IRENKA- duloxetine capsule, delayed release

Irenka by

Drug Labeling and Warnings

Irenka by is a Prescription medication manufactured, distributed, or labeled by LUPIN PHARMA, LUPIN LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • BOXED WARNING (What is this?)

    WARNING: SUICIDAL THOUGHTS AND BEHAVIORS

    Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These studies did not show an increase in the risk of suicidal thoughts and behavior with antidepressant use in patients over age 24; there was a reduction in risk with antidepressant use in patients aged 65 and older [see WARNINGS AND PRECAUTIONS (5.1)].

    In patients of all ages who are started on antidepressant therapy, monitor closely for worsening, and for emergence of suicidal thoughts and behaviors. Advise families and caregivers of the need for close observation and communication with the prescriber [see WARNINGS AND PRECAUTIONS (5.1)]. 

  • 1 INDICATIONS AND USAGE

    Irenka™ is indicated for the treatment of:

    • Major Depressive Disorder[see CLINICAL STUDIES 14.1]
    • Generalized Anxiety Disorder[see CLINICAL STUDIES 14.2]
    • Diabetic Peripheral Neuropathy[see CLINICAL STUDIES 14.3]
    • Chronic Musculoskeletal Pain[see CLINICAL STUDIES 14.5]
  • 2 DOSAGE AND ADMINISTRATION

    Swallow Irenka 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. Irenka can be given without regard to meals. If a dose of Irenka 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 Irenka at the same time.

    2.1 Dosage for Treatment of Major Depressive Disorder

    Administer duloxetine at a 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 1 week, to allow patients to adjust to the medication before increasing to 60 mg once daily. While a 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 60 mg once daily. For some patients, it may be desirable to start at 30 mg once daily for 1 week, to allow patients to adjust to the medication before increasing to 60 mg once daily. While a 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 a 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)].

    Elderly

    Initiate duloxetine at a dose of 30 mg once daily for 2 weeks before considering an increase to the target dose of 60 mg. Thereafter, patients may benefit from doses above 60 mg once daily. If a decision is made to increase the dose beyond 60 mg once daily, increase dose in increments of 30 mg once daily. The maximum dose studied was 120 mg per day. Safety of doses above 120 mg once daily has not been adequately evaluated [see CLINICAL STUDIES (14.2)].  

    Children and Adolescents (7 to 17 years of age)

    Initiate duloxetine at a dose of 30 mg once daily for 2 weeks before considering an increase to 60 mg. The recommended dose range is 30 to 60 mg once daily. Some patients may benefit from doses above 60 mg once daily. If a decision is made to increase the dose beyond 60 mg once daily, increase dose in increments of 30 mg once daily. The maximum dose studied was 120 mg per day. The safety of doses above 120 mg once daily has not been evaluated [see CLINICAL STUDIES (14.2)].

    2.3 Dosage for Treatment of Diabetic Peripheral Neuropathic Pain

    Administer duloxetine 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 a concern, a lower starting dose may be considered.

    Since diabetes is frequently complicated by renal disease, consider a 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 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 a 60 mg dose, and higher doses are associated with a 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 Irenka

    Adverse reactions after discontinuation of Irenka, after abrupt or tapered discontinuation, include: dizziness, headache, nausea, diarrhea, paresthesia, irritability, vomiting, insomnia, anxiety, hyperhidrosis, and fatigue. A gradual reduction in dosage rather than abrupt cessation is recommended whenever possible [see WARNINGS AND PRECAUTIONS (5.7)].

    2.8 Switching a Patient to or from a 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 Irenka. Conversely, at least 5 days should be allowed after stopping Irenka before starting an MAOI intended to treat psychiatric disorders [see CONTRAINDICATIONS (4)].

    2.9 Use of Irenka with Other MAOIs such as Linezolid or Methylene Blue

    Do not start Irenka in a patient who is being treated with linezolid or intravenous methylene blue because there is an increased risk of serotonin syndrome. In a patient who requires more urgent treatment of a psychiatric condition, other interventions, including hospitalization, should be considered [see CONTRAINDICATIONS (4)].

    In some cases, a patient already receiving Irenka 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 a particular patient, Irenka should be stopped promptly, and linezolid or intravenous methylene blue can be administered. The patient should be monitored for symptoms of serotonin syndrome for 5 days or until 24 hours after the last dose of linezolid or intravenous methylene blue, whichever comes first. Therapy with Irenka 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 1 mg/kg with Irenka 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)].

  • 3 DOSAGE FORMS AND STRENGTHS

    Irenka is available as delayed-release capsules:

    40 mg: Size '2' Capsules with white cap and white body imprinted with "LU" on cap and "H25" in black ink on body, containing eight white to off white mini tablets.

  • 4 CONTRAINDICATIONS

    Monoamine Oxidase Inhibitors (MAOIs)

    The use of MAOIs intended to treat psychiatric disorders with Irenka or within 5 days of stopping treatment with Irenka is contraindicated because of an increased risk of serotonin syndrome. The use of Irenka within 14 days of stopping an MAOI intended to treat psychiatric disorders is also contraindicated [see DOSAGE AND ADMINISTRATION (2.8) and WARNINGS AND PRECAUTIONS (5.4)].

    Starting Irenka in a patient who is being treated with MAOIs such as linezolid or intravenous methylene blue is also contraindicated because of an increased risk of serotonin syndrome [see DOSAGE AND ADMINISTRATION (2.9) and WARNINGS AND PRECAUTIONS (5.4)].

  • 5 WARNINGS AND PRECAUTIONS

    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 a known risk of depression and certain other psychiatric disorders, and these disorders themselves are the strongest predictors of suicide. There has been a long-standing concern, however, that antidepressants may have a 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 a 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 a total of 24 short-term trials of 9 antidepressant drugs in over 4400 patients. The pooled analyses of placebo-controlled trials in adults with MDD or other psychiatric disorders included a total of 295 short-term trials (median duration of 2 months) of 11 antidepressant drugs in over 77,000 patients. There was considerable variation in risk of suicidality among drugs, but a 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 1
    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
    		5 additional cases

    		Decreases Compared to Placebo
    25 to 64
    		1 fewer case
    ≥65
    		6 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 a 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 a 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 patient's 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 Irenka].

    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 Irenka 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

    A 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 a mixed/manic episode in patients at risk for bipolar disorder. Whether any of the symptoms described above represent such a 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 a detailed psychiatric history, including a family history of suicide, bipolar disorder, and depression. It should be noted that Irenka 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 a mixed or hepatocellular pattern of liver injury. Irenka 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 a fixed dose design, there was evidence of a 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 Irenka and alcohol may interact to cause liver injury or that Irenka may aggravate pre-existing liver disease, Irenka 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 Irenka 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 a 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 Irenka in patients who experience symptomatic orthostatic hypotension, falls and/or syncope during Irenka therapy.

    Risk of falling also appeared to be proportional to a patient's underlying risk for falls and appeared to increase steadily with age. As elderly patients tend to have a higher underlying risk for falls due to a 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 a 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, and St. John's 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 Irenka with MAOIs intended to treat psychiatric disorders is contraindicated. Irenka should also not be started in a 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 1 mg/kg to 8 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 a patient taking Irenka. Irenka should be discontinued before initiating treatment with the MAOI [see DOSAGE AND ADMINISTRATION (2.8, 2.9), and CONTRAINDICATIONS (4)].

    If concomitant use of Irenka with other serotonergic drugs including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan and St. John's Wort is clinically warranted, patients should be made aware of a potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases. Treatment with Irenka 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 Irenka, 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 Irenka 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 Irenka. The reporting rate of SJS associated with duloxetine use exceeds the general population background incidence rate for this serious skin reaction (1 to 2 cases per million person years). The reporting rate is generally accepted to be an underestimate due to underreporting.

    Irenka 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 Irenka

    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 a 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 Irenka. A gradual reduction in the dose rather than abrupt cessation is recommended whenever possible. If intolerable symptoms occur following a 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 a 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 a 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, Irenka should be used cautiously in patients with a history of mania.

    5.9 Angle-Closure Glaucoma

    The pupillary dilation that occurs following use of many antidepressant drugs including Irenka may trigger an angle closure attack in a patient with anatomically narrow angles who does not have a patent iridectomy.

    5.10 Seizures

    Duloxetine has not been systematically evaluated in patients with a 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. Irenka should be prescribed with care in patients with a history of a 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 a 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 to 6.8 beats and increases in mean blood pressure were 4.7 to 6.8 mm Hg (systolic) and 4.5 to 7 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 Irenka metabolism.

    Potential for Other Drugs to Affect Irenka

    CYP1A2 Inhibitors:

    Co-administration of Irenka with potent CYP1A2 inhibitors should be avoided [see DRUG INTERACTIONS (7.1)].

    CYP2D6 Inhibitors:

    Because CYP2D6 is involved in Irenka 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 Irenka [see DRUG INTERACTIONS (7.2)].

    Potential for Irenka to Affect Other Drugs

    Drugs Metabolized by CYP2D6:

    Co-administration of Irenka with drugs that are extensively metabolized by CYP2D6 and that have a 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 a TCA is co-administered with Irenka. Because of the risk of serious ventricular arrhythmias and sudden death potentially associated with elevated plasma levels of thioridazine, Irenka and thioridazine should not be co-administered [see DRUG INTERACTIONS (7.9)].

    Other Clinically Important Drug Interactions

    Alcohol:

    Use of Irenka concomitantly with heavy alcohol intake may be associated with severe liver injury. For this reason, Irenka 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 Irenka, it should be used with caution when it is taken in combination with or substituted for other centrally acting drugs, including those with a similar mechanism of action [see WARNINGS AND PRECAUTIONS (5.11) and DRUG INTERACTIONS (7.16)].

    5.13 Hyponatremia

    Hyponatremia may occur as a result of treatment with SSRIs and SNRIs, including Irenka. 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 Irenka 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 Irenka enteric coating. In extremely acidic conditions, Irenka, unprotected by the enteric coating, may undergo hydrolysis to form naphthol. Caution is advised in using Irenka in patients with conditions that may slow gastric emptying (e.g., some diabetics).

    Duloxetine has not been systematically evaluated in patients with a recent history of myocardial infarction or unstable coronary artery disease. Patients with these diagnoses were generally excluded from clinical studies during the product's 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 Irenka, 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 a 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

    Irenka is in a class of drugs known to affect urethral resistance. If symptoms of urinary hesitation develop during treatment with Irenka, 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.

  • 6 ADVERSE REACTIONS

    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 Irenka[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 a 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, a treatment-emergent adverse reaction of the type listed. A 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 duloxetine in placebo-controlled trials for MDD (N=3779), GAD (N=1018), OA (N=503), CLBP (N=600), and DPNP (N=906). The population studied was 17 to 89 years of age; 65.7%, 60.8%, 60.6% and 42.9% female; and 81.8%, 72.6%, 85.3%, and 74.0% Caucasian for MDD, GAD, OA and CLBP, and DPNP, respectively. Most patients received doses of a total of 60 to 120 mg per day [see CLINICAL STUDIES (14)]. The data below do not include results of the trial examining the efficacy of duloxetine in patients ≥ 65 years old for the treatment of generalized anxiety disorder; however, the adverse reactions observed in this geriatric sample were generally similar to adverse reactions in the overall adult population.

    Children and Adolescents 

    The data described below reflect exposure to duloxetine in pediatric, 10-week, placebo-controlled trials for MDD (N=341) and GAD (N=135). The population studied (N=476) was 7 to 17 years of age with 42.4% children age 7 to 11 years of age, 50.6% female, and 68.6% white. Patients received 30 to 120 mg per day during placebo-controlled acute treatment studies. Additional data come from the overall total of 822 pediatric patients (age 7 to 17 years of age) with 41.7% children age 7 to 11 years of age and 51.8% female exposed to duloxetine in MDD and GAD clinical trials up to 36-weeks in length, in which most patients received 30 to 120 mg per day.

    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 a reason for discontinuation and considered to be drug-related (i.e., discontinuation occurring in at least 1% of the duloxetine treated patients and at a 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 a 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 a 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 a 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 a 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 2 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 Indications*

    bAlso includes asthenia.

    cEvents for which there was a significant dose-dependent relationship in fixed-dose studies, excluding three MDD studies which did not have a placebo lead-in period or dose titration.

    dAlso includes initial insomnia, middle insomnia, and early morning awakening.

    eAlso includes hypersomnia and sedation.

    fAlso includes abdominal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness, and gastrointestinal pain.
  • * 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.
    		•
    Adverse Reaction
    		Percentage of Patients Reporting Reaction

    		Duloxetine (N=8100)
    		Placebo (N=5655)
    Nauseac
    		23
    		8
    Headache
    		14
    		12
    Dry mouth
    		13
    		5
    Somnolencee
    		10
    		3
    Fatigueb,c
    		9
    		5
    Insomniad
    		9
    		5
    Constipationc
    		9
    		4
    Dizzinessc
    		9
    		5
    Diarrhea
    		9
    		6
    Decreased appetitec
    		7
    		2
    Hyperhidrosisc
    		6
    		1
    Abdominal painf
    		5
    		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 3 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 Trials*,†

    cEvents for which there was a significant dose-dependent relationship in fixed-dose studies, excluding three MDD studies which did not have a placebo lead-in period or dose titration.

    dAlso includes abdominal pain upper, abdominal pain lower, abdominal tenderness, abdominal discomfort, and gastrointestinal pain

    eAlso includes asthenia

    fAlso includes hypersomnia and sedation

    gAlso includes initial insomnia, middle insomnia, and early morning awakening

    hAlso includes feeling jittery, nervousness, restlessness, tension and psychomotor hyperactivity

    iAlso includes loss of libido

    jAlso includes anorgasmia

  • * 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.
  • † For 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.
    		•

    		Percentage of Patients Reporting Reaction
    System Organ Class / Adverse Reaction
    		Duloxetine(N=4797)
    		Placebo(N=3303)
    Cardiac Disorders


    Palpitations 
    		2
    		1
    Eye Disorders


    Vision blurred 
    		3
    		1
    Gastrointestinal Disorders


    Nauseac
    		23
    		8
    Dry mouth 
    		14
    		6
    Constipationc
    		9
    		4
    Diarrhea
    		9
    		6
    Abdominal paind
    		5
    		4
    Vomiting 
    		4
    		2
    General Disorders and Administration Site Conditions

    Fatiguee
    		9
    		5
    Metabolism and Nutrition Disorders

    Decreased appetitec
    		6
    		2
    Nervous System Disorders


    Headache
    		14
    		14
    Dizzinessc
    		9
    		5
    Somnolencef9
    		3
    Tremor 
    		3
    		1
    Psychiatric Disorders


    Insomniag9
    		5
    Agitationh
    		4
    		2
    Anxiety 
    		3
    		2
    Reproductive System and Breast Disorders

    Erectile dysfunction
    		4
    		1
    Ejaculation delayedc
    		2
    		1
    Libido decreasedi
    		3
    		1
    Orgasm abnormalj
    		2
    		<1
    Respiratory, Thoracic, and Mediastinal Disorders

    Yawning 
    		2
    		<1
    Skin and Subcutaneous Tissue Disorders

    Hyperhidrosis 
    		6
    		2

    DPNP, OA, and CLBP

    Table 4 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, 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, OA, and CLBP Placebo-Controlled Trials*

    bIncidence of 120 mg/day is significantly greater than the incidence for 60 mg/day.

    cAlso includes abdominal discomfort, abdominal pain lower, abdominal pain upper, abdominal tenderness and gastrointestinal pain

    dAlso includes asthenia

    eAlso includes myalgia and neck pain

    fAlso includes hypersomnia and sedation

    gAlso includes hypoaesthesia, hypoaesthesia facial, genital hypoaesthesia and paraesthesia oral

    hAlso includes initial insomnia, middle insomnia, and early morning awakening.

    iAlso includes feeling jittery, nervousness, restlessness, tension and psychomotor hyperactivity

    jAlso includes ejaculation failure

    kAlso includes hot flush

    lAlso 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


  • * 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.
    		•

    		Percentage of Patients Reporting Reaction
    System Organ Class / Adverse Reaction
    		Duloxetine(N=3303)
    		Placebo(N=2352)
    Gastrointestinal Disorders


    Nausea
    		23
    		7
    Dry mouthb11
    		3
    Constipationb
    		10
    		3
    Diarrhea 
    		9
    		5
    Abdominal Painc
    		5
    		4
    Vomiting 
    		3
    		2
    Dyspepsia
    		2
    		1
    General Disorders and Administration Site Conditions

    Fatigued
    		11
    		5
    Infections and Infestations


    Nasopharyngitis
    		4
    		4
    Upper Respiratory Tract Infection
    		3
    		3
    Influenza
    		2
    		2
    Metabolism and Nutrition Disorders


    Decreased Appetiteb,
    		8
    		1
    Musculoskeletal and Connective Tissue


    Musculoskeletal Paine
    		3
    		3
    Muscle Spasms
    		2
    		2
    Nervous System Disorders


    Headache
    		13
    		8
    Somnolenceb,f11
    		3
    Dizziness
    		9
    		5
    Paraesthesiag
    		2
    		2
    Tremorb
    		2
    		<1
    Psychiatric Disorders


    Insomniab,h10
    		5
    Agitationi
    		3
    		1
    Reproductive System and Breast Disorders

    Erectile Dysfunctionb
    		4
    		<1
    Ejaculation Disorderj
    		2
    		<1
    Respiratory, Thoracic, and Mediastinal Disorders

    Cough
    		2
    		2
    Skin and Subcutaneous Tissue Disorders

    Hyperhidrosis 
    		6
    		1
    Vascular Disorders


    Flushingk
    		3
    		1
    Blood pressure increasedl
    		2
    		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 a consequence of pharmacologic treatment. Because adverse sexual reactions are presumed to be voluntarily underreported, the Arizona Sexual Experience Scale (ASEX), a validated measure designed to identify sexual side effects, was used prospectively in 4 MDD placebo-controlled trials. In these trials, as shown in Table 5 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 a 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 MDD Placebo-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 Patients*
    		Female Patients*

    		Duloxetine (n=175)
    		Placebo (n=83)
    		Duloxetine (n=241)
    		Placebo (n=126)
    ASEX Total (Items 1 to 5) 
    		0.56†-1.07
    		-1.15
    		-1.07
    Item 1-Sex drive 
    		-0.07
    		-0.12
    		-0.32
    		-0.24
    Item 2-Arousal 
    		0.01
    		-0.26
    		-0.21
    		-0.18
    Item 3-Ability to achieve erection (men); Lubrication (women) 
    		0.03
    		-0.25
    		-0.17
    		-0.18
    Item 4-Ease of reaching orgasm 
    		0.40‡-0.24
    		-0.09
    		-0.13
    Item 5-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 a 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, 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 a 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 a 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 6 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 a 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 a 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 6 provides the incidence of treatment-emergent adverse reactions in MDD and GAD 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 Trials*

    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.

  • * 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.
    		•
    System Organ Class/Adverse Reaction 
    		Percentage of Pediatric Patients Reporting Reaction

    		Duloxetine 
    (N=476)
    		Placebo
    (N=362)
    Gastrointestinal Disorders 
    Nausea 
    Abdominal Pain b
    Vomiting
    Diarrhea
    Dry Mouth 
    18 
    13 
    9 
    6 
    2
    8 
    10 
    4 
    3 
    1
    General Disorders and Administration Site Conditions 
    Fatigue c


    7

    5
    Investigations 
    Decreased Weight d

    14
    6
    Metabolism and Nutrition Disorders Decreased Appetite 
    10
    5
    Nervous System Disorders 
    Headache
    Somnolence e
    Dizziness
    18 
    11 
    8
    13
     6 
    4
    Psychiatric Disorders 
    Insomnia f

    7
    4
    Respiratory, Thoracic, and Mediastinal Disorders 
    Oropharyngeal Pain 
    Cough  


    4 
    3

    2 
    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. 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. Pediatric patients treated with duloxetine in clinical trials experienced a 0.1kg mean decrease in weight at 10 weeks, compared with a mean weight gain of approximately 0.9 kg in placebo-treated patients. The proportion of patients who experienced a clinically significant decrease in weight (≥3.5%) was greater in the duloxetine group than in the placebo group (14% and 6%, respectively). Subsequently, over the 4- to 6-month uncontrolled extension periods, duloxetine-treated patients on average trended toward recovery to their expected baseline weight percentile based on population data from age- and sex-matched peers. In studies up to 9 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, a 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 Irenka.

    6.12 Postmarketing Spontaneous Reports

    The following adverse reactions have been identified during postapproval use of duloxetine. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Adverse reactions reported since market introduction that were temporally related to duloxetine therapy and not mentioned elsewhere in labeling include: anaphylactic reaction, aggression and anger (particularly early in treatment or after treatment discontinuation), angioneurotic edema, angle-closure glaucoma, 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.

  • 7 DRUG INTERACTIONS

    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, a 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, a potent CYP1A2 inhibitor, to CYP2D6 poor metabolizer subjects (n=14) resulted in a 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 to 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 (AUCτ,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 Q 12 hours) and lorazepam (2 mg Q 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

    Irenka has an enteric coating that resists dissolution until reaching a segment of the gastrointestinal tract where the pH exceeds 5.5. In extremely acidic conditions, Irenka, unprotected by the enteric coating, may undergo hydrolysis to form naphthol. Caution is advised in using Irenka 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 with aluminum- and magnesium-containing antacids (51 mEq) or duloxetine with famotidine, had no significant effect on the rate or extent of duloxetine absorption after administration of a 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 a moderate inhibitor of CYP2D6. When duloxetine was administered (at a dose of 60 mg twice daily) in conjunction with a single 50 mg dose of desipramine, a 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 a clinical study, the pharmacokinetics of S-warfarin, a 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 (2.4, 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 to a 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 to 9 mg), a 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)].

  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Teratogenic Effects, Pregnancy Category C

    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 4 and 7 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 1 day postpartum were decreased at a dose 2 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. Irenka 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 a direct toxic effect of the SNRIs or SSRIs, or possibly, a 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 a mg/m2 basis, in rat; 7 times the MRHD in rabbit). However, fetal weights were decreased at this dose, with a no-effect dose of 10 mg/kg/day approximately equal to the MRHD in rats; 2 times the MRHD in rabbits).

    When duloxetine was administered orally to pregnant rats throughout gestation and lactation, the survival of pups to 1 day postpartum and pup body weights at birth and during the lactation period were decreased at a 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

    Irenka is present in human milk. In a 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 mother's clinical need for Irenka and any potential adverse effects on the milk-fed child from the drug or from the underlying maternal condition. Exercise caution when Irenka is administered to a nursing woman.

     

    Data 

    The disposition of duloxetine was studied in 6 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 a median of 3 hours after the dose. The amount of duloxetine in breast milk was approximately 7 mcg/day while on that dose; the estimated daily infant dose was approximately 2 mcg/kg/day. The presence of duloxetine metabolites in breast milk was not examined.

    8.4 Pediatric Use

    Generalized Anxiety Disorder

    In pediatric patients aged 7 to 17 years, efficacy was demonstrated in one 10-week, placebo-controlled trial. The study included 272 pediatric patients with GAD of which 47% were 7 to 11 years of age. Duloxetine demonstrated superiority over placebo as measured by greater improvement in the Pediatric Anxiety Rating Scale (PARS) for GAD severity score [see CLINICAL STUDIES (14.2)]. The safety and effectiveness in pediatric patients less than 7 years of age have not been established.

    Major Depressive Disorder

    Efficacy was not demonstrated in two 10-week, placebo-controlled trials with 800 pediatric patients with MDD, age 7 to 17. Neither duloxetine nor an active control (indicated for treatment of pediatric depression) was superior to placebo. Thus, safety and effectiveness of duloxetine have not been established in pediatric patients less than 18 years of age with MDD.

    The most frequently observed adverse reactions in the clinical trials included nausea, headache, decreased weight, and abdominal pain. 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)].

    Use of Irenka in a child or adolescent must balance the potential risks with the clinical need [see BOXED WARNING and WARNINGS AND PRECAUTIONS (5.1)].

    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 a delay in learning a 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 a child); the no-effect-level was 20 mg/kg/day (≈1 times the MRHD, for a 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, and DPNP, OA, and CLBP 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 have 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 a higher rate of falls compared to patients treated with placebo. The increased risk appears to be proportional to a patient's underlying risk for falls. Underlying risk appears to increase steadily with age. As elderly patients tend to have a 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)].

    The pharmacokinetics of duloxetine after a single dose of 40 mg were compared in healthy elderly females (65 to 77 years) and healthy middle-age females (32 to 50 years). There was no difference in the Cmax, but the AUC of duloxetine was somewhat (about 25%) higher and the half-life about 4 hours longer in the elderly females. Population pharmacokinetic analyses suggest that the typical values for clearance decrease by approximately 1% for each year of age between 25 to 75 years of age; but age as a predictive factor only accounts for a small percentage of between-patient variability. Dosage adjustment based on the age of the patient is not necessary.

    8.6 Gender

    Duloxetine's 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 a single 20 mg dose of duloxetine, 6 cirrhotic patients with moderate liver impairment (Child-Pugh Class B) had a mean plasma duloxetine clearance about 15% that of age- and gender-matched healthy subjects, with a 5-fold increase in mean exposure (AUC). Although Cmax was similar to normals in the cirrhotic patients, the half-life was about 3 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 a 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)].

  • 9 DRUG ABUSE AND DEPENDENCE

    9.2 Abuse

    In animal studies, duloxetine did not demonstrate barbiturate-like (depressant) abuse potential.

    While duloxetine has not been systematically studied in humans for its potential for abuse, there was no indication of drug-seeking behavior in the clinical trials. However, it is not possible to predict on the basis of premarketing experience the extent to which a CNS active drug will be misused, diverted, and/or abused once marketed. Consequently, physicians should carefully evaluate patients for a history of drug abuse and follow such patients closely, observing them for signs of misuse or abuse of Irenka (e.g., development of tolerance, incrementation of dose, drug-seeking behavior).

    9.3 Dependence

    In drug dependence studies, duloxetine did not demonstrate dependence-producing potential in rats.

  • 10 OVERDOSAGE

    10.1 Signs and Symptoms

    In postmarketing experience, fatal outcomes have been reported for acute overdoses, primarily with mixed overdoses, but also with duloxetine only, at doses as low as 1000 mg. Signs and symptoms of overdose (duloxetine alone or with mixed drugs) included somnolence, coma, serotonin syndrome, seizures, syncope, tachycardia, hypotension, hypertension, and vomiting.

    10.2 Management of Overdose

    There is no specific antidote to Irenka, but if serotonin syndrome ensues, specific treatment (such as with cyproheptadine and/or temperature control) may be considered. In case of acute overdose, treatment should consist of those general measures employed in the management of overdose with any drug.

    An adequate airway, oxygenation, and ventilation should be assured, and cardiac rhythm and vital signs should be monitored. Induction of emesis is not recommended. Gastric lavage with a large-bore orogastric tube with appropriate airway protection, if needed, may be indicated if performed soon after ingestion or in symptomatic patients.

    Activated charcoal may be useful in limiting absorption of duloxetine from the gastrointestinal tract. Administration of activated charcoal has been shown to decrease AUC and Cmax by an average of one-third, although some subjects had a limited effect of activated charcoal. Due to the large volume of distribution of this drug, forced diuresis, dialysis, hemoperfusion, and exchange transfusion are unlikely to be beneficial.

    In managing overdose, the possibility of multiple drug involvement should be considered. A specific caution involves patients who are taking or have recently taken Irenka and might ingest excessive quantities of a TCA. In such a case, decreased clearance of the parent tricyclic and/or its active metabolite may increase the possibility of clinically significant sequelae and extend the time needed for close medical observation [see WARNINGS AND PRECAUTIONS (5.4) and DRUG INTERACTIONS (7)]. The physician should consider contacting a poison control center  (1-800-222-1222 or www.poison.org) for additional information on the treatment of any overdose. Telephone numbers for certified poison control centers are listed in the Physicians' Desk Reference (PDR).

  • 11 DESCRIPTION

    Irenka™ (duloxetine delayed-release capsules USP) is selective serotonin and norepinephrine reuptake inhibitor (SSNRI) for oral administration. Its chemical designation is (+)-(S)-N-methyl-γ-(1-naphthyloxy)-2-thiophenepropylamine hydrochloride. The empirical formula is C18H19NOS.HCl, which corresponds to a molecular weight of 333.88. The structural formula is:

    Structure

    Duloxetine hydrochloride is a white to cream colored powder, which is soluble in methanol.

    Each capsule contains enteric-coated mini tablets comprising of duloxetine hydrochloride equivalent to 40 of duloxetine. These enteric-coated mini tablets are designed to prevent degradation of the drug in the acidic environment of the stomach. Inactive ingredients include ammonia solution, black iron oxide, croscarmellose sodium, gelatin, hypromellose, hypromellose phthalate, lactose monohydrate, magnesium stearate, polysorbate 80, potassium hydroxide, pregelatinized starch, propylene glycol, shellac, talc, titanium dioxide and triethyl citrate.

  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Although the exact mechanisms of the antidepressant, central pain inhibitory and anxiolytic actions of duloxetine in humans are unknown, these actions are believed to be related to its potentiation of serotonergic and noradrenergic activity in the CNS.

    12.2 Pharmacodynamics

    Preclinical studies have shown that duloxetine is a potent inhibitor of neuronal serotonin and norepinephrine reuptake and a less potent inhibitor of dopamine reuptake. Duloxetine has no significant affinity for dopaminergic, adrenergic, cholinergic, histaminergic, opioid, glutamate, and GABA receptors in vitro. Duloxetine does not inhibit monoamine oxidase (MAO).

    Irenka is in a class of drugs known to affect urethral resistance. If symptoms of urinary hesitation develop during treatment with Irenka, consideration should be given to the possibility that they might be drug-related.

    12.3 Pharmacokinetics

    Duloxetine has an elimination half-life of about 12 hours (range 8 to 17 hours) and its pharmacokinetics are dose proportional over the therapeutic range. Steady-state plasma concentrations are typically achieved after 3 days of dosing. Elimination of duloxetine is mainly through hepatic metabolism involving two P450 isozymes, CYP1A2 and CYP2D6.

    Absorption and Distribution

    Orally administered duloxetine hydrochloride is well absorbed. There is a median 2 hour lag until absorption begins (Tlag), with maximal plasma concentrations (Cmax) of duloxetine occurring 6 hours post dose. Food does not affect the Cmax of duloxetine, but delays the time to reach peak concentration from 6 to 10 hours and it marginally decreases the extent of absorption (AUC) by about 10%. There is a 3 hour delay in absorption and a one-third increase in apparent clearance of duloxetine after an evening dose as compared to a morning dose.

    The apparent volume of distribution averages about 1640 L. Duloxetine is highly bound (>90%) to proteins in human plasma, binding primarily to albumin and α1-acid glycoprotein. The interaction between duloxetine and other highly protein bound drugs has not been fully evaluated. Plasma protein binding of duloxetine is not affected by renal or hepatic impairment.

    Metabolism and Elimination

    Biotransformation and disposition of duloxetine in humans have been determined following oral administration of 14C-labeled duloxetine. Duloxetine comprises about 3% of the total radiolabeled material in the plasma, indicating that it undergoes extensive metabolism to numerous metabolites. The major biotransformation pathways for duloxetine involve oxidation of the naphthyl ring followed by conjugation and further oxidation. Both CYP1A2 and CYP2D6 catalyze the oxidation of the naphthyl ring in vitro. Metabolites found in plasma include 4-hydroxy duloxetine glucuronide and 5-hydroxy, 6-methoxy duloxetine sulfate. Many additional metabolites have been identified in urine, some representing only minor pathways of elimination. Only trace (<1% of the dose) amounts of unchanged duloxetine are present in the urine. Most (about 70%) of the duloxetine dose appears in the urine as metabolites of duloxetine; about 20% is excreted in the feces. Duloxetine undergoes extensive metabolism, but the major circulating metabolites have not been shown to contribute significantly to the pharmacologic activity of duloxetine.

    Children and Adolescents (ages 7 to 17 years)

    Duloxetine steady-state plasma concentration was comparable in children (7 to 12 years of age), adolescents (13 to 17 years of age) and adults. The average steady-state duloxetine concentration was approximately 30% lower in the pediatric population (children and adolescents) relative to the adults. The model-predicted duloxetine steady state plasma concentrations in children and adolescents were mostly within the concentration range observed in adult patients and did not exceed the concentration range in adults.

  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Carcinogenesis

    Duloxetine was administered in the diet to mice and rats for 2 years.

    In female mice receiving duloxetine at 140 mg/kg/day (6 times the maximum recommended human dose (MRHD) of 120 mg/day on a mg/m2 basis), there was an increased incidence of hepatocellular adenomas and carcinomas. The no-effect dose was 50 mg/kg/day (2 times the MRHD) Tumor incidence was not increased in male mice receiving duloxetine at doses up to 100 mg/kg/day (4 times the MRHD).

    In rats, dietary doses of duloxetine up to 27 mg/kg/day in females (2 times the MRHD) and up to 36 mg/kg/day in males (3 times the MRHD) did not increase the incidence of tumors.

    Mutagenesis

    Duloxetine was not mutagenic in the in vitro bacterial reverse mutation assay (Ames test) and was not clastogenic in an in vivo chromosomal aberration test in mouse bone marrow cells. Additionally, duloxetine was not genotoxic in an in vitro mammalian forward gene mutation assay in mouse lymphoma cells or in an in vitro unscheduled DNA synthesis (UDS) assay in primary rat hepatocytes, and did not induce sister chromatid exchange in Chinese hamster bone marrow in vivo.

    Impairment of Fertility

    Duloxetine administered orally to either male or female rats prior to and throughout mating at doses up to 45 mg/kg/day (4 times the MRHD) did not alter mating or fertility.

  • 14 CLINICAL STUDIES

    The efficacy of duloxetine has been established in the following adequate and well-controlled trials:

    • Major Depressive Disorder (MDD): 4 short-term and 1 maintenance trial in adults[see CLINICAL STUDIES (14.1)] .
    • Generalized Anxiety Disorder (GAD): 3 short-term trials in adults and 1 maintenance trial in adults, and 1 short term trial in children and adolescents[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 a treatment for depression was established in 4 randomized, double-blind, placebo-controlled, fixed-dose studies in adult outpatients (18 to 83 years) meeting DSM-IV criteria for major depression. In 2 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 9 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 8 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 8 weeks. There is no evidence that doses greater than 60 mg/day confer additional benefits.

    In all 4 studies, duloxetine demonstrated superiority over placebo as measured by improvement in the 17-item Hamilton Depression Rating Scale (HAMD-17) total score (Studies 1 to 4 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.

    bDoses statistically significantly superior to placebo.

    Study Number
    		Treatment Group
    		Primary Efficacy Measure: HAMD-17


    		Mean Baseline Score (SD)
    		LS Mean Change from Baseline (SE)
    		Placebo-subtracted Difference a 
    (95% CI)
    Study 1 
    		Duloxetine (60 mg/day) b Placebo 
    		21.5 (4.10) 
    21.1 (3.71)
    		-10.9 (0.70) 
    -6.1 (0.69)
    		-4.9 (-6.8, -2.9)
     -
    Study 2 
    		Duloxetine (60 mg/day) b Placebo 
    		20.3 (3.32) 
    20.5 (3.42)
    		-10.5 (0.71) 
    -8.3 (0.67)
    		-2.2 (-4.0, -0.3) 
    -
    Study 3 
    		Duloxetine (20 mg BID) b  Duloxetine (40 mg BID) b Placebo 
    		18.6 (5.85) 
    18.1 (4.52) 
    17.2 (5.11)
    		-7.4 (0.80) 
    -8.6 (0.81) 
    -5.0 (0.81)
    		-2.4 (-4.7, -0.2) 
    -3.6 (-5.9, -1.4) 
    --
    Study 4 
    		Duloxetine (40 mg BID) b  Duloxetine (60 mg BID) b Placebo 
    		19.9 (3.54) 
    20.2 (3.41) 
    19.9 (3.58)
    		-11.0 (0.49) 
    -12.1 (0.49) 
    -8.8 (0.50)
    		-2.2 (-3.6, -0.9) 
    -3.3 (-4.7, -1.9) 
    --

    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: a 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 6 months. Patients on duloxetine experienced a statistically significantly longer time to relapse of depression than did patients on placebo (Study 5 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 the DSM-IV criteria for MDD at 2 consecutive visits at least 2 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 1 fixed-dose randomized, double-blind, placebo-controlled trial and 2 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 1 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 a starting dose of 30 mg once daily for 1 week before increasing it to 60 mg once daily.

    The 2 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 a 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 a 9-week treatment period. While a 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 3 studies, duloxetine demonstrated superiority over placebo as measured by greater improvement in the Hamilton Anxiety Scale (HAM-A) total score (Studies 1 to 3 in Table 8) and by the Sheehan Disability Scale (SDS) global functional impairment score. The SDS is a composite measurement of the extent emotional symptoms disrupt patient functioning in 3 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: a decrease from baseline HAM-A total score by at least 50% to a score no higher than 11, and a Clinical Global Impressions of Improvement [CGI-Improvement] score of 1 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 a responder status for at least 10 weeks. Relapse was defined as an increase in CGI-Severity score at least 2 points to a score ≥4 and a MINI (Mini-International Neuropsychiatric Interview) diagnosis of GAD (excluding duration), or discontinuation due to lack of efficacy. Patients taking duloxetine experienced a statistically significantly longer time to relapse of GAD than did patients taking placebo (Study 4 in Figure 2).

    Subgroup analyses did not indicate that there were any differences in treatment outcomes as a function of age or gender.

    The efficacy of duloxetine in the treatment of patients ≥65 years of age with generalized anxiety disorder was established in one 10-week flexible-dose, randomized, double-blind, placebo-controlled trial in adults ≥65 years of age meeting the DSM-IV criteria for GAD. In this study, the starting dose was 30 mg once daily for 2 weeks before further dose increases in 30 mg increments at treatment weeks 2, 4, and 7 up to 120 mg once daily were allowed based on investigator judgment of clinical response and tolerability. The mean dose for patients completing the 10-week acute treatment phase was 50.95 mg. Patients treated with duloxetine (N=151) demonstrated significantly greater improvement compared with placebo (N=140) on mean change from baseline to endpoint as measured by the Hamilton Anxiety Rating Scale total score (Study 5 in Table 8).

    The efficacy of duloxetine in the treatment of pediatric patients 7 to 17 years of age with generalized anxiety disorder (GAD) was established in 1 flexible-dose randomized, double-blind, placebo-controlled trial in pediatric outpatients with GAD (based on DSM-IV criteria).

    In this study, the starting dose was 30 mg once daily for 2 weeks. Further dose increases in 30 mg increments up to 120 mg once daily were allowed based on investigator judgment of clinical response and tolerability. The mean dose for patients completing the 10-week treatment phase was 57.6 mg/day. In this study, duloxetine (N=135) demonstrated superiority over placebo (N=137) from baseline to endpoint as measured by greater improvement in the Pediatric Anxiety Rating Scale (PARS) for GAD severity score (Study 6 in Table 8).

    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 Number 
    		Treatment Group 
    		Primary Efficacy Measure


    		Mean Baseline Score (SD)
    		LS Mean Change from Baseline (SE)
    		Placebo-subtracted Difference a 
    (95% CI)
    Study 1 
    		Duloxetine (60 mg/day) b 
    		25.1 (7.18)
    		-12.8 (0.68)
    		-4.4 (-6.2, -2.5)
    (HAM-A)
    		Duloxetine (120 mg/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 2 
    		Duloxetine 
    (60 to 120 mg/day) b 
    		22.5 (7.44)
    		-8.1 (0.70)
    		-2.2 (-4.2, -0.3)
    (HAM-A)
    		Placebo 
    		23.5 (7.91)
    		-5.9 (0.70)
    		--
    Study 3 
    		Duloxetine 
    (60 to 120 mg/day) b 
    		25.8 (5.66)
    		-11.8 (0.69)
    		-2.6 (-4.5, -0.7)
    (HAM-A)
    		Placebo 
    		25.0 (5.82)
    		-9.2 (0.67)
    		--
    Study 5 (Elderly) 
    		Duloxetine 
    (60 to 120 mg/day) b 
    		24.6 (6.21)
    		-15.9 (0.63)
    		-4.2 (-5.9, -2.5)
    (HAM-A)
    		Placebo 
    		24.5 (7.05)
    		-11.7 (0.67)
    		--
    Study 6
    (Pediatric)
    		Duloxetine
    (30 to 120 mg/day) b
    		17.5 (1.98)
    		-9.7 (0.50)
    		-2.7 (-4.0, -1.3)
    (PARS for GAD)
    		Placebo
    		17.4 (2.24)
    		17.4 (2.24)
    		--
    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 2 randomized, 12-week, double-blind, placebo-controlled, fixed-dose studies in adult patients having diabetic peripheral neuropathic pain for at least 6 months. Study DPNP-1 and Study DPNP-2 enrolled a total of 791 patients of whom 592 (75%) completed the studies. Patients enrolled had Type I or II diabetes mellitus with a diagnosis of painful distal symmetrical sensorimotor polyneuropathy for at least 6 months. The patients had a baseline pain score of ≥4 on an 11-point scale ranging from 0 (no pain) to 10 (worst possible pain). Patients were permitted up to 4 g of acetaminophen per day as needed for pain, in addition to duloxetine. Patients recorded their pain daily in a 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. A total of 457 patients (342 duloxetine, 115 placebo) were enrolled in DPNP-1 and a total of 334 patients (226 duloxetine, 108 placebo) were enrolled in DPNP-2. Treatment with duloxetine 60 mg one or two times a day statistically significantly improved the endpoint mean pain scores from baseline and increased the proportion of patients with at least a 50% reduction in pain scores from baseline. For various degrees of improvement in pain from baseline to study endpoint, Figures 3 and 4 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 a decrease in pain as early as week 1, which persisted throughout the study.

    Figure 1

    Figure 3: Percentage of Patients Achieving Various Levels of Pain Relief as Measured by 24-Hour Average Pain Severity - DPNP-1

    Figure 2

    Figure 4: Percentage of Patients Achieving Various Levels of Pain Relief as Measured by 24-Hour Average Pain Severity - DPNP-2

    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 7 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 a double-blinded fashion, increased to 120 mg once daily for the remainder of the study. Patients had a mean baseline pain rating of 6 on a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain). After 13 weeks of treatment, patients taking duloxetine 60 to 120 mg daily had a significantly greater pain reduction compared to placebo. Randomization was stratified by the patient's baseline NSAIDs use status. Subgroup analyses did not indicate that there were differences in treatment outcomes as a function of NSAIDs use.

    Study CLBP-2:

    Four hundred and four patients were randomized to receive fixed doses of duloxetine daily or a 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 a 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 a mean baseline pain rating of 6 on a numerical rating scale ranging from 0 (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 7 and 8 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.

    Figure 7
    Figure 8

    Studies in Chronic Pain Due to Osteoarthritis

    The efficacy of duloxetine in chronic pain due to osteoarthritis was assessed in 2 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 a 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 7 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 7 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 a 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 a mean baseline pain rating of 6 on a numerical rating scale ranging from 0 (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 a 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 a mean baseline pain of 6 on a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain). After 13 weeks of treatment, patients taking duloxetine did not show a significantly greater pain reduction.

    In Study OA-1, for various degrees of improvement in pain from baseline to study endpoint, Figure 7 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 9
  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    16.1 How Supplied

    Irenka is available as delayed-release capsules in the following strength, color, imprint, and presentation:

  • * equivalent to duloxetine base
    		•
    Features
    		Strength

    		40 mg*
    Body color
    		White
    Cap color
    		White
    Cap imprint
    		‘LU’
    Body imprint
    		‘H25’
    Capsule number
    		2
    Presentations and NDC Codes
    Bottles of 30
    		27437-298-06

    16.2 Storage and Handling

    Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

  • 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 Irenka and counsel them in its appropriate use. A patient Medication Guide is available for Irenka. Instruct patients, their families, and their caregivers to read the Medication Guide before starting Irenka 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 ask them to alert their prescriber if these occur while taking Irenka.

    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.

    Advise families and caregivers of patients to observe for the emergence of such symptoms on a day-to-day basis, since changes may be abrupt. Such symptoms should be reported to the patient's prescriber or health professional, especially if they are severe, abrupt in onset, or were not part of the patient's presenting symptoms. Symptoms such as these may be associated with an increased risk for suicidal thinking and behavior and indicate a need for very close monitoring and possibly changes in the medication [see BOXED WARNING, and WARNINGS AND PRECAUTIONS (5.1)].

    Irenka 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 Irenka therapy in 1 to 4 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. Instruct patients to talk to their healthcare provider if they develop itching, right upper belly pain, dark urine, or yellow skin/eyes while taking Irenka, which may be signs of liver problems. Instruct patients to talk to their healthcare provider about their alcohol consumption. Use of Irenka with heavy alcohol intake may be associated with severe liver injury [see WARNINGS AND PRECAUTIONS (5.2)].  

    Alcohol

    Although Irenka does not increase the impairment of mental and motor skills caused by alcohol, use of Irenka concomitantly with heavy alcohol intake may be associated with severe liver injury. For this reason, Irenka should 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 Irenka [see WARNINGS AND PRECAUTIONS (5.3)].

    Serotonin Syndrome

    Caution patients about the risk of serotonin syndrome with the concomitant use of Irenka and other serotonergic agents including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan and St. John's 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). Caution patients to seek medical care immediately if they experience these symptoms.

    Abnormal Bleeding

    Caution patients about the concomitant use of Irenka 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 Irenka may cause serious skin reactions. This may need to be treated in a 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 Irenka 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 Irenka 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 Irenka. Advise patients to report any signs or symptoms of a 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 Irenka 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 a risk factor for angle-closure glaucoma. Patients may wish to be examined to determine whether they are susceptible to angle-closure, and have a 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 a history of seizure disorder [see WARNINGS AND PRECAUTIONS (5.10)].

    Effects on Blood Pressure

    Caution patients that Irenka 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 a 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 a result of treatment with SNRIs and SSRIs, including Irenka. 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)].

    Irenka is in a 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

    Advise patients to notify their physician if they:

    • become pregnant during therapy
    • intend to become pregnant during therapy
    • are nursing[see USE IN SPECIFIC POPULATIONS (8.1, 8.3)]

    Pediatric Use

    Safety and efficacy of duloxetine in patients 7 to 17 years of age have been established for the treatment of GAD. The types of adverse reactions observed with duloxetine in children and adolescents were generally similar to those observed in adults. The safety and effectiveness of duloxetine have not been established in pediatric patients less than 18 years of age with other indications. [See USE IN SPECIFIC POPULATIONS (8.4)].

    Interference with Psychomotor Performance

    Any psychoactive drug may impair judgment, thinking, or motor skills. Although in controlled studies duloxetine has 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 Irenka therapy does not affect their ability to engage in such activities.

    Manufactured for:

    Lupin Pharma

    Baltimore, Maryland 21202

    United States

    Manufactured by:

    Lupin Limited

    Goa 403722

    INDIA

    Revised: May 2015                                                                                      ID#: 241554

  • MEDICATION GUIDE

    Medication Guide

    Irenka™

    (eye-REN-kuh)

    (duloxetine delayed-release capsules USP)

    40 mg

    Rx Only

    Read this Medication Guide before you start taking Irenka™ and each time you get a 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 medicines
    • all treatment choices for depression or other serious mental illness

    What is the most important information I should know about antidepressant medicines, depression, other serious mental illnesses, and suicidal thoughts or actions?

    1. Irenkaand 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 a particularly high risk of having suicidal thoughts or actions.These include people who have (or have a family history of) bipolar illness (also called manic-depressive illness).
    3. How can I 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 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

    What else do I need to know about antidepressant medicines?

    • Never stop an antidepressant medicine without first talking to a 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 a list of all medicines to show your healthcare provider. Do not start new medicines without first checking with your healthcare provider.

    What are Irenka?

    Irenka is a prescription medicine used to treat a certain type of depression called Major Depressive Disorder (MDD). Irenka belongs to a class of medicines known as SNRIs (or serotonin-norepinephrine reuptake inhibitors).

    Irenka is also used to treat or manage:

    • Generalized Anxiety Disorder (GAD)
    • Diabetic Peripheral Neuropathic Pain (DPNP)
    • Chronic Musculoskeletal Pain

    Who should not take Irenka?

    Do Not take Irenka if you:

    • take a 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 5 days of stopping Irenka unless directed to do so by your healthcare provider.
    • Do not start Irenka if you stopped taking an MAOI in the last 14 days unless directed to do so by your healthcare provider.

    People who take Irenka close in time to an MAOI may have a serious problem called Serotonin Syndrome (see "What are the possible side effects of Irenka?").

    What should I tell my healthcare provider before taking Irenka?

    Before starting Irenka, tell your healthcare provider if you:

    • have heart problems or high blood pressure
    • have diabetes (Irenka 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 Irenka will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression or other conditions with Irenka 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 Irenka.

    Tell your healthcare provider about all the medicines that you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. Irenka 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 headache
    • medicines used to treat mood, anxiety, psychotic or thought disorders, including tricyclics, lithium, buspirone, SSRIs, SNRIs or MAOIs
    • tramadol and fentanyl
    • 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. John's Wort
    • thioridazine (Mellaril). Mellaril together with Irenka can cause serious heart rhythm problems or sudden death.

    Ask your healthcare provider for a list of these medicines if you are not sure.

    Do not take Irenka with any other medicine that contain duloxetine.

    How should I take Irenka?

    • Take Irenka exactly as your healthcare provider tells you to take it. Your healthcare provider may need to change the dose of Irenka until it is the right dose for you.
    • Swallow Irenka whole. Do not chew or crush Irenka.
    • Do not open the capsule and sprinkle on food or mix with liquids. Opening the capsule may affect how well Irenka works.
    • Irenka may be taken with or without food.
    • If you miss a dose of Irenka, 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 Irenka at the same time.
    • If you take too much Irenka, 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 Irenka your healthcare provider may want to lower the dose of the initial antidepressant first to potentially avoid side effects.

    What should I avoid while taking Irenka?

    • Irenka 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 Irenka affects you.
    • Use of Irenka concomitantly with heavy alcohol intake may be associated with severe liver injury. Avoid heavy alcohol use while taking Irenka.

    What are the possible side effects of Irenka?

    Irenka may cause serious side effects, including: See "What is the most important information I should know about Irenka?"

    Common possible side effects in people who take Irenka include:

    1. liver damage. Symptoms may include:

    • itching
    • right upper abdominal pain
    • dark urine
    • yellow skin or eyes
    • enlarged liver
    • increased liver enzymes

    2. changes in blood pressure and falls. Monitor your blood pressure before starting and throughout treatment. Irenka may:

    • increase your blood pressure.
    • decrease your blood pressure when standing and cause dizziness or fainting, mostly when first starting Irenka 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 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

    4. abnormal bleeding: Irenka and other antidepressant medicines may increase your risk of bleeding or bruising, especially if you take the blood thinner warfarin (Coumadin, Jantoven), a non-steroidal anti-inflammatory drug (NSAIDs, like ibuprofen or naproxen), or aspirin.

    5. severe skin reactions: Irenka may cause serious skin reactions that may require stopping its use. This may need to be treated in a 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 Irenka without first talking to your healthcare provider. Stopping Irenka too quickly or changing from another antidepressant too quickly may result in serious symptoms including:  

    • anxiety
    • irritability
    • feeling tired or problems sleeping
    • headache
    • sweating
    • dizziness
    • electric shock-like sensations
    • vomiting or nausea
    • diarrhea

    7. manic episodes:

    • greatly increased energy
    • severe trouble sleeping
    • racing thoughts
    • reckless behavior
    • unusually grand ideas
    • excessive happiness or irritability
    • talking more or faster than usual

    8. visual problems:

    • eye pain
    • changes in vision
    • swelling or redness in or around the eye

    Only 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:

    • headache
    • weakness or feeling unsteady
    • confusion, problems concentrating or thinking or memory problems

    11. problems with urination. Symptoms may include:

    • decreased urine flow
    • unable to pass any urine

    The most common side effects of Irenka include:

    • nausea
    • dry mouth
    • sleepiness
    • fatigue
    • constipation
    • loss of appetite
    • increased sweating
    • dizziness

    Common possible side effects in children and adolescents who take Irenka include:

    • Nausea
    • decreased weight
    • dizziness

    Side effects in adults may also occur in children and adolescents who take Irenka. 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 Irenka. 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 I store Irenka?

    Store at 25°C (77°F); excursions permitted to 15° to 30°C (59° to 86°F) [see USP Controlled Room Temperature].

    Keep Irenka and all medicines out of the reach of children.

    General information about the safe and effective use of Irenka.

    Medicines are sometimes prescribed for purposes other than those listed in a Medication Guide. Do not use Irenka for a condition for which it was not prescribed. Do not give Irenka 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 Irenka. If you would like more information, talk with your healthcare provider. You may ask your healthcare provider or pharmacist for information about Irenka that is written for healthcare professionals.

    For more information about Irenka call 1-800-399-2561 or go to www.lupinpharmaceuticals.com.

    What are the ingredients in Irenka?

    Active ingredient: duloxetine hydrochloride

    Inactive ingredients:

    Ammonia solution, black iron oxide, croscarmellose sodium, gelatin, hypromellose, hypromellose phthalate, lactose monohydrate, magnesium stearate, polysorbate 80, potassium hydroxide, pregelatinized starch, propylene glycol, shellac, talc, titanium dioxide and triethyl citrate.

    This Medication Guide has been approved by the U.S. Food and Drug Administration.

    Irenka™ is a trademark of Lupin Pharma.

    The brands listed are trademarks of their respective owners and are not trademarks of Lupin Pharma. The makers of these brands are not affiliated with and do not endorse Lupin Pharma or its products.

    Manufactured for:

    Lupin Pharma

    Baltimore, Maryland 21202

    United States

    Manufactured by:

    Lupin Limited

    Goa 403722

    INDIA

    Revised: May 2015                                                                                            ID#: 241555

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Irenka™ (Duloxetine Delayed-release Capsules USP)

    Rx Only

    40 mg

    NDC: 27437-298-06

    30's Bottles

    40 mg - 30s Bottle
  • INGREDIENTS AND APPEARANCE
    IRENKA 
    duloxetine capsule, delayed release
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC: 27437-298
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DULOXETINE HYDROCHLORIDE (UNII: 9044SC542W) (DULOXETINE - UNII:O5TNM5N07U) DULOXETINE40 mg
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIA (UNII: 5138Q19F1X)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    GELATIN (UNII: 2G86QN327L)  
    HYPROMELLOSE PHTHALATE (31% PHTHALATE, 40 CST) (UNII: G4U024CQK6)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SHELLAC (UNII: 46N107B71O)  
    STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
    Product Characteristics
    ColorWHITE (Cap) , WHITE (Body) Scoreno score
    ShapeCAPSULESize18mm
    FlavorImprint Code LU;H25
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 27437-298-0630 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA09069406/01/2015
    Labeler - LUPIN PHARMA (965791259)
    Registrant - LUPIN LIMITED (675923163)
    Establishment
    NameAddressID/FEIBusiness Operations
    LUPIN LIMITED677600414manufacture(27437-298) , pack(27437-298)

    • Trademark Results [Irenka]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    IRENKA
    IRENKA
    86621647 5004602 Live/Registered
    Lupin Limited
    2015-05-06
    IRENKA
    IRENKA
    85830179 not registered Dead/Abandoned
    Lupin Limited
    2013-01-23
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.