N06BA09 atomoxetine
NERVOUS SYSTEM ›PSYCHOANALEPTICS ›PSYCHOSTIMULANTS, AGENTS USED FOR ADHD AND NOOTROPICS ›Centrally acting sympathomimetics
健保收載品項 FDA 已核准 TFDA 在效許可證 12 健保給付條款 1
健保收載品名:"國嘉"思專定口服液4毫克/毫升、"應元"安妥錠40毫克、安保思定膠囊10毫克、安保思定膠囊18毫克、安保思定膠囊25毫克、安保思定膠囊40毫克、安保思定膠囊60毫克、思必靜膜衣錠40毫克、思敏膠囊10毫克、思敏膠囊18毫克、思敏膠囊25毫克、思敏膠囊40毫克、思銳膠囊10毫克、思銳膠囊18毫克、思銳膠囊25毫克、思銳膠囊40毫克
FDA 適應症
1 INDICATIONS AND USAGE Atomoxetine capsules are selective norepinephrine reuptake inhibitor indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD). ( 1.1 ) 1.1 Attention-Deficit/Hyperactivity Disorder (ADHD) Atomoxetine capsules are indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD). The efficacy of atomoxetine capsules was established in seven clinical trials in outpatients with ADHD: four 6 to 9-week trials in pediatric patients (ages 6 to 18), two 10-week trial in adults, and one maintenance trial in pediatrics (ages 6 to 15) [see Clinical Studies ( 14 )] . 1.2 Diagnostic Considerations A diagnosis of ADHD (DSM-IV) implies the presence of hyperactive-impulsive or inattentive symptoms that cause impairment and that were present before age 7 years. The symptoms must be persistent, must be more severe than is typically observed in individuals at a comparable level of development, must cause clinically significant impairment, e.g., in social, academic, or occupational functioning, and must be present in 2 or more settings, e.g., school (or work) and at home. The symptoms must not be better accounted for by another mental disorder. The specific etiology of ADHD 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. 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 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. For a Combined Type diagnosis, both inattentive and hyperactive-impulsive criteria must be met. 1.3 Need for Comprehensive Treatment Program Atomoxetine capsules are 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. Drug treatment is not intended for use in the patient who exhibits symptoms secondary to environmental factors and/or other primary psychiatric disorders, including psychosis. Appropriate educational placement is essential in children and adolescents with this diagnosis and psychosocial intervention is often helpful. When remedial measures alone are insufficient, the decision to prescribe drug treatment medication will depend upon the physician's assessment of the chronicity and severity of the patient's symptoms.
資料來源:openFDA(美國 FDA Structured Product Labeling)。為英文原文,僅供對照。
TFDA 適應症
適應症(去重後 1 項):
- 注意力缺損/過動症(ADHD)。
許可證品項:藥品外觀與仿單(12 項)
| 品名 | 外觀 | 仿單/外盒 |
|---|---|---|
| 安保思定膠囊25毫克 | 膠囊 · 藍;;;白 · 刻痕:無 · 標記:APO / AM25 · 16 外觀圖 | 仿單 · 外盒 |
| 安保思定膠囊10毫克 | 膠囊 · 白 · 刻痕:無 · 標記:APO / AM10 · 15 外觀圖 | 仿單 · 外盒 |
| 安保思定膠囊18毫克 | 膠囊 · 黃;;;白 · 刻痕:無 · 標記:APO / AM18 · 15 外觀圖 | 仿單 · 外盒 |
| 安保思定膠囊40毫克 | 膠囊 · 藍 · 刻痕:無 · 標記:APO / AM40 · 17 外觀圖 | 仿單 · 外盒 |
| 安保思定膠囊60毫克 | 膠囊 · 藍;;;黃 · 刻痕:無 · 標記:APO / AM60 · 19 外觀圖 | 仿單 · 外盒 |
| 思敏膠囊25毫克 | 膠囊 · 藍;;;白 · 刻痕:無 · 標記:AX111 / 25mg · 15 外觀圖 | 仿單 · 外盒 |
| 思敏膠囊18毫克 | — | 仿單 · 外盒 |
| 思敏膠囊40毫克 | 膠囊 · 藍;;;藍 · 刻痕:無 · 標記:AX110 / 40mg · 15 外觀圖 | 仿單 · 外盒 |
| 思敏膠囊10毫克 | — | 仿單 · 外盒 |
| "應元"安妥錠40毫克 | 圓形 · 黃 · 刻痕:直線 · 標記:S01 · 7 外觀圖 | 仿單 · 外盒 |
| 思必靜膜衣錠40毫克 | — | 仿單 · 外盒 |
| "國嘉"思專定口服液4毫克/毫升 | 液劑(包含糖漿用粉劑) · 白 · 刻痕:無 外觀圖 | 仿單 · 外盒 |
資料來源:食藥署「西藥許可證」+「藥品 ATC 碼」+「藥品仿單或外盒」+「藥品外觀」開放資料。
NHI 給付規定
直接適用條款
§ 1.3.5 Methylphenidate HCl 緩釋劑型(如Concerta Extended Release Tablets、
神經系統藥物 › 神經藥物
Methylphenidate HCl緩釋劑型(如Concerta Extended Release Tablets、Methydur Sustained Release Capsules);atomoxetine HCl(如Strattera Hard capsules、Atotine oral Solution)(93/9/1、96/5/1、96/9/1、97/5/1、106/3/1、109/9/1、111/2/1、111/8/1、113/11/1、114/10/1)
1.限6歲以上至18歲以下,依DSM或ICD標準診斷為注意力不全過動症患者,並於病歷上詳細記載其症狀、病程及診斷。(96/9/1、106/3/1、111/2/1)
2.如符合前項規定且已使用本類藥品治療半年以上,而18歲以上仍需服用者,需於病歷上詳細記載以往病史及使用理由。(96/9/1、111/2/1)
3.19歲以上至未滿41歲才第一次診斷者,須符合下列條件並檢附詳細病歷紀錄及相關資料,經事前審查核准後使用(限用含atomoxetine HCl成分一般錠劑膠囊劑藥品):(111/8/1、114/10/1)
(1)注意力測驗(Continuous Performance Test ,CPT)或Gordon Diagnostic System,GDS。
(2)世界衛生組織公告之Adult ADHD Self report Scale, ASRS (傳統中文版)、Global Assessment of Functioning Scaling ,GAF。
(3)需由精神科醫師診斷及處方,臨床醫師對個案之診斷及處方有疑慮時,宜由具有兒童青少年精神科訓練之專科醫師確認診斷。
(4)排除其他疾病因素:
Ⅰ.任何使用之藥品/物質、身體及注意力不全過動症以外之各種精神病等對注意力及衝動控制功能、症狀之影響作用。
Ⅱ.一年內患有物質使用/物質成癮、嚴重憂鬱症。
Ⅲ.思覺失調症 (Schizophrenia)、雙極性疾患(Bipolar disorder)、人格疾患、失智症及器質性因素
(5)換藥條件:若使用原藥物3個月無效(如ASRS得分大於24或較治療前增加),得以更換methylphenidate成分藥品之短效劑型。
(6)退場機制:
Ⅰ.19歲以上並已接受治療之病患,超過一年未回診,再開立藥物前,須重新經事前審查核准。
Ⅱ.換藥後半年應予評估,症狀未改善應予停用;症狀持續穩定逾一年者,得改為每年評估。
4.Atomoxetine HCl之口服錠劑、或膠囊劑原則上每日限使用1粒,惟每日劑量需超過60mg時,應於病歷中記載理由,則每日至多可使用2粒,每日最大劑量為100mg。(97/5/1、113/11/1)
5.Atomoxetine HCl口服液劑,限用於6歲以上至18歲以下無法口服錠劑之病人,每日劑量需超過60mg時,應於病歷中記載理由,每日最大劑量為100mg。(113/11/1)
6.Methydur原則上每日限使用1粒,惟每日劑量需超過33mg時,應於病歷中記載理由,則每日至多可使用2粒,每日最大劑量為44mg。(109/9/1) 歷史演變(10 次異動)
| 生效日 | 異動說明 |
|---|---|
| 93/9/1 | legacy_boan_parsed:ch01.txt |
| 96/5/1 | legacy_boan_parsed:ch01.txt |
| 96/9/1 | legacy_boan_parsed:ch01.txt |
| 97/5/1 | legacy_boan_parsed:ch01.txt |
| 106/3/1 | legacy_boan_parsed:ch01.txt |
| 109/9/1 | legacy_boan_parsed:ch01.txt |
| 111/2/1 | legacy_boan_parsed:ch01.txt |
| 111/8/1 | legacy_boan_parsed:ch01.txt |
| 113/11/1 | legacy_boan_parsed:ch01.txt |
| 114/10/1 | legacy_boan_parsed:ch01.txt |
實證補充
本藥品尚無實證補充整理(未來新增 Review/指引知識時補列)。
FDA 段:openFDA US SPL · TFDA 段:食藥署西藥許可證+ATC 分類開放資料 · NHI 段:健保署「全民健康保險藥品給付規定」(更新日 2026-05-31)· 實證補充段:人工彙整。 本頁為資訊整理,實際給付與適應症以主管機關公告為準。