Šalis: Jungtinės Valstijos
kalba: anglų
Šaltinis: NLM (National Library of Medicine)
risperidone (UNII: L6UH7ZF8HC) (risperidone - UNII:L6UH7ZF8HC)
Aphena Pharma Solutions - Tennessee, LLC
ORAL
PRESCRIPTION DRUG
Risperidone is indicated for the treatment of schizophrenia. Efficacy was established in 4 short-term trials in adults, 2 short-term trials in adolescents (ages 13 to 17 years), and one long-term maintenance trial in adults [see Clinical Studies (14.1)] . Monotherapy Risperidone is indicated for the treatment of acute manic or mixed episodes associated with Bipolar I Disorder. Efficacy was established in 2 short-term trials in adults and one short-term trial in children and adolescents (ages 10 to 17 years) [see Clinical Studies (14.2)] . Adjunctive Therapy Risperidone adjunctive therapy with lithium or valproate is indicated for the treatment of acute manic or mixed episodes associated with Bipolar I Disorder. Efficacy was established in one short-term trial in adults [see Clinical Studies (14.3)] . Risperidone is indicated for the treatment of irritability associated with autistic disorder, including symptoms of aggression towards others, deliberate self-injuriousness, temper tantrums, and quickly changing
Risperidone Tablets Risperidone Tablets are imprinted "PATR" on one side and either "Ris 0.25", "Ris 0.5", "R1", "R2", "R3", or "R4" according to their respective strengths. 0.25 mg dark yellow, capsule-shaped tablets: bottles of 60 NDC 50458-590-60, bottles of 500 NDC 50458-590-50, and hospital unit dose blister packs of 100 NDC 50458-590-10. 0.5 mg red-brown, capsule-shaped tablets: bottles of 60 NDC 50458-591-60, bottles of 500 NDC 50458-591-50, and hospital unit dose blister packs of 100 NDC 50458-591-10. 1 mg white, capsule-shaped tablets: bottles of 60 NDC 50458-592-60, bottles of 500 NDC 50458-592-50, and hospital unit dose blister packs of 100 NDC 50458-592-10. 2 mg orange, capsule-shaped tablets: bottles of 60 NDC 50458-593-60, bottles of 500 NDC 50458-593-50, and hospital unit dose blister packs of 100 NDC 50458-593-10. 3 mg yellow, capsule-shaped tablets: bottles of 60 NDC 50458-594-60, bottles of 500 NDC 50458-594-50, and hospital unit dose blister packs of 100 NDC 50458-594-10. 4 mg green, capsule-shaped tablets: bottles of 60 NDC 50458-595-60 and hospital unit dose blister packs of 100 NDC 50458-595-10. Risperidone Oral Solution Risperidone 1 mg/mL Oral Solution (NDC 50458-596-01) is supplied in 30 mL bottles with a calibrated (in milligrams and milliliters) pipette. The minimum calibrated volume is 0.25 mL, while the maximum calibrated volume is 3 mL. Risperidone Orally Disintegrating Tablets Risperidone Orally Disintegrating Tablets are etched on one side with "P0.5", "P1", "P2", "P3", or "P4" according to their respective strengths. Risperidone Orally Disintegrating Tablets 0.5 mg, 1 mg, and 2 mg are packaged in blister packs of 4 (2 × 2) tablets. Risperidone Orally Disintegrating Tablets 3 mg and 4 mg are packaged in a child-resistant pouch containing a blister with 1 tablet. 0.5 mg light coral, round, biconvex tablets: 7 blister packages (4 tablets each) per box, NDC 50458-601-28. 1 mg light coral, square, biconvex tablets: 7 blister packages (4 tablets each) per box, NDC 50458-602-28. 2 mg coral, square, biconvex tablets: 7 blister packages (4 tablets each) per box, NDC 50458-603-28. 3 mg coral, round, biconvex tablets: 28 blisters per box, NDC 50458-604-28. 4 mg coral, round, biconvex tablets: 28 blisters per box, NDC 50458-605-28. Risperidone Tablets should be stored at controlled room temperature 15°–25°C (59°–77°F). Protect from light and moisture. Risperidone 1 mg/mL Oral Solution should be stored at controlled room temperature 15°–25°C (59°–77°F). Protect from light and freezing. Risperidone Orally Disintegrating Tablets should be stored at controlled room temperature 15°–25°C (59°–77°F). Keep out of reach of children.
New Drug Application
RISPERIDONE- RISPERIDONE TABLET APHENA PHARMA SOLUTIONS - TENNESSEE, LLC ---------- HIGHLIGHTS OF PRESCRIBING INFORMATION THESE HIGHLIGHTS DO NOT INCLUDE ALL THE INFORMATION NEEDED TO USE RISPERIDONE TABLETS, ORAL SOLUTION, AND ORALLY DISINTEGRATING TABLETS SAFELY AND EFFECTIVELY. SEE FULL PRESCRIBING INFORMATION FOR RISPERIDONE TABLETS, ORAL SOLUTION, AND ORALLY DISINTEGRATING TABLETS. RISPERIDONE TABLETS, RISPERIDONE ORAL SOLUTION, RISPERIDONE ORALLY DISINTEGRATING TABLETS INITIAL U.S. APPROVAL: 1993 WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS _SEE FULL PRESCRIBING INFORMATION FOR COMPLETE BOXED WARNING._ ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS TREATED WITH ANTIPSYCHOTIC DRUGS ARE AT AN INCREASED RISK OF DEATH. RISPERIDONE IS NOT APPROVED FOR USE IN PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS. (5.1) INDICATIONS AND USAGE Risperidone is an atypical antipsychotic indicated for: Treatment of schizophrenia (1.1) As monotherapy or adjunctive therapy with lithium or valproate, for the treatment of acute manic or mixed episodes associated with Bipolar I Disorder (1.2) Treatment of irritability associated with autistic disorder (1.3) DOSAGE AND ADMINISTRATION Recommended daily dosage: INITIAL DOSE TARGET DOSE EFFECTIVE DOSE RANGE Schizophrenia: adults (2.1) 2 mg 4 to 8 mg 4 to 16 mg Schizophrenia: adolescents (2.1) 0.5 mg 3 mg 1 to 6 mg Bipolar mania: Adults (2.2) 2 to 3 mg 1 to 6 mg 1 to 6 mg Bipolar mania: in children and adolescents (2.2) 0.5 mg 1 to 2.5 mg 1 to 6 mg Irritability associated with autistic disorder (2.3) 0.25 mg (Weight < 20 kg) 0.5 mg (Weight ≥20 kg) 0.5 mg (<20 kg) 1 mg (≥20 kg) 0.5 to 3 mg Severe Renal or Hepatic Impairment in Adults: Use a lower starting dose of 0.5 mg twice daily. May increase to dosages above 1.5 mg twice daily at intervals of at least one week. (2.4) Oral Solution: Can be administered directly from calibrated pipette or mixed with beverage (water, coffee, orange juice, or low-fat milk). (2.6) Risperidone Orally Disintegrating Table Perskaitykite visą dokumentą