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Vyvanse lisdexamfetamine dimesylate 20 MG Oral Capsule Vyvanse

1 INDICATIONS AND USAGE Attention Deficit Hyperactivity Disorder Vyvanse ® is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). The efficacy of Vyvanse in the treatment of ADHD was established on the basis of three short-term controlled trials in children ages 6 to 12 years, one short-term controlled trial in adolescents ages 13 to 17 years, and two short-term controlled trials in adults who met DSM-IV-TR ® criteria for ADHD, and one maintenance trial in adults [ see CLINICAL STUDIES (14) ] . A diagnosis of Attention Deficit Hyperactivity Disorder (ADHD; DSM-IV ® ) implies the presence of hyperactive-impulsive and/or inattentive symptoms that cause impairment and were present before the age of 7 years. The symptoms must cause clinically significant impairment, e.g. in social, academic, or occupational functioning, and be present in two or more settings, e.g. school (or work) and at home. The symptoms must not be better accounted for by another mental disorder. For the Inattentive Type, at least 6 of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; easily distracted; forgetful. For the Hyperactive-Impulsive Type, at least 6 of the following symptoms (or adult equivalent symptoms) must have persisted for at least 6 months: fidgeting/squirming; leaving seat; inappropriate running/climbing; difficulty with quiet activities; "on the go"; excessive talking; blurting answers; can"t wait turn; intrusive. The Combined Type requires both inattentive and hyperactive-impulsive criteria to be met. Special Diagnostic Considerations Specific etiology of this syndrome is unknown, and there is no single diagnostic test. Adequate diagnosis requires the use not only of medical but also of special psychological, educational, and social resources. Learning may or may not be impaired. The diagnosis must be based upon a complete history and evaluation of the patient and not solely on the presence of the required number of DSM-IV characteristics. Need for Comprehensive Treatment Program Vyvanse is indicated as an integral part of a total treatment program for ADHD that may include other measures (psychological, educational, social) for patients with this syndrome. Drug treatment may not be indicated for all patients with this syndrome. Stimulants are not intended for use in patients who exhibit symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis. Appropriate educational/vocational placement is essential and psychosocial intervention is often helpful. When remedial measures alone are insufficient, the decision to prescribe stimulant medication will depend upon the physician"s assessment of the chronicity and severity of the patient"s symptoms and on the level of functional impairment. Vyvanse, is a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). ( 1 ) Children: Efficacy was established in three short-term trials in 6-12 year olds ( 14 ) Adolescents: Efficacy was established in one short-term trial in 13-17 year olds ( 14 ) Adults: Efficacy was established in two short-term and one maintenance trials ( 14 )

Lake Erie Medical & Surgical Supply DBA Q


10 months ago CAPSULE WHITE S489 20mg Vyvanse  lisdexamfetamine dimesylate 20 MG Oral Capsule Vyvanse

CAPSULE WHITE S489 20mg

10 months ago CAPSULE WHITE S489 20mg Vyvanse  lisdexamfetamine dimesylate 20 MG Oral Capsule Vyvanse

S489 20mg CAPSULE WHITE

16 HOW SUPPLIED/STORAGE AND HANDLING 16.1 How Supplied Vyvanse capsules 20 mg: ivory body/ivory cap (imprinted with NRP104/S489 and 20 mg), Bottles of 30, NDC 35356-542-30 Bottles of 60, NDC 35356-542-60 Bottles of 90, NDC 35356-542-90 Dispense in a tight, light-resistant container as defined in the USP. Store at 25º C (77º F). Excursions permitted to 15-30º C (59-86º F) [see USP Controlled Room Temperature]


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