ADVERSE REACTIONS SECTION.

6 Adverse Reactions The following clinically significant adverse reactions are discussed elsewhere in the labeling:oCardiovascular events [see Warnings and Precautions (5.1)]oHemorrhage [see Warnings and Precautions (5.2)]oHypertension [see Warnings and Precautions (5.3)]oDermatologic toxicities [see Warnings and Precautions (5.4)]oGastrointestinal perforation [see Warnings and Precautions (5.5)]oQT interval prolongation [see Warnings and Precautions (5.9) and Clinical Pharmacology (12.2)]oDrug-induced liver injury [see Warnings and Precautions (5.10)]oImpairment of TSH suppression in DTC [see Warnings and Precautions (5.12)]. oCardiovascular events [see Warnings and Precautions (5.1)]. oHemorrhage [see Warnings and Precautions (5.2)]. oHypertension [see Warnings and Precautions (5.3)]. oDermatologic toxicities [see Warnings and Precautions (5.4)]. oGastrointestinal perforation [see Warnings and Precautions (5.5)]. oQT interval prolongation [see Warnings and Precautions (5.9) and Clinical Pharmacology (12.2)]. oDrug-induced liver injury [see Warnings and Precautions (5.10)]. oImpairment of TSH suppression in DTC [see Warnings and Precautions (5.12)]. The most common adverse reactions (>=20%) are diarrhea, fatigue, infection, alopecia, hand-foot skin reaction, rash, weight loss, decreased appetite, nausea, gastrointestinal and abdominal pains, hypertension, and hemorrhage. (6) To report SUSPECTED ADVERSE REACTIONS, contact Bayer HealthCare Pharmaceuticals Inc. at 1-888-842-2937 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 data described reflect exposure to NEXAVAR in 955 patients who participated in placebo-controlled studies in hepatocellular carcinoma (N=297), advanced renal cell carcinoma (N=451), or differentiated thyroid carcinoma (N 207). The most common adverse reactions (>=20%), which were considered to be related to NEXAVAR, in patients with HCC, RCC or DTC are diarrhea, fatigue, infection, alopecia, hand-foot skin reaction, rash, weight loss, decreased appetite, nausea, gastrointestinal and abdominal pains, hypertension, and hemorrhage.. 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.. Hepatocellular Carcinoma Table shows the percentage of patients in the SHARP (HCC) study experiencing adverse reactionsthat were reported in at least 10% of patients and at higher rate in the NEXAVAR-treated group than in those receiving placebo. Table 4: Adverse Reactions Reported in at Least 10% of Patients and at Higher Rate in NEXAVAR Arm than the Placebo Arm SHARP (HCC)Adverse Reaction1 NEXAVARN=297PlaceboN=302AllGrades%Grade 3%Grade4%AllGrades%Grade3%Grade4%Any Adverse Reaction9839696248Gastrointestinal Diarrhea5510<12520 Anorexia2930183<1 Nausea24102030 Vomiting15201120 Constipation14001000Constitutional symptoms Fatigue469145122 Weight loss30201010Pain Pain, abdomen31902651Dermatology/skin Hand-foot skin reaction21803<10 Rash/desquamation19101400 Alopecia1400200 Pruritus14<1011<10 Dry skin1000600Hepatobiliary/pancreas Liver dysfunction11218211Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).Hypertension was reported in 9% of patients treated with NEXAVAR and 4% of those receiving placebo. Grade hypertension was reported in 4% of NEXAVAR-treated patients and 1% of those receiving placebo. Hemorrhage/bleeding was reported in 18% of those receiving NEXAVAR and 20% of patients receiving placebo. The rates of Grade and bleeding were also higher in patients receiving placebo (Grade - 3% NEXAVAR and 5% placebo and Grade - 2% NEXAVAR and 4% placebo). Bleeding from esophageal varices was reported in 2.4% in NEXAVAR-treated patients and 4% of patients receiving placebo.Renal failure was reported in <1% of patients treated with NEXAVAR and 3% of patients receiving placebo. Clinical pancreatitis was reported in of 297 NEXAVAR-treated patients (Grade 2).The rate of adverse reactions (including those associated with progressive disease) resulting in permanent discontinuation was similar in both the NEXAVAR-treated patients and those receiving placebo (32% of NEXAVAR-treated patients and 35% of patients receiving placebo).Laboratory test abnormalities reported in SHARP are presented in Table 5.Table 5: Laboratory Test Abnormalities Reported in SHARP (HCC)Laboratory Parameter1 NEXAVARN=297PlaceboN=302All Grades(%)Grade or (%)All Grades(%)Grade or (%)Hypoalbuminemia590470Elevated Lipase409379Lymphopenia47NR42NR Thrombocytopenia46441<1Elevated INR424342Hypophosphatemia 3511112Elevated Amylase342292Hypocalcemia 272.4151Hypokalemia10<16<11-Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).NR not reported. 1Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. Thrombocytopenia. 1-Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. Renal Cell Carcinoma Table shows the percentage of patients in the TARGET (RCC) study experiencing adverse reactions that were reported in at least 10% of patients and at higher rate in NEXAVAR-treated patients arm than in those receiving placebo. The rate of adverse reactions (including those associated with progressive disease) resulting in permanent discontinuation was similar in both the NEXAVAR-treated patients and patients receiving placebo (10% and 8%, respectively).Clinical pancreatitis was reported in of 451 NEXAVAR-treated patients (one Grade and two Grade 4). Table 6: Adverse Reactions Reported in at Least 10% of Patients and at Higher Rate in NEXAVAR Arm than the Placebo Arm TARGET (RCC)Adverse Reaction1 NEXAVARN=451PlaceboN=451All Grades%Grade 3%Grade 4%All Grades%Grade 3%Grade 4%Any Adverse Reactions9531786226Gastrointestinal symptoms Diarrhea 432013<10 Nausea 23<1019<10 Anorexia 16<101310 Vomiting16<101210 Constipation 15<1011<10Dermatology/skin Rash/desquamation40<1016<10 Hand-foot skin reaction 3060700 Alopecia27<10300 Pruritus 19<10600 Dry skin 1100400Constitutional symptoms Fatigue375<1283<1 Weight loss 10<10600Cardiovascular, General Hypertension 173<12<10Hemorrhage/bleeding Hemorrhage all sites 152081<1Pulmonary Dyspnea143<1122<1Neurology Neuropathy-sensory 13<106<10Pain Pain, abdomen 1120920 Pain, headache 10<106<10 Pain, joint 10206<101Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0). Laboratory test abnormalities reported in TARGET are presented in Table 7.Table 7: Laboratory Test Abnormalities Reported in TARGET (RCC)Laboratory Parameter1 NEXAVARN=451PlaceboN=451All Grades (%)Grade or (%)All Grades (%)Grade or (%)Hypophosphatemia4513113Anemia442494Elevated Lipase4112307Elevated Amylase301233Lymphopenia2313137Neutropenia185102 Thrombocytopenia12150Hypocalcemia 1228<1Hypokalemia51<1<11Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. 1Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. Thrombocytopenia. 1Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. Differentiated Thyroid Carcinoma The safety of NEXAVAR was evaluated in DECISION in 416 patients with locally recurrent or metastatic, progressive differentiated thyroid carcinoma (DTC) refractory to radioactive iodine (RAI) treatment randomized to receive 400 mg twice daily NEXAVAR (n=207) or matching placebo (n=209) until disease progression or intolerable toxicity in double-blind trial [see Clinical Studies (14.3)]. The data described below reflect median exposure to NEXAVAR for 46 weeks (range 0.3 to 135). The population exposed to NEXAVAR was 50% male, and had median age of 63 years.Dose interruptions for adverse reactions were required in 66% of patients receiving NEXAVAR and dose reductions were required in 64% of patients. Adverse reactions that resulted in treatment discontinuation were reported in 14% of NEXAVAR-treated patients compared to 1.4% of patients receiving placebo.Table shows the percentage of DTC patients experiencing adverse reactions at higher rate in NEXAVAR-treated patients than in patients receiving placebo in the double-blind phase of the DECISION study. Grade adverse reactions occurred in 53% of NEXAVAR-treated patients compared to 23% of patients receiving placebo. Grade adverse reactions occurred in 12% of NEXAVAR-treated patients compared to 7% of patients receiving placebo.Table 8: Selected Adverse Reactions Occurring at Higher Incidence in NEXAVAR-Treated Patients [Between Arm Difference of >= 5% (All Grades)1 or >= 2% (Grades and 4)]Adverse ReactionNEXAVARN 207PlaceboN 209All Grades(%)Grades and 4(%)All Grades(%)Grades and 4(%)Skin and subcutaneous tissue disordersPPES5 691980Alopecia67080Rash35570Pruritus200.5110Dry skin130.550Erythema1000.50Hyperkeratosis7000Gastrointestinal disordersDiarrhea686151Stomatitis3 24230Nausea210120Abdominal pain2 20171Constipation16080.5Oral pain4 140.560Vomiting11030InvestigationsWeight loss496141General disorders and administration site conditionsFatigue415201Asthenia12070Pyrexia11150Vascular disordersHypertension6 4110122Metabolism and nutrition disordersDecreased appetite30250Nervous system disordersHeadache17060Dysgeusia6000Musculoskeletal and connective tissue disordersPain in extremity15170Muscle spasms10030Respiratory, thoracic and mediastinal disordersDysphonia130.530Epistaxis7010Neoplasms benign, malignant and unspecifiedSquamous cell carcinoma of skin33001National Cancer Institute Common Terminology Criteria for Adverse Events Version 3.02Includes the following terms: abdominal pain, abdominal discomfort, hepatic pain, esophageal pain, esophageal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness, abdominal rigidity3Includes the following terms: stomatitis, aphthous stomatitis, mouth ulceration, mucosal inflammation4Includes the following terms: oral pain, oropharyngeal discomfort, glossitis, burning mouth syndrome, glossodynia5Palmar-plantar erythrodysesthesia syndrome (Hand-foot skin reaction)6Includes the following terms: hypertension, blood pressure increased, blood pressure systolic increasedThe relative increase for the following laboratory abnormalities observed in NEXAVAR-treated patients as compared to patients receiving placebo in the DECISION study is similar to that observed in the RCC and HCC studies: lipase, amylase, hypokalemia, hypophosphatemia, neutropenia, lymphopenia, anemia, and thrombocytopenia. Hypocalcemia was more frequent and more severe in patients with DTC, especially those with history of hypoparathyroidism, compared to patients with RCC or HCC. Other laboratory test abnormalities reported in DECISION are presented in Table 9Table 9: Laboratory Test Abnormalities Reported in DECISION (DTCLaboratory Parameter1 NEXAVARN=207PlaceboN=209All Grades(%)Grade or (%)All Grades (%)Grade or (%)Elevated ALT 594240Elevated AST 542150Hypocalcemia36101131Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. 1National Cancer Institute Common Terminology Criteria for Adverse Events Version 3.0. 2Includes the following terms: abdominal pain, abdominal discomfort, hepatic pain, esophageal pain, esophageal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness, abdominal rigidity. 3Includes the following terms: stomatitis, aphthous stomatitis, mouth ulceration, mucosal inflammation. 4Includes the following terms: oral pain, oropharyngeal discomfort, glossitis, burning mouth syndrome, glossodynia. 5Palmar-plantar erythrodysesthesia syndrome (Hand-foot skin reaction). 6Includes the following terms: hypertension, blood pressure increased, blood pressure systolic increased. 1Laboratory parameters graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. Additional Data from Multiple Clinical Trials The following additional drug-related adverse reactions and laboratory abnormalities were reported from clinical trials of NEXAVAR (very common 10% or greater, common to less than 10%, uncommon 0.1% to less than 1%, rare less than 0.1 %): Cardiovascular: Common: congestive heart failure+, myocardial ischemia and/or infarction Uncommon: hypertensive crisis Rare: QT prolongationDermatologic: Very common: erythema Common: exfoliative dermatitis, acne, flushing, folliculitis, hyperkeratosis Uncommon: eczema, erythema multiforme Digestive: Very common: increased lipase, increased amylase Common: mucositis, stomatitis (including dry mouth and glossodynia), dyspepsia, dysphagia, gastrointestinal reflux Uncommon: pancreatitis, gastritis, gastrointestinal perforations, cholecystitis, cholangitisNote that elevations in lipase are very common (41%, see below); diagnosis of pancreatitis should not be made solely on the basis of abnormal laboratory valuesGeneral Disorders: Very common: infection, hemorrhage (including gastrointestinal and respiratory tract and uncommon cases of cerebral hemorrhage), asthenia, pain (including mouth, bone, and tumor pain), pyrexia, decreased appetite Common: influenza-like illness Hematologic: Very common: leukopenia, lymphopenia Common: anemia, neutropenia, thrombocytopenia Uncommon: INR abnormalHepatobiliary disorders: Rare: drug-induced liver injury (including hepatic failure and death)Hypersensitivity: Uncommon: hypersensitivity reactions (including skin reactions and urticaria), anaphylactic reactionMetabolic and Nutritional: Very common: hypophosphatemia Common: transient increases in transaminases, hypocalcemia, hypokalemia, hyponatremia, hypothyroidism Uncommon: dehydration, transient increases in alkaline phosphatase, increased bilirubin (including jaundice), hyperthyroidismMusculoskeletal: Very common: arthralgia Common: myalgia, muscle spasmsNervous System and Psychiatric: Common: depression, dysgeusia Uncommon: tinnitus, reversible posterior leukoencephalopathyRenal and Genitourinary: Common: renal failure, proteinuria Rare: nephrotic syndromeReproductive: Common: erectile dysfunction Uncommon: gynecomastiaRespiratory: Common: rhinorrhea Uncommon: interstitial lung disease-like events (includes reports of pneumonitis, radiation pneumonitis, acute respiratory distress, interstitial pneumonia, pulmonitis and lung inflammation) In addition, the following medically significant adverse reactions were uncommon during clinical trials of NEXAVAR: transient ischemic attack, arrhythmia, and thromboembolism. For these adverse reactions, the causal relationship to NEXAVAR has not been established.adverse reactions may have life-threatening or fatal outcome. +reported in 1.9% of patients treated with NEXAVAR (N= 2276). 6.2 Postmarketing Experience The following adverse reactions have been identified during postapproval use of NEXAVAR. 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.Blood and lymphatic disorders: Thrombotic microangiopathy (TMA)Dermatologic: Stevens-Johnson syndrome and toxic epidermal necrolysis (TEN)Hypersensitivity: AngioedemaMusculoskeletal: Rhabdomyolysis, osteonecrosis of the jawRespiratory: Interstitial lung disease-like events (which may have life-threatening or fatal outcome)Vascular: Arterial (including aortic) aneurysms, dissections, and rupture.

CLINICAL PHARMACOLOGY SECTION.

12 Clinical Pharmacology 12.1 Mechanism of Action Sorafenib is kinase inhibitor that decreases tumor cell proliferation in vitro. Sorafenib was shown to inhibit multiple intracellular (c-CRAF, BRAF and mutant BRAF) and cell surface kinases (KIT, FLT- 3, RET, RET/PTC, VEGFR-1, VEGFR- 2, VEGFR- 3, and PDGFR-ss). Several of these kinases are thought to be involved in tumor cell signaling, angiogenesis and apoptosis. Sorafenib inhibited tumor growth of HCC, RCC, and DTC human tumor xenografts in immunocompromised mice. Reductions in tumor angiogenesis were seen in models of HCC and RCC upon sorafenib treatment, and increases in tumor apoptosis were observed in models of HCC, RCC, and DTC. 12.2 Pharmacodynamics Cardiac Electrophysiology The effect of NEXAVAR 400 mg twice daily on the QTc interval was evaluated in multi-center, open-label, non-randomized trial in 53 patients with advanced cancer. No large changes in the mean QTc intervals (that is, >20 ms) from baseline were detected in the trial. After one 28-day treatment cycle, the largest mean QTc interval change of 8.5 ms (upper bound of two-sided 90% confidence interval, 13.3 ms) was observed at hours post-dose on day of cycle [see Warnings and Precautions (5.9), Drug Interactions (7.3)]. 12.3 Pharmacokinetics Multiple doses of NEXAVAR for days resulted in 2.5- to 7-fold accumulation compared to single dose. Steady-state plasma sorafenib concentrations were achieved within days, with peak-to-trough ratio of mean concentrations of less than 2. The steady-state concentrations of sorafenib following administration of NEXAVAR 400 mg twice daily were evaluated in DTC, RCC and HCC patients. Patients with DTC have mean steady-state concentrations that are 1.8-fold higher than patients with HCC and 2.3-fold higher than those with RCC. The reason for increased sorafenib concentrations in DTC patients is unknown. Mean Cmax and AUC increased less than proportionally beyond oral doses of 400 mg administered twice daily.. Absorption After administration of NEXAVAR tablets, the mean relative bioavailability was 38-49% when compared to an oral solution. Following oral administration, sorafenib reached peak plasma levels in approximately hours. Effects of Food With moderate-fat meal (30% fat; 700 calories), bioavailability was similar to that in the fasted state. With high-fat meal (50% fat; 900 calories), bioavailability was reduced by 29% compared to that in the fasted state. Distribution In vitrobinding of sorafenib to human plasma proteins was 99.5%. Elimination The mean elimination half-life of sorafenib was approximately 25 to 48 hours. Metabolism Sorafenib undergoes oxidative metabolism by hepatic CYP3A4, as well as glucuronidation by UGT1A9.. Excretion Sorafenib accounted for approximately 70-85% of the circulating analytes in plasma at steady-state. Eight metabolites of sorafenib have been identified, of which have been detected in plasma. The main circulating metabolite of sorafenib, the pyridine N-oxide that comprises approximately 9-16% of circulating analytes at steady-state, showed in vitro potency similar to that of sorafenib. Following oral administration of 100 mg dose of solution formulation of sorafenib, 96% of the dose was recovered within 14 days, with 77% of the dose excreted in feces and 19% of the dose excreted in urine as glucuronidated metabolites. Unchanged sorafenib, accounting for 51% of the dose, was found in feces but not in urine. Specific Populations A study of the pharmacokinetics of sorafenib indicated that the mean AUC of sorafenib in Asians (N=78) was 30% lower than in Whites (N=40). Sex and age do not have clinically meaningful effect on the pharmacokinetics of sorafenib.. Patients with Renal Impairment Mild (CLcr 50-80 mL/min), moderate (CLcr 30 <50 mL/min), and severe (CLcr <30 mL/min) renal impairment do not affect the pharmacokinetics of sorafenib [see Use in Specific Populations (8.6)].. Patients with Hepatic Impairment Mild (Child-Pugh A) and moderate (Child-Pugh B) hepatic impairment do not affect the pharmacokinetics of sorafenib [see Use in Specific Populations (8.7)].. Drug Interactions Studies Effect of Strong CYP3A4 Inhibitors on Sorafenib: Ketoconazole, strong inhibitor of CYP3A4 and P-glycoprotein, administered at dose of 400 mg once daily for days did not alter the mean AUC of single oral dose of NEXAVAR 50 mg in healthy subjects. Effect of Strong CYP3A4 Inducers on Sorafenib: Concomitant use of NEXAVAR with rifampin administered at dose of 600 mg once daily for days with single oral dose of NEXAVAR 400 mg in healthy volunteers resulted in 37% decrease in the mean AUC of sorafenib. Effect of Neomycin on Sorafenib: Neomycin administered as an oral dose of g three times daily for days decreased the mean AUC of sorafenib by 54% in healthy subjects administered single oral dose of NEXAVAR 400 mg.Effect of Sorafenib on Other Drugs: NEXAVAR 400 mg twice daily for 28 days did not increase the systemic exposure of concomitantly administered midazolam (CYP3A4 substrate), dextromethorphan (CYP2D6 substrate), and omeprazole (CYP2C19 substrate) [see Clinical Pharmacology (12.3)]. Drugs that Increase Gastric pH: The aqueous solubility of sorafenib is pH dependent, with higher pH resulting in lower solubility. However, omeprazole, proton pump inhibitor, administered at dose of 40 mg once daily for days, did not result in clinically meaningful change in sorafenib single dose exposure. In Vitro Studies Sorafenib competitively inhibited CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 in vitro. However, NEXAVAR 400 mg twice daily for 28 days with substrates of CYP3A4, CYP2D6 and CYP2C19 did not increase the systemic exposure of these substrates [see Drug Interactions (7.3)]. Sorafenib did not increase CYP1A2 and CYP3A4 activities, suggesting that sorafenib is unlikely to induce CYP1A2 or CYP3A4 in humans. Sorafenib inhibits glucuronidation by UGT1A1 and UGT1A9 in vitro. NEXAVAR could increase the systemic exposure of concomitantly administered drugs that are UGT1A1 or UGT1A9 substrates.Sorafenib inhibited P-glycoprotein in vitro. NEXAVAR could increase the concentrations of concomitantly administered drugs that are P-glycoprotein substrates.

CLINICAL STUDIES SECTION.

14 Clinical Studies 14.1 Hepatocellular Carcinoma The SHARP (HCC) study (NCT00105443) was an international, multicenter, randomized, double blind, placebo-controlled trial in patients with unresectable hepatocellular carcinoma. Overall survival was the primary endpoint. total of 602 patients were randomized; 299 to NEXAVAR 400 mg twice daily and 303 to matching placebo. All 602 randomized subjects were included in the ITT population for the efficacy analyses.Demographics and baseline disease characteristics were similar between the NEXAVAR and placebo arms with regard to age, gender, race, performance status, etiology (including hepatitis B, hepatitis and alcoholic liver disease), TNM stage (stage I: <1% vs. <1%; stage II: 10.4% vs. 8.3%; stage III: 37.8% vs. 43.6%; stage IV: 50.8% vs. 46.9%), absence of both macroscopic vascular invasion and extrahepatic tumor spread (30.1% vs. 30.0%), and Barcelona Clinic Liver Cancer stage (stage B: 18.1% vs. 16.8%; stage C: 81.6% vs. 83.2%; stage D: <1% vs. 0%). Liver impairment by Child-Pugh score was comparable between the NEXAVAR and placebo arms (Class A: 95% vs. 98%; B: 5% vs. 2%). Only one patient with Child-Pugh class was entered. Prior treatments included surgical resection procedures (19.1% vs. 20.5%), locoregional therapies (including radiofrequency ablation, percutaneous ethanol injection and transarterial chemoembolization; 38.8% vs. 40.6%), radiotherapy (4.3% vs. 5.0%) and systemic therapy (3.0% vs. 5.0%). The trial was stopped for efficacy following pre-specified second interim analysis for survival showing statistically significant advantage for NEXAVAR over placebo for overall survival (HR: 0.69, p= 0.00058) (see Table 10 and Figure 1). This advantage was consistent across all subsets analyzed. Final analysis of time to tumor progression (TTP) based on data from an earlier time point (by independent radiologic review) also was significantly longer in the NEXAVAR arm (HR: 0.58, p=0.000007) (see Table 10). Table 10: Efficacy Results from SHARP (HCC)Efficacy ParameterNEXAVAR(N=299)Placebo(N=303)Overall SurvivalNumber of Events143178Median, months10.77.9(95% CI) (9.4, 13.3)(6.8, 9.1)Hazard Ratio1 (95% CI)0.69 (0.55, 0.87)P-value (log-rank test2)0.00058Time to Progression Number of Events107156Median, months5.52.8(95% CI) (4.1, 6.9)(2.7, 3.9)Hazard Ratio1 (95% CI)0.58(0.45, 0.74)P-value (log-rank test2)0.000007CI=Confidence interval1Hazard ratio, sorafenib/placebo, stratified Cox model2Stratified log rank (for the interim analysis of survival, the stopping boundary one-sided alpha 0.0077) 3The time-to-progression (TTP) analysis, based on independent radiologic review, was based on data from an earlier time point than the survival analysisFigure 1: Kaplan-Meier Curve of Overall Survival in SHARP (HCC) (Intent-to-Treat Population). 1Hazard ratio, sorafenib/placebo, stratified Cox model. 2Stratified log rank (for the interim analysis of survival, the stopping boundary one-sided alpha 0.0077) 3The time-to-progression (TTP) analysis, based on independent radiologic review, was based on data from an earlier time point than the survival analysis. Figure 1. 14.2 Renal Cell Carcinoma The safety and efficacy of NEXAVAR in the treatment of advanced renal cell carcinoma (RCC) were studied in the following two randomized controlled clinical trials. TARGET TARGET (NCT00073307)was an international, multicenter, randomized, double blind, placebo-controlled trial in patients with advanced renal cell carcinoma who had received one prior systemic therapy. Primary study endpoints included overall survival and progression-free survival (PFS). Tumor response rate was secondary endpoint. The PFS analysis included 769 patients, per protocol, stratified by MSKCC (Memorial Sloan Kettering Cancer Center) prognostic risk category (low or intermediate) and country and randomized to NEXAVAR 400 mg twice daily (N=384) or to placebo (N=385). Table 11 summarizes the demographic and disease characteristics of the study population analyzed. Baseline demographics and disease characteristics were well balanced for both treatment groups. The median time from initial diagnosis of RCC to randomization was 1.6 and 1.9 years for the NEXAVAR and placebo arms, respectively. Table 11: Demographic and Disease Characteristics TARGET (RCC)Characteristics NEXAVARN=384PlaceboN=385N(%)N(%)Gender Male 267(70)287(75) Female116(30)98(25)Race White276(72)278(73) Black/Asian/ Hispanic/Other11(3)10(2) Not reported 197(25)97(25)Age group 65 years 255(67)280(73) >= 65 years127(33)103(27)ECOG performance status at baseline 0184(48)180(47) 1191(50)201(52) 26(2)1(<1) Not reported3(<1)3(<1)MSKCC prognostic risk category Low 200(52)194(50) Intermediate 184(48)191(50)Prior IL-2 and/or interferon Yes319(83)313(81) No65(17)72(19)1Race was not collected from the 186 patients enrolled in France due to local regulations. In other patients, race was not available at the time of analysis. Progression-free survival, defined as the time from randomization to progression or death from any cause, whichever occurred earlier, was evaluated by blinded independent radiological review using RECIST criteria. Figure depicts Kaplan-Meier curves for PFS. The PFS analysis was based on two-sided Log-Rank test stratified by MSKCC prognostic risk category and country. Figure 2: Kaplan-Meier Curves for Progression-free Survival TARGET (RCC) NOTE: HR is from Cox regression model with the following covariates: MSKCC prognostic risk category and country. P-value is from two-sided Log-Rank test stratified by MSKCC prognostic risk category and country. The median PFS for patients randomized to NEXAVAR was 167 days compared to 84 days for patients randomized to placebo. The estimated hazard ratio (immediate risk of progression or death with NEXAVAR compared to placebo) was 0.44 (95% CI: 0.35, 0.55). series of patient subsets were examined in exploratory univariate analyses of PFS. The subsets included age above or below 65 years, ECOG PS or 1, MSKCC prognostic risk category, whether the prior therapy was for progressive metastatic disease or for an earlier disease setting and time from diagnosis of less than or greater than 1.5 years. The effect of NEXAVAR on PFS was consistent across these subsets, including patients with no prior IL-2 or interferon therapy (N=137; 65 patients receiving NEXAVAR and 72 placebo), for whom the median PFS was 172 days in the NEXAVAR arm compared to 85 days in the placebo arm. Tumor response was determined by independent radiologic review according to RECIST criteria. Overall, of 672 patients who were evaluable for response, (2%) patients in the NEXAVAR and no (0%) patients in the placebo arms had confirmed partial response. Thus the gain in PFS primarily reflects the stable disease population. At the time of planned interim survival analysis, based on 220 deaths, overall survival was longer for those randomized to NEXAVAR compared with placebo with hazard ratio of 0.72. This analysis did not meet the prespecified criteria for statistical significance. Additional analyses are planned as the survival data mature. Male Female. White. Black/Asian/. Hispanic/Other. Not reported 1. 65 years >= 65 years. 0. 1. 2. Not reported. Low Intermediate Yes. No. 1Race was not collected from the 186 patients enrolled in France due to local regulations. In other patients, race was not available at the time of analysis. NOTE: HR is from Cox regression model with the following covariates: MSKCC prognostic risk category and country. P-value is from two-sided Log-Rank test stratified by MSKCC prognostic risk category and country. Figure 2. BAY43-9006 BAY43-9006 (NCT00101413) was randomized discontinuation trial in patients with metastatic malignancies, including RCC. The primary endpoint was the percentage of randomized patients remaining progression-free at 24 weeks. All patients received NEXAVAR for the first 12 weeks. Radiologic assessment was repeated at week 12. Patients with <25% change in bi-dimensional tumor measurements from baseline were randomized to NEXAVAR or placebo for further 12 weeks. Patients who were randomized to placebo were permitted to cross over to open-label NEXAVAR upon progression. Patients with tumor shrinkage >=25% continued NEXAVAR, whereas patients with tumor growth >=25% discontinued treatment. total of 202 patients with advanced RCC were enrolled into BAY43-9006, including patients who had received no prior therapy and patients with tumor histology other than clear cell carcinoma. After the initial 12 weeks of NEXAVAR, 79 patients with RCC continued on open-label NEXAVAR, and 65 patients were randomized to NEXAVAR or placebo. After an additional 12 weeks, at week 24, for the 65 randomized patients, the progression-free rate was significantly higher in patients randomized to NEXAVAR (16/32, 50%) than in patients randomized to placebo (6/33, 18%) (p=0.0077). Progression-free survival was significantly longer in the NEXAVAR arm (163 days) than in the those randomized to placebo (41 days) (p=0.0001, HR=0.29).. 14.3 Differentiated Thyroid Carcinoma The safety and effectiveness of NEXAVARwas evaluated in multicenter, randomized (1:1), double-blind, placebo-controlled trial (DECISION; NCT00984282) conducted in 417 patients with locally recurrent or metastatic, progressive differentiated thyroid carcinoma (DTC) refractory to radioactive iodine (RAI) treatment. Randomization was stratified by age (< 60 years versus >= 60 years) and geographical region (North America, Europe, and Asia). All 417 subjects were included in the ITT population for the efficacy analysesAll patients were required to have actively progressing disease defined as progression within 14 months of enrollment. RAI-refractory disease was defined based on four criteria that were not mutually exclusive. All RAI treatments and diagnostic scans were to be performed under conditions of low iodine diet and adequate TSH stimulation. Following are the RAI-refractory criteria and the proportion of patients in the study that met each one: target lesion with no iodine uptake on RAI scan (68%); tumors with iodine uptake and progression after RAI treatment within 16 months of enrollment (12%); tumors with iodine uptake and multiple RAI treatments with the last treatment greater than 16 months prior to enrollment, and disease progression after each of two RAI treatments administered within 16 months of each other (7%); cumulative RAI dose >= 600 mCi administered (34%). The major efficacy outcome measure was progression-free survival (PFS) as determined by blinded, independent radiological review using modified Response Evaluation Criteria in Solid Tumors v. 1.0 (RECIST). RECIST was modified by inclusion of clinical progression of bone lesions based on the need for external beam radiation (4.4% of progression events). Additional efficacy outcomes measures included overall survival (OS), tumor response rate, and duration of response. Patients were randomized to receive NEXAVAR 400 mg twice daily (n=207) or placebo (n=210). Of the 417 patients randomized, 48% were male, the median age was 63 years, 61% were 60 years or older, 60% were white, 62% had an ECOG performance status of 0, and 99% had undergone thyroidectomy. The histological diagnoses were papillary carcinoma in 57%, follicular carcinoma (including Hurthle cell) in 25%, and poorly differentiated carcinoma in 10%, and other in 8% of the study population. Metastases were present in 96% of the patients: lungs in 86%, lymph nodes in 51%, and bone in 27%. The median cumulative RAI activity administered prior to study entry was 400 mCi.A statistically significant prolongation of PFS was demonstrated for NEXAVAR-treated patients compared to those receiving placebo (Figure 3); no statistically significant difference was seen in the final overall survival (OS) analysis (Table 121). Crossover to open label NEXAVAR occurred in 161 (77%) patients randomized to placebo after investigator-determined disease progressionTable 12: Efficacy Results from DECISION in Differentiated Thyroid CarcinomaNEXAVARN=207PlaceboN=210Progression-free Survival1 Number of Deaths or Progression113 (55%)136 (65%)Median PFS in Months (95% CI)10.8 (9.1, 12.9)5.8 5.3, 7.8)Hazard Ratio (95% CI)0.59 (0.46, 0.76)P-value <0.001Overall Survival3Number of Deaths103 (49.8%)109 (51.9%)Median OS in Months (95% CI)42.8 (34.6, 52.6)39.4 (32.7, 51.4)Hazard Ratio (95% CI)0.92 (0.71, 1.21)P-value2 0.570Objective ResponseNumber of Objective Responders 24 (12%)1 (0.5%)(95% CI)(7.6%, 16.8%)(0.01%, 2.7%)Median Duration of Response in Months (95% CI)10.2 (7.4, 16.6)NE1Independent radiological review2Two-sided log-rank test stratified by age (< 60 years, >= 60 years) and geographic region (North America, Europe, Asia)3Conducted after 212 events, which occurred 36 months after the primary PFS analysis.4All objective responses were partial responses NR Not Reached, CI Confidence interval, NE Not EstimableFigure 3: Kaplan-Meier Curve of Progression-Free Survival in DECISION (DTC)Figure 3: Kaplan-Meier Curve of Progression-Free Survival in DECISION (DTC). 1Independent radiological review. 2Two-sided log-rank test stratified by age (< 60 years, >= 60 years) and geographic region (North America, Europe, Asia). 3Conducted after 212 events, which occurred 36 months after the primary PFS analysis.. 4All objective responses were partial responses. NR Not Reached, CI Confidence interval, NE Not Estimable. Figure 3.

DOSAGE & ADMINISTRATION SECTION.

2 Dosage and Administration The recommended dosage is 400 mg orally twice daily without food. (2.1). The recommended dosage is 400 mg orally twice daily without food. (2.1). 2.1 Recommended Dosage The recommended dosage of NEXAVAR is 400 mg orally twice daily without food (at least hour before or hours after meal) until the patient is no longer clinically benfiting from therapy or until unacceptable toxicity. 2.2 Dosage Modifications for Adverse Reactions Recommended Dosage Modifications The recommended dosage modifications for adverse reactions are provided in Tables 1, 2, and 3.Table 1: Recommended Dose Reductions for Adverse ReactionsDose Reduction Hepatocellular Carcinoma andRenal Cell CarcinomaDifferentiated Thyroid CarcinomaFirst Dose Reduction400 mg orally once daily400 mg orally in the morning and 200 mg orally in the evening about 12 hours apart OR 200 mg orally in the morning and 400 mg orally in the evening about 12 hours apartSecond Dose Reduction200 mg orally once daily OR400 every other day200 mg orally twice daily Third Dose ReductionNone200 mg orally once daily Table 2: Recommended Dosage Modifications of NEXAVAR for Adverse ReactionsAdverse Reaction Severity1 NEXAVAR Dosage ModificationCardiovascular Events [see Warnings and Precautions (5.1)]Cardiac Ischemia and/or InfarctionGrade and abovePermanently discontinue.Congestive Heart FailureGrade 3Interrupt2 until Grade or less, resume at reduced dose by dose level.3 Grade 4Permanently discontinue.Hemorrhage [see Warnings and Precautions (5.2)]Grade and above requiring medical interventionPermanently discontinue.Hypertension [see Warnings and Precautions (5.3)]Grade (symptomatic/persistent)ORGrade symptomatic increase by greater than 20 mm Hg (diastolic) or greater than 140/90 mm Hg if previously within normal limitsOR Grade 3Interrupt until symptoms resolve and diastolic blood pressure less than 90 mm Hg, then resume at reduced dose by dose level.3 If needed, reduce another dose level.3 Grade 4Permanently discontinue.Gastrointestinal Perforation [see Warnings and Precautions (5.5)]Any gradePermanently discontinue.QT Interval Prolongation [see Warnings and Precautions (5.9)]Greater than 500 milliseconds ORIncrease from baseline of 60 milliseconds or greaterInterruptand correct electrolyte abnormalities (magnesium, potassium, calcium).Use medical judgement before restarting.Drug-Induced Liver Injury [see Warnings and Precautions (5.10)]Grade ALT or higher in the absence of another cause4 ORAST/ALT greater than x upper limit normal (ULN) with bilirubin greater than x ULN in the absence of another cause4 Permanently discontinue.Non-hematological toxicities [see Adverse Reactions (6.1)]Grade 2Continue treatment at reduced dose by dose level.Grade 31st occurrenceInterrupt until Grade or less, then resume at reduced dose by dose level.No improvement within days OR 2nd or 3rd occurrenceInterrupt until Grade or less, then resume at reduced dose by dose levels.4th occurrenceInterrupt until Grade or less, then resume at reduced dose by dose levels for HCC and RCC or dose levels for DTC.Grade 4Permanently discontinue.1Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).2If no recovery after 30 day interruption, discontinue treatment unless the patient is deriving clinical benefit.3If more than dose reductions are required, permanently discontinue treatment.4In addition, any grade increased alkaline phosphatase in the absence of known bone pathology and Grade or worse increased bilirubin; any of the following: INR of 1.5 or greater, ascites and/or encephalopathy in the absence of underlying cirrhosis or other organ failure considered to be due to drug-induced liver injury.Table 3: Recommended Dosage Modifications for Dermatologic ToxicitiesDermatologic Toxicity GradeOccurrenceNEXAVAR Dosage ModificationHepatocellular and Renal Cell CarcinomaDifferentiated Thyroid CarcinomaGrade 2: Painful erythema and swelling of the hands or feet and/or discomfort affecting the patients normal activities1st occurrenceContinue NEXAVAR and consider topical therapy for symptomatic relief.If no improvement within days, see below.Decrease NEXAVAR to 600 mg daily. If no improvement within days, see below.No improvement within days at reduced dose OR 2nd and 3rd occurrenceInterrupt NEXAVAR until resolved or improved to Grade to 1.Interrupt NEXAVAR until completely resolved or improved to Grade1.When resuming treatment, decrease dose by dose level.When resuming treatment, decrease dose by dose level for 2nd occurrence and doses levels for 3rd occurrence. 4th occurrenceDiscontinue NEXAVAR treatment.Grade 3: Moist desquamation, ulceration, blistering, or severe pain of the hands or feet, resulting in inability to work or perform activities of daily living 1st occurrenceInterrupt NEXAVAR until resolved or improved to Grade to Interrupt NEXAVAR until completely resolved or improved to Grade 1.When resuming treatment, decrease dose by dose level.When resuming treatment, decrease dose by dose level.2nd occurrenceInterrupt NEXAVAR until resolved or improved to Grade to 1Interrupt NEXAVAR until completely resolved or improved to Grade 1.When resuming treatment, decrease dose by dose level.When resuming treatment, decrease dose by dose levels. 3rd occurrenceDiscontinue NEXAVAR treatment.Following improvement of Grade or dermatologic toxicity to Grade or for at least 28 days on reduced dose of NEXAVAR, the dose of NEXAVAR may be increased dose level from the reduced dose. Approximately 50% of patients requiring dose reduction for dermatologic toxicity are expected to meet these criteria for resumption of the higher dose and roughly 50% of patients resuming the previous dose are expected to tolerate the higher dose (that is, maintain the higher dose level without recurrent Grade or higher dermatologic toxicity).. 1Adverse reactions graded according to National Cancer Institute Common Terminology Criteria for Adverse Events version 3.0 (NCI CTCAE v3.0).. 2If no recovery after 30 day interruption, discontinue treatment unless the patient is deriving clinical benefit.. 3If more than dose reductions are required, permanently discontinue treatment.. 4In addition, any grade increased alkaline phosphatase in the absence of known bone pathology and Grade or worse increased bilirubin; any of the following: INR of 1.5 or greater, ascites and/or encephalopathy in the absence of underlying cirrhosis or other organ failure considered to be due to drug-induced liver injury.

INFORMATION FOR PATIENTS SECTION.

17 Patient Counseling Information Advise the patient to read FDA-approved patient labeling (Patient Information).Cardiovascular EventsDiscuss with patients that cardiac ischemia and/or infarction and congestive heart failure, have been reported during NEXAVAR treatment, and that they should immediately report any episodes of chest pain or other symptoms of cardiac ischemia or congestive heart failure [see Warnings and Precautions (5.1)]. Bleeding Inform patients that NEXAVAR can increase the risk of bleeding and that they should promptly report any episodes of bleeding [see Warnings and Precautions (5.2)]. Inform patients that bleeding or elevations in the International Normalized Ratio (INR) have been reported in some patients taking warfarin while on NEXAVAR and that their INR should be monitored regularly [see Warnings and Precautions (5.6)]. HypertensionInform patients that hypertension can develop during NEXAVAR treatment, especially during the first six weeks of therapy, and that blood pressure should be monitored regularly during treatment [see Warnings and Precautions (5.3)]. Skin ReactionsAdvise patients of the possible occurrence of hand-foot skin reaction and rash during NEXAVAR treatment and appropriate countermeasures [see Warnings and Precautions (5.4)]. Gastrointestinal Perforation Advise patients that cases of gastrointestinal perforation have been reported in patients taking NEXAVAR [see Warnings and Precautions (5.5)]. Risk of Impaired Wound Healing Advise patients that NEXAVAR may impair wound healing. Advise patients to inform their healthcare provider of any planned surgical procedure [see Warnings and Precautions (5.7)]. QT Interval ProlongationInform patients with history of prolonged QT interval that NEXAVAR can worsen the condition [see Warnings and Precautions (5.9) and Clinical Pharmacology (12.2)].Drug-Induced Liver InjuryInform patients that NEXAVAR can cause hepatitis which may result in hepatic failure and death. Advise patients that liver function tests should be monitored regularly during treatment and to report signs and symptoms of hepatitis [see Warnings and Precautions (5.10)]. Embryo-Fetal ToxicityAdvise females to inform their healthcare provider if they are pregnant or become pregnant. Inform female patients of the risk to fetus and potential loss of pregnancy [see Use in Specific Populations (8.1)]. Advise females of reproductive potential to use effective contraception during treatment with NEXAVAR and for months after the last dose. Advise male patients with female partners of reproductive potential or who are pregnant to use effective contraception during treatment with NEXAVAR and for months after receiving the last dose of NEXAVAR [see Warnings and Precautions (5.11), Use in Specific Populations (8.1, 8.3)]. LactationAdvise patients not to breastfeed while taking NEXAVAR and for weeks after receiving the last dose of NEXAVAR [see Use in Specific Populations (8.2)]. Missed DosesInstruct patients that if dose of NEXAVAR is missed, the next dose should be taken at the regularly scheduled time, and not double the dose.Instruct patients to contact their healthcare provider immediately if they take too much NEXAVAR.

PHARMACOKINETICS SECTION.

12.3 Pharmacokinetics Multiple doses of NEXAVAR for days resulted in 2.5- to 7-fold accumulation compared to single dose. Steady-state plasma sorafenib concentrations were achieved within days, with peak-to-trough ratio of mean concentrations of less than 2. The steady-state concentrations of sorafenib following administration of NEXAVAR 400 mg twice daily were evaluated in DTC, RCC and HCC patients. Patients with DTC have mean steady-state concentrations that are 1.8-fold higher than patients with HCC and 2.3-fold higher than those with RCC. The reason for increased sorafenib concentrations in DTC patients is unknown. Mean Cmax and AUC increased less than proportionally beyond oral doses of 400 mg administered twice daily.. Absorption After administration of NEXAVAR tablets, the mean relative bioavailability was 38-49% when compared to an oral solution. Following oral administration, sorafenib reached peak plasma levels in approximately hours. Effects of Food With moderate-fat meal (30% fat; 700 calories), bioavailability was similar to that in the fasted state. With high-fat meal (50% fat; 900 calories), bioavailability was reduced by 29% compared to that in the fasted state. Distribution In vitrobinding of sorafenib to human plasma proteins was 99.5%. Elimination The mean elimination half-life of sorafenib was approximately 25 to 48 hours. Metabolism Sorafenib undergoes oxidative metabolism by hepatic CYP3A4, as well as glucuronidation by UGT1A9.. Excretion Sorafenib accounted for approximately 70-85% of the circulating analytes in plasma at steady-state. Eight metabolites of sorafenib have been identified, of which have been detected in plasma. The main circulating metabolite of sorafenib, the pyridine N-oxide that comprises approximately 9-16% of circulating analytes at steady-state, showed in vitro potency similar to that of sorafenib. Following oral administration of 100 mg dose of solution formulation of sorafenib, 96% of the dose was recovered within 14 days, with 77% of the dose excreted in feces and 19% of the dose excreted in urine as glucuronidated metabolites. Unchanged sorafenib, accounting for 51% of the dose, was found in feces but not in urine. Specific Populations A study of the pharmacokinetics of sorafenib indicated that the mean AUC of sorafenib in Asians (N=78) was 30% lower than in Whites (N=40). Sex and age do not have clinically meaningful effect on the pharmacokinetics of sorafenib.. Patients with Renal Impairment Mild (CLcr 50-80 mL/min), moderate (CLcr 30 <50 mL/min), and severe (CLcr <30 mL/min) renal impairment do not affect the pharmacokinetics of sorafenib [see Use in Specific Populations (8.6)].. Patients with Hepatic Impairment Mild (Child-Pugh A) and moderate (Child-Pugh B) hepatic impairment do not affect the pharmacokinetics of sorafenib [see Use in Specific Populations (8.7)].. Drug Interactions Studies Effect of Strong CYP3A4 Inhibitors on Sorafenib: Ketoconazole, strong inhibitor of CYP3A4 and P-glycoprotein, administered at dose of 400 mg once daily for days did not alter the mean AUC of single oral dose of NEXAVAR 50 mg in healthy subjects. Effect of Strong CYP3A4 Inducers on Sorafenib: Concomitant use of NEXAVAR with rifampin administered at dose of 600 mg once daily for days with single oral dose of NEXAVAR 400 mg in healthy volunteers resulted in 37% decrease in the mean AUC of sorafenib. Effect of Neomycin on Sorafenib: Neomycin administered as an oral dose of g three times daily for days decreased the mean AUC of sorafenib by 54% in healthy subjects administered single oral dose of NEXAVAR 400 mg.Effect of Sorafenib on Other Drugs: NEXAVAR 400 mg twice daily for 28 days did not increase the systemic exposure of concomitantly administered midazolam (CYP3A4 substrate), dextromethorphan (CYP2D6 substrate), and omeprazole (CYP2C19 substrate) [see Clinical Pharmacology (12.3)]. Drugs that Increase Gastric pH: The aqueous solubility of sorafenib is pH dependent, with higher pH resulting in lower solubility. However, omeprazole, proton pump inhibitor, administered at dose of 40 mg once daily for days, did not result in clinically meaningful change in sorafenib single dose exposure. In Vitro Studies Sorafenib competitively inhibited CYP2B6, CYP2C8, CYP2C9, CYP2C19, CYP2D6, and CYP3A4 in vitro. However, NEXAVAR 400 mg twice daily for 28 days with substrates of CYP3A4, CYP2D6 and CYP2C19 did not increase the systemic exposure of these substrates [see Drug Interactions (7.3)]. Sorafenib did not increase CYP1A2 and CYP3A4 activities, suggesting that sorafenib is unlikely to induce CYP1A2 or CYP3A4 in humans. Sorafenib inhibits glucuronidation by UGT1A1 and UGT1A9 in vitro. NEXAVAR could increase the systemic exposure of concomitantly administered drugs that are UGT1A1 or UGT1A9 substrates.Sorafenib inhibited P-glycoprotein in vitro. NEXAVAR could increase the concentrations of concomitantly administered drugs that are P-glycoprotein substrates.

SPL PATIENT PACKAGE INSERT SECTION.

Patient Package Insert Patient InformationNEXAVAR(R) (NEX-A-VAR)(sorafenib)tablets, oralWhat is NEXAVAR NEXAVAR is prescription medicine used to treat: oa type of liver cancer called hepatocellular carcinoma (HCC) that cannot be removed by surgeryoa type of kidney cancer called renal cell carcinoma (RCC)oa type of thyroid cancer called differentiated thyroid carcinoma (DTC) that can no longer be treated with radioactive iodine and is progressingIt is not known if NEXAVAR is safe and effective in children.Do not take NEXAVAR if you:oare allergic to sorafenib or any of the other ingredients in NEXAVAR.See the end of this leaflet for complete list of ingredients in NEXAVAR.ohave squamous cell lung cancer and receive carboplatin and paclitaxel. Before taking NEXAVAR, tell your healthcare provider about all of your medical conditions including if you:ohave heart problems including condition called congenital long QT syndromeohave chest pain ohave abnormal magnesium, potassium, or calcium blood levels ohave bleeding problems ohave high blood pressure plan to have surgery or have had recent surgery. You should stop taking NEXAVAR at least weeks before planned surgery. See What are the possible side effects of NEXAVAR oare pregnant or plan to become pregnant. NEXAVAR may harm your unborn baby. Tell your healthcare provider right away if you become pregnant during treatment with NEXAVAR. For females who are able to become pregnant:oYour healthcare should do pregnancy test before you start treatment with NEXAVAR.oUse effective birth control (contraception) during your treatment with NEXAVAR and for months after the last dose of NEXAVAR. For males with female partners who are able to become pregnant:oUse effective birth control (contraception) during your treatment with NEXAVAR and for months after the last dose of NEXAVAR.oare breastfeedingorplan to breastfeed. It is not known if NEXAVAR passes into your breast milk. Do not breastfeed during treatment with NEXAVAR and for weeks after receiving the last dose of NEXAVAR. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Especially tell your healthcare provider if you take the medicine warfarin.How should take NEXAVAR oTake NEXAVAR exactly as your healthcare provider tells you to take it. Take NEXAVAR times day. Your healthcare provider may change your dose, temporarily stop treatment or completely stop treatment with NEXAVAR if you have side effects.oTake NEXAVAR without food (at least hour before or hours after meal).oIf you miss dose of NEXAVAR, skip the missed dose, and take your next dose at your regular time. Do not double your dose of NEXAVAR. oIf you take too much NEXAVAR call your doctor or go to the nearest hospital emergency room right away. What are the possible side effects of NEXAVAR NEXAVAR may cause serious side effects, including: odecreased blood flow to the heart, heart attack and heart failure. Get emergency help right away if you get symptoms such as chest pain, shortness of breath, racing heartbeat, swelling in lower legs, feet and abdomen, feel lightheaded or faint, tiredness, nausea, vomiting, or sweat lot. oincreased risk of bleeding. Bleeding is common side effect of NEXAVAR that can be serious and can lead to death. Tell your healthcare provider right away if you have any signs of bleeding during treatment with NEXAVAR:ohigh blood pressure. High blood pressure is common side effect of NEXAVAR and can be serious.Your blood pressure should be checked every week during the first weeks of starting NEXAVAR. Your blood pressure should be checked regularly and any high blood pressure should be treated during treatment with NEXAVAR. oskin problems. condition called hand-foot skin reactions and skin rash are common with NEXAVAR treatment and can be severe.NEXAVAR may also cause severe skin and mouth reactions that can be life-threatening. Tell your healthcare provider if you have any of the following symptoms:oskin rash oskin rednessopain or swellingoblistering and peeling of your skinoblistering and peeling on the inside of your mouthoblisters on the palms of your hand or soles of your feetoan opening in the wall of your stomach or intestines (gastrointestinal perforation). Tell your healthcare provider right away if you get fever, nausea, vomiting or severe stomach (abdominal) pain. orisk of wound healing problems. Wounds may not heal properly during NEXAVAR treatment. Tell your healthcare provider if you plan to have any surgery before starting or during treatment with NEXAVAR.oYou should stop taking NEXAVAR at least 10 days before planned surgery.o Your healthcare provider should tell you when you may start taking NEXAVAR again after surgery.ochanges in the electrical activity of your heart called QT prolongation. QT prolongation can cause irregular heartbeats that can be life-threatening. Your healthcare provider may do tests during your treatment with NEXAVAR to check the levels of potassium, magnesium, and calcium in your blood, and check the electrical activity of your heart with an electrocardiogram (ECG). Tell your healthcare provider right away if you feel faint, lightheaded, dizzy or feel your heart beating irregularly or fast during your treatment with NEXAVAR.oliver problems (drug-induced hepatitis). NEXAVAR may cause liver problems that may lead to liver failure and death. Your healthcare provider will do blood tests to check your liver function regularly during your treatment with NEXAVAR. Tell your healthcare provider right away if you develop any of the following symptoms:ochange in thyroid hormone levels. If you have differentiated thyroid cancer, you can have changes in your thyroid hormone levels during treatment with NEXAVAR. Your healthcare provider may need to change your dose of thyroid medicine during treatment with NEXAVAR. Your healthcare provider should check your thyroid hormone levels every month during treatment with NEXAVAR.The most common side effects of NEXAVAR include: NEXAVAR may cause fertility problems in males. This may affect your ability to father child. Talk to your healthcare provider if this is concern for you. These are not all of the possible side effects of NEXAVAR. Call your doctor for medical advice about side effects.You may report side effects to FDA at 1-800-FDA-1088. How should store NEXAVAR oStore NEXAVAR tablets at room temperature between 68 to 77 (20 to 25 C). oStore NEXAVAR tablets in dry place. Keep NEXAVAR and all medicines out of the reach of children. General information about the safe and effective use of NEXAVAR Medicines are sometimes prescribed for purposes other than those listed in Patient Information leaflet. Do not use NEXAVAR for condition for which it is not prescribed. Do not give NEXAVAR to other people even if they have the same symptoms you have. It may harm them. You can ask your healthcare provider or pharmacist for information about NEXAVAR that is written for health professionals.What are the ingredients in NEXAVAR Active Ingredient: sorafenib tosylate Inactive Ingredients: croscarmellose sodium, ferric oxide red, hypromellose, magnesium stearate, microcrystalline cellulose, sodium lauryl sulphate, polyethylene glycol, and titanium dioxide. Manufactured for: Bayer HealthCare Pharmaceuticals Inc.Whippany, NJ 07981 Manufactured in Germany(C) 2015 Bayer HealthCare Pharmaceuticals Inc.For more information, go to www.NEXAVAR.com, or call 1-866-639-2827.This Patient Information has been approved by the U.S. Food and Drug Administration. Revised 6/2020. oa type of liver cancer called hepatocellular carcinoma (HCC) that cannot be removed by surgery. oa type of kidney cancer called renal cell carcinoma (RCC). oa type of thyroid cancer called differentiated thyroid carcinoma (DTC) that can no longer be treated with radioactive iodine and is progressing. oare allergic to sorafenib or any of the other ingredients in NEXAVAR.See the end of this leaflet for complete list of ingredients in NEXAVAR.. ohave squamous cell lung cancer and receive carboplatin and paclitaxel.. Before taking NEXAVAR, tell your healthcare provider about all of your medical conditions including if you:. ohave heart problems including condition called congenital long QT syndrome. ohave chest pain ohave abnormal magnesium, potassium, or calcium blood levels ohave bleeding problems ohave high blood pressure o plan to have surgery or have had recent surgery. You should stop taking NEXAVAR at least weeks before planned surgery. See What are the possible side effects of NEXAVAR oare pregnant or plan to become pregnant. NEXAVAR may harm your unborn baby. Tell your healthcare provider right away if you become pregnant during treatment with NEXAVAR.. For females who are able to become pregnant:. oYour healthcare should do pregnancy test before you start treatment with NEXAVAR.. oUse effective birth control (contraception) during your treatment with NEXAVAR and for months after the last dose of NEXAVAR.. For males with female partners who are able to become pregnant:. oUse effective birth control (contraception) during your treatment with NEXAVAR and for months after the last dose of NEXAVAR.. oare breastfeedingorplan to breastfeed. It is not known if NEXAVAR passes into your breast milk. Do not breastfeed during treatment with NEXAVAR and for weeks after receiving the last dose of NEXAVAR. oTake NEXAVAR exactly as your healthcare provider tells you to take it. o Take NEXAVAR times day. Your healthcare provider may change your dose, temporarily stop treatment or completely stop treatment with NEXAVAR if you have side effects.. oTake NEXAVAR without food (at least hour before or hours after meal).. oIf you miss dose of NEXAVAR, skip the missed dose, and take your next dose at your regular time. Do not double your dose of NEXAVAR. oIf you take too much NEXAVAR call your doctor or go to the nearest hospital emergency room right away. odecreased blood flow to the heart, heart attack and heart failure. Get emergency help right away if you get symptoms such as chest pain, shortness of breath, racing heartbeat, swelling in lower legs, feet and abdomen, feel lightheaded or faint, tiredness, nausea, vomiting, or sweat lot. oincreased risk of bleeding. Bleeding is common side effect of NEXAVAR that can be serious and can lead to death. Tell your healthcare provider right away if you have any signs of bleeding during treatment with NEXAVAR:. ohigh blood pressure. High blood pressure is common side effect of NEXAVAR and can be serious.Your blood pressure should be checked every week during the first weeks of starting NEXAVAR. Your blood pressure should be checked regularly and any high blood pressure should be treated during treatment with NEXAVAR. oskin problems. condition called hand-foot skin reactions and skin rash are common with NEXAVAR treatment and can be severe.NEXAVAR may also cause severe skin and mouth reactions that can be life-threatening. Tell your healthcare provider if you have any of the following symptoms:. oskin rash oskin redness. opain or swelling. oblistering and peeling of your skin. oblistering and peeling on the inside of your mouth. oblisters on the palms of your hand or soles of your feet. oan opening in the wall of your stomach or intestines (gastrointestinal perforation). Tell your healthcare provider right away if you get fever, nausea, vomiting or severe stomach (abdominal) pain. orisk of wound healing problems. Wounds may not heal properly during NEXAVAR treatment. Tell your healthcare provider if you plan to have any surgery before starting or during treatment with NEXAVAR.. oYou should stop taking NEXAVAR at least 10 days before planned surgery.. Your healthcare provider should tell you when you may start taking NEXAVAR again after surgery.. ochanges in the electrical activity of your heart called QT prolongation. QT prolongation can cause irregular heartbeats that can be life-threatening. Your healthcare provider may do tests during your treatment with NEXAVAR to check the levels of potassium, magnesium, and calcium in your blood, and check the electrical activity of your heart with an electrocardiogram (ECG). Tell your healthcare provider right away if you feel faint, lightheaded, dizzy or feel your heart beating irregularly or fast during your treatment with NEXAVAR.. oliver problems (drug-induced hepatitis). NEXAVAR may cause liver problems that may lead to liver failure and death. Your healthcare provider will do blood tests to check your liver function regularly during your treatment with NEXAVAR. Tell your healthcare provider right away if you develop any of the following symptoms:. ochange in thyroid hormone levels. If you have differentiated thyroid cancer, you can have changes in your thyroid hormone levels during treatment with NEXAVAR. Your healthcare provider may need to change your dose of thyroid medicine during treatment with NEXAVAR. Your healthcare provider should check your thyroid hormone levels every month during treatment with NEXAVAR.. oStore NEXAVAR tablets at room temperature between 68 to 77 (20 to 25 C). oStore NEXAVAR tablets in dry place.. Keep NEXAVAR and all medicines out of the reach of children. Manufactured for:. Bayer HealthCare Pharmaceuticals Inc.Whippany, NJ 07981. Manufactured in Germany. New Bayer Logo.

USE IN SPECIFIC POPULATIONS SECTION.

8 Use in Specific Populations oLactation: Advise women not to breastfeed. (8.2). oLactation: Advise women not to breastfeed. (8.2). 8.1 Pregnancy Risk Summary Based on findings from animal studies and its mechanism of action[see Clinical Pharmacology (12.1)], NEXAVAR may cause fetal harm when administered to pregnant woman. There are no available data in pregnant women to inform drug-associated risk. In animal reproduction studies, oral administration of sorafenib to pregnant rats and rabbits during the period of organogenesis resulted in embryo-fetal toxicities at maternal exposures that were significantly lower than human exposures at the recommended dose of 400 mg twice daily (see Data). Advise pregnant women and females of reproductive potential of the potential risk to fetus.The background risk of major birth defects and miscarriage for the indicated population is unknown. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively.. Data Animal Data In animal reproduction studies, sorafenib was teratogenic and induced embryo-fetal toxicity (including increased post-implantation loss, resorptions, skeletal retardations, and retarded fetal weight) when administered orally to pregnant rats and rabbits during the period of organogenesis. The effects occurred at doses considerably below the recommended human dose of 400 mg twice daily (approximately 500 mg/m2/day on body surface area basis). Adverse intrauterine development effects were seen at doses >0.2 .mg/kg/day (1.2 mg/m2/day) in rats and >=0.3 mg/kg/day (>=3.6 mg/m2/day) in rabbits. These doses result in exposures (AUC) that are approximately 0.008 times the AUC in patients at the recommended dose. 8.2 Lactation Risk Summary There are no data on the presence of sorafenib or its metabolites in human milk, or its effects on the breast-fed child or on milk production. Sorafenib was present in milk of lactating rats (see Data). Because of the potential for serious adverse reactions in breastfed child from NEXAVAR, advise women not to breastfeed during treatment with NEXAVAR and for weeks after the last dose. Data Animal Data Following administration of radiolabeled sorafenib to lactating Wistar rats, approximately 27% of the radioactivity was secreted into milk. The milk to plasma AUC ratio was approximately 5:1.. 8.3 Females and Males of Reproductive Potential NEXAVAR may cause fetal harm when administered to pregnant woman [see Use in Specific Populations (8.1)]. Pregnancy Testing Verify the pregnancy status of females of reproductive potential prior to the initiation of NEXAVAR.. Contraception Females Advise females of reproductive potential to use effective contraception during treatment and for months following the last dose of NEXAVAR. Males Based on genotoxicity and findings in animal reproduction studies, advise males with female partners of reproductive potential and pregnant partners to use effective contraception during treatment with NEXAVAR and for months following the last dose of NEXAVAR [see Use in Specific Populations (8.1), Nonclinical Toxicology (13.1)].. Infertility Males Based on findings in animal studies, NEXAVAR may impair fertility in males of reproductive potential [see Nonclinical Toxicology (13.1)].. 8.4 Pediatric Use The safety and effectiveness of NEXAVAR have not been established in pediatric patients.. Juvenile Animal Toxicity Data Repeat dosing of sorafenib to young and growing dogs resulted in irregular thickening of the femoral growth plate at daily sorafenib doses >=600 mg/m2 (approximately 0.3 times the AUC at the recommended human dose), hypocellularity of the bone marrow adjoining the growth plate at 200 mg/m2/day (approximately 0.1 times the AUC at the recommended human dose), and alterations of the dentin composition at 600 mg/m2/day. Similar effects were not observed in adult dogs when dosed for weeks or less.. 8.5 Geriatric Use In total, 59% of HCC patients treated with NEXAVAR were age 65 years or older and 19% were 75 and older. In total, 32% of RCC patients treated with NEXAVAR were age 65 years or older and 4% were 75 and older. No differences in safety or efficacy were observed between older and younger patients, and other reported clinical experience has not identified differences in responses between the elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.. 8.6 Renal Impairment No dose adjustment is necessary for patients with mild, moderate or severe renal impairment who are not on dialysis.The pharmacokinetics of sorafenib have not been studied in patients who are on dialysis [see Clinical Pharmacology (12.3)]. 8.7 Hepatic Impairment No dose adjustment is necessary for patients with mild or moderate hepatic impairment. The pharmacokinetics of sorafenib have not been studied in patients with severe (Child-Pugh C) hepatic impairment [see Clinical Pharmacology (12.3)].

WARNINGS AND PRECAUTIONS SECTION.

5 Warnings and Precautions oCardiovascular Events: Consider temporary or permanent discontinuation of NEXAVAR. (2.2, 5.1)oHemorrhage: Discontinue NEXAVAR if needed. (5.2)oHypertension: Monitor blood pressure weekly during the first weeks and periodically thereafter. Consider temporary or permanent discontinuation for severe or persistent hypertension despite antihypertensive therapy. (5.3)oDermatologic Toxicities: Interrupt and/or decrease dose. Discontinue for severe or persistent reactions, or if Stevens-Johnson syndrome and toxic epidermal necrolysis is suspected. (5.4)oGastrointestinal Perforation: Discontinue NEXAVAR. (5.5)oRisk of Impaired Wound Healing: Withhold NEXAVAR for at least 10 days prior to elective surgery. Do not administer for at least weeks following major surgery and until adequate wound healing. The safety of resumption of NEXAVAR after resolution of wound healing complications has not been established. (5.7)oQT Prolongation: Monitor electrocardiograms and electrolytes in patients at increased risk for ventricular arrhythmias. Correct electrolytes. Interrupt if QTc greater than 500 msec or increases greater than 60 msec from baseline. (2.2, 5.9, 12.2)oDrug-Induced Liver Injury: Monitor liver function tests regularly; discontinue for unexplained transaminase elevations. (5.10)oEmbryo-Fetal Toxicity: NEXAVAR may cause fetal harm. Advise patients of the potential risk to fetus and to use effective contraception. (5.11, 8.1, 8.3)oImpairment of Thyroid Stimulating Hormone Suppression (TSH) in DTC: Monitor TSH monthly and adjust thyroid replacement therapy in patients with thyroid cancer. (5.12). oCardiovascular Events: Consider temporary or permanent discontinuation of NEXAVAR. (2.2, 5.1). oHemorrhage: Discontinue NEXAVAR if needed. (5.2). oHypertension: Monitor blood pressure weekly during the first weeks and periodically thereafter. Consider temporary or permanent discontinuation for severe or persistent hypertension despite antihypertensive therapy. (5.3). oDermatologic Toxicities: Interrupt and/or decrease dose. Discontinue for severe or persistent reactions, or if Stevens-Johnson syndrome and toxic epidermal necrolysis is suspected. (5.4). oGastrointestinal Perforation: Discontinue NEXAVAR. (5.5). oRisk of Impaired Wound Healing: Withhold NEXAVAR for at least 10 days prior to elective surgery. Do not administer for at least weeks following major surgery and until adequate wound healing. The safety of resumption of NEXAVAR after resolution of wound healing complications has not been established. (5.7). oQT Prolongation: Monitor electrocardiograms and electrolytes in patients at increased risk for ventricular arrhythmias. Correct electrolytes. Interrupt if QTc greater than 500 msec or increases greater than 60 msec from baseline. (2.2, 5.9, 12.2). oDrug-Induced Liver Injury: Monitor liver function tests regularly; discontinue for unexplained transaminase elevations. (5.10). oEmbryo-Fetal Toxicity: NEXAVAR may cause fetal harm. Advise patients of the potential risk to fetus and to use effective contraception. (5.11, 8.1, 8.3). oImpairment of Thyroid Stimulating Hormone Suppression (TSH) in DTC: Monitor TSH monthly and adjust thyroid replacement therapy in patients with thyroid cancer. (5.12). 5.1 Cardiovascular Events In the SHARP (HCC) study, the incidence of cardiac ischemia/infarction was 2.7% in NEXAVAR-treated patients compared with 1.3% in those receiving placebo; in the TARGET (RCC) study, the incidence of cardiac ischemia/infarction was higher in the NEXAVAR-treated group (2.9%) compared with patients receiving placebo (0.4%), and in the DECISION (DTC) study, the incidence of cardiac ischemia/infarction was 1.9% in the NEXAVAR-treated group compared with 0% in patients receiving placebo. Patients with unstable coronary artery disease or recent myocardial infarction were excluded from this study. In multiple clinical trials, congestive heart failure has been reported in 1.9% of NEXAVAR-treated patients (N=2276) [see Adverse Reactions (6.2)]. Consider temporary or permanent discontinuation of NEXAVAR in patients who develop cardiovascular events [see Dosage and Administration (2.2)]. 5.2 Hemorrhage An increased risk of bleeding may occur following NEXAVAR administration. In the SHARP (HCC) study, the rates of bleeding from esophageal varices (2.4% and 4%) and of bleeding with fatal outcome from any site (2.4% and 4%) were similar in NEXAVAR-treated patients and those receiving placebo, respectively In the TARGET (RCC) study, bleeding was reported in 15.3% of patients in the NEXAVAR-treated group and 8.2% of patients receiving placebo. The incidence of Grade and bleeding was 2% and 0%, respectively, in NEXAVAR-treated patients, and 1.3% and 0.2%, respectively, in those receiving placebo. There was one fatal hemorrhage in each treatment group in the TARGET (RCC) study. In the DECISION (DTC) study, bleeding was reported in 17.4% of NEXAVAR-treated patients and 9.6% of those receiving placebo; however, the incidence of Grade bleeding was similar (1% and 1.4%) in NEXAVAR-treated patients and in those receiving placebo. If any bleeding necessitates medical intervention, consider permanent discontinuation of NEXAVAR [see Dosage and Administration (2.2)]. Due to the potential risk of bleeding, treat tracheal, bronchial, and esophageal infiltration with local therapy prior to administering NEXAVAR in patients with DTC.. 5.3 Hypertension In the SHARP (HCC) study, hypertension was reported in 9.4% of NEXAVAR-treated patients and 4.3% of patients receiving placebo. In the TARGET (RCC) study, hypertension was reported in 16.9% of NEXAVAR-treated patients and 1.8% of patients receiving placebo. In the DECISION (DTC) study, hypertension was reported in 40.6% of NEXAVAR-treated patients and 12.4% of patients receiving placebo. Hypertension was usually mild to moderate, occurred early in the course of treatment, and was managed with standard antihypertensive therapy. Permanent discontinuation due to hypertension occurred in of 297 NEXAVAR-treated patients in the SHARP (HCC) study, of 451 NEXAVAR-treated patients in the TARGET (RCC) study, and of 207 NEXAVAR-treated patients in the DECISION (DTC) study. Monitor blood pressure weekly during the first weeks of NEXAVAR. Thereafter, monitor blood pressure and treat hypertension, if required, in accordance with standard medical practice. In cases of severe or persistent hypertension despite institution of antihypertensive therapy, consider temporary or permanent discontinuation of NEXAVAR [see Dosage and Administration (2.2)].. 5.4 Dermatologic Toxicities Hand-foot skin reaction and rash represent the most common adverse reactions attributed to NEXAVAR. Rash and hand-foot skin reaction are usually Grade and and generally appear during the first six weeks of treatment with NEXAVAR. Permanent discontinuation of therapy due to hand-foot skin reaction occurred in (1.3%) of 297 NEXAVAR-treated patients with HCC, (0.7%) of 451 NEXAVAR-treated patients with RCC, and 11 (5.3%) of 207 NEXAVAR-treated patients with DTC. Management of dermatologic toxicities may include topical therapies for symptomatic relief, temporary treatment interruption and/or dose reduction of NEXAVAR, or in severe or persistent cases, permanent discontinuation of NEXAVAR [see Dosage and Administration (2.2)].There have been reports of severe dermatologic toxicities, including Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN). These cases may be life-threatening. Discontinue NEXAVAR if SJS or TEN are suspected. 5.5 Gastrointestinal Perforation Gastrointestinal perforation has been reported in less than 1% of patients taking NEXAVAR. In some cases this was not associated with apparent intra-abdominal tumor. In the event of gastrointestinal perforation, permanently discontinue NEXAVAR. 5.6 Increased Risk of Bleeding with Concomitant Use of Warfarin Infrequent bleeding or elevations in the International Normalized Ratio (INR) have been reported in some patients taking warfarin while on NEXAVAR. Monitor patients taking concomitant warfarin regularly for changes in prothrombin time (PT), INR or clinical bleeding episodes. 5.7 Risk of Impaired Wound Healing Impaired wound healing can occur in patients who receive drugs that inhibit the VEGF signaling pathway. Therefore, NEXAVAR has the potential to adversely affect wound healing.Withhold NEXAVAR for at least 10 days prior to elective surgery. Do not administer for at least weeks following major surgery and until adequate wound healing. The safety of resumption of NEXAVAR after resolution of wound healing complications has not been established.. 5.8 Increased Mortality Observed with NEXAVAR Administered in Combination with Carboplatin/Paclitaxel and Gemcitabine/Cisplatin in Squamous Cell Lung Cancer In subset analysis of two randomized controlled trials in chemo-naive patients with Stage IIIB-IV non-small cell lung cancer, patients with squamous cell carcinoma experienced higher mortality with the addition of NEXAVAR compared to those treated with carboplatin/paclitaxel alone (HR 1.81; 95% CI 1.19, 2.74) and gemcitabine/cisplatin alone (HR 1.22; 95% CI 0.82, 1.80). The use of NEXAVAR in combination with carboplatin/paclitaxel is contraindicated in patients with squamous cell lung cancer. NEXAVAR in combination with gemcitabine/cisplatin is not recommended in patients with squamous cell lung cancer. The safety and effectiveness of NEXAVAR has not been established in patients with non-small cell lung cancer.. 5.9 QT Interval Prolongation NEXAVAR can prolong the QT/QTc interval. QT/QTc interval prolongation increases the risk for ventricular arrhythmias. Avoid NEXAVAR in patients with congenital long QT syndrome. Monitor electrolytes and electrocardiograms in patients with congestive heart failure, bradyarrhythmias, drugs known to prolong the QT interval, including Class Ia and III antiarrhythmics. Correct electrolyte abnormalities (magnesium, potassium, calcium). Interrupt NEXAVAR if QTc interval is greater than 500 milliseconds or for an increase from baseline of 60 milliseconds or greater [see Clinical Pharmacology (12.2)]. 5.10 Drug-Induced Liver Injury Sorafenib-induced hepatitis is characterized by hepatocellular pattern of liver damage with significant increases of transaminases which may result in hepatic failure and death. Increases in bilirubin and INR may also occur. The incidence of severe drug-induced liver injury, defined as elevated transaminase levels above 20 times the upper limit of normal or transaminase elevations with significant clinical sequelae (for example, elevated INR, ascites, fatal, or transplantation), was two of 3,357 patients (0.06%) in global monotherapy database. Monitor liver function tests regularly. In case of significantly increased transaminases without alternative explanation, such as viral hepatitis or progressing underlying malignancy, discontinue NEXAVAR [see Dosage and Administration (2.2)]. 5.11 Embryo-Fetal Toxicity Based on its mechanism of action and findings in animals, NEXAVAR may cause fetal harm when administered to pregnant woman.Sorafenib caused embryo-fetal toxicities in animals at maternal exposures that were significantly lower than the human exposures at the recommended dose of 400 mg twice daily. Advise pregnant women and females of reproductive potential of the potential risk to fetus. Advise females of reproductive potential to use effective contraception during treatment and for months following the last dose of NEXAVAR. Advise male patients with female partners of reproductive potential and pregnant partners to use effective contraception during treatment and for months following the last dose of NEXAVAR [see Use in Specific Populations 8.1, 8.3)]. 5.12 Impairment of Thyroid Stimulating Hormone Suppression in Differentiated Thyroid Carcinoma NEXAVAR impairs exogenous thyroid suppression. In the DECISION (DTC) study, 99% of patients had baseline thyroid stimulating hormone (TSH) level less than 0.5 mU/L. Elevation of TSH level above 0.5 mU/L was observed in 41% of NEXAVAR-treated patients as compared with 16% of those receiving placebo patients. For patients with impaired TSH suppression while receiving NEXAVAR, the median maximal TSH was 1.6 mU/L and 25% had TSH levels greater than 4.4 mU/L.Monitor TSH levels monthly and adjust thyroid replacement medication as needed in patients with DTC.