ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. The following serious adverse reactions are discussed in greater detail in other sections of the prescribing information:oHyperlipidemia [see Warnings and Precautions (5.1) ]oPancreatitis [see Warnings and Precautions (5.2) ]oHepatotoxicity, Cholestasis, and Hepatic Failure [see Warnings and Precautions (5.3) ]oHypothyroidism [see Warnings and Precautions (5.4) ]oNeutropenia [see Warnings and Precautions (5.5) ]oCataracts [see Warnings and Precautions (5.6) ]oVitamin Supplementation Hazard [see Warnings and Precautions (5.7) ]oHypoglycemia Risk in Patients with Diabetes Mellitus [see Warnings and Precautions (5.8) ]oPhotosensitivity [see Warnings and Precautions (5.9) ]oLaboratory Tests [see Warnings and Precautions (5.10) ]oDrug/Laboratory Test Interactions [see Warnings and Precautions (5.11) ]. oHyperlipidemia [see Warnings and Precautions (5.1) ]. oPancreatitis [see Warnings and Precautions (5.2) ]. oHepatotoxicity, Cholestasis, and Hepatic Failure [see Warnings and Precautions (5.3) ]. oHypothyroidism [see Warnings and Precautions (5.4) ]. oNeutropenia [see Warnings and Precautions (5.5) ]. oCataracts [see Warnings and Precautions (5.6) ]. oVitamin Supplementation Hazard [see Warnings and Precautions (5.7) ]. oHypoglycemia Risk in Patients with Diabetes Mellitus [see Warnings and Precautions (5.8) ]. oPhotosensitivity [see Warnings and Precautions (5.9) ]. oLaboratory Tests [see Warnings and Precautions (5.10) ]. oDrug/Laboratory Test Interactions [see Warnings and Precautions (5.11) ]. The most common adverse reactions (greater than 10%) include: hyperlipidemia, hypercholesteremia, headache, hypothyroidism, asthenia, leukopenia, rash, nausea, infection, peripheral edema, abdominal pain, and dry skin. (6.1)To report SUSPECTED ADVERSE REACTIONS, contact Bausch Health US, LLC at 1-800-321-4576 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. The safety of TARGRETIN has been evaluated in two clinical trials of 152 patients with CTCL who received TARGRETIN for up to 97 weeks and in 352 patients in other trials. The mean duration of therapy for the 152 patients with CTCL was 166 days. The most common adverse events reported with an incidence of at least 10% in patients with CTCL treated at an initial dose of 300 mg/m2/day of TARGRETIN are shown in Table 2. The events at least possibly related to treatment are lipid abnormalities (elevated triglycerides, elevated total and LDL cholesterol and decreased HDL cholesterol), hypothyroidism, headache, asthenia, rash, leukopenia, anemia, nausea, infection, peripheral edema, abdominal pain, and dry skin. Most adverse events occurred at greater incidence in patients treated at starting doses of greater than 300 mg/m2/day (see Table 2). Adverse reactions leading to TARGRETIN dose reduction or discontinuation in at least two patients were hyperlipemia, neutropenia/leukopenia, diarrhea, fatigue/lethargy, hypothyroidism, headache, liver function test abnormalities, rash, pancreatitis, nausea, anemia, allergic reaction, muscle spasm, pneumonia, and confusion. The NCI Grade and NCI Grade adverse reactions reported in two or more patients with CTCL treated at an initial dose of 300 mg/m2/day of TARGRETIN (see Table 3) were hypertriglyceridemia, pruritus, headache, peripheral edema, leukopenia, rash, and hypercholesteremia. Most of these moderately severe or severe adverse events occurred at higher rate in patients treated at starting doses of greater than 300 mg/m2/day than in patients treated at starting dose of 300 mg/m2/day.In patients with CTCL receiving an initial dose of 300 mg/m2/day, the incidence of NCI Grade or elevations in triglycerides and total cholesterol was 28% and 25%, respectively (Table 4). In contrast, in patients with CTCL receiving greater than 300 mg/m2/day, the incidence of NCI Grade or elevated triglycerides and total cholesterol was 45% and 45%, respectively. Other Grade and laboratory abnormalities are shown in Table 3.In addition to the 152 patients enrolled in the two CTCL trials, 352 patients received TARGRETIN as monotherapy for various advanced malignancies at doses from mg/m2/day to 1000 mg/m2/day. The common adverse reactions (incidence greater than 10%) were similar to those seen in patients with CTCL. In the 504 patients (CTCL and non-CTCL) who received TARGRETIN as monotherapy, drug-related serious adverse reactions that were fatal, in one patient each, were acute pancreatitis, subdural hematoma, and liver failure.In the patients with CTCL receiving an initial dose of 300 mg/m2/day of TARGRETIN, adverse reactions reported at an incidence of less than 10% and not included in Tables through or discussed in other parts of labeling and possibly related to treatment were as follows:Body as Whole: chills, cellulitis, chest pain, breast pain, sepsis, and monilia infection.Cardiovascular: hemorrhage, hypertension, angina pectoris, right heart failure, syncope, and tachycardia. Digestive: constipation, dry mouth, flatulence, colitis, dyspepsia, cheilitis, gastroenteritis, gingivitis, liver failure, and melena.Hemic and Lymphatic: eosinophilia, thrombocythemia, coagulation time increased, lymphocytosis, and thrombocytopenia.Metabolic and Nutritional: LDH increased, creatinine increased, hypoproteinemia, hyperglycemia, weight decreased, weight increased, and amylase increased.Musculoskeletal: arthralgia, myalgia, bone pain, myasthenia, and arthrosis.Nervous: depression, agitation, ataxia, cerebrovascular accident, confusion, dizziness, hyperesthesia, hypesthesia, and neuropathy.Respiratory: pharyngitis, rhinitis, dyspnea, pleural effusion, bronchitis, cough increased, lung edema, hemoptysis, and hypoxia.Skin and Appendages: skin ulcer, acne, alopecia, skin nodule, macular papular rash, pustular rash, serous drainage, and vesicular bullous rash.Special Senses: dry eyes, conjunctivitis, ear pain, blepharitis, corneal lesion, keratitis, otitis externa, and visual field defect.Urogenital: albuminuria, hematuria, urinary incontinence, urinary tract infection, urinary urgency, dysuria, and kidney function abnormal.Table 2: Adverse Events with Incidence >=10% in CTCL TrialsInitial Assigned Dose Group(mg/m2/day)300>300Body SystemN=84N=53Adverse Event (AE)Preferred English term coded according to Ligand-modified COSTART Dictionary.,Patients are counted at most once in each AE category. (%)N (%)METABOLIC AND NUTRITIONAL DISORDERSHyperlipemia66 (79)42 (79)Hypercholesteremia27 (32)33 (62)Lactic dehydrogenase increased6 (7)7 (13)BODY AS WHOLEHeadache25 (30)22 (42)Asthenia17 (20)24 (45)Infection11 (13)12 (23)Abdominal pain9 (11)2 (4)Chills8 (10)7 (13)Fever4 (5)9 (17)Flu syndrome3 (4)7 (13)Back pain2 (2)6 (11)Infection bacterial (1)7 (13)ENDOCRINEHypothyroidism24 (29)28 (53)SKIN AND APPENDAGESRash14 (17)12 (23)Dry skin9 (17)5 (9)Exfoliative dermatitis8 (10)15 (28)Alopecia3 (4)6 (11)HEMIC AND LYMPHATIC SYSTEMLeukopenia14 (17)25 (47)Anemia5 (6)13 (25)Hypochromic anemia3 (4)7 (13)DIGESTIVE SYSTEMNausea13 (16)4 (8)Diarrhea6 (7)22 (42)Vomiting3 (4)7 (13)Anorexia2 (2)12 (23)CARDIOVASCULAR SYSTEMPeripheral edema11 (13)6 (11)NERVOUS SYSTEMInsomnia4 (5)6 (11)Table 3: Incidence of Moderately Severe and Severe Adverse Events Reported in at Least Two Patients (CTCL Trials)Initial Assigned Dose Group (mg/m2/day)300 (N=84)>300 (N=53)Mod SevSevereMod SevSevereBody SystemAdverse Event (AE)Preferred English term coded according to Ligand-modified COSTART Dictionary.,Patients are counted at most once in each AE category. Patients are classified by the highest severity within each row. (%)N (%)N (%)N (%)BODY AS WHOLEAsthenia1 (1)0 (0)11 (21)0 (0)Headache3 (4)0 (0)5 (9)1 (2)Infection bacterial1 (1)0 (0)0 (0)2 (4)CARDIOVASCULAR SYSTEMPeripheral edema2 (2)1 (1)0 (0)0 (0)DIGESTIVE SYSTEMAnorexia0 (0)0 (0)3 (6)0 (0)Diarrhea1 (1)1 (1)2 (4)1 (2)Pancreatitis1 (1)0 (0)3 (6)0 (0)Vomiting0 (0)0 (0)2 (4)0 (0)ENDOCRINEHypothyroidism1 (1)1 (1)2 (4)0 (0)HEMIC AND LYMPHATIC SYSTEMLeukopenia3 (4)0 (0)6 (11)1 (2)METABOLIC AND NUTRITIONAL DISORDERSBilirubinemia0 (0)1 (1)2 (4)0 (0)Hypercholesteremia2 (2)0 (0)5 (9)0 (0)Hyperlipemia16 (19)6 (7)17 (32)5 (9)SGOT/AST increased0 (0)0 (0)2 (4)0 (0)SGPT/ALT increased (0)0 (0)2 (4)0 (0)RESPIRATORY SYSTEMPneumonia0 (0)0 (0)2 (4)2 (4)SKIN AND APPENDAGESExfoliative dermatitis0 (0)1 (1)3 (6)1 (2)Rash1 (1)2 (2)1 (2)0 (0)Table 4: Treatment-Emergent Abnormal Laboratory Values in CTCL TrialsInitial Assigned Dose (mg/m2/day)300>300N=83Number of patients with at least one analyte value post-baseline. N=53 AnalyteGrade 3Adapted from NCI Common Toxicity Criteria, Grade and 4, Version 2.0. Patients are considered to have had Grade or value if either of the following occurred: a) Value becomes Grade or during the study; b) Value is abnormal at baseline and worsens to Grade or on study, including all values beyond study drug discontinuation, as defined in data handling conventions. (%)Grade (%)Grade 3(%)Grade 4(%)TriglyceridesThe denominator used to calculate the incidence rates for fasting Total Cholesterol and Triglycerides were N=75 for the 300 mg/m2/day initial dose group and N=44 for the >300 mg/m2/day initial dose group. 2173214Total cholesterol 1971630Alkaline phosphatase1002Hyperglycemia1060Hypocalcemia1000Hyponatremia1090SGPT/ALT1022Hyperkalemia0020Hypernatremia0100SGOT/AST0022Total bilirubin0002ANC decreased124198ALC decreased 70150WBC decreased40110Hemoglobin decreased0020The safety profile from the one post-approval trial with 59 subjects was generally comparable to that of the pivotal trials with the exception of serious adverse events hypertriglyceridemia, neutropenia and bone marrow failure which were observed more frequently in the TARGRETIN 300 mg/m2/day group than in the TARGRETIN 150 mg/m2/day group.Severe hypertriglyceridemia (>=800 mg/dL) was not seen in any subject in the lower dosage arm.The most common AEs by preferred term in either the TARGRETIN 300 or 150 mg/m2/day treatment group were as follows: hypertriglyceridemia (18 subjects [62.1%] and 17 subjects [56.7%], respectively); hypothyroidism (15 subjects [51.7%] and 13 subjects [43.3%], respectively); headache (9 subjects [31.0%] and subjects [23.3%], respectively); hypercholesterolemia (8 subjects [27.6%] and subjects [23.3%], respectively); neutropenia (7 subjects [24.1%] and subjects [6.7%], respectively); and skin exfoliation (5 subjects [17.2%] and subjects [16.7%], respectively).Higher percentage of subjects in the TARGRETIN 300 mg/m2/day group than in the TARGRETIN 150 mg/m2/day group experienced SAEs (13 subjects [44.8%] vs 11 subjects [36.7%], respectively.Of the SAEs of special interest, there were more events in the TARGRETIN 300 mg/m2/day group than in TARGRETIN 150 mg/m2/day group of bone marrow failure (3 [10.3%] vs [3.3%, respectively]), neutropenia (3 [10.3%] vs [0%], respectively), and hypertriglyceridemia (9 [31%] vs [6.7%], respectively).

CLINICAL PHARMACOLOGY SECTION.

12 CLINICAL PHARMACOLOGY. 12.1 Mechanism of Action. Bexarotene selectively binds and activates retinoid receptor subtypes (RXR, RXRss, RXR). RXRs can form heterodimers with various receptor partners such as retinoic acid receptors (RARs), vitamin receptor, thyroid receptor, and peroxisome proliferator activator receptors (PPARs). Once activated, these receptors function as transcription factors that regulate the expression of genes that control cellular differentiation and proliferation. Bexarotene inhibits the growth in vitro of some tumor cell lines of hematopoietic and squamous cell origin. It also induces tumor regression in vivo in some animal models. The exact mechanism of action of bexarotene in the treatment of cutaneous T-cell lymphoma (CTCL) is unknown.. 12.3 Pharmacokinetics. Terminal half-life of bexarotene is approximately hours. Studies in patients with advanced malignancies show approximate single dose linearity within the therapeutic range.Absorption After oral administration of TARGRETIN, bexarotene is absorbed with Tmax of about hours. Plasma bexarotene AUC and Cmax values resulting from 75 to 300 mg dose were 35% and 48% higher, respectively, after fat-containing meal than after glucose solution.Distribution Bexarotene is highly bound (>99%) to plasma proteins. The plasma proteins to which bexarotene binds have not been elucidated, and the ability of bexarotene to displace drugs bound to plasma proteins and the ability of drugs to displace bexarotene binding have not been studied.EliminationMetabolismFour bexarotene metabolites have been identified in plasma: 6- and 7-hydroxy-bexarotene and 6- and 7-oxo-bexarotene. In vitro studies suggest that cytochrome P450 3A4 is the major cytochrome P450 responsible for formation of the oxidative metabolites and that the oxidative metabolites may be glucuronidated. The oxidative metabolites are active in in vitro assays of retinoid receptor activation, but the relative contribution of the parent and any metabolites to the efficacy and safety of TARGRETIN is unknown.ExcretionThe renal elimination of bexarotene and its metabolites was examined in patients with Type diabetes mellitus. Urinary elimination of bexarotene and its known metabolites is minor excretory pathway (<1% of administered dose).Pharmacokinetics in Specific PopulationsAge: Based on the population pharmacokinetic analysis of data for 232 patients aged >=65 years and 343 patients aged <65 years, age has no statistically significant effect on bexarotene pharmacokinetics.Body Weight and Gender: Based on the population pharmacokinetics analysis of data for 614 patients with weight range of 26 to 145 kg, the bexarotene apparent clearance increases with increasing body weight. Gender has no statistically significant effect on bexarotene pharmacokinetics.Race: Based on the population pharmacokinetic analysis of data for 540 Caucasian and 44 Black patients, bexarotene pharmacokinetics are similar in Blacks and Caucasians. There are insufficient data to evaluate potential differences in the pharmacokinetics of bexarotene for other races.Renal Impairment: No formal studies have been conducted with TARGRETIN in patients with renal impairment. Urinary elimination of bexarotene and its known metabolites is minor excretory pathway (<1% of administered dose), but because renal impairment can result in significant protein binding changes, pharmacokinetics may be altered in patients with renal impairment. Hepatic Impairment: No specific studies have been conducted with TARGRETIN in patients with hepatic impairment. Because less than 1% of the dose is excreted in the urine unchanged and there is in vitro evidence of extensive hepatic contribution to bexarotene elimination, hepatic impairment would be expected to lead to greatly decreased clearance.Drug InteractionsEffect of Other Drugs on TARGRETINCYP3A4 Inhibitors/Inducers: In clinical study, concomitant administration of multiple doses of ketoconazole with TARGRETIN did not alter bexarotene plasma concentrations. This suggests that bexarotene elimination is not dependent on CYP3A4 metabolism.Paclitaxel plus Carboplatin: The co-administration of paclitaxel (200 mg/m2 IV dose over hours) plus carboplatin (at dose expected to achieve an AUC of mgmin/mL) with TARGRETIN (400 mg/m2 orally once daily) increased the exposure to bexarotene (AUC0-24 and Cmax) by 2-fold compared to TARGRETIN alone.Atorvastatin: Bexarotene concentrations were not affected by concomitant atorvastatin administration. Effect of TARGRETIN on Other DrugsBexarotene did not significantly inhibit the following enzymes in human liver microsomes: CYP1A2, CYP2A6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4. In vitro data suggested potential for bexarotene to inhibit CYP2C8 and induce CYP3A4. Atorvastatin: The exposure (AUC) to atorvastatin (a substrate for CYP3A4) decreased by half when atorvastatin was co-administered with TARGRETIN (400 mg/m2 orally once daily).Tamoxifen: Based on interim data, concomitant administration of TARGRETIN and tamoxifen resulted in approximately 35% decrease in plasma concentrations of tamoxifen, possibly through induction of CYP3A4 by bexarotene.Paclitaxel: The exposure (AUC) to paclitaxel (a substrate for CYP3A4 and CYP2C8) decreased by 19% when paclitaxel (200 mg/m2 IV dose over hours) was co-administered with TARGRETIN (400 mg/m2 orally once daily). Carboplatin: The co-administration of TARGRETIN (400 mg/m2 orally once daily) had no effect on the exposure to free or total carboplatin.

CLINICAL STUDIES SECTION.

14 CLINICAL STUDIES. TARGRETIN was evaluated in two clinical trials in 152 patients with advanced and early stage cutaneous T-cell lymphoma (CTCL) in two multicenter, open-label, historically controlled clinical trials conducted in the U.S., Canada, Europe, and Australia.The advanced disease patients had disease refractory to at least one prior systemic therapy (median of two, range to prior systemic therapies) and had been treated with median of five (range to 11) prior systemic, irradiation, and/or topical therapies. Early disease patients were intolerant to, had disease that was refractory to, or had reached response plateau of months on, at least two prior therapies. The patients entered had been treated with median of 3.5 (range to 12) therapies (systemic, irradiation, and/or topical).The two clinical trials enrolled total of 152 patients, 102 of whom had disease refractory to at least one prior systemic therapy, 90 with advanced disease and 12 with early disease. This is the patient population for whom TARGRETIN is indicated.Patients were initially treated with starting dose of 650 mg/m2/day with subsequent reduction of starting dose to 500 mg/m2/day. Neither of these starting doses was tolerated, and the starting dose was then reduced to 300 mg/m2/day. If, however, patient on 300 mg/m2/day of TARGRETIN showed no response after or more weeks of therapy, the dose could be increased to 400 mg/m2/day.Tumor response was assessed in both trials by observation of up to five baseline-defined index lesions using Composite Assessment of Index Lesion Disease Severity (CA). This endpoint was based on summation of the grades, for all index lesions, of erythema, scaling, plaque elevation, hypopigmentation or hyperpigmentation, and area of involvement. Also considered in response assessment was the presence or absence of cutaneous tumors and extracutaneous disease manifestations.All tumor responses required confirmation over at least two assessments separated by at least weeks. partial response was defined as an improvement of at least 50% in the index lesions without worsening, or development of new cutaneous tumors or non-cutaneous manifestations. complete clinical response required complete disappearance of all manifestations of disease, but did not require confirmation by biopsy.At the initial dose of 300 mg/m2/day, 1/62 (1.6%) of patients had complete clinical tumor response and 19/62 (30%) of patients had partial tumor response. The rate of relapse (25% increase in CA or worsening of other aspects of disease) in the 20 patients who had tumor response was 6/20 (30%) over median duration of observation of 21 weeks, and the median duration of tumor response had not been reached. Responses were seen as early as weeks and new responses continued to be seen at later visits.In one post-approval clinical trial with total of 59 subjects (29 in 300 mg/m2/day dose group and 30 in the 150 mg/m2/day dose), the objective response rate was higher in the TARGRETIN 300 mg/m2/day group than in the TARGRETIN 150 mg/m2/day group with respect to the CA (34.5% vs 23.3%), Physicians Global Assessment (PGA) (37.9% vs 20.0%), and percent BSA involvement (34.5% vs 23.3%).The median duration of response in the TARGRETIN 300 mg/m2/day group based on the CA, PGA, and percent BSA involvement was 86.5 days, 72.0 days and 60.0 days, respectively. While in the TARGRETIN 150 mg/m2/day group the median duration of response based on the CA, PGA, and percent BSA involvement was 55 days, 119.0 days and 118.0 days, respectively.The median time to cutaneous tumor response (the time to cutaneous tumor response for given subject is defined as the time interval from the first day of TARGRETIN treatment to the time of the first observation when the subject with subsequent confirmation of response meets criteria for CR, CCR or PR) in the TARGRETIN 300 mg/m2/day group based on the CA, PGA, and percent BSA involvement was 85 days, 98 days and 117.5 days, respectively. While in the TARGRETIN 150 mg/m2/day group the median time to cutaneous tumor response based on the CA, PGA, and percent BSA involvement was 87 days, 57 days and 57 days, respectively. In the TARGRETIN 300 mg/m2/day group, the median time to cutaneous tumor progression based on the CA, PGA, and percent BSA involvement was 77.5, 115.5, and 88.0 days, respectively. In the TARGRETIN 150 mg/m2/day group, the median time to cutaneous tumor progression was 203.0 days based on the CA and 86.0 days based on percent BSA involvement; no subject in this treatment group had cutaneous tumor progression based on the PGA.

INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. Advise the patient to read the FDA-approved patient labeling (Patient Information).Inform the patient or caregiver about the following:Birth DefectsAdvise patients that TARGRETIN is contraindicated in pregnancy [see Contraindications (4.1)]. TARGRETIN is member of the retinoid class of drugs that is associated with birth defects in humans [see Use In Specific Populations (8.1)]. oAdvise females of reproductive potential that they must avoid pregnancy while taking TARGRETIN and for at least month following discontinuation of therapy.oAdvise females of reproductive potential of the importance of monthly pregnancy testing while taking TARGRETIN.oAdvise females of reproductive potential to use effective contraception for month prior to the initiation of therapy, during therapy, and for at least month following discontinuation of therapy and that two reliable forms of contraception should be used simultaneously, one of which should be non-hormonal.oAdvise females of reproductive potential that TARGRETIN therapy should be initiated on the second or third day of normal menstrual period.oInstruct patient to immediately stop taking TARGRETIN if she becomes pregnant while taking this drug.oAdvise male patients with sexual partners who are pregnant, possibly pregnant, or who could become pregnant that they must use condoms during sexual intercourse while taking TARGRETIN and for at least month after the last dose of the drug.PancreatitisAdvise patients of the risk of developing pancreatitis, which may be accompanied by nausea, vomiting, and abdominal or back pain and to immediately contact their healthcare provider if these symptoms occur [see Warnings and Precautions (5.2)]. HepatotoxicityInform patients of the possibility of developing liver function abnormalities and serious hepatic toxicity. Advise patients to immediately contact their healthcare provider if signs of liver failure occur, including jaundice, anorexia, bleeding, or bruising [see Warnings and Precautions (5.3)]. NeutropeniaAdvise patients of the possibility of developing neutropenia and to immediately contact their healthcare provider should they develop fever, particularly in association with any suggestion of infection [see Warnings and Precautions (5.5)]. CataractsAdvise patients of the possibility of developing new or worsening cataracts and to inform their healthcare provider about any changes in their vision during treatment with TARGRETIN [see Warnings and Precautions (5.6)]. Vitamin Supplementation HazardAdvise patients to limit vitamin intake to <=15,000 IU/day to avoid potential additive toxic effects.Hypoglycemia and Diabetes MellitusAdvise patients of the possibility of developing hypoglycemia when using insulin, agents enhancing insulin secretion, or insulin sensitizers while on TARGRETIN therapy. Instruct patients on these medications to check their blood sugar frequently and to notify their physicians of any changes in blood sugar level [see Warnings and Precautions (5.8)]. PhotosensitivityAdvise patients of potential increased skin sensitivity to sunlight while taking TARGRETIN and to minimize exposure to sunlight and artificial ultraviolet light [see Warnings and Precautions (5.9)]. Laboratory TestsAdvise patients of laboratory testing which will occur during therapy to monitor lipids, liver function, thyroid function, and white blood cell counts [see Warnings and Precautions (5.10)]. If applicable, advise patients of monthly pregnancy testing [see Use In Specific Populations (8.3)]. Administration InstructionsAdvise patients to take TARGRETIN with meal [see DOSAGE AND ADMINISTRATION]. Distributed by:Bausch Health US, LLC Bridgewater, NJ 08807 USAManufactured by:Catalent Pharma Solutions LLCSt. Petersburg, FL 33716 USATARGRETIN is trademark of Bausch Health Companies Inc. or its affiliates. Any other product/brand names are trademarks of their respective owners.(C) 2020 Bausch Health Companies Inc. or its affiliates9436601. oAdvise females of reproductive potential that they must avoid pregnancy while taking TARGRETIN and for at least month following discontinuation of therapy.. oAdvise females of reproductive potential of the importance of monthly pregnancy testing while taking TARGRETIN.. oAdvise females of reproductive potential to use effective contraception for month prior to the initiation of therapy, during therapy, and for at least month following discontinuation of therapy and that two reliable forms of contraception should be used simultaneously, one of which should be non-hormonal.. oAdvise females of reproductive potential that TARGRETIN therapy should be initiated on the second or third day of normal menstrual period.. oInstruct patient to immediately stop taking TARGRETIN if she becomes pregnant while taking this drug.. oAdvise male patients with sexual partners who are pregnant, possibly pregnant, or who could become pregnant that they must use condoms during sexual intercourse while taking TARGRETIN and for at least month after the last dose of the drug.

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics. Terminal half-life of bexarotene is approximately hours. Studies in patients with advanced malignancies show approximate single dose linearity within the therapeutic range.Absorption After oral administration of TARGRETIN, bexarotene is absorbed with Tmax of about hours. Plasma bexarotene AUC and Cmax values resulting from 75 to 300 mg dose were 35% and 48% higher, respectively, after fat-containing meal than after glucose solution.Distribution Bexarotene is highly bound (>99%) to plasma proteins. The plasma proteins to which bexarotene binds have not been elucidated, and the ability of bexarotene to displace drugs bound to plasma proteins and the ability of drugs to displace bexarotene binding have not been studied.EliminationMetabolismFour bexarotene metabolites have been identified in plasma: 6- and 7-hydroxy-bexarotene and 6- and 7-oxo-bexarotene. In vitro studies suggest that cytochrome P450 3A4 is the major cytochrome P450 responsible for formation of the oxidative metabolites and that the oxidative metabolites may be glucuronidated. The oxidative metabolites are active in in vitro assays of retinoid receptor activation, but the relative contribution of the parent and any metabolites to the efficacy and safety of TARGRETIN is unknown.ExcretionThe renal elimination of bexarotene and its metabolites was examined in patients with Type diabetes mellitus. Urinary elimination of bexarotene and its known metabolites is minor excretory pathway (<1% of administered dose).Pharmacokinetics in Specific PopulationsAge: Based on the population pharmacokinetic analysis of data for 232 patients aged >=65 years and 343 patients aged <65 years, age has no statistically significant effect on bexarotene pharmacokinetics.Body Weight and Gender: Based on the population pharmacokinetics analysis of data for 614 patients with weight range of 26 to 145 kg, the bexarotene apparent clearance increases with increasing body weight. Gender has no statistically significant effect on bexarotene pharmacokinetics.Race: Based on the population pharmacokinetic analysis of data for 540 Caucasian and 44 Black patients, bexarotene pharmacokinetics are similar in Blacks and Caucasians. There are insufficient data to evaluate potential differences in the pharmacokinetics of bexarotene for other races.Renal Impairment: No formal studies have been conducted with TARGRETIN in patients with renal impairment. Urinary elimination of bexarotene and its known metabolites is minor excretory pathway (<1% of administered dose), but because renal impairment can result in significant protein binding changes, pharmacokinetics may be altered in patients with renal impairment. Hepatic Impairment: No specific studies have been conducted with TARGRETIN in patients with hepatic impairment. Because less than 1% of the dose is excreted in the urine unchanged and there is in vitro evidence of extensive hepatic contribution to bexarotene elimination, hepatic impairment would be expected to lead to greatly decreased clearance.Drug InteractionsEffect of Other Drugs on TARGRETINCYP3A4 Inhibitors/Inducers: In clinical study, concomitant administration of multiple doses of ketoconazole with TARGRETIN did not alter bexarotene plasma concentrations. This suggests that bexarotene elimination is not dependent on CYP3A4 metabolism.Paclitaxel plus Carboplatin: The co-administration of paclitaxel (200 mg/m2 IV dose over hours) plus carboplatin (at dose expected to achieve an AUC of mgmin/mL) with TARGRETIN (400 mg/m2 orally once daily) increased the exposure to bexarotene (AUC0-24 and Cmax) by 2-fold compared to TARGRETIN alone.Atorvastatin: Bexarotene concentrations were not affected by concomitant atorvastatin administration. Effect of TARGRETIN on Other DrugsBexarotene did not significantly inhibit the following enzymes in human liver microsomes: CYP1A2, CYP2A6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4. In vitro data suggested potential for bexarotene to inhibit CYP2C8 and induce CYP3A4. Atorvastatin: The exposure (AUC) to atorvastatin (a substrate for CYP3A4) decreased by half when atorvastatin was co-administered with TARGRETIN (400 mg/m2 orally once daily).Tamoxifen: Based on interim data, concomitant administration of TARGRETIN and tamoxifen resulted in approximately 35% decrease in plasma concentrations of tamoxifen, possibly through induction of CYP3A4 by bexarotene.Paclitaxel: The exposure (AUC) to paclitaxel (a substrate for CYP3A4 and CYP2C8) decreased by 19% when paclitaxel (200 mg/m2 IV dose over hours) was co-administered with TARGRETIN (400 mg/m2 orally once daily). Carboplatin: The co-administration of TARGRETIN (400 mg/m2 orally once daily) had no effect on the exposure to free or total carboplatin.

SPL PATIENT PACKAGE INSERT SECTION.

Patient InformationTARGRETIN(R) (tar-GRET-in)(bexarotene)CapsulesWhat is the most important information should know about TARGRETINTARGRETIN can cause serious side effects, including major birth defects to an unborn baby, if taken during pregnancy.For females who can become pregnant:oYou should avoid becoming pregnant during treatment with TARGRETIN.oDo not take TARGRETIN if you are pregnant or plan to become pregnant.oYour healthcare provider will do pregnancy test, within week before you start TARGRETIN, and each month during treatment with TARGRETIN to make sure that you are not pregnant.oYou must use two effective forms of birth control together starting month before you begin treatment with TARGRETIN, during treatment, and for month after stopping TARGRETIN. Birth control pills (oral contraceptives) and other hormonal forms of birth control may not be effective if used with TARGRETIN. At least one of the forms of birth control that you choose should not contain hormones. Talk to your healthcare provider about what forms of birth control may be right for you during treatment with TARGRETIN. oYou should start taking TARGRETIN on the second or third day of normal menstrual period. Follow your healthcare providers instructions about when to start TARGRETIN.oCall your healthcare provider right away, if you become pregnant or think that you are pregnant during treatment with TARGRETIN, and for month after you stop taking TARGRETIN.For males:oYou must use condom with female partners who are pregnant, might be pregnant, or who are able to become pregnant, during treatment with TARGRETIN and for at least month after your last dose.What is TARGRETINTARGRETIN is prescription medicine used to treat the skin problems that happen with type of cancer called cutaneous T-cell lymphoma (CTCL) after treatment with at least one other type of medicine by mouth or injection, did not work or has stopped working.It is not known if TARGRETIN is safe and effective in children.Who should not take TARGRETINDo not take TARGRETIN:oif you are pregnant or plan to become pregnant. See What is the most important information should know about TARGRETINoif you are allergic to bexarotene or any of the ingredients in TARGRETIN. See the end of this leaflet for complete list of ingredients in TARGRETIN.Before taking TARGRETIN, tell your healthcare provider about all of your medical conditions, including if you:ohave or have had problems with your pancreas, including pancreatitisohave or have had gallbladder problemsohave or have had liver problemsohave thyroid problemsohave diabetesohave high levels of fats (lipids) called cholesterol or triglycerides in your bloodohave cataracts or history of cataractsodrink alcoholoare pregnant, plan to become pregnant, or think you may be pregnant. See What is the most important information should know about TARGRETINoare breastfeeding or plan to breastfeed. It is not known if TARGRETIN passes into your breast milk. You should not breastfeed during treatment with TARGRETIN. Talk to your healthcare provider about the best way to feed your baby during treatment with TARGRETIN.Tell your healthcare provider about all of the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Using TARGRETIN with certain other medicines can affect each other.How should take TARGRETINoTake TARGRETIN exactly as your healthcare provider tells you.oYour healthcare provider will tell you how many TARGRETIN capsules to take each day. Your healthcare provider may change your daily dose of TARGRETIN as needed to treat your CTCL or if you get certain side effects. You should not change your dose unless your healthcare provider tells you to.Take your dose of TARGRETIN one time day with meal. Your healthcare provider will do blood tests before you start TARGRETIN and during treatment to check for side effects.What should avoid while taking TARGRETINoLimit your exposure to sunlight and artificial types of sunlight. TARGRETIN can make your skin more sensitive to sunlight and you can get sunburn.oLimit the amount of vitamin that you take during treatment with TARGRETIN. Large doses of vitamin may cause side effects that are similar to side effects that can happen in people who take TARGRETIN.What are the possible side effects of TARGRETINTARGRETIN can cause serious side effects, including: oSee What is the most important information should know about TARGRETINoIncreased levels of fats (lipids) called cholesterol or triglycerides, in your blood are common with TARGRETIN, but can also be serious. Your healthcare provider may prescribe you medicines to treat high cholesterol or triglycerides levels, reduce your dose, temporarily stop treatment or completely stop treatment with TARGRETIN if you have this problem.oInflammation of the pancreas (acute pancreatitis). TARGRETIN can sometimes cause pancreatitis that comes on suddenly (acute), and that can lead to death. Your risk of developing acute pancreatitis may be greater if you:ohave had pancreatitis in the pastohigh levels of fats in your blood that are not controlledodrink large amounts of alcoholohave gallbladder problemsohave diabetes that is not controlledotake certain medicines that can increase the amount of triglycerides in your bloodotake medicines that can harm your pancreasTell your healthcare provider right away if you develop signs or symptoms of pancreatitis during treatment with TARGRETIN, including: onausea that will not go awayovomitingostomach-area (abdominal) or back painoLiver problems, including liver failure. TARGRETIN can cause increased liver function blood test results, or liver problems that can lead to death.oThyroid problems (hypothyroidism) are common with TARGRETIN. Your healthcare provider may prescribe thyroid hormone treatment for you if needed.oLow white blood cell count is common with TARGRETIN, but may sometimes be severe.oNew or worse cataracts. Tell your healthcare provider about any changes in your vision during treatment with TARGRETIN. You may need to have an eye examination.oRisk of low blood sugar in people who have diabetes. TARGRETIN can interact with certain medicines used to treat diabetes, such as insulin, sulfonylurea medicines, and thiazolinedione medicines. If you have diabetes, talk to your healthcare provider about your diabetes medicines and your risk for low blood sugar if you take TARGRETIN.The most common side effects of TARGRETIN include:oheadacheoastheniaorashonauseaoinfectionostomach-area (abdomen) painoswelling of your hands, arms, feet or legsodry skinThese are not all the possible side effects of TARGRETIN. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.How should store TARGRETINoStore TARGRETIN between 36 to 77F (2 to 25C). oStore the TARGRETIN bottle away from light, heat, and humidity.oThe capsules should not be taken after the expiration date printed on the bottle.Keep TARGRETIN and all medicines out of the reach of children.General information about the safe and effective use of TARGRETINMedicines are sometimes prescribed for purposes other than those listed in Patient Information leaflet. Do not use TARGRETIN for condition for which it was not prescribed. Do not give TARGRETIN to other people, even if they have the same symptoms that you have. It may harm them. You can ask your pharmacist or healthcare provider for information about TARGRETIN that is written for health professionals.What are the ingredients in TARGRETINActive ingredient: bexaroteneInactive ingredients: butylated hydroxyanisole, polyethylene glycol 400, polysorbate 20, and povidone. The capsule shell contains gelatin, sorbitol special-glycerin blend, and titanium dioxide.Distributed by: Bausch Health US, LLC, Bridgewater, NJ 08807 USAManufactured by: Catalent Pharma Solutions LLC, St. Petersburg, FL 33716 USATARGRETIN is trademark of Bausch Health Companies Inc. or its affiliates.Any other product/brand names are trademarks of their respective owners.(C) 2020 Bausch Health Companies Inc. or its affiliatesFor more information, call 1-800-321-4576.This Patient Information has been approved by the U.S. Food and Drug Administration.Rev. 04/20209436601. oYou should avoid becoming pregnant during treatment with TARGRETIN.. oDo not take TARGRETIN if you are pregnant or plan to become pregnant.. oYour healthcare provider will do pregnancy test, within week before you start TARGRETIN, and each month during treatment with TARGRETIN to make sure that you are not pregnant.. oYou must use two effective forms of birth control together starting month before you begin treatment with TARGRETIN, during treatment, and for month after stopping TARGRETIN. Birth control pills (oral contraceptives) and other hormonal forms of birth control may not be effective if used with TARGRETIN. At least one of the forms of birth control that you choose should not contain hormones. Talk to your healthcare provider about what forms of birth control may be right for you during treatment with TARGRETIN. oYou should start taking TARGRETIN on the second or third day of normal menstrual period. Follow your healthcare providers instructions about when to start TARGRETIN.. oCall your healthcare provider right away, if you become pregnant or think that you are pregnant during treatment with TARGRETIN, and for month after you stop taking TARGRETIN.. oYou must use condom with female partners who are pregnant, might be pregnant, or who are able to become pregnant, during treatment with TARGRETIN and for at least month after your last dose.. oif you are pregnant or plan to become pregnant. See What is the most important information should know about TARGRETIN. oif you are allergic to bexarotene or any of the ingredients in TARGRETIN. See the end of this leaflet for complete list of ingredients in TARGRETIN.. ohave or have had problems with your pancreas, including pancreatitis. ohave or have had gallbladder problems. ohave or have had liver problems. ohave thyroid problems. ohave diabetes. ohave high levels of fats (lipids) called cholesterol or triglycerides in your blood. ohave cataracts or history of cataracts. odrink alcohol. oare pregnant, plan to become pregnant, or think you may be pregnant. See What is the most important information should know about TARGRETIN. oare breastfeeding or plan to breastfeed. It is not known if TARGRETIN passes into your breast milk. You should not breastfeed during treatment with TARGRETIN. Talk to your healthcare provider about the best way to feed your baby during treatment with TARGRETIN.. oTake TARGRETIN exactly as your healthcare provider tells you.. oYour healthcare provider will tell you how many TARGRETIN capsules to take each day. Your healthcare provider may change your daily dose of TARGRETIN as needed to treat your CTCL or if you get certain side effects. You should not change your dose unless your healthcare provider tells you to.. oLimit your exposure to sunlight and artificial types of sunlight. TARGRETIN can make your skin more sensitive to sunlight and you can get sunburn.. oLimit the amount of vitamin that you take during treatment with TARGRETIN. Large doses of vitamin may cause side effects that are similar to side effects that can happen in people who take TARGRETIN.. oSee What is the most important information should know about TARGRETIN. oIncreased levels of fats (lipids) called cholesterol or triglycerides, in your blood are common with TARGRETIN, but can also be serious. Your healthcare provider may prescribe you medicines to treat high cholesterol or triglycerides levels, reduce your dose, temporarily stop treatment or completely stop treatment with TARGRETIN if you have this problem.. oInflammation of the pancreas (acute pancreatitis). TARGRETIN can sometimes cause pancreatitis that comes on suddenly (acute), and that can lead to death. Your risk of developing acute pancreatitis may be greater if you:ohave had pancreatitis in the pastohigh levels of fats in your blood that are not controlledodrink large amounts of alcoholohave gallbladder problemsohave diabetes that is not controlledotake certain medicines that can increase the amount of triglycerides in your bloodotake medicines that can harm your pancreas. ohave had pancreatitis in the past. ohigh levels of fats in your blood that are not controlled. odrink large amounts of alcohol. ohave gallbladder problems. ohave diabetes that is not controlled. otake certain medicines that can increase the amount of triglycerides in your blood. otake medicines that can harm your pancreas. onausea that will not go awayovomitingostomach-area (abdominal) or back pain. onausea that will not go away. ovomiting. ostomach-area (abdominal) or back pain. oLiver problems, including liver failure. TARGRETIN can cause increased liver function blood test results, or liver problems that can lead to death.. oThyroid problems (hypothyroidism) are common with TARGRETIN. Your healthcare provider may prescribe thyroid hormone treatment for you if needed.. oLow white blood cell count is common with TARGRETIN, but may sometimes be severe.. oNew or worse cataracts. Tell your healthcare provider about any changes in your vision during treatment with TARGRETIN. You may need to have an eye examination.. oRisk of low blood sugar in people who have diabetes. TARGRETIN can interact with certain medicines used to treat diabetes, such as insulin, sulfonylurea medicines, and thiazolinedione medicines. If you have diabetes, talk to your healthcare provider about your diabetes medicines and your risk for low blood sugar if you take TARGRETIN.. oheadache. oasthenia. orash. onausea. oinfection. ostomach-area (abdomen) pain. oswelling of your hands, arms, feet or legs. odry skin. oStore TARGRETIN between 36 to 77F (2 to 25C). oStore the TARGRETIN bottle away from light, heat, and humidity.. oThe capsules should not be taken after the expiration date printed on the bottle.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. 8.1 Pregnancy. Risk SummaryTARGRETIN, retinoid, can cause fetal harm based on findings from animal studies when administered to pregnant female and is contraindicated during pregnancy. Bexarotene was teratogenic and caused developmental mortality in rats following oral administration during organogenesis [see Data]. TARGRETIN must not be given to pregnant female or female who intends to become pregnant. If pregnancy does occur during treatment with TARGRETIN, immediately discontinue the drug and advise the pregnant female of the potential risk to fetus.The background risk of major birth defects and miscarriage for the indicated populations is unknown. However, the background risk in the U.S. general population of major birth defects is 2-4% and of miscarriage is 15-20% of clinically recognized pregnancies.DataAnimal DataBexarotene caused malformations when administered orally to pregnant rats during days 7-17 of gestation. Developmental abnormalities included incomplete ossification at mg/kg/day and cleft palate, depressed eye bulge/microphthalmia, and small ears at 16 mg/kg/day. The plasma AUC of bexarotene in rats at mg/kg/day is approximately one third the AUC in humans at the recommended daily dose. At doses greater than 10 mg/kg/day, bexarotene caused developmental mortality. The no effect dose for fetal effects in rats was mg/kg/day (producing an AUC approximately one sixth of the AUC at the recommended human daily dose).. 8.2 Lactation. Risk SummaryThere is no information regarding the presence of TARGRETIN in human milk, the effects on the breast fed infant, or the effects on milk production. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from TARGRETIN, discontinue breastfeeding during treatment with TARGRETIN.. 8.3 Females and Males of Reproductive Potential. Pregnancy TestingObtain negative serum pregnancy test (e.g., serum beta-human chorionic gonadotropin [beta-HCG]) with sensitivity of at least 50 mIU/L within week prior to TARGRETIN therapy. Obtain another pregnancy test at monthly intervals while the patient remains on TARGRETIN.ContraceptionFemalesTARGRETIN can cause fetal harm when administered to pregnant female [see Use in Specific Populations (8.1) ]. Females of reproductive potential should be advised to avoid becoming pregnant when TARGRETIN is used. Effective contraception must be used for month prior to the initiation of therapy, during therapy and for at least month following discontinuation of therapy; it is recommended that two reliable forms of contraception be used simultaneously unless abstinence is the chosen method. Bexarotene can potentially induce metabolic enzymes and thereby theoretically reduce the plasma concentrations of oral or other systemic hormonal contraceptives [see Drug Interactions (7) ]. Thus, if treatment with TARGRETIN is intended in female with reproductive potential, it is strongly recommended that one of the two reliable forms of contraception should be non-hormonal. TARGRETIN therapy should be initiated on the second or third day of normal menstrual period. No more than 1-month supply of TARGRETIN should be given to the patient so that the results of pregnancy testing can be assessed and counseling regarding avoidance of pregnancy and birth defects can be reinforced.MalesMale patients with sexual partners who are pregnant, possibly pregnant, or who could become pregnant must use condoms during sexual intercourse while taking TARGRETIN and for at least month after the last dose of drug.. 8.4 Pediatric Use. Safety and effectiveness of TARGRETIN in pediatric patients have not been established.. 8.5 Geriatric Use. Of the total patients with CTCL in clinical trials of TARGRETIN, 64% were 60 years or older, while 33% were 70 years or older. No overall differences in safety were observed between patients 70 years or older and younger patients, but greater sensitivity of some older individuals to TARGRETIN cannot be ruled out. Responses to TARGRETIN were observed across all age group decades, without preference for any individual age group decade.. 8.6 Hepatic Impairment. No specific studies have been conducted with TARGRETIN in subjects with hepatic impairment. Hepatic impairment is expected to lead to decreased clearance [see Clinical Pharmacology (12.3) ]. If TARGRETIN is used in patients with hepatic impairment, monitor for signs of toxicity that may be due to increased exposure.

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. oHyperlipidemia: TARGRETIN causes elevations in blood lipids. Obtain baseline values, monitor, and manage elevations during therapy by dose reduction, interruption, discontinuation and/or lipid lowering therapy. (5.1, 5.11)oPancreatitis: Interrupt TARGRETIN and evaluate if suspected. (5.2)oHepatotoxicity, Cholestasis, and Hepatic Failure: Interrupt or discontinue TARGRETIN and evaluate if liver chemistry tests exceed three times the upper limit of normal values. (5.3)oHypothyroidism: TARGRETIN therapy can cause hypothyroidism. Monitor and replace thyroid hormone if needed. (5.5)oNeutropenia: Monitor for neutropenia. Reduce TARGRETIN dose or interrupt as indicated. (5.6)oPhotosensitivity: Minimize exposure to sunlight and artificial ultraviolet light during treatment. (5.10). oHyperlipidemia: TARGRETIN causes elevations in blood lipids. Obtain baseline values, monitor, and manage elevations during therapy by dose reduction, interruption, discontinuation and/or lipid lowering therapy. (5.1, 5.11). oPancreatitis: Interrupt TARGRETIN and evaluate if suspected. (5.2). oHepatotoxicity, Cholestasis, and Hepatic Failure: Interrupt or discontinue TARGRETIN and evaluate if liver chemistry tests exceed three times the upper limit of normal values. (5.3). oHypothyroidism: TARGRETIN therapy can cause hypothyroidism. Monitor and replace thyroid hormone if needed. (5.5). oNeutropenia: Monitor for neutropenia. Reduce TARGRETIN dose or interrupt as indicated. (5.6). oPhotosensitivity: Minimize exposure to sunlight and artificial ultraviolet light during treatment. (5.10). 5.1 Hyperlipidemia. TARGRETIN induces substantial elevations in lipids in most patients. About 70% of patients with CTCL who received an initial dose of >300 mg/m2/day of TARGRETIN had fasting triglyceride levels greater than 2.5 times the upper limit of normal. About 55% had values over 800 mg/dL with median of about 1200 mg/dL in those patients. Cholesterol elevations above 300 mg/dL occurred in approximately 60% and 75% of patients with CTCL who received an initial dose of 300 mg/m2/day or greater than 300 mg/m2/day, respectively. Decreases in high density lipoprotein (HDL) cholesterol to less than 25 mg/dL were seen in about 55% and 90% of patients receiving an initial dose of 300 mg/m2/day or greater than 300 mg/m2/day, respectively, of TARGRETIN. Monitor lipid changes and treat abnormalities during therapy. The effects on triglycerides, HDL cholesterol, and total cholesterol were reversible with cessation of therapy, and could generally be mitigated by dose reduction and/or concomitant antilipemic therapy.Perform fasting blood lipid determinations before TARGRETIN therapy is initiated and weekly until the lipid response to TARGRETIN is established, which usually occurs within to weeks, and monitor at 8-week intervals thereafter. Fasting triglycerides should be normal or normalized with appropriate intervention prior to initiating TARGRETIN therapy. Maintain triglyceride levels below 400 mg/dL to reduce the risk of clinical sequelae [see Warnings and Precautions (5.2) ]. If fasting triglycerides are elevated or become elevated during treatment, institute antilipemic therapy, and if necessary, reduce or interrupt the dose of TARGRETIN. In the 300 mg/m2/day initial dose group, 60% of patients were given lipid lowering drugs. Atorvastatin was used in 48% (73/152) of patients with CTCL. Because of potential drug-drug interaction, avoid gemfibrozil use with TARGRETIN [see Drug Interactions (7) ].. 5.2 Pancreatitis. Acute pancreatitis, including fatal case, has been reported in four patients with CTCL and in six patients with non-CTCL cancers treated with TARGRETIN; the cases were associated with marked elevations of fasting serum triglycerides, the lowest being 770 mg/dL in one patient. One patient with advanced non-CTCL cancer died of pancreatitis. Interrupt TARGRETIN and evaluate if pancreatitis is suspected. Patients with CTCL who have risk factors for pancreatitis (e.g., prior pancreatitis, uncontrolled hyperlipidemia, excessive alcohol consumption, uncontrolled diabetes mellitus, biliary tract disease, and medications known to increase triglyceride levels or to be associated with pancreatic toxicity) may be at greater risk for pancreatitis associated with TARGRETIN [see Warnings and Precautions (5.1) ].. 5.3 Hepatotoxicity, Cholestasis, and Hepatic Failure. TARGRETIN caused elevations in liver chemistry tests (LFTs) in 5% (AST), 2% (ALT), and 0% (bilirubin) in patients with CTCL receiving an initial dose of 300 mg/m2/day. In contrast, with an initial dose greater than 300 mg/m2/day of TARGRETIN, the incidence of LFT elevations was higher at 7% (SGOT/AST), 9% (SGPT/ALT), and 6% (bilirubin). Two patients developed cholestasis, including one patient who died of liver failure. In clinical trials, elevated LFTs resolved within month in 80% of patients following decrease in dose or discontinuation of therapy. Obtain baseline LFTs and monitor LFTs after 1, 2, and weeks of treatment initiation, and if stable, at least every weeks thereafter during treatment. Interrupt or discontinue TARGRETIN if test results exceed three times the upper limit of normal values for AST, ALT, or bilirubin.. 5.4 Hypothyroidism. TARGRETIN induces hypothyroidism in about half of all patients treated by causing reversible reduction in levels of thyroid hormone (total thyroxine [total T4]) and thyroid-stimulating hormone (TSH). The incidence of decreases in TSH and total T4 were about 60% and 45%, respectively, in patients with CTCL receiving an initial dose of 300 mg/m2/day. Hypothyroidism was reported as an adverse event in 29% of patients. Consider treatment with thyroid hormone supplementation in patients with hypothyroidism. In the 300 mg/m2/day initial dose group, 37% of patients were treated with thyroid hormone replacement. Obtain baseline thyroid function tests and patients monitor during treatment.. 5.5 Neutropenia. Leukopenia in the range of 1000 to <3000 WBC 106/L occurred in 18% of patients with CTCL receiving an initial dose of 300 mg/m2/day of TARGRETIN. Patients receiving an initial dose greater than 300 mg/m2/day of TARGRETIN had an incidence of leukopenia of 43%. No patient with CTCL treated with TARGRETIN developed leukopenia of less than 1000 WBC 106/L. The usual time to onset of leukopenia was to weeks after initiating TARGRETIN. The leukopenia observed in most patients was predominantly neutropenia. In the 300 mg/m2/day initial dose group, the incidence of NCI Grade and Grade neutropenia, respectively, was 12% and 4%. The leukopenia and neutropenia experienced during TARGRETIN therapy resolved after dose reduction or discontinuation of treatment, on average within 30 days in 93% of the patients with CTCL and 82% of patients with non-CTCL cancers. Leukopenia and neutropenia were rarely associated with severe sequelae or serious adverse events. Obtain complete blood counts (CBC) at baseline and periodically during treatment.. 5.6 Cataracts. Posterior subcapsular cataracts occurred in preclinical toxicity studies in rats and dogs administered bexarotene daily for months. New cataracts or worsening of previous cataracts occurred in 15 of 79 patients who were monitored with serial slit lamp examinations. Because of the high prevalence and rate of cataract formation in older patient populations, the relationship of TARGRETIN and cataracts cannot be determined in the absence of an appropriate control group. Patients treated with TARGRETIN who experience visual difficulties should have an appropriate ophthalmologic evaluation.. 5.7 Vitamin Supplementation Hazard. In clinical studies, patients were advised to limit vitamin intake to <=15,000 IU/day. Because of the relationship of bexarotene to vitamin A, patients should be advised to limit vitamin supplements to avoid potential additive toxic effects.. 5.8 Hypoglycemia Risk in Patients with Diabetes Mellitus. In patients using insulin, agents enhancing insulin secretion (e.g., sulfonylureas), or insulin sensitizers (e.g., thiazolidinedione class), based on the mechanism of action, TARGRETIN could enhance the action of these agents, resulting in hypoglycemia. Hypoglycemia has not been associated with the use of TARGRETIN as monotherapy.. 5.9 Photosensitivity. Retinoids as class have been associated with photosensitivity. In vitro assays indicate that bexarotene is potential photosensitizing agent. Phototoxicity manifested as sunburn and skin sensitivity to sunlight occurred in patients who were exposed to direct sunlight while receiving TARGRETIN. Advise patients to minimize exposure to sunlight and artificial ultraviolet light while receiving TARGRETIN. 5.10 Laboratory Tests. Before initiating TARGRETIN therapy, obtain CBC, fasting lipid profile, liver function tests, and thyroid profile. Fasting triglycerides should be normal or normalized with appropriate intervention prior to therapy. Monitor lab tests during TARGRETIN therapy as described above.Hyperlipidemia usually occurs within the initial to weeks. Therefore, weekly lipid determinations are recommended during this interval. Subsequently, in patients not hyperlipidemic, determinations can be performed less frequently [see Warnings and Precautions (5.1) ].A white blood cell count with differential should be obtained at baseline and periodically during treatment. Baseline liver function tests should be obtained and should be carefully monitored after 1, 2, and weeks of treatment initiation, and if stable, periodically thereafter during treatment. Baseline thyroid function tests should be obtained and then monitored during treatment as indicated [see Warnings and Precautions (5.3, 5.4, 5.5, 5.6)].. 5.11 Drug/Laboratory Test Interactions. CA125 assay values in patients with ovarian cancer may be increased by TARGRETIN therapy.