ADVERSE REACTIONS SECTION.

ADVERSE REACTIONS. Associated with Discontinuation of TreatmentApproximately 16% of the 453 patients who received Mirtazapine tablets, USP in US 6-week controlled clinical trials discontinued treatment due to an adverse experience, compared to 7% of the 361 placebo-treated patients in those studies. The most common events (>=1%) associated with discontinuation and considered to be drug related (i.e., those events associated with dropout at rate at least twice that of placebo) are included in Table 2. Table 2: Common Adverse Events Associated with Discontinuation of Treatment in 6-Week US Mirtazapine Trials Commonly Observed Adverse Events in US Controlled Clinical Trials The most commonly observed adverse events associated with the use of Mirtazapine tablets, USP (incidence of 5% or greater) and not observed at an equivalent incidence among placebo-treated patients (mirtazapine incidence at least twice that for placebo) are listed in Table 3. Table 3: Common Treatment-Emergent Adverse Events Associated With the Use of Mirtazapine in 6-Week US Trials Adverse Events Occurring at an Incidence of 1% or More Among Mirtazapine-Treated Patients Table enumerates adverse events that occurred at an incidence of 1% or more, and were more frequent than in the placebo group, among Mirtazapine tablets, USP-treated patients who participated in short-term US placebo-controlled trials in which patients were dosed in range of to 60 mg/day. This table shows the percentage of patients in each group who had at least episode of an event at some time during their treatment. Reported adverse events were classified using standard COSTART-based dictionary terminology. The prescriber should be aware that these figures cannot be used to predict the incidence of side effects in the course of usual medical practice where patient characteristics and other factors differ from those which prevailed in the clinical trials. Similarly, the cited frequencies cannot be compared with figures obtained from other investigations involving different treatments, uses and investigators. The cited figures, however, do provide the prescribing physician with some basis for estimating the relative contribution of drug and nondrug factors to the side-effect incidence rate in the population studied. Table 4: Incidence of Adverse Clinical Experiences (>=1%) in Short-Term US Controlled Studies Events reported by at least 1% of patients treated with mirtazapine are included, except the following events which had an incidence on placebo greater than or equal to mirtazapine: headache, infection, pain, chest pain, palpitation, tachycardia, postural hypotension, nausea, dyspepsia, diarrhea, flatulence, insomnia, nervousness, libido decreased, hypertonia, pharyngitis, rhinitis, sweating, amblyopia, tinnitus, taste perversion. ECG Changes The electrocardiograms for 338 patients who received Mirtazapine tablets, USP and 261 patients who received placebo in 6-week, placebo-controlled trials were analyzed. Prolongation in QTc >= 500 msec was not observed among mirtazapine-treated patients; mean change in QTc was +1.6 msec for mirtazapine and -3.1 msec for placebo. Mirtazapine was associated with mean increase in heart rate of 3.4 bpm, compared to 0.8 bpm for placebo. The clinical significance of these changes is unknown. Other Adverse Events Observed During the Premarketing Evaluation of Mirtazapine During its premarketing assessment, multiple doses of Mirtazapine tablets, USP were administered to 2,796 patients in clinical studies. The conditions and duration of exposure to mirtazapine varied greatly, and included (in overlapping categories) open and double-blind studies, uncontrolled and controlled studies, inpatient and outpatient studies, fixed-dose and titration studies. Untoward events associated with this exposure were recorded by clinical investigators using terminology of their own choosing. Consequently, it is not possible to provide meaningful estimate of the proportion of individuals experiencing adverse events without first grouping similar types of untoward events into smaller number of standardized event categories. In the tabulations that follow, reported adverse events were classified using standard COSTART-based dictionary terminology. The frequencies presented, therefore, represent the proportion of the 2,796 patients exposed to multiple doses of mirtazapine who experienced an event of the type cited on at least one occasion while receiving mirtazapine. All reported events are included except those already listed in Table 4, those adverse experiences subsumed under COSTART terms that are either overly general or excessively specific so as to be uninformative, and those events for which drug cause was very remote. It is important to emphasize that, although the events reported occurred during treatment with mirtazapine, they were not necessarily caused by it. Events are further categorized by body system and listed in order of decreasing frequency according to the following definitions: frequent adverse events are those occurring on or more occasions in at least 1/100 patients; infrequent adverse events are those occurring in 1/100 to 1/1000 patients; rare events are those occurring in fewer than 1/1000 patients. Only those events not already listed in Table appear in this listing. Events of major clinical importance are also described in the WARNINGS and PRECAUTIONS sections. Body as Whole: frequent: malaise, abdominal pain, abdominal syndrome acute; infrequent: chills, fever, face edema, ulcer, photosensitivity reaction, neck rigidity, neck pain, abdomen enlarged; rare: cellulitis, chest pain substernal. Cardiovascular System: frequent: hypertension, vasodilatation; infrequent: angina pectoris, myocardial infarction, bradycardia, ventricular extrasystoles, syncope, migraine, hypotension; rare: atrial arrhythmia, bigeminy, vascular headache, pulmonary embolus, cerebral ischemia, cardiomegaly, phlebitis, left heart failure. Digestive System: frequent: vomiting, anorexia; infrequent: eructation, glossitis, cholecystitis, nausea and vomiting, gum hemorrhage, stomatitis, colitis, liver function tests abnormal; rare: tongue discoloration, ulcerative stomatitis, salivary gland enlargement, increased salivation, intestinal obstruction, pancreatitis, aphthous stomatitis, cirrhosis of liver, gastritis, gastroenteritis, oral moniliasis, tongue edema. Endocrine System: rare: goiter, hypothyroidism. Hemic and Lymphatic System: rare: lymphadenopathy, leukopenia, petechia, anemia, thrombocytopenia, lymphocytosis, pancytopenia. Metabolic and Nutritional Disorders: frequent: thirst; infrequent: dehydration, weight loss; rare: gout, SGOT increased, healing abnormal, acid phosphatase increased, SGPT increased, diabetes mellitus, hyponatremia. Musculoskeletal System: frequent: myasthenia, arthralgia; infrequent: arthritis, tenosynovitis; rare: pathologic fracture, osteoporosis fracture, bone pain, myositis, tendon rupture, arthrosis, bursitis. Nervous System: frequent: hypesthesia, apathy, depression, hypokinesia, vertigo, twitching, agitation, anxiety, amnesia, hyperkinesia, paresthesia; infrequent: ataxia, delirium, delusions, depersonalization, dyskinesia, extrapyramidal syndrome, libido increased, coordination abnormal, dysarthria, hallucinations, manic reaction, neurosis, dystonia, hostility, reflexes increased, emotional lability, euphoria, paranoid reaction; rare: aphasia, nystagmus, akathisia (psychomotor restlessness), stupor, dementia, diplopia, drug dependence, paralysis, grand mal convulsion, hypotonia, myoclonus, psychotic depression, withdrawal syndrome, serotonin syndrome. Respiratory System: frequent: cough increased, sinusitis; infrequent: epistaxis, bronchitis, asthma, pneumonia; rare: asphyxia, laryngitis, pneumothorax, hiccup. Skin and Appendages: frequent: pruritus, rash; infrequent: acne, exfoliative dermatitis, dry skin, herpes simplex, alopecia; rare: urticaria, herpes zoster, skin hypertrophy, seborrhea, skin ulcer. Special Senses: infrequent: eye pain, abnormality of accommodation, conjunctivitis, deafness, keratoconjunctivitis, lacrimation disorder, angle-closure glaucoma, hyperacusis, ear pain; rare: blepharitis, partial transitory deafness, otitis media, taste loss, parosmia. Urogenital System: frequent: urinary tract infection; infrequent: kidney calculus, cystitis, dysuria, urinary incontinence, urinary retention, vaginitis, hematuria, breast pain, amenorrhea, dysmenorrhea, leukorrhea, impotence; rare: polyuria, urethritis, metrorrhagia, menorrhagia, abnormal ejaculation, breast engorgement, breast enlargement, urinary urgency. Other Adverse Events Observed During Postmarketing Evaluation of Mirtazapine Adverse events reported since market introduction, which were temporally (but not necessarily causally) related to mirtazapine therapy, include cases of the ventricular arrhythmia torsades de pointes. In of the cases, however, concomitant drugs were implicated. All patients recovered. Cases of severe skin reactions, including Stevens-Johnson syndrome, bullous dermatitis, erythema multiforme and toxic epidermal necrolysis have also been reported. Increased creatine kinase blood levels and rhabdomyolysis have also been reported.. Mirtazapine-table2. Mirtazapine-table3. Mirtazapine-table4.

CLINICAL PHARMACOLOGY SECTION.

CLINICAL PHARMACOLOGY. PharmacodynamicsThe mechanism of action of Mirtazapine tablets, USP as with other drugs effective in the treatment of major depressive disorder, is unknown. Evidence gathered in preclinical studies suggests that mirtazapine enhances central noradrenergic and serotonergic activity. These studies have shown that mirtazapine acts as an antagonist at central presynaptic 2-adrenergic inhibitory autoreceptors and heteroreceptors, an action that is postulated to result in an increase in central noradrenergic and serotonergic activity. Mirtazapine, is potent antagonist of 5-HT2 and 5-HT3 receptors. Mirtazapine has no significant affinity for the 5-HT1A and 5-HT1B receptors. Mirtazapine, is potent antagonist of histamine (H1) receptors, property that may explain its prominent sedative effects. Mirtazapine, is moderate peripheral 1-adrenergic antagonist, property that may explain the occasional orthostatic hypotension reported in association with its use. Mirtazapine, is moderate antagonist at muscarinic receptors, property that may explain the relatively low incidence of anticholinergic side effects associated with its use. Pharmacokinetics Mirtazapine tablets, USP are rapidly and completely absorbed following oral administration and have half-life of about 20 to 40 hours. Peak plasma concentrations are reached within about hours following an oral dose. The presence of food in the stomach has minimal effect on both the rate and extent of absorption and does not require dosage adjustment. Mirtazapine is extensively metabolized after oral administration. Major pathways of biotransformation are demethylation and hydroxylation followed by glucuronide conjugation. In vitro data from human liver microsomes indicate that cytochrome 2D6 and 1A2 are involved in the formation of the 8-hydroxy metabolite of mirtazapine, whereas cytochrome 3A is considered to be responsible for the formation of the N-desmethyl and N-oxide metabolite. Mirtazapine has an absolute bioavailability of about 50%. It is eliminated predominantly via urine (75%) with 15% in feces. Several unconjugated metabolites possess pharmacological activity but are present in the plasma at very low levels. The (-) enantiomer has an elimination half-life that is approximately twice as long as the (+) enantiomer and therefore achieves plasma levels that are about three times as high as that of the (+) enantiomer. Plasma levels are linearly related to dose over dose range of 15 to 80 mg. The mean elimination half-life of mirtazapine after oral administration ranges from approximately 20 to 40 hours across age and gender subgroups, with females of all ages exhibiting significantly longer elimination half-lives than males (mean half-life of 37 hours for females vs. 26 hours for males). Steady state plasma levels of mirtazapine are attained within days, with about 50% accumulation (accumulation ratio 1.5). Mirtazapine is approximately 85% bound to plasma proteins over concentration range of 0.01 to 10 mcg/mL. Special Populations Geriatric Following oral administration of Mirtazapine tablets, USP 20 mg/day for days to subjects of varying ages (range, 25-74), oral clearance of mirtazapine was reduced in the elderly compared to the younger subjects. The differences were most striking in males, with 40% lower clearance in elderly males compared to younger males, while the clearance in elderly females was only 10% lower compared to younger females. Caution is indicated in administering mirtazapine to elderly patients (see PRECAUTIONS and DOSAGE AND ADMINISTRATION). Pediatrics Safety and effectiveness of mirtazapine in the pediatric population have not been established (see PRECAUTIONS). Gender The mean elimination half-life of mirtazapine after oral administration ranges from approximately 20 to 40 hours across age and gender subgroups, with females of all ages exhibiting significantly longer elimination half-lives than males (mean half-life of 37 hours for females vs. 26 hours for males) (see Pharmacokinetics). Race There have been no clinical studies to evaluate the effect of race on the pharmacokinetics of mirtazapine. Renal Insufficiency The disposition of mirtazapine was studied in patients with varying degrees of renal function. Elimination of mirtazapine is correlated with creatinine clearance. Total body clearance of mirtazapine was reduced approximately 30% in patients with moderate (Clcr 11-39 mL/min/1.73 m2) and approximately 50% in patients with severe (Clcr < 10 mL/min/1.73 m2) renal impairment when compared to normal subjects. Caution is indicated in administering mirtazapine to patients with compromised renal function (see PRECAUTIONS and DOSAGE AND ADMINISTRATION). Hepatic Insufficiency Following single 15 mg oral dose of mirtazapine, the oral clearance of mirtazapine was decreased by approximately 30% in hepatically impaired patients compared to subjects with normal hepatic function. Caution is indicated in administering mirtazapine to patients with compromised hepatic function (see PRECAUTIONS and DOSAGE AND ADMINISTRATION). Clinical Trials Showing Effectiveness The efficacy of Mirtazapine tablets, USP as treatment for major depressive disorder was established in four placebo-controlled, 6-week trials in adult outpatients meeting DSM-III criteria for major depressive disorder. Patients were titrated with mirtazapine from dose range of mg up to 35 mg/day. Overall, these studies demonstrated mirtazapine to be superior to placebo on at least three of the following four measures: 21 -Item Hamilton Depression Rating Scale (HDRS) total score; HDRS Depressed Mood Item; CGI Severity score; and Montgomery and Asberg Depression Rating Scale (MADRS). Superiority of mirtazapine over placebo was also found for certain factors of the HDRS, including anxiety/somatization factor and sleep disturbance factor. The mean mirtazapine dose for patients who completed these four studies ranged from 21 to 32 mg/day. fifth study of similar design utilized higher dose (up to 50 mg) per day and also showed effectiveness. Examination of age and gender subsets of the population did not reveal any differential responsiveness on the basis of these subgroupings. In longer-term study, patients meeting (DSM-IV) criteria for major depressive disorder who had responded during an initial to 12 weeks of acute treatment on mirtazapine were randomized to continuation of mirtazapine or placebo for up to 40 weeks of observation for relapse. Response during the open phase was defined as having achieved HAM-D 17 total score of <= and CGI-Improvement score of or at two consecutive visits beginning with week of the to 12 weeks in the open-label phase of the study. Relapse during the double-blind phase was determined by the individual investigators. Patients receiving continued mirtazapine treatment experienced significantly lower relapse rates over the subsequent 40 weeks compared to those receiving placebo. This pattern was demonstrated in both male and female patients.

DOSAGE & ADMINISTRATION SECTION.

DOSAGE ADMINISTRATION. Initial Treatment The recommended starting dose for Mirtazapine tablets, USP is 15 mg/day, administered in single dose, preferably in the evening prior to sleep. In the controlled clinical trials establishing the efficacy of mirtazapine in the treatment of major depressive disorder, the effective dose range was generally 15 to 45 mg/day. While the relationship between dose and satisfactory response in the treatment of major depressive disorder for mirtazapine has not been adequately explored, patients not responding to the initial 15-mg dose may benefit from dose increases up to maximum of 45 mg/day. Mirtazapine has an elimination half-life of approximately 20 to 40 hours; therefore, dose changes should not be made at intervals of less than to weeks in order to allow sufficient time for evaluation of the therapeutic response to given dose.Elderly and Patients with Renal or Hepatic Impairment The clearance of mirtazapine is reduced in elderly patients and in patients with moderate to severe renal or hepatic impairment. Consequently, the prescriber should be aware that plasma mirtazapine levels may be increased in these patient groups, compared to levels observed in younger adults without renal or hepatic impairment (see PRECAUTIONS and CLINICAL PHARMACOLOGY). Maintenance/Extended TreatmentIt is generally agreed that acute episodes of depression require several months or longer of sustained pharmacological therapy beyond response to the acute episode. Systematic evaluation of Mirtazapine tablets, USP has demonstrated that its efficacy in major depressive disorder is maintained for periods of up to 40 weeks following to 12 weeks of initial treatment at dose of 15 to 45 mg/ day (see CLINICAL PHARMACOLOGY). Based on these limited data, it is unknown whether or not the dose of mirtazapine needed for maintenance treatment is identical to the dose needed to achieve an initial response. Patients should be periodically reassessed to determine the need for maintenance treatment and the appropriate dose for such treatment. Switching Patient To or From Monoamine Oxidase Inhibitor (MAOI) Intended to Treat Psychiatric Disorders At least 14 days should elapse between discontinuation of an MAOI intended to treat psychiatric disorders and initiation of therapy with Mirtazapine tablets, USP. Conversely, at least 14 days should be allowed after stopping mirtazapine before starting an MAOI intended to treat psychiatric disorders (see CONTRAINDICATIONS). Use of Mirtazapine With Other MAOIs, Such as Linezolid or Methylene Blue Do not start mirtazapine in patient who is being treated with linezolid or intravenous methylene blue because there is an increased risk of serotonin syndrome. In patient who requires more urgent treatment of psychiatric condition, other interventions, including hospitalization, should be considered (see CONTRAINDICATIONS). In some cases, patient already receiving therapy with mirtazapine may require urgent treatment with linezolid or intravenous methylene blue. If acceptable alternatives to linezolid or intravenous methylene blue treatment are not available and the potential benefits of linezolid or intravenous methylene blue treatment are judged to outweigh the risks of serotonin syndrome in particular patient, mirtazapine should be stopped promptly, and linezolid or intravenous methylene blue can be administered. The patient should be monitored for symptoms of serotonin syndrome for weeks or until 24 hours after the last dose of linezolid or intravenous methylene blue, whichever comes first. Therapy with mirtazapine may be resumed 24 hours after the last dose of linezolid or intravenous methylene blue (see WARNINGS). The risk of administering methylene blue by non-intravenous routes (such as oral tablets or by local injection) or in intravenous doses much lower than mg/kg with mirtazapine is unclear. The clinician should, nevertheless, be aware of the possibility of emergent symptoms of serotonin syndrome with such use (see WARNINGS). Discontinuation of Mirtazapine Treatment Symptoms associated with the discontinuation or dose reduction of Mirtazapine tablets, USP have been reported. Patients should be monitored for these and other symptoms when discontinuing treatment or during dosage reduction. gradual reduction in the dose over several weeks, rather than abrupt cessation, is recommended whenever possible. If intolerable symptoms occur following decrease in the dose or upon discontinuation of treatment, dose titration should be managed on the basis of the patients clinical response (see PRECAUTIONS and ADVERSE REACTIONS). Information for PatientsPatients should be advised that taking mirtazapine can cause mild pupillary dilation, which in susceptible individuals, can lead to an episode of angle-closure glaucoma. Pre-existing glaucoma is almost always open-angle glaucoma because angle-closure glaucoma, when diagnosed, can be treated definitively with iridectomy. Open-angle glaucoma is not risk factor for angle-closure glaucoma. Patients may wish to be examined to determine whether they are susceptible to angle-closure, and have prophylactic procedure (e.g., iridectomy), if they are susceptible.

DRUG INTERACTIONS SECTION.

DRUG INTERACTIONS. As with other drugs, the potential for interaction by variety of mechanisms (e.g., pharmacodynamic, pharmacokinetic inhibition or enhancement, etc.) is possibility (see CLINICAL PHARMACOLOGY). Monoamine Oxidase Inhibitors (See CONTRAINDICATIONS, WARNINGS and DOSAGE AND ADMINISTRATION.) Serotonergic Drugs (See CONTRAINDICATIONS and WARNINGS.) Drugs Affecting Hepatic Metabolism The metabolism and pharmacokinetics of Mirtazapine tablets, USP may be affected by the induction or inhibition of drug-metabolizing enzymes. Drugs that are Metabolized by and/or Inhibit Cytochrome P450 Enzymes CYP Enzyme Inducers (these studies used both drugs at steady state) Phenytoin In healthy male patients (n=18), phenytoin (200 mg daily) increased mirtazapine (30 mg daily) clearance about 2-fold, resulting in decrease in average plasma mirtazapine concentrations of 45%. Mirtazapine did not significantly affect the pharmacokinetics of phenytoin. CarbamazepineIn healthy male patients (n=24), carbamazepine (400 mg b.i.d.) increased mirtazapine (15 mg b.i.d.) clearance about 2-fold, resulting in decrease in average plasma mirtazapine concentrations of 60%. When phenytoin, carbamazepine, or another inducer of hepatic metabolism (such as rifampicin) is added to mirtazapine therapy, the mirtazapine dose may have to be increased. If treatment with such medicinal product is discontinued, it may be necessary to reduce the mirtazapine dose. CYP Enzyme Inhibitors CimetidineIn healthy male patients (n=12), when cimetidine, weak inhibitor of CYP1A2, CYP2D6, and CYP3A4, given at 800 mg b.i.d. at steady state was coadministered with mirtazapine (30 mg daily) at steady state, the Area Under the Curve (AUC) of mirtazapine increased more than 50%. Mirtazapine did not cause relevant changes in the pharmacokinetics of cimetidine. The mirtazapine dose may have to be decreased when concomitant treatment with cimetidine is started, or increased when cimetidine treatment is discontinued. Ketoconazole In healthy, male, Caucasian patients (n=24), coadministration of the potent CYP3A4 inhibitor ketoconazole (200 mg b.i.d. for 6.5 days) increased the peak plasma levels and the AUC of single 30 mg dose of mirtazapine by approximately 40% and 50% respectively. Caution should be exercised when coadministering mirtazapine with potent CYP3A4 inhibitors, HIV protease inhibitors, azole antifungals, erythromycin, or nefazodone. Paroxetine In an in vivo interaction study in healthy, CYP2D6 extensive metabolizer patients (n=24), mirtazapine (30 mg/day), at steady state, did not cause relevant changes in the pharmacokinetics of steady state paroxetine (40 mg/day), CYP2D6 inhibitor. Other Drug-Drug Interactions AmitriptylineIn healthy, CYP2D6 extensive metabolizer patients (n=32), amitriptyline (75 mg daily), at steady state, did not cause relevant changes in the pharmacokinetics of steady state mirtazapine (30 mg daily); mirtazapine also did not cause relevant changes in the pharmacokinetics of amitriptyline. WarfarinIn healthy male subjects (n=16), mirtazapine (30 mg daily), at steady state, caused small (0.2) but statistically significant increase in the International Normalized Ratio (INR) in subjects treated with warfarin. As at higher dose of mirtazapine, more pronounced effect can not be excluded, it is advisable to monitor the INR in case of concomitant treatment of warfarin with mirtazapine. Lithium No relevant clinical effects or significant changes in pharmacokinetics have been observed in healthy male subjects on concurrent treatment with subtherapeutic levels of lithium (600 mg/day for 10 days) at steady state and single 30-mg dose of mirtazapine. The effects of higher doses of lithium on the pharmacokinetics of mirtazapine are unknown. Risperidone In an in vivo, nonrandomized, interaction study, subjects (n=6) in need of treatment with an antipsychotic and antidepressant drug, showed that mirtazapine (30 mg daily) at steady state did not influence the pharmacokinetics of risperidone (up to mg b.i.d.). Alcohol Concomitant administration of alcohol (equivalent to 60 g) had minimal effect on plasma levels of mirtazapine (15 mg) in healthy male subjects. However, the impairment of cognitive and motor skills produced by mirtazapine were shown to be additive with those produced by alcohol. Accordingly, patients should be advised to avoid alcohol while taking mirtazapine. Diazepam Concomitant administration of diazepam (15 mg) had minimal effect on plasma levels of mirtazapine (15 mg) in 12 healthy subjects. However, the impairment of motor skills produced by mirtazapine has been shown to be additive with those caused by diazepam. Accordingly, patients should be advised to avoid diazepam and other similar drugs while taking mirtazapine.

GENERAL PRECAUTIONS SECTION.

GENERAL PRECAUTIONS. Discontinuation Symptoms There have been reports of adverse reactions upon the discontinuation of mirtazapine tablets (particularly when abrupt), including but not limited to the following: dizziness, abnormal dreams, sensory disturbances (including paresthesia and electric shock sensations), agitation, anxiety, fatigue, confusion, headache, tremor, nausea, vomiting, and sweating, or other symptoms which may be of clinical significance. The majority of the reported cases are mild and self-limiting. Even though these have been reported as adverse reactions, it should be realized that these symptoms may be related to underlying disease.Patients currently taking mirtazapine should NOT discontinue treatment abruptly, due to risk of discontinuation symptoms. At the time that medical decision is made to discontinue treatment with mirtazapine, gradual reduction in the dose, rather than an abrupt cessation, is recommended.Akathisia/Psychomotor Restlessness The use of antidepressants has been associated with the development of akathisia, characterized by subjectively unpleasant or distressing restlessness and need to move, often accompanied by an inability to sit or stand still. This is most likely to occur within the first few weeks of treatment. In patients who develop these symptoms, increasing the dose may be detrimental.Hyponatremia Hyponatremia has been reported very rarely with the use of mirtazapine. Caution should be exercised in patients at risk, such as elderly patients or patients concomitantly treated with medications known to cause hyponatremia.Somnolence In US controlled studies, somnolence was reported in 54% of patients treated with Mirtazapine tablets, USP compared to 18% for placebo and 60% for amitriptyline. In these studies, somnolence resulted in discontinuation for 10.4% of mirtazapine-treated patients, compared to 2.2% for placebo. It is unclear whether or not tolerance develops to the somnolent effects of mirtazapine. Because of the potentially significant effects of mirtazapine on impairment of performance, patients should be cautioned about engaging in activities requiring alertness until they have been able to assess the drugs effect on their own psychomotor performance (see PRECAUTIONS: Information for Patients).DizzinessIn US controlled studies, dizziness was reported in 7% of patients treated with mirtazapine, compared to 3% for placebo and 14% for amitriptyline. It is unclear whether or not tolerance develops to the dizziness observed in association with the use of mirtazapine. Increased Appetite/Weight Gain In US controlled studies, appetite increase was reported in 17% of patients treated with mirtazapine, compared to 2% for placebo and 6% for amitriptyline. In these same trials, weight gain of >=7% of body weight was reported in 7.5% of patients treated with mirtazapine, compared to 0% for placebo and 5.9% for amitriptyline. In pool of premarketing US studies, including many patients for long-term, open-label treatment, 8% of patients receiving mirtazapine discontinued for weight gain. In an 8-week-long pediatric clinical trial of doses between 15 to 45 mg/day, 49% of mirtazapine-treated patients had weight gain of at least 7%, compared to 5.7% of placebo-treated patients (see PRECAUTIONS: Pediatric Use).Cholesterol/Triglycerides In US controlled studies, nonfasting cholesterol increases to >=20% above the upper limits of normal were observed in 15% of patients treated with mirtazapine, compared to 7% for placebo and 8% for amitriptyline. In these same studies, nonfasting triglyceride increases to >=500 mg/dL were observed in 6% of patients treated with mirtazapine, compared to 3% for placebo and 3% for amitriptyline.Transaminase Elevations Clinically significant ALT (SGPT) elevations (>=3 times the upper limit of the normal range) were observed in 2.0% (8/424) of patients exposed to mirtazapine in pool of short-term US controlled trials, compared to 0.3% (1/328) of placebo patients and 2.0% (3/181) of amitriptyline patients. Most of these patients with ALT increases did not develop signs or symptoms associated with compromised liver function. While some patients were discontinued for the ALT increases, in other cases, the enzyme levels returned to normal despite continued mirtazapine treatment. Mirtazapine should be used with caution in patients with impaired hepatic function (see CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).Activation of Mania/Hypomania Mania/hypomania occurred in approximately 0.2% (3/1,299 patients) of mirtazapine-treated patients in US studies. Although the incidence of mania/hypomania was very low during treatment with mirtazapine, it should be used carefully in patients with history of mania/hypomania.SeizureIn premarketing clinical trials, only one seizure was reported among the 2,796 US and non-US patients treated with mirtazapine. However, no controlled studies have been carried out in patients with history of seizures. Therefore, care should be exercised when mirtazapine is used in these patients.Use in Patients with Concomitant IllnessClinical experience with mirtazapine in patients with concomitant systemic illness is limited. Accordingly, care is advisable in prescribing mirtazapine for patients with diseases or conditions that affect metabolism or hemodynamic responses. Mirtazapine has not been systematically evaluated or used to any appreciable extent in patients with recent history of myocardial infarction or other significant heart disease. Mirtazapine was associated with significant orthostatic hypotension in early clinical pharmacology trials with normal volunteers. Orthostatic hypotension was infrequently observed in clinical trials with depressed patients. Mirtazapine should be used with caution in patients with known cardiovascular or cerebrovascular disease that could be exacerbated by hypotension (history of myocardial infarction, angina, or ischemic stroke) and conditions that would predispose patients to hypotension (dehydration, hypovolemia, and treatment with antihypertensive medication). Mirtazapine clearance is decreased in patients with moderate [glomerular filtration rate (GFR) 11-39 mL/min/1.73 m2] and severe [GFR 10 mL/min/1.73 m2] renal impairment, and also in patients with hepatic impairment. Caution is indicated in administering mirtazapine to such patients (see CLINICAL PHARMACOLOGY and DOSAGE And ADMINISTRATION).

PRECAUTIONS SECTION.

PRECAUTIONS. GENERAL PRECAUTIONS. Discontinuation Symptoms There have been reports of adverse reactions upon the discontinuation of mirtazapine tablets (particularly when abrupt), including but not limited to the following: dizziness, abnormal dreams, sensory disturbances (including paresthesia and electric shock sensations), agitation, anxiety, fatigue, confusion, headache, tremor, nausea, vomiting, and sweating, or other symptoms which may be of clinical significance. The majority of the reported cases are mild and self-limiting. Even though these have been reported as adverse reactions, it should be realized that these symptoms may be related to underlying disease.Patients currently taking mirtazapine should NOT discontinue treatment abruptly, due to risk of discontinuation symptoms. At the time that medical decision is made to discontinue treatment with mirtazapine, gradual reduction in the dose, rather than an abrupt cessation, is recommended.Akathisia/Psychomotor Restlessness The use of antidepressants has been associated with the development of akathisia, characterized by subjectively unpleasant or distressing restlessness and need to move, often accompanied by an inability to sit or stand still. This is most likely to occur within the first few weeks of treatment. In patients who develop these symptoms, increasing the dose may be detrimental.Hyponatremia Hyponatremia has been reported very rarely with the use of mirtazapine. Caution should be exercised in patients at risk, such as elderly patients or patients concomitantly treated with medications known to cause hyponatremia.Somnolence In US controlled studies, somnolence was reported in 54% of patients treated with Mirtazapine tablets, USP compared to 18% for placebo and 60% for amitriptyline. In these studies, somnolence resulted in discontinuation for 10.4% of mirtazapine-treated patients, compared to 2.2% for placebo. It is unclear whether or not tolerance develops to the somnolent effects of mirtazapine. Because of the potentially significant effects of mirtazapine on impairment of performance, patients should be cautioned about engaging in activities requiring alertness until they have been able to assess the drugs effect on their own psychomotor performance (see PRECAUTIONS: Information for Patients).DizzinessIn US controlled studies, dizziness was reported in 7% of patients treated with mirtazapine, compared to 3% for placebo and 14% for amitriptyline. It is unclear whether or not tolerance develops to the dizziness observed in association with the use of mirtazapine. Increased Appetite/Weight Gain In US controlled studies, appetite increase was reported in 17% of patients treated with mirtazapine, compared to 2% for placebo and 6% for amitriptyline. In these same trials, weight gain of >=7% of body weight was reported in 7.5% of patients treated with mirtazapine, compared to 0% for placebo and 5.9% for amitriptyline. In pool of premarketing US studies, including many patients for long-term, open-label treatment, 8% of patients receiving mirtazapine discontinued for weight gain. In an 8-week-long pediatric clinical trial of doses between 15 to 45 mg/day, 49% of mirtazapine-treated patients had weight gain of at least 7%, compared to 5.7% of placebo-treated patients (see PRECAUTIONS: Pediatric Use).Cholesterol/Triglycerides In US controlled studies, nonfasting cholesterol increases to >=20% above the upper limits of normal were observed in 15% of patients treated with mirtazapine, compared to 7% for placebo and 8% for amitriptyline. In these same studies, nonfasting triglyceride increases to >=500 mg/dL were observed in 6% of patients treated with mirtazapine, compared to 3% for placebo and 3% for amitriptyline.Transaminase Elevations Clinically significant ALT (SGPT) elevations (>=3 times the upper limit of the normal range) were observed in 2.0% (8/424) of patients exposed to mirtazapine in pool of short-term US controlled trials, compared to 0.3% (1/328) of placebo patients and 2.0% (3/181) of amitriptyline patients. Most of these patients with ALT increases did not develop signs or symptoms associated with compromised liver function. While some patients were discontinued for the ALT increases, in other cases, the enzyme levels returned to normal despite continued mirtazapine treatment. Mirtazapine should be used with caution in patients with impaired hepatic function (see CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).Activation of Mania/Hypomania Mania/hypomania occurred in approximately 0.2% (3/1,299 patients) of mirtazapine-treated patients in US studies. Although the incidence of mania/hypomania was very low during treatment with mirtazapine, it should be used carefully in patients with history of mania/hypomania.SeizureIn premarketing clinical trials, only one seizure was reported among the 2,796 US and non-US patients treated with mirtazapine. However, no controlled studies have been carried out in patients with history of seizures. Therefore, care should be exercised when mirtazapine is used in these patients.Use in Patients with Concomitant IllnessClinical experience with mirtazapine in patients with concomitant systemic illness is limited. Accordingly, care is advisable in prescribing mirtazapine for patients with diseases or conditions that affect metabolism or hemodynamic responses. Mirtazapine has not been systematically evaluated or used to any appreciable extent in patients with recent history of myocardial infarction or other significant heart disease. Mirtazapine was associated with significant orthostatic hypotension in early clinical pharmacology trials with normal volunteers. Orthostatic hypotension was infrequently observed in clinical trials with depressed patients. Mirtazapine should be used with caution in patients with known cardiovascular or cerebrovascular disease that could be exacerbated by hypotension (history of myocardial infarction, angina, or ischemic stroke) and conditions that would predispose patients to hypotension (dehydration, hypovolemia, and treatment with antihypertensive medication). Mirtazapine clearance is decreased in patients with moderate [glomerular filtration rate (GFR) 11-39 mL/min/1.73 m2] and severe [GFR 10 mL/min/1.73 m2] renal impairment, and also in patients with hepatic impairment. Caution is indicated in administering mirtazapine to such patients (see CLINICAL PHARMACOLOGY and DOSAGE And ADMINISTRATION).. INFORMATION FOR PATIENTS. Prescribers or other health professionals should inform patients, their families, and their caregivers about the benefits and risks associated with treatment with Mirtazapine tablets, USP and should counsel them in its appropriate use. patient Medication Guide about Antidepressant Medicines, Depression and other Serious Mental Illnesses, and Suicidal Thoughts or Actions is available for mirtazapine. The prescriber or health professional should instruct patients, their families, and their caregivers to read the Medication Guide and should assist them in understanding its contents. Patients should be given 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.Patients should be advised of the following issues and asked to alert their prescriber if these occur while taking Mirtazapine tablets, USP. Clinical Worsening and Suicide RiskPatients, their families, and their caregivers should be encouraged 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. Families and caregivers of patients should be advised to look for the emergence of such symptoms on day-to-day basis, since changes may be abrupt. Such symptoms should be reported to the patients prescriber or health professional, especially if they are severe, abrupt in onset, or were not part of the patients presenting symptoms. Symptoms such as these may be associated with an increased risk for suicidal thinking and behavior and indicate need for very close monitoring and possibly changes in the medication. AgranulocytosisPatients who are to receive mirtazapine should be warned about the risk of developing agranulocytosis. Patients should be advised to contact their physician if they experience any indication of infection such as fever, chills, sore throat, mucous membrane ulceration, or other possible signs of infection. Particular attention should be paid to any flu-like complaints or other symptoms that might suggest infection.Interference with Cognitive and Motor Performance Mirtazapine may impair judgment, thinking and particularly, motor skills, because of its prominent sedative effect. The drowsiness associated with mirtazapine use may impair patients ability to drive, use machines, or perform tasks that require alertness. Thus, patients should be cautioned about engaging in hazardous activities until they are reasonably certain that mirtazapine therapy does not adversely affect their ability to engage in such activities. Completing Course of TherapyWhile patients may notice improvement with Mirtazapine tablets, USP therapy in to weeks, they should be advised to continue therapy as directed.Concomitant Medication Patients should be advised to inform their physician if they are taking, or intend to take, any prescription or over-the-counter drugs, since there is potential for mirtazapine to interact with other drugs.Patients should be made aware of potential increased risk for serotonin syndrome if concomitant use of mirtazapine with other serotonergic drugs, including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, and St. Johns wort, is clinically warranted, particularly during treatment initiation and dose increases.AlcoholThe impairment of cognitive and motor skills produced by mirtazapine has been shown to be additive with those produced by alcohol. Accordingly, patients should be advised to avoid alcohol while taking mirtazapine.PregnancyPatients should be advised to notify their physician if they become pregnant or intend to become pregnant during mirtazapine therapy.NursingPatients should be advised to notify their physician if they are breast-feeding an infant.. LABORATORY TESTS. There are no routine laboratory tests recommended.. DRUG INTERACTIONS. As with other drugs, the potential for interaction by variety of mechanisms (e.g., pharmacodynamic, pharmacokinetic inhibition or enhancement, etc.) is possibility (see CLINICAL PHARMACOLOGY). Monoamine Oxidase Inhibitors (See CONTRAINDICATIONS, WARNINGS and DOSAGE AND ADMINISTRATION.) Serotonergic Drugs (See CONTRAINDICATIONS and WARNINGS.) Drugs Affecting Hepatic Metabolism The metabolism and pharmacokinetics of Mirtazapine tablets, USP may be affected by the induction or inhibition of drug-metabolizing enzymes. Drugs that are Metabolized by and/or Inhibit Cytochrome P450 Enzymes CYP Enzyme Inducers (these studies used both drugs at steady state) Phenytoin In healthy male patients (n=18), phenytoin (200 mg daily) increased mirtazapine (30 mg daily) clearance about 2-fold, resulting in decrease in average plasma mirtazapine concentrations of 45%. Mirtazapine did not significantly affect the pharmacokinetics of phenytoin. CarbamazepineIn healthy male patients (n=24), carbamazepine (400 mg b.i.d.) increased mirtazapine (15 mg b.i.d.) clearance about 2-fold, resulting in decrease in average plasma mirtazapine concentrations of 60%. When phenytoin, carbamazepine, or another inducer of hepatic metabolism (such as rifampicin) is added to mirtazapine therapy, the mirtazapine dose may have to be increased. If treatment with such medicinal product is discontinued, it may be necessary to reduce the mirtazapine dose. CYP Enzyme Inhibitors CimetidineIn healthy male patients (n=12), when cimetidine, weak inhibitor of CYP1A2, CYP2D6, and CYP3A4, given at 800 mg b.i.d. at steady state was coadministered with mirtazapine (30 mg daily) at steady state, the Area Under the Curve (AUC) of mirtazapine increased more than 50%. Mirtazapine did not cause relevant changes in the pharmacokinetics of cimetidine. The mirtazapine dose may have to be decreased when concomitant treatment with cimetidine is started, or increased when cimetidine treatment is discontinued. Ketoconazole In healthy, male, Caucasian patients (n=24), coadministration of the potent CYP3A4 inhibitor ketoconazole (200 mg b.i.d. for 6.5 days) increased the peak plasma levels and the AUC of single 30 mg dose of mirtazapine by approximately 40% and 50% respectively. Caution should be exercised when coadministering mirtazapine with potent CYP3A4 inhibitors, HIV protease inhibitors, azole antifungals, erythromycin, or nefazodone. Paroxetine In an in vivo interaction study in healthy, CYP2D6 extensive metabolizer patients (n=24), mirtazapine (30 mg/day), at steady state, did not cause relevant changes in the pharmacokinetics of steady state paroxetine (40 mg/day), CYP2D6 inhibitor. Other Drug-Drug Interactions AmitriptylineIn healthy, CYP2D6 extensive metabolizer patients (n=32), amitriptyline (75 mg daily), at steady state, did not cause relevant changes in the pharmacokinetics of steady state mirtazapine (30 mg daily); mirtazapine also did not cause relevant changes in the pharmacokinetics of amitriptyline. WarfarinIn healthy male subjects (n=16), mirtazapine (30 mg daily), at steady state, caused small (0.2) but statistically significant increase in the International Normalized Ratio (INR) in subjects treated with warfarin. As at higher dose of mirtazapine, more pronounced effect can not be excluded, it is advisable to monitor the INR in case of concomitant treatment of warfarin with mirtazapine. Lithium No relevant clinical effects or significant changes in pharmacokinetics have been observed in healthy male subjects on concurrent treatment with subtherapeutic levels of lithium (600 mg/day for 10 days) at steady state and single 30-mg dose of mirtazapine. The effects of higher doses of lithium on the pharmacokinetics of mirtazapine are unknown. Risperidone In an in vivo, nonrandomized, interaction study, subjects (n=6) in need of treatment with an antipsychotic and antidepressant drug, showed that mirtazapine (30 mg daily) at steady state did not influence the pharmacokinetics of risperidone (up to mg b.i.d.). Alcohol Concomitant administration of alcohol (equivalent to 60 g) had minimal effect on plasma levels of mirtazapine (15 mg) in healthy male subjects. However, the impairment of cognitive and motor skills produced by mirtazapine were shown to be additive with those produced by alcohol. Accordingly, patients should be advised to avoid alcohol while taking mirtazapine. Diazepam Concomitant administration of diazepam (15 mg) had minimal effect on plasma levels of mirtazapine (15 mg) in 12 healthy subjects. However, the impairment of motor skills produced by mirtazapine has been shown to be additive with those caused by diazepam. Accordingly, patients should be advised to avoid diazepam and other similar drugs while taking mirtazapine.. CARCINOGENESIS MUTAGENESIS IMPAIRMENT OF FERTILITY. Carcinogenesis Carcinogenicity studies were conducted with mirtazapine given in the diet at doses of 2, 20, and 200 mg/kg/day to mice and 2, 20, and 60 mg/kg/day to rats. The highest doses used are approximately 20 and 12 times the maximum recommended human dose (MRHD) of 45 mg/day on an mg/m2 basis in mice and rats, respectively. There was an increased incidence of hepatocellular adenoma and carcinoma in male mice at the high dose. In rats, there was an increase in hepatocellular adenoma in females at the mid and high doses and in hepatocellular tumors and thyroid follicular adenoma/cystadenoma and carcinoma in males at the high dose. The data suggest that the above effects could possibly be mediated by non-genotoxic mechanisms, the relevance of which to humans is not known. The doses used in the mouse study may not have been high enough to fully characterize the carcinogenic potential of Mirtazapine tablets, USP. Mutagenesis Mirtazapine was not mutagenic or clastogenic and did not induce general DNA damage as determined in several genotoxicity tests: Ames test, in vitro gene mutation assay in Chinese hamster 79 cells, in vitro sister chromatid exchange assay in cultured rabbit lymphocytes, in vivo bone marrow micronucleus test in rats, and unscheduled DNA synthesis assay in HeLa cells. Impairment of Fertility In fertility study in rats, mirtazapine was given at doses up to 100 mg/kg [20 times the maximum recommended human dose (MRHD) on an mg/m2 basis]. Mating and conception were not affected by the drug, but estrous cycling was disrupted at doses that were or more times the MRHD and pre-implantation losses occurred at 20 times the MRHD.. PREGNANCY. Teratogenic Effects -Pregnancy Category Reproduction studies in pregnant rats and rabbits at doses up to 100 mg/kg and 40 mg/kg, respectively [20 and 17 times the maximum recommended human dose (MRHD) on an mg/m2 basis, respectively], have revealed no evidence of teratogenic effects. However, in rats, there was an increase in postimplantation losses in dams treated with mirtazapine. There was an increase in pup deaths during the first days of lactation and decrease in pup birth weights. The cause of these deaths is not known. The effects occurred at doses that were 20 times the MRHD, but not at times the MRHD, on an mg/m2 basis. There are no adequate and well-controlled studies in pregnant women. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed.. NURSING MOTHERS. Because some mirtazapine may be excreted into breast milk, caution should be exercised when Mirtazapine tablets, USP are administered to nursing women.. PEDIATRIC USE. Safety and effectiveness in the pediatric population have not been established (see BOXED WARNING and WARNINGS: Clinical Worsening and Suicide Risk). Two placebo-controlled trials in 258 pediatric patients with MDD have been conducted with Mirtazapine tablets, USP, and the data were not sufficient to support claim for use in pediatric patients. Anyone considering the use of mirtazapine in child or adolescent must balance the potential risks with the clinical need. In an 8-week-long pediatric clinical trial of doses between 15 to 45 mg/day, 49% of mirtazapine-treated patients had weight gain of at least 7%, compared to 5.7% of placebo-treated patients. The mean increase in weight was kg (2 kg SD) for mirtazapine-treated patients versus kg (2 kg SD) for placebo-treated patients (see PRECAUTIONS: Increased Appetite/Weight Gain).. GERIATRIC USE. Approximately 190 elderly individuals (>=65 years of age) participated in clinical studies with Mirtazapine tablets, USP. This drug is known to be substantially excreted by the kidney (75%), and the risk of decreased clearance of this drug is greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection. Sedating drugs may cause confusion and over-sedation in the elderly. No unusual adverse age-related phenomena were identified in this group. Pharmacokinetic studies revealed decreased clearance in the elderly. Caution is indicated in administering mirtazapine to elderly patients (see CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION).

SPL MEDGUIDE SECTION.

SPL MEDGUIDE. Medication Guide Mirtazapine (mir taz peen) tablets, USPRead the Medication Guide that comes with Mirtazapine tablets, USP before you start taking it and each time you get refill. There may be new information. This Medication Guide does not take the place of talking to your healthcare provider about your medical condition or treatment. If you have any questions about Mirtazapine tablets, USP, talk to your healthcare provider.What is the most important information should know about Mirtazapine tablets, USPMirtazapine tablets, USP and other antidepressant medicines may cause serious side effects, including:1. Suicidal thoughts or actions:Mirtazapine tablets, USP and other antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, or young adults within the first few months of treatment or when the dose is changed. Depression or other serious mental illnesses are the most important causes of suicidal thoughts or actions.Watch for these changes and call your healthcare provider right away if you notice:New or sudden changes in mood, behavior, actions, thoughts, or feelings, especially if severe.Pay particular attention to such changes when Mirtazapine tablets, USP is started or when the dose is changed. Keep all follow-up visits with your healthcare provider and call between visits if you are worried about symptoms.Call your healthcare provider right away if you have any of the following symptoms, or call 911 if an emergency, especially if they are new, worse, or worry you:attempts to commit suicide acting on dangerous impulsesacting aggressive or violentthoughts about suicide or dyingnew or worse depressionnew or worse anxiety or panic attacksfeeling agitated, restless, angry or irritabletrouble sleepingan increase in activity or talking more than what is normal for youother unusual changes in behavior or moodCall your healthcare provider right away if you have any of the following symptoms, or call 911 if an emergency. Mirtazapine tablets, USP may be associated with these serious side effects: 2. Manic episodes:greatly increased energysevere trouble sleepingracing thoughtsreckless behaviorunusually grand ideasexcessive happiness or irritabilitytalking more or faster than usual3. Decreased White Blood Cells called neutrophils, which are needed to fight infections. Tell your doctor if you have any indication of infection such as fever, chills, sore throat, or mouth or nose sores, especially symptoms which are flu-like. 4. Serotonin Syndrome. This condition can be life-threatening and may include:agitation, hallucinations, coma or other changes in mental statuscoordination problems or muscle twitching (overactive reflexes)racing heartbeat, high or low blood pressuresweating or fevernausea, vomiting, or diarrheamuscle rigidity5. Visual problemseye painchanges in visionswelling or redness in or around the eyeOnly some people are at risk for these problems. You may want to undergo an eye examination to see if you are at risk and receive preventative treatment if you are. 6. Seizures 7. Low salt (sodium) levels in the blood. Elderly people may be at greater risk for this. Symptoms may include:headacheweakness or feeling unsteadyconfusion, problems concentrating or thinking or memory problems8. Sleepiness. It is best to take Mirtazapine tablets, USP close to bedtime.9. Severe skin reactions: Call your doctor right away if you have any or all of the following symptoms:severe rash with skin swelling (including on the palms of the hands and soles of the feet)painful reddening of the skin and/or blisters/ulcers on the body or in the mouth10. Severe allergic reactions: trouble breathing, swelling of the face, tongue, eyes or mouthrash, itchy welts (hives) or blisters, alone or with fever or joint pain11. Increases in appetite or weight. Children and adolescents should have height and weight monitored during treatment. 12. Increased cholesterol and triglyceride levels in your bloodDo not stop Mirtazapine tablets, USP without first talking to your healthcare provider. Stopping Mirtazapine tablets, USP too quickly may cause potentially serious symptoms including:dizzinessabnormal dreamsagitationanxietyfatigueconfusionheadacheshakingtingling sensationnausea, vomitingsweatingWhat is Mirtazapine tablets, USPMirtazapine tablets, USP is prescription medicine used to treat depression. It is important to talk with your healthcare provider about the risks of treating depression and also the risks of not treating it. You should discuss all treatment choices with your healthcare provider.Talk to your healthcare provider if you do not think that your condition is getting better with Mirtazapine tablets, USP treatment.Who should not take Mirtazapine tablets, USPDo not take Mirtazapine tablets, USP:if you are allergic to mirtazapine or any of the ingredients in Mirtazapine tablets, USP. See the end of this Medication Guide for complete list of ingredients in Mirtazapine tablets, USP.If you take monoamine oxidase inhibitor (MAOI). Ask your healthcare provider or pharmacist if you are not sure if you take an MAOI, including the antibiotic linezolid.Do not take an MAOI within weeks of stopping Mirtazapine tablets, USP unless directed to do so by your physician.Do not start Mirtazapine tablets, USP if you stopped taking an MAOI in the last weeks unless directed to do so by your physician.People who take Mirtazapine tablets, USP close in time to an MAOI may have serious or even life-threatening side effects. Get medical help right away if you have any of these symptoms:high feveruncontrolled muscle spasmsstiff musclesrapid changes in heart rate or blood pressureconfusionloss of consciousness (pass out)What should tell my healthcare provider before taking Mirtazapine tablets, USPAsk if you are not sure.Before starting Mirtazapine tablets, USP, tell your healthcare provider if you:Are taking certain drugs such as:Triptans used to treat migraine headacheMedicines used to treat mood, anxiety, psychotic or thought disorders, including tricyclics, lithium, SSRIs, SNRIs, or antipsychoticsTramadol used to treat painOver-the-counter supplements such as tryptophan or St. Johns wortPhenytoin, carbamazepine, or rifampicin (these drugs can decrease your blood level of Mirtazapine tablets, USP)Cimetidine or ketoconazole (these drugs can increase your blood level of Mirtazapine tablets, USP)Have or had:liver problemskidney problemsheart problemsseizures or convulsionsbipolar disorder or maniaa tendency to get dizzy or faintare pregnant or plan to become pregnant. It is not known if Mirtazapine tablets, USP will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression during pregnancyare breastfeeding or plan to breastfeed. Some Mirtazapine tablets, USP may pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby while taking Mirtazapine tablets, USP Tell your healthcare provider about all the medicines that you take, including prescription and non-prescription medicines, vitamins, and herbal supplements. Mirtazapine tablets, USP and some medicines may interact with each other, may not work as well, or may cause serious side effects.Your healthcare provider or pharmacist can tell you if it is safe to take Mirtazapine tablets, USP with your other medicines. Do not start or stop any medicine while taking Mirtazapine tablets, USP without talking to your healthcare provider first. How should take Mirtazapine tablets, USPTake Mirtazapine tablets, USP exactly as prescribed. Your healthcare provider may need to change the dose of Mirtazapine tablets, USP until it is the right dose for you.Take Mirtazapine tablets, USP at the same time each day, preferably in the evening at bedtime.Swallow Mirtazapine tablets, USP as directed.It is common for antidepressant medicines such as Mirtazapine tablets, USP to take up to few weeks before you start to feel better. Do not stop taking Mirtazapine tablets, USP if you do not feel results right away.Do not stop taking or change the dose of Mirtazapine tablets, USP without first talking to your doctor, even if you feel better.Mirtazapine tablets, USP may be taken with or without food.If you miss dose of Mirtazapine tablets, USP, 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 Mirtazapine tablets, USP at the same time.If you take too much Mirtazapine tablets, USP, call your healthcare provider or poison control center right away, or get emergency treatment. What should avoid while taking Mirtazapine tablets, USPMirtazapine tablets, USP 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 Mirtazapine tablets, USP affects you.Avoid drinking alcohol or taking diazepam (a medicine used for anxiety, insomnia and seizures, for example) or similar medicines while taking Mirtazapine tablets, USP. If you are uncertain about whether certain medication can be taken with Mirtazapine tablets, USP, please discuss with your doctor.What are the possible side effects of Mirtazapine tablets, USPMirtazapine tablets, USP may cause serious side effects, including all of those described in the section entextd What is the most important information should know about Mirtazapine tablets, USPCommon possible side effects in people who take Mirtazapine tablets, USP include:sleepinessincreased appetite, weight gaindry mouthconstipationdizzinessabnormal dreamsTell 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 Mirtazapine tablets, USP. For more information, ask your healthcare provider or pharmacist.CALL YOUR DOCTOR FOR MEDICAL ADVICE ABOUT SIDE EFFECTS. YOU MAY REPORT SIDE EFFECTS TO THE FDA AT 1-800-FDA-1088.How should store Mirtazapine tablets, USPStore at 20 to 25C (68 to 77F); excursions permitted 15 to 30C (59 to 86F). [see USP Controlled Room Temperature]. Protect from light and moisture.Keep Mirtazapine tablets, USP and all medicines out of the reach of children.General information about Mirtazapine tablets, USPMedicines are sometimes prescribed for purposes other than those listed in Medication Guide. Do not use Mirtazapine tablets, USP for condition for which it was not prescribed. Do not give Mirtazapine tablets, USP to other people, even if they have the same condition. It may harm them.This Medication Guide summarizes the most important information about Mirtazapine tablets, USP. If you would like more information, talk with your healthcare provider. You may ask your healthcare provider or pharmacist for information about Mirtazapine tablets, USP that is written for healthcare professionals.To report SUSPECTED ADVERSE REACTIONS, contact Sun Pharmaceutical Industries, Inc. at 1-800-818-4555. What are the ingredients in Mirtazapine tablets, USPActive ingredient: mirtazapineInactive ingredients:7.5 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A52767 that is made of iron oxide yellow, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide.15 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A52767 that is made of iron oxide yellow, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. 30 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A56666 that is made of iron oxides yellow, red and black, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. 45 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A58916 that is made of hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. This Medication Guide has been approved by the U.S. Food and Drug Administration.Manufactured by: ALKALOIDA Chemical Company Zrt.4440 TiszavasvariKabay Janos u. 29.HungaryDistributed by:Sun Pharmaceutical Industries, Inc.Cranbury, NJ 08512Revised: 03/2015. Mirtazapine tablets, USP and other antidepressant medicines may increase suicidal thoughts or actions in some children, teenagers, or young adults within the first few months of treatment or when the dose is changed. Depression or other serious mental illnesses are the most important causes of suicidal thoughts or actions.. Watch for these changes and call your healthcare provider right away if you notice:New or sudden changes in mood, behavior, actions, thoughts, or feelings, especially if severe.Pay particular attention to such changes when Mirtazapine tablets, USP is started or when the dose is changed. New or sudden changes in mood, behavior, actions, thoughts, or feelings, especially if severe.. Pay particular attention to such changes when Mirtazapine tablets, USP is started or when the dose is changed.. attempts to commit suicide acting on dangerous impulses. acting aggressive or violent. thoughts about suicide or dying. new or worse depression. new or worse anxiety or panic attacks. feeling agitated, restless, angry or irritable. trouble sleeping. an increase in activity or talking more than what is normal for you. other unusual changes in behavior or mood. greatly increased energy. severe trouble sleeping. racing thoughts. reckless behavior. unusually grand ideas. excessive happiness or irritability. talking more or faster than usual. 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. eye pain. changes in vision. swelling or redness in or around the eye. headache. weakness or feeling unsteady. confusion, problems concentrating or thinking or memory problems. severe rash with skin swelling (including on the palms of the hands and soles of the feet). painful reddening of the skin and/or blisters/ulcers on the body or in the mouth. rash, itchy welts (hives) or blisters, alone or with fever or joint pain. dizziness. abnormal dreams. agitation. anxiety. fatigue. confusion. headache. shaking. tingling sensation. nausea, vomiting. sweating. if you are allergic to mirtazapine or any of the ingredients in Mirtazapine tablets, USP. See the end of this Medication Guide for complete list of ingredients in Mirtazapine tablets, USP.. If you take monoamine oxidase inhibitor (MAOI). Ask your healthcare provider or pharmacist if you are not sure if you take an MAOI, including the antibiotic linezolid.. Do not take an MAOI within weeks of stopping Mirtazapine tablets, USP unless directed to do so by your physician.. Do not start Mirtazapine tablets, USP if you stopped taking an MAOI in the last weeks unless directed to do so by your physician.. high fever. uncontrolled muscle spasms. stiff muscles. rapid changes in heart rate or blood pressure. confusion. loss of consciousness (pass out). Are taking certain drugs such as:. Triptans used to treat migraine headache. Medicines used to treat mood, anxiety, psychotic or thought disorders, including tricyclics, lithium, SSRIs, SNRIs, or antipsychotics. Tramadol used to treat pain. Over-the-counter supplements such as tryptophan or St. Johns wort. Phenytoin, carbamazepine, or rifampicin (these drugs can decrease your blood level of Mirtazapine tablets, USP). Cimetidine or ketoconazole (these drugs can increase your blood level of Mirtazapine tablets, USP). Have or had:liver problemskidney problemsheart problemsseizures or convulsionsbipolar disorder or maniaa tendency to get dizzy or faintare pregnant or plan to become pregnant. It is not known if Mirtazapine tablets, USP will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression during pregnancyare breastfeeding or plan to breastfeed. Some Mirtazapine tablets, USP may pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby while taking Mirtazapine tablets, USP liver problems. kidney problems. heart problems. seizures or convulsions. bipolar disorder or mania. tendency to get dizzy or faint. are pregnant or plan to become pregnant. It is not known if Mirtazapine tablets, USP will harm your unborn baby. Talk to your healthcare provider about the benefits and risks of treating depression during pregnancy. are breastfeeding or plan to breastfeed. Some Mirtazapine tablets, USP may pass into your breast milk. Talk to your healthcare provider about the best way to feed your baby while taking Mirtazapine tablets, USP. Take Mirtazapine tablets, USP exactly as prescribed. Your healthcare provider may need to change the dose of Mirtazapine tablets, USP until it is the right dose for you.. Take Mirtazapine tablets, USP at the same time each day, preferably in the evening at bedtime.Swallow Mirtazapine tablets, USP as directed.It is common for antidepressant medicines such as Mirtazapine tablets, USP to take up to few weeks before you start to feel better. Do not stop taking Mirtazapine tablets, USP if you do not feel results right away.Do not stop taking or change the dose of Mirtazapine tablets, USP without first talking to your doctor, even if you feel better.Mirtazapine tablets, USP may be taken with or without food.If you miss dose of Mirtazapine tablets, USP, 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 Mirtazapine tablets, USP at the same time.If you take too much Mirtazapine tablets, USP, call your healthcare provider or poison control center right away, or get emergency treatment. Swallow Mirtazapine tablets, USP as directed.. It is common for antidepressant medicines such as Mirtazapine tablets, USP to take up to few weeks before you start to feel better. Do not stop taking Mirtazapine tablets, USP if you do not feel results right away.. Do not stop taking or change the dose of Mirtazapine tablets, USP without first talking to your doctor, even if you feel better.Mirtazapine tablets, USP may be taken with or without food.If you miss dose of Mirtazapine tablets, USP, 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 Mirtazapine tablets, USP at the same time.If you take too much Mirtazapine tablets, USP, call your healthcare provider or poison control center right away, or get emergency treatment. Mirtazapine tablets, USP may be taken with or without food.. If you miss dose of Mirtazapine tablets, USP, 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 Mirtazapine tablets, USP at the same time.. If you take too much Mirtazapine tablets, USP, call your healthcare provider or poison control center right away, or get emergency treatment.. Mirtazapine tablets, USP 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 Mirtazapine tablets, USP affects you.. Avoid drinking alcohol or taking diazepam (a medicine used for anxiety, insomnia and seizures, for example) or similar medicines while taking Mirtazapine tablets, USP. If you are uncertain about whether certain medication can be taken with Mirtazapine tablets, USP, please discuss with your doctor.. sleepiness. increased appetite, weight gain. dry mouth. constipation. dizziness. abnormal dreams. Store at 20 to 25C (68 to 77F); excursions permitted 15 to 30C (59 to 86F). [see USP Controlled Room Temperature]. Protect from light and moisture.. 7.5 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A52767 that is made of iron oxide yellow, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide.. 15 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A52767 that is made of iron oxide yellow, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. 30 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A56666 that is made of iron oxides yellow, red and black, hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. 45 mg tablets: lactose monohydrate, corn starch, pregelatinized starch, colloidal silicon dioxide, magnesium stearate, opadry 20A58916 that is made of hydroxypropyl cellulose, hypromellose 2910 and titanium dioxide. Mirtazapine-box.

WARNINGS SECTION.

WARNINGS. Clinical Worsening and Suicide Risk Patients with major depressive disorder (MDD), both adult and pediatric, may experience worsening of their depression and/or the emergence of suicidal ideation and behavior (suicidality) or unusual changes in behavior, whether or not they are taking antidepressant medications, and this risk may persist until significant remission occurs. Suicide is known risk of depression and certain other psychiatric disorders, and these disorders themselves are the strongest predictors of suicide. There has been long-standing concern, however, that antidepressants may have role in inducing worsening of depression and the emergence of suicidality in certain patients during the early phases of treatment. Pooled analyses of short-term placebo-controlled trials of antidepressant drugs (SSRIs and others) showed that these drugs increase the risk of suicidal thinking and behavior (suicidality) in children, adolescents, and young adults (ages 18 to 24) with major depressive disorder (MDD) and other psychiatric disorders. Short-term studies did not show an increase in the risk of suicidality with antidepressants compared to placebo in adults beyond age 24; there was reduction in risk with antidepressants compared to placebo in adults aged 65 and older. The pooled analyses of placebo-controlled trials in children and adolescents with MDD, obsessive compulsive disorder (OCD), or other psychiatric disorders included total of 24 short-term trials of antidepressant drugs in over 4400 patients. The pooled analyses of placebo-controlled trials in adults with MDD or other psychiatric disorders included total of 295 short-term trials (median duration of months) of 11 antidepressant drugs in over 77,000 patients. There was considerable variation in risk of suicidality among drugs, but tendency toward an increase in the younger patients for almost all drugs studied. There were differences in absolute risk of suicidality across different indications, with the highest incidence in MDD. The risk 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.No suicides occurred in any of the pediatric trials. There were suicides in the adult trials, but the number was not sufficient to reach any conclusion about drug effect on suicide. It is unknown whether the suicidality risk extends to longer-term use, i.e., beyond several months. However, there is substantial evidence from placebo-controlled maintenance trials in adults with depression that the use of antidepressants can delay the recurrence of depression. All patients being treated with antidepressants for any indication should be monitored appropriately and observed closely for clinical worsening, suicidality, and unusual changes in behavior, especially during the initial few months of course of drug therapy, or at times of dose changes, either increases or decreases. The following symptoms, anxiety, agitation, panic attacks, insomnia, irritability, hostility, aggressiveness, impulsivity, akathisia (psychomotor restlessness), hypomania, and mania, have been reported in adult and pediatric patients being treated with antidepressants for major depressive disorder as well as for other indications, both psychiatric and nonpsychiatric. Although causal link between the emergence of such symptoms and either the worsening of depression and/or the emergence of suicidal impulses has not been established, there is concern that such symptoms may represent precursors to emerging suicidality. Consideration should be given to changing the therapeutic regimen, including possibly discontinuing the medication, in patients whose depression is persistently worse, or who are experiencing emergent suicidality or symptoms that might be precursors to worsening depression or suicidality, especially if these symptoms are severe, abrupt in onset, or were not part of the patients presenting symptoms.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 Mirtazapine tablets, USP should be written for the smallest quantity of tablets consistent with good patient management, in order to reduce the risk of overdose.Screening Patients for Bipolar Disorder: major depressive episode may be the initial presentation of bipolar disorder. It is generally believed (though not established in controlled trials) that treating such an episode with an antidepressant alone may increase the likelihood of precipitation of mixed/manic episode in patients at risk for bipolar disorder. Whether any of the symptoms described above represent such conversion is unknown. However, prior to initiating treatment with an antidepressant, patients with depressive symptoms should be adequately screened to determine if they are at risk for bipolar disorder; such screening should include detailed psychiatric history, including family history of suicide, bipolar disorder, and depression. It should be noted that Mirtazapine tablets, USP are not approved for use in treating bipolar depression.Agranulocytosis In premarketing clinical trials, (1 with Sjogrens Syndrome) out of 2796 patients treated with Mirtazapine tablets, USP developed agranulocytosis [absolute neutrophil count (ANC) 500/mm3 with associated signs and symptoms, e.g., fever, infection, etc.] and third patient developed severe neutropenia (ANC 500/mm3 without any associated symptoms). For these three patients, onset of severe neutropenia was detected on days 61, 9, and 14 of treatment, respectively. All patients recovered after mirtazapine was stopped. These cases yield crude incidence of severe neutropenia (with or without associated infection) of approximately 1.1 per thousand patients exposed, with very wide 95% confidence interval, i.e., 2.2 cases per 10,000 to 3.1 cases per 1000. If patient develops sore throat, fever, stomatitis or other signs of infection, along with low WBC count, treatment with mirtazapine should be discontinued and the patient should be closely monitored. Serotonin Syndrome The development of potentially life-threatening serotonin syndrome has been reported with SNRIs and SSRIs, including mirtazapine, alone but particularly with concomitant use of other serotonergic drugs (including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, tryptophan, buspirone, and St. Johns wort), and with drugs that impair metabolism of serotonin (in particular, MAOIs, both those intended to treat psychiatric disorders and also others, such as linezolid and intravenous methylene blue). Serotonin syndrome symptoms may include mental status changes (e.g., agitation, hallucinations, delirium, and coma), autonomic instability (e.g., tachycardia, labile blood pressure, dizziness, diaphoresis, flushing, hyperthermia), neuromuscular symptoms (e.g., tremor, rigidity, myoclonus, hyperreflexia, incoordination), seizures, and/or gastrointestinal symptoms (e.g., nausea, vomiting, diarrhea). Patients should be monitored for the emergence of serotonin syndrome.The concomitant use of mirtazapine with MAOIs intended to treat psychiatric disorders is contraindicated. Mirtazapine tablets, USP should also not be started in patient who is being treated with MAOIs such as linezolid or intravenous methylene blue. All reports with methylene blue that provided information on the route of administration involved intravenous administration in the dose range of mg/kg to mg/kg. No reports involved the administration of methylene blue by other routes (such as oral tablets or local tissue injection) or at lower doses. There may be circumstances when it is necessary to initiate treatment with an MAOI such as linezolid or intravenous methylene blue in patient taking Mirtazapine tablets, USP. Mirtazapine tablets, USP should be discontinued before initiating treatment with the MAOI (see CONTRAINDICATIONS and DOSAGE AND ADMINISTRATION). If concomitant use of mirtazapine with other serotonergic drugs, including triptans, tricyclic antidepressants, fentanyl, lithium, tramadol, buspirone, tryptophan, and St. Johns wort, is clinically warranted, be aware of potential increased risk for serotonin syndrome, particularly during treatment initiation and dose increases. Treatment with mirtazapine and any concomitant serotonergic agents should be discontinued immediately if the above events occur and supportive symptomatic treatment should be initiated. Angle-closure Glaucoma The pupillary dilation that occurs following use of many antidepressant drugs including Mirtazapine tablets, USP may trigger an angle-closure attack in patient with anatomically narrow angles who does not have patent iridectomy.. Mirtazapine-table1.