimus cream, 1% in your eyes, nose, mouth, vagina, or rectum (mucous membranes). If you get pimecrolimus cream, 1% in any of these areas, burning or irritation can happen. Wipe off any pimecrolimus cream, 1% from the affected area and then rinse the area well with cold water. Pimecrolimus cream, 1% is for external use only. A patient should use pimecrolimus cream, 1% for short periods, and if needed, treatment may be repeated with breaks in between. Wash hands before using pimecrolimus cream, 1%. When applying pimecrolimus cream, 1% after bath or shower, the skin should be dry. Apply thin layer of pimecrolimus cream, 1% only to the affected skin areas, twice day, as directed by the physician. Use the smallest amount of pimecrolimus cream, 1% needed to control the signs and symptoms of eczema. A patient should not bathe, shower or swim right after applying pimecrolimus cream, 1%. This could wash off the cream. A patient can use moisturizers with pimecrolimus cream, 1%. They should be sure to check with the physician first about the products that are right for them. Because the skin of patients with eczema can be very dry, it is important they keep up good skin care practices. If patient uses moisturizers, he or she should apply them after pimecrolimus cream, 1%.

NONCLINICAL TOXICOLOGY SECTION.

13 NONCLINICAL TOXICOLOGY. 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility. In 2-year rat dermal carcinogenicity study using pimecrolimus cream, 1%, statistically significant increase in the incidence of follicular cell adenoma of the thyroid was noted in low, mid and high dose male animals compared to vehicle and saline control male animals. Follicular cell adenoma of the thyroid was noted in the dermal rat carcinogenicity study at the lowest dose of mg/kg/day [0.2% pimecrolimus cream; 1.5X the Maximum Recommended Human Dose (MRHD) based on AUC comparisons]. No increase in the incidence of follicular cell adenoma of the thyroid was noted in the oral carcinogenicity study in male rats up to 10 mg/kg/day (66X MRHD based on AUC comparisons). However, oral studies may not reflect continuous exposure or the same metabolic profile as by the dermal route. In mouse dermal carcinogenicity study using pimecrolimus in an ethanolic solution, no increase in incidence of neoplasms was observed in the skin or other organs up to the highest dose of mg/kg/day (0.32% pimecrolimus in ethanol) 27X MRHD based on AUC comparisons. However, lymphoproliferative changes (including lymphoma) were noted in 13 week repeat dose dermal toxicity study conducted in mice using pimecrolimus in an ethanolic solution at dose of 25 mg/kg/day (47X MRHD based on AUC comparisons). No lymphoproliferative changes were noted in this study at dose of 10 mg/kg/day (17X MRHD based on AUC comparison). However, the latency time to lymphoma formation was shortened to weeks after dermal administration of pimecrolimus dissolved in ethanol at dose of 100 mg/kg/day (179-217X MRHD based on AUC comparisons).In mouse oral (gavage) carcinogenicity study, statistically significant increase in the incidence of lymphoma was noted in high dose male and female animals compared to vehicle control male and female animals. Lymphomas were noted in the oral mouse carcinogenicity study at dose of 45 mg/kg/day (258-340X MRHD based on AUC comparisons). No drug-related tumors were noted in the mouse oral carcinogenicity study at dose of 15 mg/kg/day (60-133X MRHD based on AUC comparisons).In an oral (gavage) rat carcinogenicity study, statistically significant increase in the incidence of benign thymoma was noted in 10 mg/kg/day pimecrolimus treated male and female animals compared to vehicle control treated male and female animals. In addition, significant increase in the incidence of benign thymoma was noted in another oral (gavage) rat carcinogenicity study in mg/kg/day pimecrolimus treated male animals compared to vehicle control treated male animals. No drug-related tumors were noted in the rat oral carcinogenicity study at dose of mg/kg/day male animals (1.1X MRHD based on AUC comparisons) and at dose of mg/kg/day for female animals (21X MRHD based on AUC comparisons).In 52-week dermal photo-carcinogenicity study, the median time to onset of skin tumor formation was decreased in hairless mice following chronic topical dosing with concurrent exposure to UV radiation (40 weeks of treatment followed by 12 weeks of observation) with the pimecrolimus cream, 1% vehicle alone. No additional effect on tumor development beyond the vehicle effect was noted with the addition of the active ingredient, pimecrolimus, to the vehicle cream.A 39-week oral monkey toxicology study was conducted with pimecrolimus doses of 15 mg/kg/day, 45 mg/kg/day and 120 mg/kg/day. dose dependent increase in expression of immunosuppressive-related lymphoproliferative disorder (IRLD) associated with lymphocryptovirus (a monkey strain of virus related to human Epstein Barr virus) was observed. IRLD in monkeys mirrors what has been noted in human transplant patients after chronic systemic immunosuppressive therapy, post transplantation lymphoproliferative disease (PTLD), after treatment with chronic systemic immunosuppressive therapy. Both IRLD and PTLD can progress to lymphoma, which is dependent on the dose and duration of systemic immunosuppressive therapy. dose dependent increase in opportunistic infections (a signal of systemic immunosuppression) was also noted in this monkey study. no observed adverse effect level (NOAEL) for IRLD and opportunistic infections was not established in this study. IRLD occurred at the lowest dose of 15 mg/kg/day for 39 weeks [31X the Maximum Recommended Human Dose (MRHD) of pimecrolimus cream, 1% based on AUC comparisons] in this study. partial recovery from IRLD was noted upon cessation of dosing in this study. battery of in vitro genotoxicity tests, including Ames assay, mouse lymphoma L5178Y assay, and chromosome aberration test in V79 Chinese hamster cells and an in vivo mouse micronucleus test revealed no evidence for mutagenic or clastogenic potential for the drug. An oral fertility and embryofetal developmental study in rats revealed estrus cycle disturbances, post-implantation loss and reduction in litter size at the 45 mg/kg/day dose (38X MRHD based on AUC comparisons). No effect on fertility in female rats was noted at 10 mg/kg/day (12X MRHD based on AUC comparisons). No effect on fertility in male rats was noted at 45 mg/kg/day (23X MRHD based on AUC comparisons), which was the highest dose tested in this study.A second oral fertility and embryofetal developmental study in rats revealed reduced testicular and epididymal weights, reduced testicular sperm counts and motile sperm for males and estrus cycle disturbances, decreased corpora lutea, decreased implantations and viable fetuses for females at 45 mg/kg/day dose (123X MRHD for males and 192X MRHD for females based on AUC comparisons). No effect on fertility in female rats was noted at 10 mg/kg/day (5X MRHD based on AUC comparisons). No effect on fertility in male rats was noted at mg/kg/day (0.7X MRHD based on AUC comparisons).

PREGNANCY SECTION.

8.1 Pregnancy. Pregnancy Category CThere are no adequate and well-controlled studies with pimecrolimus cream, 1% in pregnant women. Therefore, pimecrolimus cream, 1% should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.In dermal embryofetal developmental studies, no maternal or fetal toxicity was observed up to the highest practicable doses tested, 10 mg/kg/day (1% pimecrolimus cream) in rats (0.14X MRHD based on body surface area) and 10 mg/kg/day (1% pimecrolimus cream) in rabbits (0.65X MRHD based on AUC comparisons). The 1% pimecrolimus cream was administered topically for hours/day during the period of organogenesis in rats and rabbits (gestational days to 21 in rats and gestational days to 20 in rabbits).A second dermal embryofetal development study was conducted in rats using pimecrolimus cream applied dermally to pregnant rats (1 cream/kg body weight of 0.2%, 0.6% and 1.0% pimecrolimus cream) from gestation day to 17 at doses of 2, 6, and 10 mg/kg/day with daily exposure of approximately 22 hours. No maternal, reproductive, or embryo-fetal toxicity attributable to pimecrolimus was noted at 10 mg/kg/day (0.66X MRHD based on AUC comparisons), the highest dose evaluated in this study. No teratogenicity was noted in this study at any dose.A combined oral fertility and embryofetal developmental study was conducted in rats and an oral embryofetal developmental study was conducted in rabbits. Pimecrolimus was administered during the period of organogenesis (2 weeks prior to mating until gestational day 16 in rats, gestational days to 18 in rabbits) up to dose levels of 45 mg/kg/day in rats and 20 mg/kg/day in rabbits. In the absence of maternal toxicity, indicators of embryofetal toxicity (post-implantation loss and reduction in litter size) were noted at 45 mg/kg/day (38X MRHD based on AUC comparisons) in the oral fertility and embryofetal developmental study conducted in rats. No malformations in the fetuses were noted at 45 mg/kg/day (38X MRHD based on AUC comparisons) in this study. No maternal toxicity, embryotoxicity or teratogenicity were noted in the oral rabbit embryofetal developmental toxicity study at 20 mg/kg/day (3.9X MRHD based on AUC comparisons), which was the highest dose tested in this study.A second oral embryofetal development study was conducted in rats. Pimecrolimus was administered during the period of organogenesis (gestational days to 17) at doses of 2, 10 and 45 mg/kg/day. Maternal toxicity, embryolethality and fetotoxicity were noted at 45 mg/kg/day (271X MRHD based on AUC comparisons). slight increase in skeletal variations that were indicative of delayed skeletal ossification was also noted at this dose. No maternal toxicity, embryolethality or fetotoxicity were noted at 10 mg/kg/day (16X MRHD based on AUC comparisons). No teratogenicity was noted in this study at any dose.A second oral embryofetal development study was conducted in rabbits. Pimecrolimus was administered during the period of organogenesis (gestational days to 20) at doses of 2, and 20 mg/kg/day. Maternal toxicity, embryotoxicity and fetotoxicity were noted at 20 mg/kg/day (12X MRHD based on AUC comparisons). slight increase in skeletal variations that were indicative of delayed skeletal ossification was also noted at this dose. No maternal toxicity, embryotoxicity or fetotoxicity were noted at mg/kg/day (5X MRHD based on AUC comparisons). No teratogenicity was noted in this study at any dose.An oral peri- and post-natal developmental study was conducted in rats. Pimecrolimus was administered from gestational day through lactational day 21 up to dose level of 40 mg/kg/day. Only of 22 females delivered live pups at the highest dose of 40 mg/kg/day. Postnatal survival, development of the F1 generation, their subsequent maturation and fertility were not affected at 10 mg/kg/day (12X MRHD based on AUC comparisons), the highest dose evaluated in this study.Pimecrolimus was transferred across the placenta in oral rat and rabbit embryofetal developmental studies.

SPL MEDGUIDE SECTION.

MEDICATION GUIDEPimecrolimus (pim kroe li mus) Cream, 1%Important: Pimecrolimus cream, 1% is for use on the skin only (topical). Do not get pimecrolimus cream, 1% in your eyes, nose, mouth, vagina, or rectum. What is the most important information should know about pimecrolimus cream, 1%It is not known if pimecrolimus cream, 1% is safe to use for long period of time. very small number of people who have used pimecrolimus cream, 1% have developed cancer (for example, skin cancer or lymphoma). But link that pimecrolimus cream, 1% use caused these cancers has not been shown. Because of this concern:Do not use pimecrolimus cream, 1% continuously for long time. Use pimecrolimus cream, 1% only on areas of your skin that have eczema. Do not use pimecrolimus cream, 1% on child under years of age.What is pimecrolimus cream, 1%Pimecrolimus cream, 1% is prescription medicine used on the skin (topical) to treat mild to moderate eczema (atopic dermatitis). Pimecrolimus cream, 1% is for adults and children age years and older who do not have weakened immune system. Pimecrolimus cream, 1% is used on the skin for short periods, and if needed, treatment may be repeated with breaks in between. Pimecrolimus cream, 1% is for use after other prescription medicines have not worked for you or if your doctor recommends that other prescription medicines should not be used.It is not known if pimecrolimus cream, 1% is safe and effective in people who have weakened immune system.Pimecrolimus cream, 1% is not for use in children under years of age.Who should not use pimecrolimus cream, 1%Do not use pimecrolimus cream, 1% if you are allergic to pimecrolimus or any of the ingredients in pimecrolimus cream, 1%. See the end of this Medication Guide for complete list of ingredients in pimecrolimus cream, 1%. What should tell my doctor before using pimecrolimus cream, 1%Before using pimecrolimus cream, 1%, tell your doctor about all of your medical conditions, including if you:have skin disease called Nethertons syndrome (a rare inherited condition) have any infection on your skin including chicken pox or herpes have been told you have weakened immune system are pregnant or plan to become pregnant. It is not known if pimecrolimus cream, 1% will harm your unborn baby. are breastfeeding or plan to breastfeed. It is not known if pimecrolimus, 1% passes into your breast milk. You and your doctor should decide if you will use pimecrolimus cream, 1% or breastfeed. You should not do both.Tell your doctor about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Tell your doctor about all the skin medicines and products you use. Know the medicines you take. Keep list of them with you to show your doctor and pharmacist each time you get new medicine.How should use pimecrolimus cream, 1%Use pimecrolimus cream, 1% exactly as your doctor tells you to use it. Stop pimecrolimus cream, 1% when the signs and symptoms of eczema, such as itching, rash, and redness go away, or as directed by your doctor. Wash your hands before using pimecrolimus cream, 1%. If you apply pimecrolimus cream, 1% after bath or shower, make sure your skin is dry. Apply thin layer of pimecrolimus cream, 1% only to the affected skin areas, two times each day, as directed by your doctor. Use the smallest amount of pimecrolimus cream, 1% to help control the signs and symptoms of eczema. If you apply pimecrolimus cream, 1% to another person, or if you have eczema and are not treating your hands, it is important for you to wash your hands with soap and water after applying pimecrolimus cream, 1%. This should remove any cream left on your hands. Do not bathe, shower or swim right after applying pimecrolimus cream, 1%. This could wash off the cream. You can use moisturizers with pimecrolimus cream, 1%. Ask your doctor first about the products that are right for you. People with eczema can have very dry skin, so it is important to keep up good skin care practices. If you use moisturizers, apply them after pimecrolimus cream, 1%. Call your doctor if your symptoms get worse with pimecrolimus cream, 1% or your symptoms do not improve after weeks of treatment.What should avoid while using pimecrolimus cream, 1%You should not use sun lamps, tanning beds, or get treatment with ultraviolet light therapy during treatment with pimecrolimus cream, 1%. Limit your time in the sun during treatment with pimecrolimus cream, 1% even when the medicine is not on your skin. If you need to be outdoors after applying pimecrolimus cream, 1%, wear loose fitting clothing that protects the treated area from the sun. Ask your doctor what other types of protection from the sun you should use. It is not known how pimecrolimus cream, 1% may affect your skin with exposure to ultraviolet light. Do not cover the skin being treated with bandages, dressings or wraps. You can wear normal clothing. Pimecrolimus cream, 1% is for use on the skin only. Do not get pimecrolimus cream, 1% in your eyes, nose, mouth, vagina, or rectum (mucous membranes). If you get pimecrolimus cream, 1% in any of these areas, burning or irritation can happen. Wipe off any pimecrolimus cream, 1% from the affected area and then rinse the area well with cold water. Do not swallow pimecrolimus cream, 1%. If you do, call your doctor. Avoid using pimecrolimus cream, 1% on skin areas that have cancers or pre-cancers.What are the possible side effects of pimecrolimus cream, 1% Pimecrolimuscream, 1% may cause serious side effects.See What is the most important information should know about pimecrolimus cream, 1% The most common side effect at the skin application site is burning or feeling of warmth. These side effects are usually mild or moderate, happen during the first few days of treatment, and usually clear up in few days.Other common side effects include:headache common cold or stuffy nose, sore throat cough flu (influenza) fever viral infection. Some people may get viral skin infections (like cold sores, chicken pox, shingles, or warts) or swollen lymph nodes (glands).Tell your doctor if you get skin infection or if you have any side effect (for example, swollen glands) that bothers you or that does not go away.These are not all the possible side effects with pimecrolimus cream, 1%. Ask your doctor or pharmacist for more information.Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should store pimecrolimus cream, 1%Store pimecrolimus cream, 1% at room temperature between 68 to 77F (20 to 25C). Do not freeze pimecrolimus cream, 1%.Keep pimecrolimus cream, 1% and all medicines out of the reach of children. General information about the safe and effective use of pimecrolimus cream, 1%Medicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use pimecrolimus cream, 1% for conditions other than which it was prescribed. Do not give pimecrolimus cream, 1% to other people even if they have the same symptoms you have. It may harm them.You can ask your doctor or pharmacist for information about pimecrolimus cream, 1% that is written for health professionals.For more information call Teva Pharmaceuticals USA, Inc. at 1-888-838-2872.What are the ingredients in pimecrolimus cream, 1% Active ingredient: pimecrolimus Inactive ingredients: benzyl alcohol, cetyl alcohol, cetostearyl alcohol (type A), citric acid anhydrous, medium-chain triglycerides, mono- and di-glycerides, oleyl alcohol, propylene glycol, sodium hydroxide, stearyl alcohol, and water. This Medication Guide has been approved by the U.S. Food and Drug Administration.Repackaged and Distributed By:Remedy Repack, Inc.625 Kolter Dr. Suite Indiana, PA 1-724-465-8762. Do not use pimecrolimus cream, 1% continuously for long time. Use pimecrolimus cream, 1% only on areas of your skin that have eczema. Do not use pimecrolimus cream, 1% on child under years of age.. have skin disease called Nethertons syndrome (a rare inherited condition) have any infection on your skin including chicken pox or herpes have been told you have weakened immune system are pregnant or plan to become pregnant. It is not known if pimecrolimus cream, 1% will harm your unborn baby. are breastfeeding or plan to breastfeed. It is not known if pimecrolimus, 1% passes into your breast milk. You and your doctor should decide if you will use pimecrolimus cream, 1% or breastfeed. You should not do both.. Use pimecrolimus cream, 1% exactly as your doctor tells you to use it. Stop pimecrolimus cream, 1% when the signs and symptoms of eczema, such as itching, rash, and redness go away, or as directed by your doctor. Wash your hands before using pimecrolimus cream, 1%. If you apply pimecrolimus cream, 1% after bath or shower, make sure your skin is dry. Apply thin layer of pimecrolimus cream, 1% only to the affected skin areas, two times each day, as directed by your doctor. Use the smallest amount of pimecrolimus cream, 1% to help control the signs and symptoms of eczema. If you apply pimecrolimus cream, 1% to another person, or if you have eczema and are not treating your hands, it is important for you to wash your hands with soap and water after applying pimecrolimus cream, 1%. This should remove any cream left on your hands. Do not bathe, shower or swim right after applying pimecrolimus cream, 1%. This could wash off the cream. You can use moisturizers with pimecrolimus cream, 1%. Ask your doctor first about the products that are right for you. People with eczema can have very dry skin, so it is important to keep up good skin care practices. If you use moisturizers, apply them after pimecrolimus cream, 1%. Call your doctor if your symptoms get worse with pimecrolimus cream, 1% or your symptoms do not improve after weeks of treatment.. You should not use sun lamps, tanning beds, or get treatment with ultraviolet light therapy during treatment with pimecrolimus cream, 1%. Limit your time in the sun during treatment with pimecrolimus cream, 1% even when the medicine is not on your skin. If you need to be outdoors after applying pimecrolimus cream, 1%, wear loose fitting clothing that protects the treated area from the sun. Ask your doctor what other types of protection from the sun you should use. It is not known how pimecrolimus cream, 1% may affect your skin with exposure to ultraviolet light. Do not cover the skin being treated with bandages, dressings or wraps. You can wear normal clothing. Pimecrolimus cream, 1% is for use on the skin only. Do not get pimecrolimus cream, 1% in your eyes, nose, mouth, vagina, or rectum (mucous membranes). If you get pimecrolimus cream, 1% in any of these areas, burning or irritation can happen. Wipe off any pimecrolimus cream, 1% from the affected area and then rinse the area well with cold water. Do not swallow pimecrolimus cream, 1%. If you do, call your doctor. Avoid using pimecrolimus cream, 1% on skin areas that have cancers or pre-cancers.. See What is the most important information should know about pimecrolimus cream, 1% The most common side effect at the skin application site is burning or feeling of warmth. These side effects are usually mild or moderate, happen during the first few days of treatment, and usually clear up in few days.. headache common cold or stuffy nose, sore throat cough flu (influenza) fever viral infection. Some people may get viral skin infections (like cold sores, chicken pox, shingles, or warts) or swollen lymph nodes (glands).. Store pimecrolimus cream, 1% at room temperature between 68 to 77F (20 to 25C). Do not freeze pimecrolimus cream, 1%.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. 8.1 Pregnancy. Pregnancy Category CThere are no adequate and well-controlled studies with pimecrolimus cream, 1% in pregnant women. Therefore, pimecrolimus cream, 1% should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.In dermal embryofetal developmental studies, no maternal or fetal toxicity was observed up to the highest practicable doses tested, 10 mg/kg/day (1% pimecrolimus cream) in rats (0.14X MRHD based on body surface area) and 10 mg/kg/day (1% pimecrolimus cream) in rabbits (0.65X MRHD based on AUC comparisons). The 1% pimecrolimus cream was administered topically for hours/day during the period of organogenesis in rats and rabbits (gestational days to 21 in rats and gestational days to 20 in rabbits).A second dermal embryofetal development study was conducted in rats using pimecrolimus cream applied dermally to pregnant rats (1 cream/kg body weight of 0.2%, 0.6% and 1.0% pimecrolimus cream) from gestation day to 17 at doses of 2, 6, and 10 mg/kg/day with daily exposure of approximately 22 hours. No maternal, reproductive, or embryo-fetal toxicity attributable to pimecrolimus was noted at 10 mg/kg/day (0.66X MRHD based on AUC comparisons), the highest dose evaluated in this study. No teratogenicity was noted in this study at any dose.A combined oral fertility and embryofetal developmental study was conducted in rats and an oral embryofetal developmental study was conducted in rabbits. Pimecrolimus was administered during the period of organogenesis (2 weeks prior to mating until gestational day 16 in rats, gestational days to 18 in rabbits) up to dose levels of 45 mg/kg/day in rats and 20 mg/kg/day in rabbits. In the absence of maternal toxicity, indicators of embryofetal toxicity (post-implantation loss and reduction in litter size) were noted at 45 mg/kg/day (38X MRHD based on AUC comparisons) in the oral fertility and embryofetal developmental study conducted in rats. No malformations in the fetuses were noted at 45 mg/kg/day (38X MRHD based on AUC comparisons) in this study. No maternal toxicity, embryotoxicity or teratogenicity were noted in the oral rabbit embryofetal developmental toxicity study at 20 mg/kg/day (3.9X MRHD based on AUC comparisons), which was the highest dose tested in this study.A second oral embryofetal development study was conducted in rats. Pimecrolimus was administered during the period of organogenesis (gestational days to 17) at doses of 2, 10 and 45 mg/kg/day. Maternal toxicity, embryolethality and fetotoxicity were noted at 45 mg/kg/day (271X MRHD based on AUC comparisons). slight increase in skeletal variations that were indicative of delayed skeletal ossification was also noted at this dose. No maternal toxicity, embryolethality or fetotoxicity were noted at 10 mg/kg/day (16X MRHD based on AUC comparisons). No teratogenicity was noted in this study at any dose.A second oral embryofetal development study was conducted in rabbits. Pimecrolimus was administered during the period of organogenesis (gestational days to 20) at doses of 2, and 20 mg/kg/day. Maternal toxicity, embryotoxicity and fetotoxicity were noted at 20 mg/kg/day (12X MRHD based on AUC comparisons). slight increase in skeletal variations that were indicative of delayed skeletal ossification was also noted at this dose. No maternal toxicity, embryotoxicity or fetotoxicity were noted at mg/kg/day (5X MRHD based on AUC comparisons). No teratogenicity was noted in this study at any dose.An oral peri- and post-natal developmental study was conducted in rats. Pimecrolimus was administered from gestational day through lactational day 21 up to dose level of 40 mg/kg/day. Only of 22 females delivered live pups at the highest dose of 40 mg/kg/day. Postnatal survival, development of the F1 generation, their subsequent maturation and fertility were not affected at 10 mg/kg/day (12X MRHD based on AUC comparisons), the highest dose evaluated in this study.Pimecrolimus was transferred across the placenta in oral rat and rabbit embryofetal developmental studies.. 8.3 Nursing Mothers. It is not known whether this drug is excreted in human milk. Because of the potential for serious adverse reactions in nursing infants from pimecrolimus, decision should be made whether to discontinue nursing or to discontinue the drug, taking into account the importance of the drug to the mother.. 8.4 Pediatric Use. Pimecrolimus cream, 1% is not indicated for use in children less than years of age.The long-term safety and effects of pimecrolimus cream, 1% on the developing immune system are unknown.Three Phase pediatric trials were conducted involving 1,114 subjects to 17 years of age. Two trials were 6-week randomized vehicle-controlled trials with 20-week open-label phase and one was vehicle-controlled (up to year) safety trial with the option for sequential topical corticosteroid use. Of these subjects 542 (49%) were to years of age. In the short-term trials, 11% of pimecrolimus subjects did not complete these trials and 1.5% of pimecrolimus subjects discontinued due to adverse events. In the one-year trial, 32% of pimecrolimus subjects did not complete this trial and 3% of pimecrolimus subjects discontinued due to adverse events. Most discontinuations were due to unsatisfactory therapeutic effect.The most common local adverse event in the short-term trials of pimecrolimus cream, 1% in pediatric subjects ages to 17 was application site burning (10% vs. 13% vehicle); the incidence in the long-term trial was 9% pimecrolimus vs. 7% vehicle [see Adverse Reactions (6.1)]. Adverse events that were more frequent (greater than 5%) in subjects treated with pimecrolimus cream, 1% compared to vehicle were headache (14% vs. 9%) in the short-term trial. Nasopharyngitis (26% vs. 21%), influenza (13% vs. 4%), pharyngitis (8% vs. 3%), viral infection (7% vs. 1%), pyrexia (13% vs. 5%), cough (16% vs. 11%), and headache (25% vs. 16%) were increased over vehicle in the 1-year safety trial [see Adverse Reactions (6.1)]. In 843 subjects ages to 17 years treated with pimecrolimus cream, 1%, (0.8%) developed eczema herpeticum (5 on pimecrolimus cream, 1% alone and on pimecrolimus cream, 1% used in sequence with corticosteroids). In 211 subjects on vehicle alone, there were no cases of eczema herpeticum. The majority of adverse events were mild to moderate in severity. Two Phase trials were conducted involving 436 infants age months-23 months. One 6-week randomized vehicle-controlled trial with 20-week open-label phase and one safety trial, up to one year, were conducted. In the 6-week trial, 11% of pimecrolimus and 48% of vehicle subjects did not complete this trial; no subject in either group discontinued due to adverse events. Infants on pimecrolimus cream, 1% had an increased incidence of some adverse events compared to vehicle. In the 6-week vehicle-controlled trial these adverse events included pyrexia (32% vs. 13% vehicle), URI (24% vs. 14%), nasopharyngitis (15% vs. 8%), gastroenteritis (7% vs. 3%), otitis media (4% vs. 0%), and diarrhea (8% vs. 0%). In the open-label phase of the trial, for infants who switched to pimecrolimus cream, 1% from vehicle, the incidence of the above-cited adverse events approached or equaled the incidence of those subjects who remained on pimecrolimus cream, 1%. In the month safety data, 16% of pimecrolimus and 35% of vehicle subjects discontinued early and 1.5% of pimecrolimus and 0% of vehicle subjects discontinued due to adverse events. Infants on pimecrolimus cream, 1% had greater incidence of some adverse events as compared to vehicle. These included pyrexia (30% vs. 20%), URI (21% vs. 17%), cough (15% vs. 9%), hypersensitivity (8% vs. 2%), teething (27% vs. 22%), vomiting (9% vs. 4%), rhinitis (13% vs. 9%), viral rash (4% vs. 0%), rhinorrhea (4% vs. 0%), and wheezing (4% vs. 0%).The systemic exposure to pimecrolimus from pimecrolimus cream, 1% was investigated in 28 pediatric subjects with atopic dermatitis (20% to 80% BSA involvement) between the ages of months to 14 yrs. Following twice daily application for three weeks, blood concentrations of pimecrolimus were less than ng/mL with 60% (96/161) of the blood samples having blood concentration below the limit of quantification (0.5 ng/mL). However, more children (23 children out of the total 28 children investigated) had at least one detectable blood level as compared to the adults (12 adults out of the total 52 adults investigated) over 3-week treatment period. Due to the erratic nature of the blood levels observed, no correlation could be made between amount of cream, degree of BSA involvement, and blood concentrations. In general, the blood concentrations measured in adult atopic dermatitis subjects were comparable to those seen in the pediatric population.In second group of 30 pediatric subjects aged to 23 months with 10% to 92% BSA involvement, following twice daily application for three weeks, blood concentrations of pimecrolimus were less than 2.6 ng/mL with 65% (75/116) of the blood samples having blood concentration below 0.5ng/mL, and 27% (31/116) below the limit of quantification (0.1 ng/mL) for these trials.Overall, higher proportion of detectable blood levels was seen in the pediatric subject population as compared to adult population. This increase in the absolute number of positive blood levels may be due to the larger surface area to body mass ratio seen in these younger subjects. In addition, higher incidence of upper respiratory symptoms/infections was also seen relative to the older age group in the PK trials. At this time, causal relationship between these findings and pimecrolimus use cannot be ruled out.. 8.5 Geriatric Use. Nine (9) subjects greater than or equal to 65 years old received pimecrolimus cream, 1% in Phase trials. Clinical trials of pimecrolimus cream, 1% did not include sufficient numbers of subjects aged 65 and over to assess efficacy and safety.

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. Should not be used in immunocompromised adults and children, including patients on systemic immunosuppressive medications. 5.1) Avoid treatment on malignant or pre-malignant skin conditions, as these can present as dermatitis. 5.2) Should not be used in patients with Nethertons Syndrome or skin diseases with potential for increased systemic absorption. 5.2) Should not be used in immunocompromised adults and children, including patients on systemic immunosuppressive medications. 5.1) Avoid treatment on malignant or pre-malignant skin conditions, as these can present as dermatitis. 5.2) Should not be used in patients with Nethertons Syndrome or skin diseases with potential for increased systemic absorption. 5.2) 5.1 Risk of Immunosuppression. Prolonged systemic use of calcineurin inhibitors for sustained immunosuppression in animal studies and transplant patients following systemic administration has been associated with an increased risk of infections, lymphomas, and skin malignancies. These risks are associated with the intensity and duration of immunosuppression.Based on this information and the mechanism of action, there is concern about potential risk with the use of topical calcineurin inhibitors, including pimecrolimus cream, 1%. While causal relationship has not been established, rare cases of skin malignancy and lymphoma have been reported in patients treated with topical calcineurin inhibitors, including pimecrolimus cream, 1%. Therefore:Continuous long-term use of topical calcineurin inhibitors, including pimecrolimus cream, 1%, in any age group should be avoided, and application limited to areas of involvement with atopic dermatitis Pimecrolimus cream, 1% is not indicated for use in children less than years of age Pimecrolimus cream, 1% should not be used in immunocompromised adults and children, including patients on systemic immunosuppressive medications. If signs and symptoms of atopic dermatitis do not improve within weeks, patients should be re-examined by their healthcare provider and their diagnosis be confirmed. The safety of pimecrolimus cream, 1% has not been established beyond one year of non-continuous use.. Continuous long-term use of topical calcineurin inhibitors, including pimecrolimus cream, 1%, in any age group should be avoided, and application limited to areas of involvement with atopic dermatitis Pimecrolimus cream, 1% is not indicated for use in children less than years of age Pimecrolimus cream, 1% should not be used in immunocompromised adults and children, including patients on systemic immunosuppressive medications. If signs and symptoms of atopic dermatitis do not improve within weeks, patients should be re-examined by their healthcare provider and their diagnosis be confirmed. The safety of pimecrolimus cream, 1% has not been established beyond one year of non-continuous use.. 5.2 Application to Malignant or Pre-malignant Skin Conditions. The use of pimecrolimus cream, 1% should be avoided on malignant or pre-malignant skin conditions. Malignant or pre-malignant skin conditions, such as cutaneous T-cell lymphoma (CTCL), can present as dermatitis.Pimecrolimus cream, 1% should not be used in patients with Nethertons Syndrome or other skin diseases where there is the potential for increased systemic absorption of pimecrolimus. The safety of pimecrolimus cream, 1% has not been established in patients with generalized erythroderma.The use of pimecrolimus cream, 1% may cause local symptoms such as skin burning (burning sensation, stinging, soreness) or pruritus. Localized symptoms are most common during the first few days of pimecrolimus cream, 1% application and typically improve as the lesions of atopic dermatitis resolve [see Adverse Reactions (6.1)]. 5.3 Bacterial and Viral Skin Infections. Before commencing treatment with pimecrolimus cream, 1%, bacterial or viral infections at treatment sites should be resolved. Trials have not evaluated the safety and efficacy of pimecrolimus cream, 1% in the treatment of clinically infected atopic dermatitis.While patients with atopic dermatitis are predisposed to superficial skin infections including eczema herpeticum (Kaposis varicelliform eruption), treatment with pimecrolimus cream, 1% may be independently associated with an increased risk of varicella zoster virus infection (chicken pox or shingles), herpes simplex virus infection, or eczema herpeticum.In clinical trials, 15/1,544 (1%) cases of skin papilloma (warts) were observed in subjects using pimecrolimus cream, 1%. The youngest subject was age and the oldest was age 12. In cases where there is worsening of skin papillomas or they do not respond to conventional therapy, discontinuation of pimecrolimus cream, 1% should be considered until complete resolution of the warts is achieved.. 5.4 Patients with Lymphadenopathy. In clinical trials, 14/1,544 (0.9%) cases of lymphadenopathy were reported while using pimecrolimus cream, 1%. These cases of lymphadenopathy were usually related to infections and noted to resolve upon appropriate antibiotic therapy. Of these 14 cases, the majority had either clear etiology or were known to resolve. Patients who receive pimecrolimus cream, 1% and who develop lymphadenopathy should have the etiology of their lymphadenopathy investigated. In the absence of clear etiology for the lymphadenopathy, or in the presence of acute infectious mononucleosis, pimecrolimus cream, 1% should be discontinued. Patients who develop lymphadenopathy should be monitored to ensure that the lymphadenopathy resolves.. 5.5 Sun Exposure. During the course of treatment, it is prudent for patients to minimize or avoid natural or artificial sunlight exposure, even while pimecrolimus cream, 1% is not on the skin. The potential effects of pimecrolimus cream, 1% on skin response to ultraviolet damage are not known.. 5.6 Immunocompromised Patients. The safety and efficacy of pimecrolimus cream, 1% in immunocompromised patients have not been studied.