olanzapine 5 MG Disintegrating Oral Tablet
1 INDICATIONS AND USAGE Olanzapine is an atypical antipsychotic indicated: As oral formulation for the: • Treatment of schizophrenia. ( 1.1 ) Adults: Efficacy was established in three clinical trials in patients with schizophrenia: two 6-week trials and one maintenance trial. ( 14.1 ) Adolescents (ages 13 to 17): Efficacy was established in one 6week trial in patients with schizophrenia (14.1) . The increased potential (in adolescents compared with adults) for weight gain and dyslipidemia may lead clinicians to consider prescribing other drugs first in adolescents. (1.1) • Acute treatment of manic or mixed episodes associated with bipolar I disorder and maintenance treatment of bipolar I disorder. ( 1.2 ) Adults: Efficacy was established in three clinical trials in patients with manic or mixed episodes of bipolar I disorder: two 3- to 4-week trials and one maintenance trial. ( 14.2 ) Adolescents (ages 13 to 17): Efficacy was established in one 3-week trial in patients with manic or mixed episodes associated with bipolar I disorder (14.2) . The increased potential (in adolescents compared with adults) for weight gain and dyslipidemia may lead clinicians to consider prescribing other drugs first in adolescents. (1.2) Medication therapy for pediatric patients with schizophrenia or bipolar I disorder should be undertaken only after a thorough diagnostic evaluation and with careful consideration of the potential risks. (1.3) Adjunct to valproate or lithium in the treatment of manic or mixed episodes associated with bipolar I disorder. ( 1.2 ) Efficacy was established in two 6-week clinical trials in adults. ( 14.2 ). Maintenance efficacy has not been systematically evaluated. As Olanzapine and Fluoxetine in Combination for the: Treatment of depressive episodes associated with bipolar I disorder. (1.5) Efficacy was established with Symbyax (olanzapine and fluoxetine in combination); refer to the product label for Symbyax. Treatment of treatment resistant depression. (1.6) Efficacy was established with Symbyax (olanzapine and fluoxetine combination) in adults; refer to the product label for Symbyax. 1.1 Schizophrenia Oral olanzapine is indicated for the treatment of schizophrenia. Efficacy was established in three clinical trials in adult patients with schizophrenia: two 6-week trials and one maintenance trial. In adolescent patients with schizophrenia (ages 13 to 17), efficacy was established in one 6-week trial [ see Clinical Studies ( 14.1 )]. When deciding among the alternative treatments available for adolescents, clinicians should consider the increased potential (in adolescents as compared with adults) for weight gain and dyslipidemia. Clinicians should consider the potential long-term risks when prescribing to adolescents, and in many cases this may lead them to consider prescribing other drugs first in adolescents [see Warnings and Precautions ( 5.5 )]. 1.2 Bipolar I Disorder (Manic or Mixed Episodes) Monotherapy Oral olanzapine is indicated for the Acute treatment of manic or mixed episodes associated with bipolar I disorder and maintenance treatment of bipolar I disorder. Efficacy was established in three clinical trials in adult patients with manic or mixed episodes of bipolar I disorder: two 3- to 4-week trials and one monotherapy maintenance trial. In adolescent patients with manic or mixed episodes associated with bipolar I disorder (ages 13 to 17), efficacy was established in one 3-week trial [see Clinical Studies ( 14.2 ) ]. When deciding among the alternative treatments available for adolescents, clinicians should consider the increased potential (in adolescents as compared with adults) for weight gain and dyslipidemia. Clinicians should consider the potential long-term risks when prescribing to adolescents, and in many cases this may lead them to consider prescribing other drugs first in adolescents [see Warnings and Precautions (5.5) ]. Adjunctive Therapy to Lithium or Valproate Oral olanzapine is indicated for the treatment of manic or mixed episodes associated with bipolar I disorder as an adjunct to lithium or valproate. Efficacy was established in two 6-week clinical trials in adults. The effectiveness of adjunctive therapy for longer-term use has not been systematically evaluated in controlled trials [see Clinical Studies (14.2) ]. 1.3 Special Considerations in Treating Pediatric Schizophrenia and Bipolar I Disorder Pediatric schizophrenia and bipolar I disorder are serious mental disorders; however, diagnosis can be challenging. For pediatric schizophrenia, symptom profiles can be variable, and for bipolar I disorder, pediatric patients may have variable patterns of periodicity of manic or mixed symptoms. It is recommended that medication therapy for pediatric schizophrenia and bipolar I disorder be initiated only after a thorough diagnostic evaluation has been performed and careful consideration given to the risks associated with medication treatment. Medication treatment for both pediatric schizophrenia and bipolar I disorder should be part of a total treatment program that often includes psychological, educational and social interventions. 1.5 Olanzapine and Fluoxetine in Combination: Depressive Episodes Associated with Bipolar I Disorder Oral olanzapine and fluoxetine in combination is indicated for the treatment of depressive episodes associated with bipolar I disorder, based on clinical studies. When using olanzapine and fluoxetine in combination, refer to the Clinical Studies section of the package insert for Symbyax. Olanzapine monotheraphy is not indicated for the treatment of depressive episodes associated with bipolar I disorder. 1.6 Olanzapine and Fluoxetine in Combination: Treatment Resistant Depression Oral olanzapine and fluoxetine in combination is indicated for the treatment of treatment resistant depression (major depressive disorder in patients who do not respond to 2 separate trials of different antidepressants of adequate dose and duration in the current episode), based on clinical studies in adult patients. When using olanzapine and fluoxetine in combination, refer to the Clinical Studies section of the package insert for Symbyax. Olanzapine monotherapy is not indicated for the treatment of treatment resistant depression.
Dr.Reddy's Laboratories Limited
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olanzapine tablet orally disintegrating
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16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied
OLANZAPINE orally disintegrating tablets USP, 5 mg are yellow-colored, capsule-shaped tablets, flat on one side and concave on the other side, debossed with R-262 on the flat side and plain on the concave side and are supplied in bottles of 30, carton of 10 packs containing 10 tablets each, carton of 30 packs containing 1 tablet each and carton of 3 packs containing 10 tablets each. Bottles of 30 NDC 55111-262-30 Carton of 10 packs (NDC 55111-262-78), each pack containing 10 tablets (NDC 55111-262-79) Carton of 30 packs (NDC 55111-262-31), each pack containing 1 tablet (NDC 55111-262-11) Carton of 3 packs (NDC 55111-262-81), each pack containing 10 tablets (NDC 55111-262-79)
OLANZAPINE orally disintegrating tablets 10 mg USP, are yellow-colored, capsule-shaped tablets, flat on one side and concave on the other side, debossed with R-263 on the flat side and plain on the concave side and are supplied in bottles of 30, carton of 10 packs containing 10 tablets each, carton of 30 packs containing 1 tablet each and carton of 3 packs containing 10 tablets each. Bottles of 30 NDC 55111-263-30 Carton of 10 packs (NDC 55111-263-78), each pack containing 10 tablets (NDC 55111-263-79) Carton of 30 packs (NDC 55111-263-31), each pack containing 1 tablet (NDC 55111-263-11) Carton of 3 packs (NDC 55111-263-81), each pack containing 10 tablets (NDC 55111-263-79)
OLANZAPINE orally disintegrating tablets USP, 15 mg are yellow-colored, capsule-shaped tablets, flat on one side and concave on the other side, debossed with R-264 on the flat side and plain on the concave side and are supplied in bottles of 30, carton of 10 packs containing 10 tablets each, carton of 30 packs containing 1 tablet each and carton of 3 packs containing 10 tablets each. Bottles of 30 NDC 55111-264-30 Carton of 10 packs (NDC 55111-264-78), each pack containing 10 tablets (NDC 55111-264-79) Carton of 30 packs (NDC 55111-264-31), each pack containing 1 tablet (NDC 55111-264-11) Carton of 3 packs (NDC 55111-264-81), each pack containing 10 tablets (NDC 55111-264-79)
OLANZAPINE orally disintegrating tablets USP, 20 mg are yellow-colored, capsule-shaped tablets, flat on one side and concave on the other side, debossed with R-265 on the flat side and plain on the concave side and are supplied in bottles of 30, carton of 10 packs containing 10 tablets each, carton of 30 packs containing 1 tablet each and carton of 3 packs containing 10 tablets each. Bottles of 30 NDC 55111-265-30 Carton of 10 packs (NDC 55111-265-78), each pack containing 10 tablets (NDC 55111-265-79) Carton of 30 packs (NDC 55111-265-31), each pack containing 1 tablet (NDC 55111-265-11) Carton of 3 packs (NDC 55111-265-81), each pack containing 10 tablets (NDC 55111-265-79) 16.2 Storage and Handling Store
OLANZAPINE orally disintegrating tablets, USP at controlled room temperature, 20° to 25°C (68° to 77°F) [see USP]. The USP defines controlled room temperature as a temperature maintained thermostatically that encompasses the usual and customary working environment of 20° to 25°C (68° to 77°F); that results in a mean kinetic temperature calculated to be not more than 25°C; and that allows for excursions between 15° and 30°C (59° and 86°F) that are experienced in pharmacies, hospitals, and warehouses. Protect
OLANZAPINE orally disintegrating tablets, USP from light and moisture.
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