INFORMATION FOR PATIENTS SECTION.

17 PATIENT COUNSELING INFORMATION. See FDA-approved patient labeling (Medication Guide). Information on Medication Guide- Inform patients, their families, and their caregivers about the benefits and risks associated with treatment with duloxetine delayed-release capsules and counsel them in its appropriate use. patient Medication Guide is available for duloxetine delayed-release capsules. Instruct patients, their families, and their caregivers to read the Medication Guide before starting duloxetine delayed-release capsules and each time their prescription is renewed, and assist them in understanding its contents. Give patients the opportunity to discuss the contents of the Medication Guide and to obtain answers to any questions they may have. The complete text of the Medication Guide is reprinted at the end of this document.Advise patients of the following issues and asked to alert their prescriber if these occur while taking duloxetine delayed-release capsules. Suicidal Thoughts and Behaviors- Encourage patients, their families, and their caregivers to be alert to the emergence of anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, mania, other unusual changes in behavior, worsening of depression, and suicidal ideation, especially early during antidepressant treatment and when the dose is adjusted up or downAdvise families and caregivers of patients to observe for the emergence of such symptoms on day-to-day basis, since changes may be abrupt. Such symptoms should be reported to the patients prescriber or health professional, especially if they are severe, abrupt in onset, or were not part of the patients presenting symptoms. Symptoms such as these may be associated with an increased risk for suicidal thinking and behavior and indicate need for very close monitoring and possibly changes in the medication [see Boxed Warning, and Warnings and Precautions (5.1)]. Duloxetine delayed-release capsules should be swallowed whole and should not be chewed or crushed, nor should the capsule be opened and its contents be sprinkled on food or mixed with liquids. All of these might affect the enteric coating. Continuing the Therapy Prescribed While patients may notice improvement with duloxetine delayed-release capsule therapy in to weeks, advise patients to continue therapy as directed. Hepatotoxicity Inform patients that severe liver problems, sometimes fatal, have been reported in patients treated with duloxetine delayed-release capsules. Instruct patients to talk to their healthcare provider if they develop itching, right upper belly pain, dark urine, or yellow skin/eyes while taking duloxetine delayed-release capsules, which may be signs of liver problems. Instruct patients to talk to their healthcare provider about their alcohol consumption. Use of duloxetine delayed-release capsules with heavy alcohol intake may be associated with severe liver injury [see Warnings and Precautions (5.2)] Alcohol Although duloxetine delayed-release capsules do not increase the impairment of mental and motor skills caused by alcohol, use of duloxetine delayed-release capsules concomitantly with heavy alcohol intake may be associated with severe liver injury. For this reason, duloxetine delayed-release capsules should ordinarily not be prescribed for patients with substantial alcohol use [see Warnings and Precautions (5.2) and Drug Interactions (7.15)] Orthostatic Hypotension, Falls and Syncope Advise patients of the risk of orthostatic hypotension, falls and syncope, especially during the period of initial use and subsequent dose escalation, and in association with the use of concomitant drugs that might potentiate the orthostatic effect of duloxetine [see Warnings and Precautions (5.3)] Serotonin Syndrome Caution patients about the risk of serotonin syndrome with the concomitant use of duloxetine delayed-release capsules and other serotonergic agents including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, amphetamines and St. Johns Wort [see Contraindications (4), Warnings and Precautions (5.4), and Drug Interactions (7.14)] .Advise patients of the signs and symptoms associated with serotonin syndrome that may include mental status changes (e.g., agitation, hallucinations, delirium, and coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular changes (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Patients should be cautioned to seek medical care immediately if they experience these symptoms.Abnormal Bleeding Caution patients about the concomitant use of duloxetine and NSAIDs, aspirin, warfarin, or other drugs that affect coagulation since combined use of psychotropic drugs that interfere with serotonin reuptake and these agents has been associated with an increased risk of bleeding[see Warnings and Precautions (5.5)]. Severe Skin Reactions Caution patients that duloxetine delayed-release capsules may cause serious skin reactions. This may need to be treated in hospital and may be life-threatening. Counsel patients to call their doctor right away or get emergency help if they have skin blisters, peeling rash, sores in their mouth, hives, or any other allergic reactions[see Warnings and Precautions (5.6)]. Discontinuation of Treatment Instruct patients that discontinuation of duloxetine delayed-release capsules may be associated with symptoms such as dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue, and should be advised not to alter their dosing regimen, or stop taking duloxetine delayed-release capsules without consulting their physician[see Warnings and Precautions (5.7)]. Activation of Mania or Hypomania Adequately screen patients with depressive symptoms for risk of bipolar disorder (e.g. family history of suicide, bipolar disorder, and depression) prior to initiating treatment with duloxetine delayed-release capsules. Advise patients to report any signs or symptoms of manic reaction such as greatly increased energy, severe trouble sleeping, racing thoughts, reckless behavior, talking more or faster than usual, unusually grand ideas, and excessive happiness or irritability[see Warnings and Precautions (5.8)]. Angle-Closure Glaucoma Advise patients that taking duloxetine delayed-release capsules can cause mild pupillary dilation, which in susceptible individuals, can lead to an episode of angle-closure glaucoma. Pre-existing glaucoma is almost always open-angle glaucoma because angle-closure glaucoma, when diagnosed, can be treated definitively with iridectomy. Open-angle glaucoma is not risk factor for angle-closure glaucoma. Patients may wish to be examined to determine whether they are susceptible to angle-closure, and have prophylactic procedure (e.g., iridectomy), if they are susceptible.[See Warnings and Precautions (5.9)]. Seizures Advise patients to inform their physician if they have history of seizure disorder[see Warnings and Precautions (5.10)]. Effects on Blood Pressure Caution patients that duloxetine delayed-release capsules may cause an increase in blood pressure[see Warnings and Precautions (5.11)]. Concomitant Medications Advise patients to inform their physicians if they are taking, or plan to take, any prescription or over-the-counter medications, since there is potential for interactions[see Dosage and Administration (2.8, 2.9), Contraindications (4), Warnings and Precautions (5.4, 5.12), and Drug Interactions (7)]. Hyponatremia Advise patients that hyponatremia has been reported as result of treatment with SNRIs and SSRIs, including duloxetine delayed-release capsules. Advise patients of the signs and symptoms of hyponatremia[see Warnings and Precautions (5.13)]. Concomitant Illnesses Advise patients to inform their physicians about all of their medical conditions[see Warnings and Precautions (5.14)]. Duloxetine delayed-release capsules are in class of medicines that may affect urination. Instruct patients to consult with their healthcare provider if they develop any problems with urine flow[see Warnings and Precautions (5.15)]. Pregnancy and Nursing MothersAdvise patients to notify their physician if they become pregnant during therapyintend to become pregnant during therapyare nursing [see Use in Specific Populations (8.1, 8.3)].Pediatric Use -Pediatric use information for patients ages to 17 years with GAD is approved for Eli Lilly and Company, Inc.s Cymbalta(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information. The safety and effectiveness of CYMBALTA have not been established in pediatric patients less than 18 years of age with other indications. [See Use in Specific Populations (8.4)]. The safety and effectiveness of duloxetine have not been established in pediatric patients less than 18 years of age with other indications.Interference with Psychomotor Performance Any psychoactive drug may impair judgment, thinking, or motor skills. Although in controlled studies duloxetine delayed-release capsules have not been shown to impair psychomotor performance, cognitive function, or memory, it may be associated with sedation and dizziness. Therefore, caution patients about operating hazardous machinery including automobiles, until they are reasonably certain that duloxetine therapy does not affect their ability to engage in such activities.Manufactured by:TORRENT PHARMACEUTICALS LTD., Indrad-382 721, Dist. Mehsana, INDIA.For:TORRENT PHARMA INC., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920.8063354 Revised February 2017. Information on Medication Guide- Inform patients, their families, and their caregivers about the benefits and risks associated with treatment with duloxetine delayed-release capsules and counsel them in its appropriate use. patient Medication Guide is available for duloxetine delayed-release capsules. Instruct patients, their families, and their caregivers to read the Medication Guide before starting duloxetine delayed-release capsules and each time their prescription is renewed, and assist them in understanding its contents. Give patients the opportunity to discuss the contents of the Medication Guide and to obtain answers to any questions they may have. The complete text of the Medication Guide is reprinted at the end of this document.. Suicidal Thoughts and Behaviors- Encourage patients, their families, and their caregivers to be alert to the emergence of anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, mania, other unusual changes in behavior, worsening of depression, and suicidal ideation, especially early during antidepressant treatment and when the dose is adjusted up or down. Duloxetine delayed-release capsules should be swallowed whole and should not be chewed or crushed, nor should the capsule be opened and its contents be sprinkled on food or mixed with liquids. All of these might affect the enteric coating.. Continuing the Therapy Prescribed While patients may notice improvement with duloxetine delayed-release capsule therapy in to weeks, advise patients to continue therapy as directed.. Hepatotoxicity Inform patients that severe liver problems, sometimes fatal, have been reported in patients treated with duloxetine delayed-release capsules. Instruct patients to talk to their healthcare provider if they develop itching, right upper belly pain, dark urine, or yellow skin/eyes while taking duloxetine delayed-release capsules, which may be signs of liver problems. Instruct patients to talk to their healthcare provider about their alcohol consumption. Use of duloxetine delayed-release capsules with heavy alcohol intake may be associated with severe liver injury [see Warnings and Precautions (5.2)] .. Alcohol Although duloxetine delayed-release capsules do not increase the impairment of mental and motor skills caused by alcohol, use of duloxetine delayed-release capsules concomitantly with heavy alcohol intake may be associated with severe liver injury. For this reason, duloxetine delayed-release capsules should ordinarily not be prescribed for patients with substantial alcohol use [see Warnings and Precautions (5.2) and Drug Interactions (7.15)] .. Orthostatic Hypotension, Falls and Syncope Advise patients of the risk of orthostatic hypotension, falls and syncope, especially during the period of initial use and subsequent dose escalation, and in association with the use of concomitant drugs that might potentiate the orthostatic effect of duloxetine [see Warnings and Precautions (5.3)] .. Serotonin Syndrome Caution patients about the risk of serotonin syndrome with the concomitant use of duloxetine delayed-release capsules and other serotonergic agents including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, amphetamines and St. Johns Wort [see Contraindications (4), Warnings and Precautions (5.4), and Drug Interactions (7.14)] .. Abnormal Bleeding Caution patients about the concomitant use of duloxetine and NSAIDs, aspirin, warfarin, or other drugs that affect coagulation since combined use of psychotropic drugs that interfere with serotonin reuptake and these agents has been associated with an increased risk of bleeding[see Warnings and Precautions (5.5)]. Severe Skin Reactions Caution patients that duloxetine delayed-release capsules may cause serious skin reactions. This may need to be treated in hospital and may be life-threatening. Counsel patients to call their doctor right away or get emergency help if they have skin blisters, peeling rash, sores in their mouth, hives, or any other allergic reactions[see Warnings and Precautions (5.6)]. Discontinuation of Treatment Instruct patients that discontinuation of duloxetine delayed-release capsules may be associated with symptoms such as dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue, and should be advised not to alter their dosing regimen, or stop taking duloxetine delayed-release capsules without consulting their physician[see Warnings and Precautions (5.7)]. Activation of Mania or Hypomania Adequately screen patients with depressive symptoms for risk of bipolar disorder (e.g. family history of suicide, bipolar disorder, and depression) prior to initiating treatment with duloxetine delayed-release capsules. Advise patients to report any signs or symptoms of manic reaction such as greatly increased energy, severe trouble sleeping, racing thoughts, reckless behavior, talking more or faster than usual, unusually grand ideas, and excessive happiness or irritability[see Warnings and Precautions (5.8)]. Angle-Closure Glaucoma Advise patients that taking duloxetine delayed-release capsules can cause mild pupillary dilation, which in susceptible individuals, can lead to an episode of angle-closure glaucoma. Pre-existing glaucoma is almost always open-angle glaucoma because angle-closure glaucoma, when diagnosed, can be treated definitively with iridectomy. Open-angle glaucoma is not risk factor for angle-closure glaucoma. Patients may wish to be examined to determine whether they are susceptible to angle-closure, and have prophylactic procedure (e.g., iridectomy), if they are susceptible.[See Warnings and Precautions (5.9)]. Seizures Advise patients to inform their physician if they have history of seizure disorder[see Warnings and Precautions (5.10)]. Effects on Blood Pressure Caution patients that duloxetine delayed-release capsules may cause an increase in blood pressure[see Warnings and Precautions (5.11)]. Concomitant Medications Advise patients to inform their physicians if they are taking, or plan to take, any prescription or over-the-counter medications, since there is potential for interactions[see Dosage and Administration (2.8, 2.9), Contraindications (4), Warnings and Precautions (5.4, 5.12), and Drug Interactions (7)]. Hyponatremia Advise patients that hyponatremia has been reported as result of treatment with SNRIs and SSRIs, including duloxetine delayed-release capsules. Advise patients of the signs and symptoms of hyponatremia[see Warnings and Precautions (5.13)]. Concomitant Illnesses Advise patients to inform their physicians about all of their medical conditions[see Warnings and Precautions (5.14)]. Duloxetine delayed-release capsules are in class of medicines that may affect urination. Instruct patients to consult with their healthcare provider if they develop any problems with urine flow[see Warnings and Precautions (5.15)]. Pregnancy and Nursing Mothers. become pregnant during therapy. intend to become pregnant during therapy. are nursing [see Use in Specific Populations (8.1, 8.3)].. Pediatric Use -. Interference with Psychomotor Performance Any psychoactive drug may impair judgment, thinking, or motor skills. Although in controlled studies duloxetine delayed-release capsules have not been shown to impair psychomotor performance, cognitive function, or memory, it may be associated with sedation and dizziness. Therefore, caution patients about operating hazardous machinery including automobiles, until they are reasonably certain that duloxetine therapy does not affect their ability to engage in such activities.. logo.

ADVERSE REACTIONS SECTION.

6 ADVERSE REACTIONS. Most common adverse reactions (>=5% and at least twice the incidence of placebo patients): nausea, dry mouth, somnolence, constipation, decreased appetite, and hyperhidrosis (6.3). To report SUSPECTED ADVERSE REACTIONS, contact Torrent Pharma Inc. at 1-269-544-2299 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.. Most common adverse reactions (>=5% and at least twice the incidence of placebo patients): nausea, dry mouth, somnolence, constipation, decreased appetite, and hyperhidrosis (6.3). . The following serious adverse reactions are described below and elsewhere in the labeling:Suicidal Thoughts and Behaviors in Children, Adolescents, and Young Adults [see Boxed Warning and Warnings and Precautions (5.1)]Hepatotoxicity [see Warnings and Precautions (5.2)] Orthostatic Hypotension, Falls and Syncope [see Warnings and Precautions (5.3)] Serotonin Syndrome [see Warnings and Precautions (5.4)] Abnormal Bleeding [see Warnings and Precautions (5.5)] Severe Skin Reactions [see Warnings and Precautions (5.6)] Discontinuation of Treatment with duloxetine delayed-release capsules [see Warnings and Precautions (5.7)] Activation of Mania/Hypomania [see Warnings and Precautions (5.8)] Angle-Closure Glaucoma [see Warnings and Precautions (5.9)] Seizures [see Warnings and Precautions (5.10)] Effect on Blood Pressure [see Warnings and Precautions (5.11)] Clinically Important Drug Interactions [see Warnings and Precautions (5.12)] Hyponatremia [see Warnings and Precautions (5.13)] Urinary Hesitation and Retention [see Warnings and Precautions (5.15)] Suicidal Thoughts and Behaviors in Children, Adolescents, and Young Adults [see Boxed Warning and Warnings and Precautions (5.1)]. Hepatotoxicity [see Warnings and Precautions (5.2)] Orthostatic Hypotension, Falls and Syncope [see Warnings and Precautions (5.3)] Serotonin Syndrome [see Warnings and Precautions (5.4)] Abnormal Bleeding [see Warnings and Precautions (5.5)] Severe Skin Reactions [see Warnings and Precautions (5.6)] Discontinuation of Treatment with duloxetine delayed-release capsules [see Warnings and Precautions (5.7)] Activation of Mania/Hypomania [see Warnings and Precautions (5.8)] Angle-Closure Glaucoma [see Warnings and Precautions (5.9)] Seizures [see Warnings and Precautions (5.10)] Effect on Blood Pressure [see Warnings and Precautions (5.11)] Clinically Important Drug Interactions [see Warnings and Precautions (5.12)] Hyponatremia [see Warnings and Precautions (5.13)] Urinary Hesitation and Retention [see Warnings and Precautions (5.15)] 6.1 Clinical Trial Data Sources. 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 stated frequencies of adverse reactions represent the proportion of individuals who experienced, at least once, treatment-emergent adverse reaction of the type listed. reaction was considered treatment-emergent if it occurred for the first time or worsened while receiving therapy following baseline evaluation. Reactions reported during the studies were not necessarily caused by the therapy, and the frequencies do not reflect investigator impression (assessment) of causality.Adults -- The data described below reflect exposure to duloxetin in placebo-controlled trials for MDD (N=3779), GAD (N=1018), OA (N=503), CLBP (N=600), DPNP (N=906), and another indication (N=1294). The population studied was 17 to 89 years of age; 65.7%, 60.8%, 60.6%, 42.9%, and 94.4% female; and 81.8%, 72.6%, 85.3%, 74.0%, and 85.7% Caucasian for MDD, GAD, OA and CLBP, DPNP, and another indication, respectively. Most patients received doses of total of 60 to 120 mg per day [see Clinical Studies (14)].Information describing two additional clinical studies in which efficacy was not demonstrated in patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. Other pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. 6.2 Adverse Reactions Reported as Reasons for Discontinuation of Treatment in Adult Placebo-Controlled Trials. Major Depressive Disorder -- Approximately 8.4% (319/3779) of the patients who received duloxetine in placebo-controlled trials for MDD discontinued treatment due to an adverse reaction, compared with 4.6% (117/2536) of the patients receiving placebo. Nausea (duloxetine 1.1%, placebo 0.4%) was the only common adverse reaction reported as reason for discontinuation and considered to be drug-related (i.e., discontinuation occurring in at least 1% of the duloxetine-treated patients and at rate of at least twice that of placebo).Generalized Anxiety Disorder -- Approximately 13.7% (139/1018) of the patients who received duloxetine in placebo-controlled trials for GAD discontinued treatment due to an adverse reaction, compared with 5.0% (38/767) for placebo. Common adverse reactions reported as reason for discontinuation and considered to be drug-related (as defined above) included nausea (duloxetine 3.3%, placebo 0.4%), and dizziness (duloxetine 1.3%, placebo 0.4%).Diabetic Peripheral Neuropathic Pain -- Approximately 12.9% (117/906) of the patients who received duloxetine in placebo-controlled trials for DPNP discontinued treatment due to an adverse reaction, compared with 5.1% (23/448) for placebo. Common adverse reactions reported as reason for discontinuation and considered to be drug-related (as defined above) included nausea (duloxetine 3.5%, placebo 0.7%), dizziness (duloxetine 1.2%, placebo 0.4%), and somnolence (duloxetine 1.1%, placebo 0.0%). Chronic Pain due to Osteoarthritis -- Approximately 15.7% (79/503) of the patients who received duloxetine in 13-week, placebo-controlled trials for chronic pain due to OA discontinued treatment due to an adverse reaction, compared with 7.3% (37/508) for placebo. Common adverse reactions reported as reason for discontinuation and considered to be drug-related (as defined above) included nausea (duloxetine 2.2%, placebo 1.0%).Chronic Low Back Pain -- Approximately 16.5% (99/600) of the patients who received duloxetine in 13-week, placebo-controlled trials for CLBP discontinued treatment due to an adverse reaction, compared with 6.3% (28/441) for placebo. Common adverse reactions reported as reason for discontinuation and considered to be drug-related (as defined above) included nausea (duloxetine 3.0%, placebo 0.7%), and somnolence (duloxetine 1.0%, placebo 0.0%). 6.3 Most Common Adult Adverse Reactions. Pooled Trials for all Approved Indications -- The most commonly observed adverse reactions in duloxetine-treated patients (incidence of at least 5% and at least twice the incidence in placebo patients) were nausea, dry mouth, somnolence, constipation, decreased appetite, and hyperhidrosis. Diabetic Peripheral Neuropathic Pain -- The most commonly observed adverse reactions in duloxetine-treated patients (as defined above) were nausea, somnolence, decreased appetite, constipation, hyperhidrosis, and dry mouth.Chronic Pain due to Osteoarthritis -- The most commonly observed adverse reactions in duloxetine-treated patients (as defined above) were nausea, fatigue, constipation, dry mouth, insomnia, somnolence, and dizziness.Chronic Low Back Pain -- The most commonly observed adverse reactions in duloxetine-treated patients (as defined above) were nausea, dry mouth, insomnia, somnolence, constipation, dizziness, and fatigue. 6.4 Adverse Reactions Occurring at an Incidence of 5% or More Among Duloxetine-Treated Patients in Adult Placebo-Controlled Trials. Table gives the incidence of treatment-emergent adverse reactions in placebo-controlled trials for approved indications that occurred in 5% or more of patients treated with duloxetine and with an incidence greater than placebo.Table 2: Treatment-Emergent Adverse Reactions: Incidence of 5% or More and Greater than Placebo in Placebo-Controlled Trials of Approved Indicationsa aThe inclusion of an event in the table is determined based on the percentages before rounding; however, the percentages displayed in the table are rounded to the nearest integer. Also includes asthenia. Events for which there was significant dose-dependent relationship in fixed-dose studies, excluding three MDD studies which did not have placebo lead-in period or dose titration. Also includes initial insomnia, middle insomnia, and early morning awakening. Also includes hypersomnia and sedation. Also includes abdominal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness, and gastrointestinal pain. Percentage of Patients Reporting Reaction Adverse Reaction Duloxetine N 8100 Placebo N 5655 Nauseac 23 Headache 14 12 Dry mouth 13 Somnolencee 10 Fatigueb c 5 Insomniad 5 Constipationc 4 Dizzinessc 5 Diarrhea 6 Decreased appetitec 2 Hyperhidrosisc 1 Abdominal painf 4 6.5 Adverse Reactions Occurring at an Incidence of 2% or More Among Duloxetine-Treated Patients in Adult Placebo-Controlled Trials. Pooled MDD and GAD Trials -- Table gives the incidence of treatment-emergent adverse reactions in MDD and GAD placebo-controlled trials for approved indications that occurred in 2% or more of patients treated with duloxetine and with an incidence greater than placebo. Table 3: Treatment-Emergent Adverse Reactions: Incidence of 2% or More and Greater than Placebo in MDD and GAD Placebo-Controlled Trialsa b The inclusion of an event in the table is determined based on the percentages before rounding; however, the percentages displayed in the table are rounded to the nearest integer. bFor GAD, there were no adverse events that were significantly different between treatments in adults >=65 years that were also not significant in the adults <65 years. cEvents for which there was significant dose-dependent relationship in fixed-dose studies, excluding three MDD studies which did not have placebo lead-in period or dose titration. dAlso includes abdominal pain upper, abdominal pain lower, abdominal tenderness, abdominal discomfort, and gastrointestinal pain Also includes asthenia Also includes hypersomnia and sedation Also includes initial insomnia, middle insomnia, and early morning awakening hAlso includes feeling jittery, nervousness, restlessness, tension and psychomotor hyperactivity Also includes loss of libido Also includes anorgasmia System Organ Class Adverse Reaction Percentage of Patients Reporting Reaction Duloxetine N 4797 Placebo N 3303 Cardiac Disorders Palpitations 1 Eye Disorders Vision blurred 1 Gastrointestinal Disorders Nauseac 25 Dry mouth 14 Constipationc 4 Diarrhea 6 Abdominal paind 4 Vomiting 2 General Disorders and Administration Site Conditions Fatiguee 5 Metabolism and Nutrition Disorders Decreased appetitec 2 Nervous System Disorders Headache 14 14 Dizzinessc 5 Somnolencef 3 Tremor 1 Psychiatric Disorders Insomniag 5 Agitationh 2 Anxiety 2 Reproductive System and Breast Disorders Erectile dysfunction 1 Ejaculation delayedc 1 Libido decreasedi 1 Orgasm abnormalj <1 Respiratory Thoracic and Mediastinal Disorders Yawning <1 Skin and Subcutaneous Tissue Disorders Hyperhidrosis 2 DPNP, another indication, OA, and CLBP -- Table gives the incidence of treatment-emergent adverse events that occurred in 2% or more of patients treated with duloxetine (determined prior to rounding) in the premarketing acute phase of DPNP, another indication, OA, and CLBP placebo-controlled trials and with an incidence greater than placebo.Table 4: Treatment-Emergent Adverse Reactions: Incidence of 2% or More and Greater than Placebo in DPNP, Another Indication, OA and CLBP Placebo-Controlled Trialsa The inclusion of an event in the table is determined based on the percentages before rounding; however, the percentages displayed in the table are rounded to the nearest integer. Incidence of 120 mg/day is significantly greater than the incidence for 60 mg/day. Also includes abdominal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness and gastrointestinal pain Also includes asthenia Also includes myalgia and neck pain Also includes hypersomnia and sedation Also includes hypoaesthesia, hypoaesthesia facial, genital hypoaesthesia and paraesthesia oral Also includes initial insomnia, middle insomnia, and early morning awakening. iAlso includes feeling jittery, nervousness, restlessness, tension and psychomotor hyperactivity Also includes ejaculation failure Also includes hot flush Also includes blood pressure diastolic increased, blood pressure systolic increased, diastolic hypertension, essential hypertension, hypertension, hypertensive crisis, labile hypertension, orthostatic hypertension, secondary hypertension, and systolic hypertension System Organ Class Adverse Reaction Percentage of Patients Reporting Reaction Duloxetine N 3303 Placebo N 2352 Gastrointestinal Disorders Nausea 23 Dry Mouthb 11 Constipationb 10 Diarrhea 5 Abdominal Painc 4 Vomiting 2 Dyspepsia 1 General Disorders and Administration Site Conditions Fatigued 11 Infections and Infestations Nasopharyngitis 4 Upper Respiratory Tract Infection 3 Influenza 0 Metabolism and Nutrition Disorders Decreased Appetiteb 1 Musculoskeletal and Connective Tissue Musculoskeletal Paine 3 Muscle Spasms 2 Nervous System Disorders Headache 13 Somnolenceb f 11 Dizziness 5 Paraesthesiag 2 Tremorb <1 Psychiatric Disorders Insomniab h 10 Agitationi 1 Reproductive System and Breast Disorders Erectile dysfunctionb <1 Ejaculation Disorderj <1 Respiratory Thoracic and Mediastinal Disorders Cough 2 Skin and Subcutaneous Tissue Disorders Hyperhidrosis 1 Vascular Disorders Flushingk 1 Blood pressure increasedl 1 6.6 Effects on Male and Female Sexual Function in Adults. Changes in sexual desire, sexual performance and sexual satisfaction often occur as manifestations of psychiatric disorders or diabetes, but they may also be consequence of pharmacologic treatment. Because adverse sexual reactions are presumed to be voluntarily underreported, the Arizona Sexual Experience Scale (ASEX), validated measure designed to identify sexual side effects, was used prospectively in MDD placebo-controlled trials. In these trials, as shown in Table below, patients treated with duloxetine experienced significantly more sexual dysfunction, as measured by the total score on the ASEX, than did patients treated with placebo. Gender analysis showed that this difference occurred only in males. Males treated with duloxetine experienced more difficulty with ability to reach orgasm (ASEX Item 4) than males treated with placebo. Females did not experience more sexual dysfunction on duloxetine than on placebo as measured by ASEX total score. Negative numbers signify an improvement from baseline level of dysfunction, which is commonly seen in depressed patients. Physicians should routinely inquire about possible sexual side effects. Table 5: Mean Change in ASEX Scores by Gender in MDDPlacebo-Controlled Trials n=Number of patients with non-missing change score for ASEX total p=0.013 versus placebo p<0.001 versus placebo Male Patientsa Female Patientsa Duloxetine n 175 Placebo n 83 Duloxetine n 241 Placebo n 126 ASEX Total (Items to 5) 0.56b -1.07 -1.15 -1.07 Item -- Sex drive -0.07 -0.12 -0.32 -0.24 Item -- Arousal 0.01 -0.26 -0.21 -0.18 Item -- Ability to achieve erection (men); Lubrication (women) 0.03 -0.25 -0.17 -0.18 Item -- Ease of reaching orgasm 0.40c -0.24 -0.09 -0.13 Item -- Orgasm satisfaction 0.09 -0.13 -0.11 -0.17 6.7 Vital Sign Changes in Adults. In placebo-controlled clinical trials across approved indications for change from baseline to endpoint, duloxetine treatment was associated with mean increases of 0.23 mm Hg in systolic blood pressure and 0.73 mm Hg in diastolic blood pressure compared to mean decreases of 1.09 mm Hg systolic and 0.55 mm Hg diastolic in placebo-treated patients. There was no significant difference in the frequency of sustained (3 consecutive visits) elevated blood pressure [see Warnings and Precautions (5.3, 5.11)]. Duloxetine treatment, for up to 26 weeks in placebo-controlled trials across approved indications, typically caused small increase in heart rate for change from baseline to endpoint compared to placebo of up to 1.37 beats per minute (increase of 1.20 beats per minute in duloxetine-treated patients, decrease of 0.17 beats per minute in placebo-treated patients).. 6.8 Laboratory Changes in Adults. Duloxetine treatment in placebo-controlled clinical trials across approved indications, was associated with small mean increases from baseline to endpoint in ALT, AST, CPK, and alkaline phosphatase; infrequent, modest, transient, abnormal values were observed for these analytes in duloxetine-treated patients when compared with placebo-treated patients [see Warnings and Precautions (5.2)]. High bicarbonate, cholesterol, and abnormal (high or low) potassium, were observed more frequently in duloxetine treated patients compared to placebo. 6.9 Electrocardiogram Changes in Adults. The effect of duloxetine 160 mg and 200 mg administered twice daily to steady state was evaluated in randomized, double-blinded, two-way crossover study in 117 healthy female subjects. No QT interval prolongation was detected. Duloxetine appears to be associated with concentration-dependent but not clinically meaningful QT shortening.. 6.10 Other Adverse Reactions Observed During the Premarketing and Postmarketing Clinical Trial Evaluation of Duloxetine in Adults. Following is list of treatment-emergent adverse reactions reported by patients treated with duloxetine in clinical trials. In clinical trials of all indications, 34,756 patients were treated with duloxetine. Of these, 26.9% (9337) took duloxetine for at least months, and 12.4% (4317) for at least one year. The following listing is not intended to include reactions (1) already listed in previous tables or elsewhere in labeling, (2) for which drug cause was remote, (3) which were so general as to be uninformative, (4) which were not considered to have significant clinical implications, or (5) which occurred at rate equal to or less than placebo. Reactions are categorized by body system according to the following definitions: frequent adverse reactions are those occurring in at least 1/100 patients; infrequent adverse reactions are those occurring in 1/100 to 1/1000 patients; rare reactions are those occurring in fewer than 1/1000 patients. Cardiac Disorders -- Frequent: palpitations; Infrequent: myocardial infarction and tachycardia. Ear and Labyrinth Disorders -- Frequent: vertigo; Infrequent: ear pain and tinnitus. Endocrine Disorders -- Infrequent: hypothyroidism. Eye Disorders -- Frequent: vision blurred; Infrequent: diplopia, dry eye, and visual impairment.Gastrointestinal Disorders -- Frequent: flatulence; Infrequent: dysphagia, eructation, gastritis, gastrointestinal hemorrhage, halitosis, and stomatitis; Rare: gastric ulcer. General Disorders and Administration Site Conditions -- Frequent: chills/rigors; Infrequent: falls, feeling abnormal, feeling hot and/or cold, malaise, and thirst; Rare: gait disturbance. Infections and Infestations -- Infrequent: gastroenteritis and laryngitis. Investigations -- Frequent: weight increased, weight decreased; Infrequent: blood cholesterol increased. Metabolism and Nutrition Disorders -- Infrequent: dehydration and hyperlipidemia; Rare: dyslipidemia. Musculoskeletal and Connective Tissue Disorders -- Frequent: musculoskeletal pain; Infrequent: muscle tightness and muscle twitching.Nervous System Disorders -- Frequent: dysgeusia, lethargy, and paraesthesia/hypoesthesia; Infrequent: disturbance in attention, dyskinesia, myoclonus, and poor quality sleep; Rare: dysarthria. Psychiatric Disorders -- Frequent: abnormal dreams and sleep disorder; Infrequent: apathy, bruxism, disorientation/confusional state, irritability, mood swings, and suicide attempt; Rare: completed suicide. Renal and Urinary Disorders -- Frequent: urinary frequency; Infrequent: dysuria, micturition urgency, nocturia, polyuria, and urine odor abnormal. Reproductive System and Breast Disorders -- Frequent: anorgasmia/orgasm abnormal; Infrequent: menopausal symptoms, sexual dysfunction, and testicular pain; Rare: menstrual disorder. Respiratory, Thoracic and Mediastinal Disorders -- Frequent: yawning, oropharyngeal pain; Infrequent: throat tightness. Skin and Subcutaneous Tissue Disorders -- Frequent: pruritus; Infrequent: cold sweat, dermatitis contact, erythema, increased tendency to bruise, night sweats, and photosensitivity reaction; Rare: ecchymosis. Vascular Disorders -- Frequent: hot flush; Infrequent: flushing, orthostatic hypotension, and peripheral coldness.. 6.11 Adverse Reactions Observed in Children and Adolescent Placebo-Controlled Clinical Trials. The adverse drug reaction profile observed in pediatric clinical trials (children and adolescents) was consistent with the adverse drug reaction profile observed in adult clinical trials. The specific adverse drug reactions observed in adult patients can be expected to be observed in pediatric patients (children and adolescents) [see Adverse Reactions (6.5)]. The most common (>=5% and twice placebo) adverse reactions observed in pediatric clinical trials include: nausea, diarrhea, decreased weight, and dizziness. Table provides the incidence of treatment-emergent adverse reactions in pediatric placebo- controlled trials that occurred in greater than 2% of patients treated with duloxetine and with an incidence greater than placebo.Table 6: Treatment-Emergent Adverse Reactions: Incidence of 2% or More and Greater than Placebo in three 10- week Pediatric Placebo-Controlled Trialsa aThe inclusion of an event in the table is determined based on the percentages before rounding; however, the percentages displayed in the table are rounded to the nearest integer. bAlso includes abdominal pain upper, abdominal pain lower, abdominal tenderness, abdominal discomfort, and gastrointestinal pain. cAlso includes asthenia. dFrequency based on weight measurement meeting potentially clinically significant threshold of >=3.5% weight loss (N=467 duloxetine; N=354 Placebo). eAlso includes hypersomnia and sedation. fAlso includes initial insomnia, insomnia, middle insomnia, and terminal insomnia. System Organ Class Adverse Reaction Percentage of Pediatric Patients Reporting Reaction Duloxetine N 476 Placebo N 362 Gastrointestinal Disorders Nausea 18 Abdominal Painb 13 10 Vomiting 4 Diarrhea 3 Dry Mouth 1 General Disorders and Administration Site Conditions Fatiguec 5 Investigations Decreased Weightd 14 Metabilism and Nutrition Disorders Decreased Appetite 10 Nervous System Disorders Headache 18 13 Somnolence 11 Dizziness 4 Psychiatric Disorders Insomniaf 4 Respiratory Thoracic and Mediastinal Disorders Oropharyngeal Pain 2 Cough 1 Other adverse reactions that occurred at an incidence of less than 2% but were reported by more duloxetine treated patients than placebo treated patients and are associated duloxetine treatment: abnormal dreams (including nightmare), anxiety, flushing (including hot flush), hyperhidrosis, palpitations, pulse increased, and tremor. Discontinuation-emergent symptoms have been reported when stopping duloxetine delayed-release capsules. The most commonly reported symptoms following discontinuation of duloxetine in pediatric clinical trials have included headache, dizziness, insomnia, and abdominal pain [see Warnings and Precautions (5.7) and Adverse Reactions (6.2)]. Growth (Height and Weight) -- Decreased appetite and weight loss have been observed in association with the use of SSRIs and SNRIs. In studies up to months, duloxetine-treated pediatric patients experienced an increase in height of 1.7 cm on average (2.2 cm increase in children [7 to 11 years of age] and 1.3 cm increase in adolescents [12 to 17 years of age]). While height increase was observed during these studies, mean decrease of 1% in height percentile was observed (decrease of 2% in children [7 to 11 years of age] and increase of 0.3% in adolescents [12 to 17 years of age]). Weight and height should be monitored regularly in children and adolescents treated with duloxetine. Information describing two additional clinical studies in which efficacy was not demonstrated in patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. Other pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. 6.12 Postmarketing Spontaneous Reports. The following adverse reactions have been identified during post approval use of duloxetine delayed-release capsules. 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. Adverse reactions reported since market introduction that were temporally related to duloxetine therapy and not mentioned elsewhere in labeling include: acute pancreatitis, anaphylactic reaction, aggression and anger (particularly early in treatment or after treatment discontinuation), angioneurotic edema, angle-closure glaucoma, colitis (microscopic or unspecified), cutaneous vasculitis (sometimes associated with systemic involvement), extrapyramidal disorder, galactorrhea, gynecological bleeding, hallucinations, hyperglycemia, hyperprolactinemia, hypersensitivity, hypertensive crisis, muscle spasm, rash, restless legs syndrome, seizures upon treatment discontinuation, supraventricular arrhythmia, tinnitus (upon treatment discontinuation), trismus, and urticaria.

CLINICAL STUDIES SECTION.

14 CLINICAL STUDIES. The efficacy of duloxetine has been established in the following adequate and well-controlled trials: Major Depressive Disorder (MDD): short-term and maintenance trial in adults [see Clinical Studies (14.1)] .Generalized Anxiety Disorder (GAD): short-term trials in adults, maintenance trial in adults [see Clinical Studies (14.2)] .Diabetic Peripheral Neuropathic Pain (DPNP): Two 12-week trials in adults [see Clinical Studies (14.3)] .Chronic Musculoskeletal Pain: Two 12- to 13-week trials in adult patients with chronic low back pain (CLBP) and one 13-week trial in adult patients with chronic pain due to osteoarthritis [see Clinical Studies (14.5)] .Pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. Major Depressive Disorder (MDD): short-term and maintenance trial in adults [see Clinical Studies (14.1)] .. Generalized Anxiety Disorder (GAD): short-term trials in adults, maintenance trial in adults [see Clinical Studies (14.2)] .. Diabetic Peripheral Neuropathic Pain (DPNP): Two 12-week trials in adults [see Clinical Studies (14.3)] .. Chronic Musculoskeletal Pain: Two 12- to 13-week trials in adult patients with chronic low back pain (CLBP) and one 13-week trial in adult patients with chronic pain due to osteoarthritis [see Clinical Studies (14.5)] .. 14.1 Major Depressive Disorder. The efficacy of duloxetine as treatment for depression was established in randomized, double-blind, placebo-controlled, fixed-dose studies in adult outpatients (18 to 83 years) meeting DSM-IV criteria for major depression. In studies, patients were randomized to duloxetine 60 mg once daily (N=123 and N=128, respectively) or placebo (N=122 and N=139, respectively) for weeks; in the third study, patients were randomized to duloxetine 20 or 40 mg twice daily (N=86 and N=91, respectively) or placebo (N=89) for weeks; in the fourth study, patients were randomized to duloxetine 40 or 60 mg twice daily (N=95 and N=93, respectively) or placebo (N=93) for weeks. There is no evidence that doses greater than 60 mg/day confer additional benefits. In all studies, duloxetine demonstrated superiority over placebo as measured by improvement in the 17-text Hamilton Depression Rating Scale (HAMD-17) total score (Studies to in Table 7). In all of these clinical studies, analyses of the relationship between treatment outcome and age, gender, and race did not suggest any differential responsiveness on the basis of these patient characteristics.Table 7: Summary of the Primary Efficacy Results for Studies in Major Depressive Disorder SD: standard deviation; SE: standard error; LS Mean: least-squares mean; CI: confidence interval, not adjusted for multiplicity in trials where multiple dose groups were included. aDifference (drug minus placebo) in least-squares mean change from baseline. Doses statistically significantly superior to placebo. Primary Efficacy Measure HAMD 17 Study Number Treatment Group Mean Baseline Score SD LS Mean Change from Baseline SE Placebo subtracted Differencea 95 Cl Study Duloxetine (60 mg/day) 21.5 (4.10) -10.9 (0.70) -4.9 (-6.8, -2.9) Placebo 21.1 (3.71) -6.1 (0.69) -- Study Duloxetine (60 mg/day) 20.3 (3.32) -10.5 (0.71) -2.2 (-4.0, -0.3) Placebo 20.5 (3.42) -8.3 (0.67) Study Duloxetine (20 mg BID) 18.6 (5.85) -7.4 (0.80) -2.4 (-4.7, -0.2) Duloxetine (40 mg BID) 18.1 (4.52) -8.6 (0.81) -3.6 (-5.9, -1.4) Placebo 17.2 (5.11) -5.0 (0.81) -- Study Duloxetine (40 mg BID) 19.9 (3.54) -11.0 (0.49) -2.2 (-3.6, -0.9) Duloxetine (60 mg BID) 20.2 (3.41) -12.1 (0.49) -3.3 (-4.7, -1.9) Placebo 19.9 (3.58) -8.8 (0.50) -- In another study, 533 patients meeting DSM-IV criteria for MDD received duloxetine 60 mg once daily during an initial 12-week open-label treatment phase. Two hundred and seventy-eight patients who responded to open label treatment (defined as meeting the following criteria at weeks 10 and 12: HAMD-17 total score <=9, Clinical Global Impressions of Severity (CGI-S) <=2, and not meeting the DSM-IV criteria for MDD) were randomly assigned to continuation of duloxetine at the same dose (N=136) or to placebo (N=142) for months. Patients on duloxetine experienced statistically significantly longer time to relapse of depression than did patients on placebo (Study in Figure 1). Relapse was defined as an increase in the CGI-S score of >=2 points compared with that obtained at week 12, as well as meeting theDSM-IV criteria for MDD at consecutive visits at least weeks apart, where the 2-week temporal criterion had to be satisfied at only the second visit. The effectiveness of duloxetine in hospitalized patients with major depressive disorder has not been studied.. Figure 1. 14.2 Generalized Anxiety Disorder. The efficacy of duloxetine in the treatment of generalized anxiety disorder (GAD) was established in fixed-dose randomized, double-blind, placebo-controlled trial and flexible-dose randomized, double-blind, placebo-controlled trials in adult outpatients between 18 and 83 years of age meeting the DSM-IV criteria for GAD. In flexible-dose study and in the fixed-dose study, the starting dose was 60 mg once daily where down titration to 30 mg once daily was allowed for tolerability reasons before increasing it to 60 mg once daily. Fifteen percent of patients were down titrated. One flexible-dose study had starting dose of 30 mg once daily for week before increasing it to 60 mg once daily. The flexible-dose studies involved dose titration with duloxetine doses ranging from 60 mg once daily to 120 mg once daily (N=168 and N=162) compared to placebo (N=159 and N=161) over 10-week treatment period. The mean dose for completers at endpoint in the flexible-dose studies was 104.75 mg/day. The fixed-dose study evaluated duloxetine doses of 60 mg once daily (N=168) and 120 mg once daily (N=170) compared to placebo (N=175) over 9-week treatment period. While 120 mg/day dose was shown to be effective, there is no evidence that doses greater than 60 mg/day confer additional benefit. In all studies, duloxetine demonstrated superiority over placebo as measured by greater improvement in the Hamilton Anxiety Scale (HAM-A) total score (Studies to in Table 8) and by the Sheehan Disability Scale (SDS) global functional impairment score. The SDS is composite measurement of the extent emotional symptoms disrupt patient functioning in life domains: work/school, social life/leisure activities, and family life/home responsibilities.In another study, 887 patients meeting DSM-IV-TR criteria for GAD received duloxetine 60 mg to 120 mg once daily during an initial 26-week open-label treatment phase. Four hundred and twenty-nine patients who responded to open-label treatment (defined as meeting the following criteria at weeks 24 and 26: decrease from baseline HAM-A total score by at least 50% to score no higher than 11, and Clinical Global Impressions of Improvement [CGI-Improvement] score of or 2) were randomly assigned to continuation of duloxetine at the same dose (N=216) or to placebo (N=213) and were observed for relapse. Of the patients randomized, 73% had been in responder status for at least 10 weeks. Relapse was defined as an increase in CGI-Severity score at least points to score >=4 and MINI (Mini-International Neuropsychiatric Interview) diagnosis of GAD (excluding duration), or discontinuation due to lack of efficacy. Patients taking duloxetine experienced statistically significantly longer time to relapse of GAD than did patients taking placebo (Study in Figure 2).Subgroup analyses did not indicate that there were any differences in treatment outcomes as function of age or gender. Table 8: Summary of the Primary Efficacy Results for Studies in General Anxiety Disorder SD: standard deviation; SE: standard error; LS Mean: least-squares mean; CI: confidence interval, not adjusted for multiplicity in trials where multiple dose groups were included. aDifference (drug minus placebo) in least squares mean change from baseline. bDose statistically significantly superior to placebo. Study Treatment Group Primary Efficacy Measure Number Mean Baseline Score SD LS Mean Change from Baseline SE Placebo substracted Differencea 95 Cl Study (HAM-A) Duloxetine (60mg/day)b 25.1 (7.18) -12.8 (0.68) -4.4 (-6.2, -2.5) Duloxetine (120mg/day)b 25.1 (7.24) -12.5 (0.67) -4.1 (-5.9, -2.3) Placebo 25.8 (7.66) -8.4 (0.67) -- Study (HAM-A) Duloxetine (60 to 120mg/day)b 22.5 (7.44) -8.1 (0.70) -2.2 (-4.2, -0.3) Placebo 23.5 (7.91) -5.9 (0.70) -- Study (HAM-A) Duloxetine (60 to 120mg/day)b 25.8 (5.66) -11.8 (0.69) -2.6 (-4.5, -0.7) Placebo 25.0 (5.82) -9.2 (0.67) -- Figure 2: Kaplan-Meier Estimation of Cumulative Proportion of Patients with Relapse (GAD Study 4)Pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. Figure 2. 14.3 Diabetic Peripheral Neuropathic Pain. The efficacy of duloxetine for the management of neuropathic pain associated with diabetic peripheral neuropathy was established in randomized, 12-week, double-blind, placebo-controlled, fixed-dose studies in adult patients having diabetic peripheral neuropathic pain for at least months. Study DPNP-1 and Study DPNP-2 enrolled total of 791 patients of whom 592 (75%) completed the studies. Patients enrolled had Type or II diabetes mellitus with diagnosis of painful distal symmetrical sensorimotor polyneuropathy for at least months. The patients had baseline pain score of >=4 on an 11-point scale ranging from (no pain) to 10 (worst possible pain). Patients were permitted up to g of acetaminophen per day as needed for pain, in addition to duloxetine. Patients recorded their pain daily in diary. Both studies compared duloxetine 60 mg once daily or 60 mg twice daily with placebo. DPNP-1 additionally compared duloxetine 20 mg with placebo. total of 457 patients (342 duloxetine, 115 placebo) were enrolled in DPNP-1 and total of 334 patients (226 duloxetine, 108 placebo) were enrolled in DPNP-2. Treatment with duloxetine 60 mg one or two times day statistically significantly improved the endpoint mean pain scores from baseline and increased the proportion of patients with at least 50% reduction in pain scores from baseline. For various degrees of improvement in pain from baseline to study endpoint, Figures and show the fraction of patients achieving that degree of improvement. The figures are cumulative, so that patients whose change from baseline is, for example, 50%, are also included at every level of improvement below 50%. Patients who did not complete the study were assigned 0% improvement. Some patients experienced decrease in pain as early as week 1, which persisted throughout the study.. Figure 3. Figure 4. 14.5 Chronic Musculoskeletal Pain. Duloxetine is indicated for the management of chronic musculoskeletal pain. This has been established in studies in patients with chronic low back pain and chronic pain due to osteoarthritis.Studies in Chronic Low Back Pain The efficacy of duloxetine in chronic low back pain (CLBP) was assessed in two double-blind, placebo-controlled, randomized clinical trials of 13-weeks duration (Study CLBP-1 and Study CLBP-2), and one of 12-weeks duration (CLBP-3). CLBP-1 and CLBP-3 demonstrated efficacy of duloxetine in the treatment of chronic low back pain. Patients in all studies had no signs of radiculopathy or spinal stenosis.Study CLBP-1: Two hundred thirty-six adult patients (N=115 on duloxetine, N=121 on placebo) enrolled and 182 (77%) completed 13-week treatment phase. After weeks of treatment, duloxetine patients with less than 30% reduction in average daily pain and who were able to tolerate duloxetine 60 mg once daily had their dose of duloxetine, in double-blinded fashion, increased to 120 mg once daily for the remainder of the study. Patients had mean baseline pain rating of on numerical rating scale ranging from (no pain) to 10 (worst possible pain). After 13 weeks of treatment, patients taking duloxetine 60 to 120 mg daily had significantly greater pain reduction compared to placebo. Randomization was stratified by the patients baseline NSAIDs-use status. Subgroup analyses did not indicate that there were differences in treatment outcomes as function of NSAIDs use.Study CLBP-2: Four hundred and four patients were randomized to receive fixed doses of duloxetine daily or matching placebo (N=59 on duloxetine 20 mg, N=116 on duloxetine 60 mg, N=112 on duloxetine 120 mg, N=117 on placebo) and 267 (66%) completed the entire 13-week study. After 13 weeks of treatment, none of the three duloxetine doses showed statistically significant difference in pain reduction compared to placebo.Study CLBP-3: Four hundred and one patients were randomized to receive fixed doses of duloxetine 60 mg daily or placebo (N=198 on duloxetine, N=203 on placebo), and 303 (76%) completed the study. Patients had mean baseline pain rating of on numerical rating scale ranging from (no pain) to 10 (worst possible pain). After 12 weeks of treatment, patients taking duloxetine 60 mg daily had significantly greater pain reduction compared to placebo. For various degrees of improvement in pain from baseline to study endpoint, Figures and show the fraction of patients in CLBP-1 and CLBP-3 achieving that degree of improvement. The figures are cumulative, so that patients whose change from baseline is, for example, 50%, are also included at every level of improvement below 50%. Patients who did not complete the study were assigned the value of 0% improvement.Studies in Chronic Pain Due to Osteoarthritis The efficacy of duloxetine in chronic pain due to osteoarthritis was assessed in double-blind, placebo-controlled, randomized clinical trials of 13-weeks duration (Study OA-1 and Study OA-2). All patients in both studies fulfilled the ACR clinical and radiographic criteria for classification of idiopathic osteoarthritis of the knee. Randomization was stratified by the patients baseline NSAIDs-use status. Patients assigned to duloxetine started treatment in both studies at dose of 30 mg once daily for one week. After the first week, the dose of duloxetine was increased to 60 mg once daily. After weeks of treatment with duloxetine 60 mg once daily, in OA-1 patients with sub-optimal response to treatment (<30% pain reduction) and tolerated duloxetine 60 mg once daily had their dose increased to 120 mg. However, in OA-2, all patients, regardless of their response to treatment after weeks, were re-randomized to either continue receiving duloxetine 60 mg once daily or have their dose increased to 120 mg once daily for the remainder of the study. Patients in the placebo treatment groups in both studies received matching placebo for the entire duration of studies. For both studies, efficacy analyses were conducted using 13-week data from the combined duloxetine 60 mg and 120 mg once daily treatment groups compared to the placebo group. Study OA-1: Two hundred fifty-six patients (N=128 on duloxetine, N=128 on placebo) enrolled and 204 (80%) completed the study. Patients had mean baseline pain rating of on numerical rating scale ranging from (no pain) to 10 (worst possible pain). After 13 weeks of treatment, patients taking duloxetine had significantly greater pain reduction. Subgroup analyses did not indicate that there were differences in treatment outcomes as function of NSAIDs use. Study OA-2: Two hundred thirty-one patients (N=111 on duloxetine, N=120 on placebo) enrolled and 173 (75%) completed the study. Patients had mean baseline pain of on numerical rating scale ranging from (no pain) to 10 (worst possible pain). After 13 weeks of treatment, patients taking duloxetine did not show significantly greater pain reduction. In Study OA-1, for various degrees of improvement in pain from baseline to study endpoint, Figure shows the fraction of patients achieving that degree of improvement. The figure is cumulative, so that patients whose change from baseline is, for example, 50%, are also included at every level of improvement below 50%. Patients who did not complete the study were assigned the value of 0% improvement.. Figure 7. Figure 8. Figure 9.

DOSAGE & ADMINISTRATION SECTION.

2 DOSAGE AND ADMINISTRATION. Take duloxetine delayed-release capsule once daily, with or without food. Swallow duloxetine delayed-release capsule whole; do not crush or chew, do not open capsule. Take missed dose as soon as it is remembered. Do not take two doses of duloxetine delayed-release capsules at the same time. (2)Indication Starting Dose Target Dose Maximum Dose MDD (2.1) 40 mg/day to 60 mg/day AcuteTreatment:40 mg/day (20 mg twice daily) to 60 mg/day (once daily or as 30 mg twice daily); Maintenance Treatment: 60 mg/day 120 mg/day GAD (2.2)Adults 60 mg/day 60 mg/day(once daily) 120 mg/day DPNP (2.3) 60 mg/day 60 mg/day (once daily) 60 mg/day Chronic Musculoskeletal Pain (2.5) 30 mg/day 60 mg/day (once daily) 60 mg/daySome patients may benefit from starting at 30 mg once daily (2)There is no evidence that doses greater than 60 mg/day confers additional benefit, while some adverse reactions were observed to be dose-dependent (2)Discontinuing duloxetine delayed-release capsules: Gragually reduce dosage to avoid discontinuation symptoms (2.7, 5.7)Hepatic Impairment: Avoid use in patients with chronic liver disease or cirrhosis (5.14)Renal Impairment: Avoid use in patients with severe renal impairment, GFR <30 mL/min (5.14). Take duloxetine delayed-release capsule once daily, with or without food. Swallow duloxetine delayed-release capsule whole; do not crush or chew, do not open capsule. Take missed dose as soon as it is remembered. Do not take two doses of duloxetine delayed-release capsules at the same time. (2). Some patients may benefit from starting at 30 mg once daily (2). There is no evidence that doses greater than 60 mg/day confers additional benefit, while some adverse reactions were observed to be dose-dependent (2). Discontinuing duloxetine delayed-release capsules: Gragually reduce dosage to avoid discontinuation symptoms (2.7, 5.7). Hepatic Impairment: Avoid use in patients with chronic liver disease or cirrhosis (5.14). Renal Impairment: Avoid use in patients with severe renal impairment, GFR <30 mL/min (5.14). Swallow duloxetine delayed-release capsules whole. Do not chew or crush. Do not open the capsule and sprinkle its contents on food or mix with liquids. All of these might affect the enteric coating. Duloxetine delayed-release capsules can be given without regard to meals. If dose of duloxetine delayed-release capsules is missed, take the missed dose as soon as it is remembered. If it is almost time for the next dose, skip the missed dose and take the next dose at the regular time. Do not take two doses of duloxetine delayed-release capsules at the same time.. 2.1 Dosage for Treatment of Major Depressive Disorder. Administer duloxetine delayed-release capsules at total dose of 40 mg/day (given as 20 mg twice daily) to 60 mg/day (given either once daily or as 30 mg twice daily). For some patients, it may be desirable to start at 30 mg once daily for week, to allow patients to adjust to the medication before increasing to 60 mg once daily. While 120 mg/day dose was shown to be effective, there is no evidence that doses greater than 60 mg/day confer any additional benefits. The safety of doses above 120 mg/day has not been adequately evaluated. Periodically reassess to determine the need for maintenance treatment and the appropriate dose for such treatment [see Clinical Studies (14.1)]. 2.2 Dosage for Treatment of Generalized Anxiety Disorder. Adults -- For most patients, initiate duloxetine delayed-release capsules 60 mg once daily. For some patients, it may be desirable to start at 30 mg once daily for week, to allow patients to adjust to the medication before increasing to 60 mg once daily. While 120 mg once daily dose was shown to be effective, there is no evidence that doses greater than 60 mg/day confer additional benefit. Nevertheless, if decision is made to increase the dose beyond 60 mg once daily, increase dose in increments of 30 mg once daily. The safety of doses above 120 mg once daily has not been adequately evaluated. Periodically reassess to determine the continued need for maintenance treatment and the appropriate dose for such treatment [see Clinical Studies (14.2)].Pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. 2.3 Dosage for Treatment of Diabetic Peripheral Neuropathic Pain. Administer duloxetine delayed-release capsules 60 mg once daily. There is no evidence that doses higher than 60 mg confer additional significant benefit and the higher dose is clearly less well tolerated [see Clinical Studies (14.3)]. For patients for whom tolerability is concern, lower starting dose may be considered. Since diabetes is frequently complicated by renal disease, consider lower starting dose and gradual increase in dose for patients with renal impairment [see Dosage and Administration (2.6), Use in Specific Populations (8.10), and Clinical Pharmacology (12.3)]. 2.5 Dosage for Treatment of Chronic Musculoskeletal Pain. Administer duloxetine delayed-release capsules 60 mg once daily. Begin treatment at 30 mg for one week, to allow patients to adjust to the medication before increasing to 60 mg once daily. There is no evidence that higher doses confer additional benefit, even in patients who do not respond to 60 mg dose, and higher doses are associated with higher rate of adverse reactions [see Clinical Studies (14.5)].. 2.6 Dosing in Special Populations. Hepatic Impairment -- Avoid use in patients with chronic liver disease or cirrhosis [see Warnings and Precautions (5.14) and Use in Specific Populations (8.9)]. Severe Renal Impairment -- Avoid use in patients with severe renal impairment, GFR <30 mL/min [see Warnings and Precautions (5.14) and Use in Specific Populations (8.10)]. 2.7 Discontinuing duloxetine delayed-release capsules. Adverse reactions after discontinuation of duloxetine delayed-release capsules, after abrupt or tapered discontinuation, include: dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue. gradual reduction in dosage rather than abrupt cessation is recommended whenever possible [see Warnings and Precautions (5.7)]. 2.8 Switching Patient to or from Monoamine Oxidase Inhibitor (MAOI) Intended to Treat Psychiatric Disorders. At least 14 days should elapse between discontinuation of an MAOI intended to treat psychiatric disorders and initiation of therapy with duloxetine delayed-release capsules. Conversely, at least days should be allowed after stopping duloxetine delayed-release capsules before starting an MAOI intended to treat psychiatric disorders [see Contraindications (4)]. 2.9 Use of Duloxetine Delayed-Release Capsules with Other MAOIs such as Linezolid or Methylene Blue. Do not start duloxetine delayed-release capsules in patient who is being treated with linezolid or intravenous methylene blue because there is an increased risk of serotonin syndrome. In patient who requires more urgent treatment of psychiatric condition, other interventions, including hospitalization, should be considered [see Contraindications (4)]. In some cases, patient already receiving duloxetine delayed-release capsules therapy may require urgent treatment with linezolid or intravenous methylene blue. If acceptable alternatives to linezolid or intravenous methylene blue treatment are not available and the potential benefits of linezolid or intravenous methylene blue treatment are judged to outweigh the risks of serotonin syndrome in particular patient, duloxetine delayed-release capsules should be stopped promptly, and linezolid or intravenous methylene blue can be administered. The patient should be monitored for symptoms of serotonin syndrome for days or until 24 hours after the last dose of linezolid or intravenous methylene blue, whichever comes first. Therapy with duloxetine delayed-release capsules may be resumed 24 hours after the last dose of linezolid or intravenous methylene blue [see Warnings and Precautions (5.4)]. The risk of administering methylene blue by non-intravenous routes (such as oral tablets or by local injection) or in intravenous doses much lower than mg/kg with duloxetine delayed-release capsules is unclear. The clinician should, nevertheless, be aware of the possibility of emergent symptoms of serotonin syndrome with such use [see Warnings and Precautions (5.4)].

DRUG INTERACTIONS SECTION.

7 DRUG INTERACTIONS. Potent inhibitors of CYP1A2 should be avoided (7.1).Potent inhibitors of CYP2D6 may increase duloxetine concentrations (7.2).Duloxetine is moderate inhibitor of CYP2D6 (7.9).. Potent inhibitors of CYP1A2 should be avoided (7.1).. Potent inhibitors of CYP2D6 may increase duloxetine concentrations (7.2).. Duloxetine is moderate inhibitor of CYP2D6 (7.9).. Both CYP1A2 and CYP2D6 are responsible for duloxetine metabolism. 7.1 Inhibitors of CYP1A2. When duloxetine 60 mg was co-administered with fluvoxamine 100 mg, potent CYP1A2 inhibitor, to male subjects (n=14) duloxetine AUC was increased approximately 6-fold, the Cmax was increased about 2.5-fold, and duloxetine t1/2 was increased approximately 3-fold. Other drugs that inhibit CYP1A2 metabolism include cimetidine and quinolone antimicrobials such as ciprofloxacin and enoxacin [see Warnings and Precautions (5.12)]. 7.2 Inhibitors of CYP2D6. Concomitant use of duloxetine (40 mg once daily) with paroxetine (20 mg once daily) increased the concentration of duloxetine AUC by about 60%, and greater degrees of inhibition are expected with higher doses of paroxetine. Similar effects would be expected with other potent CYP2D6 inhibitors (e.g., fluoxetine, quinidine) [see Warnings and Precautions (5.12)]. 7.3 Dual Inhibition of CYP1A2 and CYP2D6. Concomitant administration of duloxetine 40 mg twice daily with fluvoxamine 100 mg, potent CYP1A2 inhibitor, to CYP2D6 poor metabolizer subjects (n=14) resulted in 6-fold increase in duloxetine AUC and Cmax.. 7.4 Drugs that Interfere with Hemostasis (e.g., NSAIDs, Aspirin, and Warfarin). Serotonin release by platelets plays an important role in hemostasis. Epidemiological studies of the case-control and cohort design that have demonstrated an association between use of psychotropic drugs that interfere with serotonin reuptake and the occurrence of upper gastrointestinal bleeding have also shown that concurrent use of an NSAID or aspirin may potentiate this risk of bleeding. Altered anticoagulant effects, including increased bleeding, have been reported when SSRIs or SNRIs are co-administered with warfarin. Concomitant administration of warfarin (2-9 mg once daily) under steady state conditions with duloxetine 60 or 120 mg once daily for up to 14 days in healthy subjects (n=15) did not significantly change INR from baseline (mean INR changes ranged from 0.05 to +0.07). The total warfarin (protein bound plus free drug) pharmacokinetics (AUCT,ss, Cmax,ss or tmax,ss) for both R- and S-warfarin were not altered by duloxetine. Because of the potential effect of duloxetine on platelets, patients receiving warfarin therapy should be carefully monitored when duloxetine is initiated or discontinued [see Warnings and Precautions (5.5)]. 7.5 Lorazepam. Under steady-state conditions for duloxetine (60 mg 12 hours) and lorazepam (2 mg 12 hours), the pharmacokinetics of duloxetine were not affected by co-administration. 7.6 Temazepam. Under steady-state conditions for duloxetine (20 mg qhs) and temazepam (30 mg qhs), the pharmacokinetics of duloxetine were not affected by co-administration. 7.7 Drugs that Affect Gastric Acidity. Duloxetine delayed-release capsules have an enteric coating that resists dissolution until reaching segment of the gastrointestinal tract where the pH exceeds 5.5. In extremely acidic conditions, duloxetine delayed-release capsules, unprotected by the enteric coating, may undergo hydrolysis to form naphthol. Caution is advised in using duloxetine delayed-release capsules in patients with conditions that may slow gastric emptying (e.g., some diabetics). Drugs that raise the gastrointestinal pH may lead to an earlier release of duloxetine. However, co-administration of duloxetine delayed-release capsules with aluminum- and magnesium-containing antacids (51 mEq) or duloxetine delayed-release capsules with famotidine, had no significant effect on the rate or extent of duloxetine absorption after administration of 40 mg oral dose. It is unknown whether the concomitant administration of proton pump inhibitors affects duloxetine absorption [see Warnings and Precautions (5.14)]. 7.8 Drugs Metabolized by CYP1A2. In vitro drug interaction studies demonstrate that duloxetine does not induce CYP1A2 activity. Therefore, an increase in the metabolism of CYP1A2 substrates (e.g., theophylline, caffeine) resulting from induction is not anticipated, although clinical studies of induction have not been performed. Duloxetine is an inhibitor of the CYP1A2 isoform in in vitro studies, and in two clinical studies the average (90% confidence interval) increase in theophylline AUC was 7% (1% to 15%) and 20% (13% to 27%) when co-administered with duloxetine (60 mg twice daily).. 7.9 Drugs Metabolized by CYP2D6. Duloxetine is moderate inhibitor of CYP2D6. When duloxetine was administered (at dose of 60 mg twice daily) in conjunction with single 50 mg dose of desipramine, CYP2D6 substrate, the AUC of desipramine increased 3-fold [see Warnings and Precautions (5.12)]. 7.10 Drugs Metabolized by CYP2C9. Results of in vitro studies demonstrate that duloxetine does not inhibit activity. In clinical study, the pharmacokinetics of S-warfarin, CYP2C9 substrate, were not significantly affected by duloxetine [see Drug Interactions (7.4)].. 7.11 Drugs Metabolized by CYP3A. Results of in vitro studies demonstrate that duloxetine does not inhibit or induce CYP3A activity. Therefore, an increase or decrease in the metabolism of CYP3A substrates (e.g., oral contraceptives and other steroidal agents) resulting from induction or inhibition is not anticipated, although clinical studies have not been performed. 7.12 Drugs Metabolized by CYP2C19. Results of in vitro studies demonstrate that duloxetine does not inhibit CYP2C19 activity at therapeutic concentrations. Inhibition of the metabolism of CYP2C19 substrates is therefore not anticipated, although clinical studies have not been performed. 7.13 Monoamine Oxidase Inhibitors (MAOIs). [see Dosage and Administration (2.8, 2.9), Contraindications (4), and Warnings and Precautions (5.4)].. 7.14 Serotonergic Drugs. [see Dosage and Administration (2.8, 2.9), Contraindications (4), and Warnings and Precautions (5.4)].. 7.15 Alcohol. When duloxetine and ethanol were administered several hours apart so that peak concentrations of each would coincide, duloxetine did not increase the impairment of mental and motor skills caused by alcohol.In the duloxetine clinical trials database, three duloxetine-treated patients had liver injury as manifested by ALT and total bilirubin elevations, with evidence of obstruction. Substantial intercurrent ethanol use was present in each of these cases, and this may have contributed to the abnormalities seen [see Warnings and Precautions (5.2, 5.12)]. 7.16 CNS Drugs. [see Warnings and Precautions (5.12)]. 7.17 Drugs Highly Bound to Plasma Protein. Because duloxetine is highly bound to plasma protein, administration of duloxetine delayed-release capsules to patient taking another drug that is highly protein bound may cause increased free concentrations of the other drug, potentially resulting in adverse reactions. However, co-administration of duloxetine (60 or 120 mg) with warfarin (2-9 mg), highly protein-bound drug, did not result in significant changes in INR and in the pharmacokinetics of either total S-or total R-warfarin (protein bound plus free drug) [see Drug Interactions (7.4)].

SPL MEDGUIDE SECTION.

Medication Guide. Duloxetine (doo-LOX-e-teen) Delayed-Release Capsules, USP Read the Medication Guide before you start taking duloxetine delayed-release capsules and each time you get refill. There may be new information. This information does not take the place of talking to your healthcare provider about your medical condition or treatment. Talk to your healthcare provider about: all risks and benefits of treatment with antidepressant medicinesall treatment choices for depression or other serious mental illnessWhat is the most important information should know about antidepressant medicines, depression, other serious mental illnesses, and suicidal thoughts or actions1. Duloxetine delayed-release capsules and other antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, or young adults within the first few months of treatment or when the dose is changed. 2. Depression and other serious mental illnesses are the most important causes of suicidal thoughts or actions. Some people may have particularly high risk of having suicidal thoughts or actions. These include people who have (or have family history of) bipolar illness (also called manic-depressive illness).3. How can watch for and try to prevent suicidal thoughts and actions Pay close attention to any changes in mood, behavior, actions, thoughts, or feelings, especially sudden changes. This is very important when an antidepressant medicine is started or when the dose is changed.Call your healthcare provider right away to report new or sudden changes in mood, behavior, thoughts, or feelings.Keep all follow-up visits with your healthcare provider as scheduled. Call your healthcare provider between visits as needed, especially if you have concerns about symptoms.Call your healthcare provider right away if you have any of the following symptoms, or feelings, especially if they are new, worse, or worry you. In an emergency, call 911.attempts to commit suicideacting on dangerous impulsesacting aggressive, being angry, or violentthoughts about suicide or dyingnew or worse depressionnew or worse anxietypanic attacksfeeling very agitated or restlessnew or worse irritabilitytrouble sleepingan extreme increase in activity or talking (mania)other unusual changes in behavior or moodWhat else do need to know about antidepressant medicinesNever stop an antidepressant medicine without first talking to healthcare provider. Stopping an antidepressant medicine suddenly can cause other symptoms.Antidepressants are medicines used to treat depression and other illnesses. It is important to discuss all the risks of treating depression and also the risks of not treating it. Patients should discuss all treatment choices with your healthcare provider, not just the use of antidepressants.Antidepressant medicines have other side effects. Talk to your healthcare provider about the side effects of the medicine prescribed for you or your family member.Antidepressant medicines can interact with other medicines. Know all of the medicines that you or your family member takes. Keep list of all medicines to show your healthcare provider. Do not start new medicines without first checking with your healthcare provider..What are duloxetine delayed-release capsulesDuloxetine delayed-release capsules is prescription medicine used to treat certain type of depression called Major Depressive Disorder (MDD). Duloxetine delayed-release capsules belongs to class of medicines known as SNRIs (or serotonin-norepinephrine reuptake inhibitors).Duloxetine delayed-release capsules are also used to treat or manage:Generalized Anxiety Disorder (GAD)Diabetic Peripheral Neuropathic Pain (DPNP)Chronic Musculoskeletal PainWho should not take duloxetine delayed-release capsulesDo Not take duloxetine delayed-release capsules if you:take Monoamine Oxidase Inhibitor (MAOI). Ask your healthcare provider or pharmacist if you are not sure if you take an MAOI, including the antibiotic linezolid or intravenous methylene blue.Do not take an MAOI within days of stopping duloxetine delayed-release capsules unless directed to do so by your healthcare provider.Do not start duloxetine delayed-release capsules if you stopped taking an MAOI in the last 14 days unless directed to do so by your healthcare provider.People who take duloxetine delayed-release capsules close in time to an MAOI may have serious problem called Serotonin Syndrome (see What are the possible side effects of duloxetine delayed-release capsules).What should tell my healthcare provider before taking duloxetine delayed-release capsulesBefore starting duloxetine delayed-release capsules, tell your healthcare provider if you:have heart problems or high blood pressurehave diabetes (duloxetine delayed-release capsule treatment makes it harder for some people with diabetes to control their blood sugar)have liver problemshave kidney problemshave glaucomahave or had seizures or convulsionshave bipolar disorder or maniahave low sodium levels in your bloodhave delayed stomach emptyinghave or had bleeding problemsare pregnant or plan to become pregnant. It is not known if duloxetine delayed-release capsules will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression or other conditions with duloxetine delayed-release capsules during pregnancy.are breastfeeding or plan to breastfeed. Duloxetine can pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby while taking duloxetine delayed-release capsules.Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Duloxetine delayed-release capsules and some medicines may interact with each other, may not work as well, or may cause serious side effects. Especially tell your healthcare provider if you take: triptans used to treat migraine headachemedicines used to treat mood, anxiety, psychotic or thought disorders, including tricyclics, lithium, buspirone, SSRIs, SNRIs or MAOIstramadol and fentanylamphetaminescimetidinethe antibiotics ciprofloxacin, enoxacinmedicine to treat irregular heart rate (like propafenone, flecainide, quinidine)theophyllinethe blood thinner warfarin (Coumadin, Jantoven)non-steroidal anti-inflammatory drug (NSAID) (like ibuprofen, naproxen or aspirin).over-the-counter supplements such as tryptophan or St. Johns Wortthioridazine (Mellaril). Mellaril together with duloxetine delayed-release capsules can cause serious heart rhythm problems or sudden death.Ask your healthcare provider for list of these medicines if you are not sure. Do not take duloxetine delayed-release capsules with any other medicine that contain duloxetine.How should take duloxetine delayed-release capsulesTake duloxetine delayed-release capsules exactly as your healthcare provider tells you to take it. Your healthcare provider may need to change the dose of duloxetine delayed-release capsules until it is the right dose for you.Swallow duloxetine delayed-release capsules whole. Do not chew or crush duloxetine delayed-release capsules.Do not open the capsule and sprinkle on food or mix with liquids. Opening the capsule may affect how well duloxetine delayed-release capsules works.Duloxetine delayed-release capsules may be taken with or without food.If you miss dose of duloxetine delayed-release capsules, take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take your next dose at the regular time. Do not take two doses of duloxetine delayed-release capsules at the same time.If you take too many duloxetine delayed-release capsules, call your healthcare provider or poison control center at 1-800-222-1222 right away, or get emergency treatment.When switching from another antidepressant to duloxetine delayed-release capsules your heathcare provider may want to lower the dose of the initial antidepressant first to potentially avoid side effects.What should avoid while taking duloxetine delayed-release capsulesDuloxetine delayed-release capsules can cause sleepiness or may affect your ability to make decisions, think clearly, or react quickly. You should not drive, operate heavy machinery, or do other dangerous activities until you know how duloxetine delayed-release capsules affect you.Use of duloxetine delayed-release capsules concomitantly with heavy alcohol intake may be associated with severe liver injury. Avoid heavy alcohol use while taking duloxetine delayed-release capsules.What are the possible side effects of duloxetine delayed-release capsulesDuloxetine delayed-release capsules may cause serious side effects, including: See What is the most important information should know about duloxetine delayed-release capsules Common possible side effects in people who take duloxetine delayed-release capsules include:1. liver damage. Symptoms may include: itchingright upper abdominal paindark urineyellow skin or eyesenlarged liverincreased liver enzymes2. changes in blood pressure and falls. Monitor your blood pressure before starting and throughout treatment. Duloxetine delayed-release capsules may: increase your blood pressure.decrease your blood pressure when standing and cause dizziness or fainting, mostly when first starting duloxetine delayed-release capsules or when increasing the dose.increase risk of falls, especially in elderly.3. Serotonin Syndrome: This condition can be life-threatening and symptoms may include: agitation, hallucinations, coma or other changes in mental statuscoordination problems or muscle twitching (overactive reflexes)racing heartbeat, high or low blood pressuresweating or fevernausea, vomiting, or diarrheamuscle rigiditydizzinessflushingtremorseizures4. abnormal bleeding: Duloxetine delayed-release capsules and other antidepressant medicines may increase your risk of bleeding or bruising, especially if you take the blood thinner warfarin (Coumadin, Jantoven), non-steroidal anti-inflammatory drug (NSAIDs, like ibuprofen or naproxen), or aspirin. 5. severe skin reactions: Duloxetine delayed-release capsules may cause serious skin reactions that may require stopping its use. This may need to be treated in hospital and may be life-threatening. Call your healthcare provider right away or get emergency help if you have skin blisters, peeling rash, sores in the mouth, hives or any other allergic reactions. 6. discontinuation symptoms: Do not stop duloxetine delayed-release capsules without first talking to your healthcare provider. Stopping duloxetine delayed-release capsules too quickly or changing from another antidepressant too quickly may result in serious symptoms including:anxietyirritabilityfeeling tired or problems sleepingheadachesweatingdizzinesselectric shock-like sensationsvomiting or nauseadiarrhea7. manic episodes:greatly increased energysevere trouble sleepingracing thoughtsreckless behaviorunusually grand ideasexcessive happiness or irritabilitytalking more or faster than usual8. visual problems: eye painchanges in visionswelling or redness in or around the eyeOnly some people are at risk for these problems. You may want to undergo an eye examination to see if you are at risk and receive preventative treatment if you are. 9. seizures or convulsions 10. low salt (sodium) levels in the blood. Elderly people may be at greater risk for this. Symptoms may include: Headacheweakness or feeling unsteadyconfusion, problems concentrating or thinking or memory problems11. problems with urination. Symptoms may include: decreased urine flowunable to pass any urineThe most common side effects of duloxetine delayed-release capsules include: nauseadry mouthsleepinessfatigueconstipationloss of appetiteincreased sweatingdizzinessCommon possible side effects in children and adolescents who take duloxetine delayed-release capsules include:nauseadecreased weightdizzinessSide effects in adults may also occur in children and adolescents who take duloxetine delayed-release capsules. Children and adolescents should have height and weight monitored during treatment.Tell your healthcare provider if you have any side effect that bothers you or that does not go away. These are not all the possible side effects of duloxetine delayed-release capsules. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to 1-800-FDA- 1088. How should store duloxetine delayed-release capsulesStore duloxetine delayed-release capsules at 20 to 25C (68 to 77F); excursions permitted to 15 to 30C (59 to 86F) [see USP Controlled Room Temperature].Keep duloxetine delayed-release capsules and all medicines out of the reach of children. General information about the safe and effective use of duloxetine delayed-release capsulesMedicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use duloxetine delayed-release capsules for condition for which it was not prescribed. Do not give duloxetine delayed-release capsules to other people, even if they have the same symptoms that you have. It may harm them. This Medication Guide summarizes the most important information about duloxetine delayed-release capsules. If you would like more information, talk with your healthcare provider. You may ask your healthcare provider or pharmacist for information about duloxetine delayed-release capsules that is written for healthcare professionals. For more information about duloxetine delayed-release capsules call 1-269-544-2299.What are the ingredients in duloxetine delayed-release capsulesActive ingredient: duloxetine hydrochloride, USPInactive ingredients: Gelatin, hypromellose, methacrylic acid copolymer dispersion, polyethylene glycol 400, sodium lauryl sulfate, sucrose, sugar spheres, talc, titanium dioxide, triethyl citrate. Additionally, the 20 mg capsules contain FD&C Blue No. and black imprinting ink (It contains black iron oxide, potassium hydroxide, propylene glycol, and shellac), the 30 mg capsules contain FD&C Blue No. 1, FD&C Red No. 40, black imprinting ink (It contains black iron oxide, potassium hydroxide, propylene glycol, and shellac) and white imprinting ink (It contains povidone, shellac, sodium hydroxide, and titanium dioxide), and the 60 mg capsules contain FD&C Blue No. 2, iron oxide yellow and white imprinting ink (It contains povidone, shellac, sodium hydroxide, and titanium dioxide).This Medication Guide has been approved by the U.S. Food and Drug Administration.The brands listed are trademarks of their respective owners.Manufactured by:TORRENT PHARMACEUTICALS LTD., Indrad-382 721, Dist. Mehsana, INDIA.For:TORRENT PHARMA INC., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920.8063412 Revised February 2017. all risks and benefits of treatment with antidepressant medicines. all treatment choices for depression or other serious mental illness. Pay close attention to any changes in mood, behavior, actions, thoughts, or feelings, especially sudden changes. This is very important when an antidepressant medicine is started or when the dose is changed.. Call your healthcare provider right away to report new or sudden changes in mood, behavior, thoughts, or feelings.. Keep all follow-up visits with your healthcare provider as scheduled. Call your healthcare provider between visits as needed, especially if you have concerns about symptoms.. attempts to commit suicide. acting on dangerous impulses. acting aggressive, being angry, or violent. thoughts about suicide or dying. new or worse depression. new or worse anxiety. panic attacks. feeling very agitated or restless. new or worse irritability. trouble sleeping. an extreme increase in activity or talking (mania). other unusual changes in behavior or mood. Never stop an antidepressant medicine without first talking to healthcare provider. Stopping an antidepressant medicine suddenly can cause other symptoms.. Antidepressants are medicines used to treat depression and other illnesses. It is important to discuss all the risks of treating depression and also the risks of not treating it. Patients should discuss all treatment choices with your healthcare provider, not just the use of antidepressants.. Antidepressant medicines have other side effects. Talk to your healthcare provider about the side effects of the medicine prescribed for you or your family member.. Antidepressant medicines can interact with other medicines. Know all of the medicines that you or your family member takes. Keep list of all medicines to show your healthcare provider. Do not start new medicines without first checking with your healthcare provider... Generalized Anxiety Disorder (GAD). Diabetic Peripheral Neuropathic Pain (DPNP). Chronic Musculoskeletal Pain. take Monoamine Oxidase Inhibitor (MAOI). Ask your healthcare provider or pharmacist if you are not sure if you take an MAOI, including the antibiotic linezolid or intravenous methylene blue.. Do not take an MAOI within days of stopping duloxetine delayed-release capsules unless directed to do so by your healthcare provider.. Do not start duloxetine delayed-release capsules if you stopped taking an MAOI in the last 14 days unless directed to do so by your healthcare provider.. have heart problems or high blood pressure. have diabetes (duloxetine delayed-release capsule treatment makes it harder for some people with diabetes to control their blood sugar). have liver problems. have kidney problems. have glaucoma. have or had seizures or convulsions. have bipolar disorder or mania. have low sodium levels in your blood. have delayed stomach emptying. have or had bleeding problems. are pregnant or plan to become pregnant. It is not known if duloxetine delayed-release capsules will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression or other conditions with duloxetine delayed-release capsules during pregnancy.. are breastfeeding or plan to breastfeed. Duloxetine can pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby while taking duloxetine delayed-release capsules.. triptans used to treat migraine headache. medicines used to treat mood, anxiety, psychotic or thought disorders, including tricyclics, lithium, buspirone, SSRIs, SNRIs or MAOIs. tramadol and fentanyl. amphetamines. cimetidine. the antibiotics ciprofloxacin, enoxacin. medicine to treat irregular heart rate (like propafenone, flecainide, quinidine). theophylline. the blood thinner warfarin (Coumadin, Jantoven). non-steroidal anti-inflammatory drug (NSAID) (like ibuprofen, naproxen or aspirin).. over-the-counter supplements such as tryptophan or St. Johns Wort. thioridazine (Mellaril). Mellaril together with duloxetine delayed-release capsules can cause serious heart rhythm problems or sudden death.. Take duloxetine delayed-release capsules exactly as your healthcare provider tells you to take it. Your healthcare provider may need to change the dose of duloxetine delayed-release capsules until it is the right dose for you.. Swallow duloxetine delayed-release capsules whole. Do not chew or crush duloxetine delayed-release capsules.. Do not open the capsule and sprinkle on food or mix with liquids. Opening the capsule may affect how well duloxetine delayed-release capsules works.. Duloxetine delayed-release capsules may be taken with or without food.. If you miss dose of duloxetine delayed-release capsules, take the missed dose as soon as you remember. If it is almost time for the next dose, skip the missed dose and take your next dose at the regular time. Do not take two doses of duloxetine delayed-release capsules at the same time.. If you take too many duloxetine delayed-release capsules, call your healthcare provider or poison control center at 1-800-222-1222 right away, or get emergency treatment.. When switching from another antidepressant to duloxetine delayed-release capsules your heathcare provider may want to lower the dose of the initial antidepressant first to potentially avoid side effects.. Duloxetine delayed-release capsules can cause sleepiness or may affect your ability to make decisions, think clearly, or react quickly. You should not drive, operate heavy machinery, or do other dangerous activities until you know how duloxetine delayed-release capsules affect you.. Use of duloxetine delayed-release capsules concomitantly with heavy alcohol intake may be associated with severe liver injury. Avoid heavy alcohol use while taking duloxetine delayed-release capsules.. itching. right upper abdominal pain. dark urine. yellow skin or eyes. enlarged liver. increased liver enzymes. increase your blood pressure.. decrease your blood pressure when standing and cause dizziness or fainting, mostly when first starting duloxetine delayed-release capsules or when increasing the dose.. increase risk of falls, especially in elderly.. agitation, hallucinations, coma or other changes in mental status. coordination problems or muscle twitching (overactive reflexes). racing heartbeat, high or low blood pressure. sweating or fever. nausea, vomiting, or diarrhea. muscle rigidity. dizziness. flushing. tremor. seizures. anxiety. irritability. feeling tired or problems sleeping. headache. sweating. dizziness. electric shock-like sensations. vomiting or nausea. diarrhea. greatly increased energy. severe trouble sleeping. racing thoughts. reckless behavior. unusually grand ideas. excessive happiness or irritability. talking more or faster than usual. eye pain. changes in vision. swelling or redness in or around the eye. Headache. weakness or feeling unsteady. confusion, problems concentrating or thinking or memory problems. decreased urine flow. unable to pass any urine. nausea. dry mouth. sleepiness. fatigue. constipation. loss of appetite. increased sweating. dizziness. nausea. decreased weight. dizziness. Torrent logo.

USE IN SPECIFIC POPULATIONS SECTION.

8 USE IN SPECIFIC POPULATIONS. Pregnancy: Based on animal data may cause fetal harm (8.1)Nursing Mothers: Exercise caution when administered to nursing woman (8.3)Pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information.. Pregnancy: Based on animal data may cause fetal harm (8.1). Nursing Mothers: Exercise caution when administered to nursing woman (8.3). 8.1 Pregnancy. Pregnancy Category Risk Summary -- There are no adequate and well-controlled studies of duloxetine administration in pregnant women. In animal studies with duloxetine, fetal weights were decreased but there was no evidence of teratogenicity in pregnant rats and rabbits at oral doses administered during the period of organogenesis up to and times the maximum recommended human dose (MRHD) of 120 mg/day, respectively. When duloxetine was administered orally to pregnant rats throughout gestation and lactation, pup weights at birth and pup survival to day postpartum were decreased at dose times the MRHD. At this dose, pup behaviors consistent with increased reactivity, such as increased startle response to noise and decreased habituation of locomotor activity were observed. Post-weaning growth was not adversely affected. Duloxetine should be used in pregnancy only if the potential benefit justifies the potential risk to the fetus. Clinical Considerations Fetal/Neonatal Adverse Reaction -- Neonates exposed during pregnancy to serotonin norepinephrine reuptake inhibitors (SNRIs) or selective serotonin reuptake inhibitors (SSRIs) have developed complications requiring prolonged hospitalization, respiratory support, and tube feeding which can arise immediately upon delivery. Reported clinical findings have included respiratory distress, cyanosis, apnea, seizures, temperature instability, feeding difficulty, vomiting, hypoglycemia, hypotonia, hypertonia, hyperreflexia, tremor, jitteriness, irritability, and constant crying. These features are consistent with either direct toxic effect of the SNRIs or SSRIs, or possibly, drug discontinuation syndrome. It should be noted that, in some cases, the clinical picture is consistent with serotonin syndrome [see Warnings and Precautions (5.4)]. Data Animal Data -- In animal reproduction studies, duloxetine has been shown to have adverse effects on embryo/fetal and postnatal development. When duloxetine was administered orally to pregnant rats and rabbits during the period of organogenesis, there was no evidence of teratogenicity at doses up to 45 mg/kg/day (4 times the maximum recommended human dose (MRHD) of 120 mg/day on mg/m2 basis, in rat; times the MRHD in rabbit). However, fetal weights were decreased at this dose, with no-effect dose of 10 mg/kg/day approximately equal to the MRHD in rats; times the MRHD in rabbits). When duloxetine was administered orally to pregnant rats throughout gestation and lactation, the survival of pups to day postpartum and pup body weights at birth and during the lactation period were decreased at dose of 30 mg/kg/day (2 times the MRHD); the no-effect dose was 10 mg/kg/day. Furthermore, behaviors consistent with increased reactivity, such as increased startle response to noise and decreased habituation of locomotor activity, were observed in pups following maternal exposure to 30 mg/kg/day. Post-weaning growth and reproductive performance of the progeny were not affected adversely by maternal duloxetine treatment.. 8.3 Nursing Mothers. Risk Summary Duloxetine is present in human milk. In published study, lactating women who were weaning their infants were given duloxetine. At steady state, the concentration of duloxetine in breast milk was approximately 25% that of maternal plasma. The estimated daily infant dose was approximately 0.14% of the maternal dose. The developmental and health benefits of human milk feeding should be considered along with the mothers clinical need for duloxetine and any potential adverse effects on the milk-fed child from the drug or from the underlying maternal condition. Exercise caution when duloxetine is administered to nursing woman. Data The disposition of duloxetine was studied in lactating women who were at least 12 weeks postpartum and had elected to wean their infants. The women were given 40 mg of duloxetine twice daily for 3.5 days. The peak concentration measured in breast milk occurred at median of hours after the dose. The amount of duloxetine in breast milk was approximately mcg/day while on that dose; the estimated daily infant dose was approximately mcg/kg/day. The presence of duloxetine metabolites in breast milk was not examined.. 8.4 Pediatric Use. The safety and effectiveness in pediatric patients less than years of age have not been established. The safety and effectiveness in pediatric patients less than years of age have not been established. Decreased appetite and weight loss have been observed in association with the use of SSRIs and SNRIs. Perform regular monitoring of weight and growth in children and adolescents treated with an SNRI such as duloxetine [see Adverse Reactions (6.11)]. Information describing two additional clinical studies in which efficacy was not demonstrated in patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. Other pediatric use information for patients ages to 17 years is approved for Eli Lilly and Company, Inc.s CYMBALTA(R) (duloxetine) delayed-release capsules. However, due to Eli Lilly and Company, Inc.s marketing exclusivity rights, this drug product is not labeled with that pediatric information. Animal Data -- Duloxetine administration to young rats from post-natal day 21 (weaning) through post-natal day 90 (adult) resulted in decreased body weights that persisted into adulthood, but recovered when drug treatment was discontinued; slightly delayed (~1.5 days) sexual maturation in females, without any effect on fertility; and delay in learning complex task in adulthood, which was not observed after drug treatment was discontinued. These effects were observed at the high dose of 45 mg/kg/day (2 times the MRHD, for child); the no-effect-level was 20 mg/kg/day (1 times the MRHD, for child).. 8.5 Geriatric Use. Of the 2,418 patients in premarketing clinical studies of duloxetine for MDD, 5.9% (143) were 65 years of age or over. Of the 1041 patients in CLBP premarketing studies, 21.2% (221) were 65 years of age or over. Of the 487 patients in OA premarketing studies, 40.5% (197) were 65 years of age or over. Of the 1,074 patients in the DPNP premarketing studies, 33% (357) were 65 years of age or over. In the MDD, GAD, DPNP, OA, CLBP and other studies, no overall differences in safety or effectiveness were generally observed between these subjects and younger subjects, 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. SSRIs and SNRIs, including duloxetine has been associated with cases of clinically significant hyponatremia in elderly patients, who may be at greater risk for this adverse event [see Warnings and Precautions (5.13)]. In an analysis of data from all placebo-controlled-trials, patients treated with duloxetine reported higher rate of falls compared to patients treated with placebo. The increased risk appears to be proportional to patients underlying risk for falls. Underlying risk appears to increase steadily with age. As elderly patients tend to have higher prevalence of risk factors for falls such as medications, medical comorbidities and gait disturbances, the impact of increasing age by itself on falls during treatment with duloxetine is unclear. Falls with serious consequences including bone fractures and hospitalizations have been reported [see Warnings and Precautions (5.3) and Adverse Reactions (6.10)].. 8.6 Gender. Duloxetines half-life is similar in men and women. Dosage adjustment based on gender is not necessary.. 8.7 Smoking Status. Duloxetine bioavailability (AUC) appears to be reduced by about one-third in smokers. Dosage modifications are not recommended for smokers.. 8.8 Race. No specific pharmacokinetic study was conducted to investigate the effects of race. 8.9 Hepatic Impairment. Patients with clinically evident hepatic impairment have decreased duloxetine metabolism and elimination. After single 20 mg dose of duloxetine, cirrhotic patients with moderate liver impairment (Child-Pugh Class B) had mean plasma duloxetine clearance about 15% that of age- and gender-matched healthy subjects, with 5-fold increase in mean exposure (AUC). Although Cmax was similar to normals in the cirrhotic patients, the half-life was about times longer [see Dosage and Administration (2.6) and Warnings and Precautions (5.14)]. 8.10 Severe Renal Impairment. Limited data are available on the effects of duloxetine in patients with end-stage renal disease (ESRD). After single 60 mg dose of duloxetine, Cmax and AUC values were approximately 100% greater in patients with end-stage renal disease receiving chronic intermittent hemodialysis than in subjects with normal renal function. The elimination half-life, however, was similar in both groups. The AUCs of the major circulating metabolites, 4-hydroxy duloxetine glucuronide and 5-hydroxy, 6-methoxy duloxetine sulfate, largely excreted in urine, were approximately 7- to 9-fold higher and would be expected to increase further with multiple dosing. Population PK analyses suggest that mild to moderate degrees of renal impairment (estimated CrCl 30 to 80 mL/min) have no significant effect on duloxetine apparent clearance [see Dosage and Administration (2.6) and Warnings and Precautions (5.14)].

WARNINGS AND PRECAUTIONS SECTION.

5 WARNINGS AND PRECAUTIONS. Hepatotoxicity: Hepatic failure, sometimes fatal, has been reported in patients treated with duloxetine delayed-release capsules. Duloxetine delayed-release capsules should be discontinued in patients who develop jaundice or other evidence of clinically significant liver dysfunction and should not be resumed unless another cause can be established. Duloxetine delayed-release capsules should not be prescribed to patients with substantial alcohol use or evidence of chronic liver disease (5.2)Orthostatic Hypotension, Falls and Syncope: Cases have been reported with duloxetine therapy (5.3)Serotonin Syndrome: Serotonin syndrome has been reported with SSRIs and SNRIs, including with duloxetine delayed-release capsules, both when taken alone, but especially when co-administered with other serotonergic agents (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines and St. Johns Wort). If such symptoms occur, discontinue duloxetine and initiate supportive treatment. If concomitant use of duloxetine delayed-release capsules with other serotonergic drugs is clinically warranted, patients should be made aware of potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases (5.4)Abnormal Bleeding: Duloxetine delayed-release capsules may increase the risk of bleeding events. Patients should be cautioned about the risk of bleeding associated with the concomitant use of duloxetine and NSAIDs, aspirin, or other drugs that affect coagulation (5.5, 7.4)Severe Skin Reactions: Severe skin reactions, including erythema multiforme and Stevens-Johnson Syndrome (SJS), can occur with duloxetine delayed-release capsules. Duloxetine delayed-release capsules should be discontinued at the first appearance of blisters, peeling rash, mucosal erosions, or any other sign of hypersensitivity if no other etiology can be identified. (5.6)Discontinuation: May result in symptoms, including dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue (5.7)Activation of mania or hypomania has occurred (5.8)Angle-Closure Glaucoma: Angle-closure glaucoma has occurred in patients with untreated anatomically narrow angles treated with antidepressants. (5.9)Seizures: Prescribe with care in patients with history of seizure disorder (5.10)Blood Pressure: Monitor blood pressure prior to initiating treatment and periodically throughout treatment (5.11)Inhibitors of CYP1A2 or Thioridazine: Should not administer with duloxetine delayed-release capsules (5.12)Hyponatremia: Cases of hyponatremia have been reported (5.13)Glucose Control in Diabetes: In diabetic peripheral neuropathic pain patients, small increases in fasting blood glucose, and HbA1chave been observed (5.14)Conditions that Slow Gastric Emptying: Use cautiously in these patients (5.14)Urinary Hesitation and Retention (5.15). Hepatotoxicity: Hepatic failure, sometimes fatal, has been reported in patients treated with duloxetine delayed-release capsules. Duloxetine delayed-release capsules should be discontinued in patients who develop jaundice or other evidence of clinically significant liver dysfunction and should not be resumed unless another cause can be established. Duloxetine delayed-release capsules should not be prescribed to patients with substantial alcohol use or evidence of chronic liver disease (5.2). Orthostatic Hypotension, Falls and Syncope: Cases have been reported with duloxetine therapy (5.3). Serotonin Syndrome: Serotonin syndrome has been reported with SSRIs and SNRIs, including with duloxetine delayed-release capsules, both when taken alone, but especially when co-administered with other serotonergic agents (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines and St. Johns Wort). If such symptoms occur, discontinue duloxetine and initiate supportive treatment. If concomitant use of duloxetine delayed-release capsules with other serotonergic drugs is clinically warranted, patients should be made aware of potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases (5.4). Abnormal Bleeding: Duloxetine delayed-release capsules may increase the risk of bleeding events. Patients should be cautioned about the risk of bleeding associated with the concomitant use of duloxetine and NSAIDs, aspirin, or other drugs that affect coagulation (5.5, 7.4). Severe Skin Reactions: Severe skin reactions, including erythema multiforme and Stevens-Johnson Syndrome (SJS), can occur with duloxetine delayed-release capsules. Duloxetine delayed-release capsules should be discontinued at the first appearance of blisters, peeling rash, mucosal erosions, or any other sign of hypersensitivity if no other etiology can be identified. (5.6). Discontinuation: May result in symptoms, including dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue (5.7). Activation of mania or hypomania has occurred (5.8). Angle-Closure Glaucoma: Angle-closure glaucoma has occurred in patients with untreated anatomically narrow angles treated with antidepressants. (5.9). Seizures: Prescribe with care in patients with history of seizure disorder (5.10). Blood Pressure: Monitor blood pressure prior to initiating treatment and periodically throughout treatment (5.11). Inhibitors of CYP1A2 or Thioridazine: Should not administer with duloxetine delayed-release capsules (5.12). Hyponatremia: Cases of hyponatremia have been reported (5.13). Glucose Control in Diabetes: In diabetic peripheral neuropathic pain patients, small increases in fasting blood glucose, and HbA1chave been observed (5.14). Conditions that Slow Gastric Emptying: Use cautiously in these patients (5.14). Urinary Hesitation and Retention (5.15). 5.1 Suicidal Thoughts and Behaviors in Children, Adolescents, and Young Adults. Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications, and this risk may persist until significant remission occurs. Suicide is known risk of depression and certain other psychiatric disorders, and these disorders themselves are the strongest predictors of suicide. There has been long-standing concern, however, that antidepressants may have role in inducing worsening of depression and the emergence of suicidality in certain patients during the early phases of treatment. Pooled analyses of short-term placebo-controlled trials of antidepressant drugs (SSRIs and others) showed that these drugs increase the risk of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults (ages 18 to 24) with major depressive disorder (MDD) and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was reduction with antidepressants compared to placebo in adults aged 65 and older. The pooled analyses of placebo-controlled trials in children and adolescents with MDD, obsessive compulsive disorder (OCD), or other psychiatric disorders included total of 24 short-term trials of antidepressant drugs in over 4400 patients. The pooled analyses of placebo-controlled trials in adults with MDD or other psychiatric disorders included total of 295 short-term trials (median duration of months) of 11 antidepressant drugs in over 77,000 patients. There was considerable variation in risk of suicidality among drugs, but tendency toward an increase in the younger patients for almost all drugs studied. There were differences in absolute risk of suicidality across the different indications, with the highest incidence in MDD. The risk of differences (drug vs placebo), however, were relatively stable within age strata and across indications. These risk differences (drug-placebo difference in the number of cases of suicidality per 1000 patients treated) are provided in Table 1.Table Age Range Drug Placebo Difference in Number of Cases of Suicidality per 1000 Patients Treated Increases Compared to Placebo <18 14 additional cases 18 to 24 additional cases Decreases Compared to Placebo 25 to 64 fewer case >=65 fewer cases No suicides occurred in any of the pediatric trials. There were suicides in the adult trials, but the number was not sufficient to reach any conclusion about drug effect on suicide. It is unknown whether the suicidality risk extends to longer-term use, i.e., beyond several months. However, there is substantial evidence from placebo-controlled maintenance trials in adults with depression that the use of antidepressants can delay the recurrence of depression. All patients being treated with antidepressants for any indication should be monitored appropriately and observed closely for clinical worsening, suicidality, and unusual changes in behavior, especially during the initial few months of course of drug therapy, or at times of dose changes, either increases or decreases. The following symptoms, anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, and mania, have been reported in adult and pediatric patients being treated with antidepressants for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric. Although causal link between the emergence of such symptoms and either the worsening of depression and/or the emergence of suicidal impulses has not been established, there is concern that such symptoms may represent precursors to emerging suicidality.Consideration should be given to changing the therapeutic regimen, including possibly discontinuing the medication, in patients whose depression is persistently worse, or who are experiencing emergent suicidality or symptoms that might be precursors to worsening depression or suicidality, especially if these symptoms are severe, abrupt in onset, or were not part of the patients presenting symptoms.If the decision has been made to discontinue treatment, medication should be tapered, as rapidly as is feasible, but with recognition that discontinuation can be associated with certain symptoms [see Dosage and Administration (2.7) and Warnings and Precautions (5.7) for descriptions of the risks of discontinuation of duloxetine delayed-release capsules].Families and caregivers of patients being treated with antidepressants for major depressive disorder or other indications, both psychiatric and nonpsychiatric, should be alerted about the need to monitor patients for the emergence of agitation, irritability, unusual changes in behavior, and the other symptoms described above, as well as the emergence of suicidality, and to report such symptoms immediately to health care providers. Such monitoring should include daily observation by families and caregivers. Prescriptions for duloxetine delayed-release capsules should be written for the smallest quantity of capsules consistent with good patient management, in order to reduce the risk of overdose. Screening Patients for Bipolar Disorder -- major depressive episode may be the initial presentation of bipolar disorder. It is generally believed (though not established in controlled trials) that treating such an episode with an antidepressant alone may increase the likelihood of precipitation of mixed/manic episode in patients at risk for bipolar disorder. Whether any of the symptoms described above represent such conversion is unknown. However, prior to initiating treatment with an antidepressant, patients with depressive symptoms should be adequately screened to determine if they are at risk for bipolar disorder; such screening should include detailed psychiatric history, including family history of suicide, bipolar disorder, and depression. It should be noted that duloxetine is not approved for use in treating bipolar depression.. 5.2 Hepatotoxicity. There have been reports of hepatic failure, sometimes fatal, in patients treated with duloxetine. These cases have presented as hepatitis with abdominal pain, hepatomegaly, and elevation of transaminase levels to more than twenty times the upper limit of normal with or without jaundice, reflecting mixed or hepatocellular pattern of liver injury. Duloxetine should be discontinued in patients who develop jaundice or other evidence of clinically significant liver dysfunction and should not be resumed unless another cause can be established. Cases of cholestatic jaundice with minimal elevation of transaminase levels have also been reported. Other postmarketing reports indicate that elevated transaminases, bilirubin, and alkaline phosphatase have occurred in patients with chronic liver disease or cirrhosis. Duloxetine increased the risk of elevation of serum transaminase levels in development program clinical trials. Liver transaminase elevations resulted in the discontinuation of 0.3% (92/34,756) of duloxetine-treated patients. In most patients, the median time to detection of the transaminase elevation was about two months. In adult placebo-controlled trials in any indication, for patients with normal and abnormal baseline ALT values, elevation of ALT >3 times the upper limit of normal occurred in 1.25% (144/11,496) of duloxetine-treated patients compared to 0.45% (39/8716) of placebo-treated patients. In adult placebo-controlled studies using fixed dose design, there was evidence of dose response relationship for ALT and AST elevation of >3 times the upper limit of normal and >5 times the upper limit of normal, respectively. Because it is possible that duloxetine and alcohol may interact to cause liver injury or that duloxetine may aggravate pre-existing liver disease, duloxetine delayed-release capsules should not be prescribed to patients with substantial alcohol use or evidence of chronic liver disease.. 5.3 Orthostatic Hypotension, Falls and Syncope. Orthostatic hypotension, falls and syncope have been reported with therapeutic doses of duloxetine. Syncope and orthostatic hypotension tend to occur within the first week of therapy but can occur at any time during duloxetine treatment, particularly after dose increases. The risk of falling appears to be related to the degree of orthostatic decrease in blood pressure as well as other factors that may increase the underlying risk of falls.In an analysis of patients from all placebo-controlled trials, patients treated with duloxetine reported higher rate of falls compared to patients treated with placebo. Risk appears to be related to the presence of orthostatic decrease in blood pressure. The risk of blood pressure decreases may be greater in patients taking concomitant medications that induce orthostatic hypotension (such as antihypertensives) or are potent CYP1A2 inhibitors [see Warnings and Precautions (5.12) and Drug Interactions (7.1)] and in patients taking duloxetine at doses above 60 mg daily. Consideration should be given to dose reduction or discontinuation of duloxetine in patients who experience symptomatic orthostatic hypotension, falls and/or syncope during duloxetine therapy. Risk of falling also appeared to be proportional to patients underlying risk for falls and appeared to increase steadily with age. As elderly patients tend to have higher underlying risk for falls due to higher prevalence of risk factors such as use of multiple medications, medical comorbidities and gait disturbances, the impact of increasing age by itself is unclear. Falls with serious consequences including bone fractures and hospitalizations have been reported [see Adverse Reactions (6.10) and Patient Counseling Information (17)]. 5.4 Serotonin Syndrome. The development of potentially life-threatening serotonin syndrome has been reported with SNRIs and SSRIs, including duloxetine, alone but particularly with concomitant use of other serotonergic drugs (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, amphetamines and St. Johns Wort) and with drugs that impair metabolism of serotonin (in particular, MAOIs, both those intended to treat psychiatric disorders and also others, such as linezolid and intravenous methylene blue).Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, delirium, and coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Patients should be monitored for the emergence of serotonin syndrome. The concomitant use of duloxetine with MAOIs intended to treat psychiatric disorders is contraindicated. Duloxetine should also not be started in patient who is being treated with MAOIs such as linezolid or intravenous methylene blue. All reports with methylene blue that provided information on the route of administration involved intravenous administration in the dose range of mg/kg to mg/kg. No reports involved the administration of methylene blue by other routes (such as oral tablets or local tissue injection) or at lower doses. There may be circumstances when it is necessary to initiate treatment with an MAOI such as linezolid or intravenous methylene blue in patient taking duloxetine. Duloxetine should be discontinued before initiating treatment with the MAOI [see Dosage and Administration (2.8, 2.9), and Contraindications (4)]. If concomitant use of duloxetine with other serotonergic drugs including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, amphetamines and St. Johns Wort is clinically warranted, patients should be made aware of potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases. Treatment with duloxetine and any concomitant serotonergic agents, should be discontinued immediately if the above events occur and supportive symptomatic treatment should be initiated. 5.5 Abnormal Bleeding. SSRIs and SNRIs, including duloxetine, may increase the risk of bleeding events. Concomitant use of aspirin, nonsteroidal anti-inflammatory drugs, warfarin, and other anti-coagulants may add to this risk. Case reports and epidemiological studies (case-control and cohort design) have demonstrated an association between use of drugs that interfere with serotonin reuptake and the occurrence of gastrointestinal bleeding. Bleeding events related to SSRIs and SNRIs use have ranged from ecchymoses, hematomas, epistaxis, and petechiae to life-threatening hemorrhages. Patients should be cautioned about the risk of bleeding associated with the concomitant use of duloxetine and NSAIDs, aspirin, or other drugs that affect coagulation. 5.6 Severe Skin Reactions. Severe skin reactions, including erythema multiforme and Stevens-Johnson Syndrome (SJS), can occur with duloxetine. The reporting rate of SJS associated with duloxetine use exceeds the general population background incidence rate for this serious skin reaction (1 to cases per million person years). The reporting rate is generally accepted to be an underestimate due to underreporting. Duloxetine should be discontinued at the first appearance of blisters, peeling rash, mucosal erosions, or any other sign of hypersensitivity if no other etiology can be identified. 5.7 Discontinuation of Treatment with Duloxetine Delayed-Release Capsules. Discontinuation symptoms have been systematically evaluated in patients taking duloxetine. Following abrupt or tapered discontinuation in adult placebo-controlled clinical trials, the following symptoms occurred at 1% or greater and at significantly higher rate in duloxetine-treated patients compared to those discontinuing from placebo: dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue. During marketing of other SSRIs and SNRIs (serotonin and norepinephrine reuptake inhibitors), there have been spontaneous reports of adverse events occurring upon discontinuation of these drugs, particularly when abrupt, including the following: dysphoric mood, irritability, agitation, dizziness, sensory disturbances (e.g., paresthesias such as electric shock sensations), anxiety, confusion, headache, lethargy, emotional lability, insomnia, hypomania, tinnitus, and seizures. Although these events are generally self-limiting, some have been reported to be severe. Patients should be monitored for these symptoms when discontinuing treatment with duloxetine. gradual reduction in the dose rather than abrupt cessation is recommended whenever possible. If intolerable symptoms occur following decrease in the dose or upon discontinuation of treatment, then resuming the previously prescribed dose may be considered. Subsequently, the physician may continue decreasing the dose but at more gradual rate [see Dosage and Administration (2.7)]. 5.8 Activation of Mania/Hypomania. In adult placebo-controlled trials in patients with major depressive disorder, activation of mania or hypomania was reported in 0.1% (4/3779) of duloxetine-treated patients and 0.04% (1/2536) of placebo-treated patients. No activation of mania or hypomania was reported in DPNP, GAD, or chronic musculoskeletal pain placebo-controlled trials. Activation of mania or hypomania has been reported in small proportion of patients with mood disorders who were treated with other marketed drugs effective in the treatment of major depressive disorder. As with these other agents, duloxetine should be used cautiously in patients with history of mania. 5.9 Angle-Closure Glaucoma. The pupillary dilation that occurs following use of many antidepressant drugs including duloxetine may trigger an angle closure attack in patient with anatomically narrow angles who does not have patent iridectomy.. 5.10 Seizures. Duloxetine has not been systematically evaluated in patients with seizure disorder, and such patients were excluded from clinical studies. In adult placebo-controlled clinical trials, seizures/convulsions occurred in 0.02% (3/12,722) of patients treated with duloxetine and 0.01% (1/9513) of patients treated with placebo. Duloxetine delayed-release capsules should be prescribed with care in patients with history of seizure disorder. 5.11 Effect on Blood Pressure. In adult placebo-controlled clinical trials across indications from baseline to endpoint, duloxetine treatment was associated with mean increases of 0.5 mm Hg in systolic blood pressure and 0.8 mm Hg in diastolic blood pressure compared to mean decreases of 0.6 mm Hg systolic and 0.3 mm Hg diastolic in placebo-treated patients. There was no significant difference in the frequency of sustained (3 consecutive visits) elevated blood pressure. In clinical pharmacology study designed to evaluate the effects of duloxetine on various parameters, including blood pressure at supratherapeutic doses with an accelerated dose titration, there was evidence of increases in supine blood pressure at doses up to 200 mg twice daily. At the highest 200 mg twice daily dose, the increase in mean pulse rate was 5.0 to 6.8 beats and increases in mean blood pressure were 4.7 to 6.8 mm Hg (systolic) and 4.5 to mm Hg (diastolic) up to 12 hours after dosing. Blood pressure should be measured prior to initiating treatment and periodically measured throughout treatment [see Adverse Reactions (6.7)].. 5.12 Clinically Important Drug Interactions. Both CYP1A2 and CYP2D6 are responsible for duloxetine metabolism. Potential for Other Drugs to Affect Duloxetine CYP1A2 Inhibitors -- Co-administration of duloxetine with potent CYP1A2 inhibitors should be avoided [see Drug Interactions (7.1)]. CYP2D6 Inhibitors -- Because CYP2D6 is involved in duloxetine metabolism, concomitant use of duloxetine with potent inhibitors of CYP2D6 would be expected to, and does, result in higher concentrations (on average of 60%) of duloxetine [see Drug Interactions (7.2)]. Potential for Duloxetine to Affect Other Drugs Drugs Metabolized by CYP2D6 -- Co-administration of duloxetine with drugs that are extensively metabolized by CYP2D6 and that have narrow therapeutic index, including certain antidepressants (tricyclic antidepressants [TCAs], such as nortriptyline, amitriptyline, and imipramine), phenothiazines and Type 1C antiarrhythmics (e.g., propafenone, flecainide), should be approached with caution. Plasma TCA concentrations may need to be monitored and the dose of the TCA may need to be reduced if TCA is co-administered with duloxetine. Because of the risk of serious ventricular arrhythmias and sudden death potentially associated with elevated plasma levels of thioridazine, duloxetine and thioridazine should not be co-administered [see Drug Interactions (7.9)]. Other Clinically Important Drug Interactions Alcohol -- Use of duloxetine concomitantly with heavy alcohol intake may be associated with severe liver injury. For this reason, duloxetine delayed-release capsules should not be prescribed for patients with substantial alcohol use [see Warnings and Precautions (5.2) and Drug Interactions (7.15)]. CNS Acting Drugs -- Given the primary CNS effects of duloxetine, it should be used with caution when it is taken in combination with or substituted for other centrally acting drugs, including those with similar mechanism of action [see Warnings and Precautions (5.12) and Drug Interactions (7.16)]. 5.13 Hyponatremia. Hyponatremia may occur as result of treatment with SSRIs and SNRIs, including duloxetine. In many cases, this hyponatremia appears to be the result of the syndrome of inappropriate antidiuretic hormone secretion (SIADH). Cases with serum sodium lower than 110 mmol/L have been reported and appeared to be reversible when duloxetine was discontinued. Elderly patients may be at greater risk of developing hyponatremia with SSRIs and SNRIs. Also, patients taking diuretics or who are otherwise volume depleted may be at greater risk [see Use in Specific Populations (8.5)]. Discontinuation of duloxetine should be considered in patients with symptomatic hyponatremia and appropriate medical intervention should be instituted. Signs and symptoms of hyponatremia include headache, difficulty concentrating, memory impairment, confusion, weakness, and unsteadiness, which may lead to falls. More severe and/or acute cases have been associated with hallucination, syncope, seizure, coma, respiratory arrest, and death. 5.14 Use in Patients with Concomitant Illness. Clinical experience with duloxetine in patients with concomitant systemic illnesses is limited. There is no information on the effect that alterations in gastric motility may have on the stability of duloxetines enteric coating. In extremely acidic conditions, duloxetine, unprotected by the enteric coating, may undergo hydrolysis to form naphthol. Caution is advised in using duloxetine in patients with conditions that may slow gastric emptying (e.g., some diabetics). Duloxetine has not been systematically evaluated in patients with recent history of myocardial infarction or unstable coronary artery disease. Patients with these diagnoses were generally excluded from clinical studies during the products premarketing testing.Hepatic Impairment-- Avoid use in patients with chronic liver disease or cirrhosis [see Dosage and Administration (2.6), Warnings and Precautions (5.2), and Use in Specific Populations (8.9)]. Severe Renal Impairment -- Avoid use in patients with severe renal impairment, GFR <30 mL/min. Increased plasma concentration of duloxetine, and especially of its metabolites, occur in patients with end-stage renal disease (requiring dialysis) [see Dosage and Administration (2.6) and Use in Specific Populations (8.10)]. Glycemic Control in Patients with Diabetes -- As observed in DPNP trials, duloxetine treatment worsens glycemic control in some patients with diabetes. In three clinical trials of duloxetine for the management of neuropathic pain associated with diabetic peripheral neuropathy, the mean duration of diabetes was approximately 12 years, the mean baseline fasting blood glucose was 176 mg/dL, and the mean baseline hemoglobin A1c (HbA1c) was 7.8%. In the 12-week acute treatment phase of these studies, duloxetine was associated with small increase in mean fasting blood glucose as compared to placebo. In the extension phase of these studies, which lasted up to 52 weeks, mean fasting blood glucose increased by 12 mg/dL in the duloxetine group and decreased by 11.5 mg/dL in the routine care group. HbA1c increased by 0.5% in the duloxetine and by 0.2% in the routine care groups.. 5.15 Urinary Hesitation and Retention. Duloxetine is in class of drugs known to affect urethral resistance. If symptoms of urinary hesitation develop during treatment with duloxetine, consideration should be given to the possibility that they might be drug-related. In post marketing experience, cases of urinary retention have been observed. In some instances of urinary retention associated with duloxetine use, hospitalization and/or catheterization has been needed. 5.16 Laboratory Tests. No specific laboratory tests are recommended.