N06AB06 sertraline

NERVOUS SYSTEM PSYCHOANALEPTICS ANTIDEPRESSANTS Selective serotonin reuptake inhibitors

健保收載品項 TFDA 在效許可證 16 FDA 已核准 健保給付條款 1

台灣藥品與外觀

台灣食藥署在效西藥許可證 16 張;以下列出 16 個品項(8 項有外觀照)。

健保收載品名:"晟德"聖憂復液 20 毫克/毫升、"瑞安"克憂寧膜衣錠50毫克、"皇佳"耐憂解膜衣錠50毫克、憂必晴膜衣錠100毫克、憂必晴膜衣錠50毫克、憂解膜衣錠 100 毫克、憂解膜衣錠50毫克、抗憂服膜衣錠 100 毫克、抗憂服膜衣錠50毫克、樂寶寧 膜衣錠50毫克、樂復得膜衣錠100毫克、樂復得膜衣錠50公絲(思卓林)、樂復得膜衣錠50毫克、釋憂膜衣錠50毫克

樂復得膜衣錠50毫克 外觀
樂復得膜衣錠50毫克
橢圓形 · 白 · 刻痕:直線 · 標記:VLE / ZLT50 · 10 mm
樂復得膜衣錠100毫克 外觀
樂復得膜衣錠100毫克
橢圓形 · 白 · 刻痕:無 · 標記:VLE / ZLT 100 · 15 mm
無外觀照
釋憂膜衣錠50毫克
無外觀照
施特瓦林
無外觀照
施特瓦林
無外觀照
施特瓦林
無外觀照
抗憂服膜衣錠50毫克
憂解膜衣錠50毫克 外觀
憂解膜衣錠50毫克
橢圓形 · 白 · 刻痕:無 · 標記:NK / 380 · 11 mm
憂必晴膜衣錠50毫克 外觀
憂必晴膜衣錠50毫克
橢圓形 · 白 · 刻痕:直線 · 標記:ZAP 50 / MACRO · 10 mm
無外觀照
樂寶寧 膜衣錠50毫克
無外觀照
“晟德”聖憂復液 20 毫克/毫升
憂解膜衣錠 100 毫克 外觀
憂解膜衣錠 100 毫克
橢圓形 · 黃 · 刻痕:直線 · 標記:N K / 489 · 13 mm
“瑞安”克憂寧膜衣錠50毫克 外觀
“瑞安”克憂寧膜衣錠50毫克
四邊形 · 白 · 刻痕:直線 · 標記:S 02 · 10.4 mm
無外觀照
抗憂服膜衣錠 100 毫克
"皇佳"耐憂解膜衣錠50毫克 外觀
"皇佳"耐憂解膜衣錠50毫克
橢圓形 · 白 · 刻痕:直線 · 10.5 mm
憂必晴膜衣錠100毫克 外觀
憂必晴膜衣錠100毫克
橢圓形 · 白 · 刻痕:直線 · 標記:ZAP 100 / MACRO · 13 mm

資料來源:食藥署「西藥許可證」+「藥品 ATC 碼」+「藥品外觀」+「藥品仿單或外盒」開放資料。外觀照與仿單連結指向食藥署原始檔。

適應症

台灣 TFDA 核准適應症

  1. 鬱症、強迫症、恐慌症、創傷後壓力症候群(PSTD)、社交恐懼症及經前不悅症(PMDDPremenstrualDysphoricDisorder)。
  2. 鬱症、強迫症、恐慌症、創傷後壓力症候群(PTSD)、社交恐懼症及經前不悅症(PMDDPremenstrualDysphoricDisorder)。
  3. 鬱症、強迫症、恐慌症、創傷後壓力症候群、社交恐懼症及經前不悅症。
  4. 鬱症、強迫症、恐慌症、創傷後壓力症候群(PTSD)及社交恐懼症及經前不悅症(PMDDPremenstrualDysphoricDisorder)。
  5. 抗憂鬱劑。

美國 FDA 適應症(英文原文對照)

美國 FDA 核准成分 sertraline hydrochloride (商品名 SERTRALINE / SERTRALINE HYDROCHLORIDE / Sertraline / Sertraline HCL / Sertraline Hydrochloride) · 仿單更新 2026-03-30

INDICATIONS AND USAGE Major Depressive Disorder – Sertraline hydrochloride is indicated for the treatment of major depressive disorder in adults. The efficacy of Sertraline hydrochloride in the treatment of a major depressive episode was established in six to eight week controlled trials of adult outpatients whose diagnoses corresponded most closely to the DSM-III category of major depressive disorder (see Clinical Trials under CLINICAL PHARMACOLOGY ). A major depressive episode implies a prominent and relatively persistent depressed or dysphoric mood that usually interferes with daily functioning (nearly every day for at least 2 weeks); it should include at least 4 of the following 8 symptoms: change in appetite, change in sleep, psychomotor agitation or retardation, loss of interest in usual activities or decrease in sexual drive, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, and a suicide attempt or suicidal ideation. The antidepressant action of sertraline hydrochloride in hospitalized depressed patients has not been adequately studied. The efficacy of sertraline hydrochloride in maintaining an antidepressant response for up to 44 weeks following 8 weeks of open-label acute treatment (52 weeks total) was demonstrated in a placebo-controlled trial. The usefulness of the drug in patients receiving sertraline hydrochloride for extended periods should be reevaluated periodically (see Clinical Trials under CLINICAL PHARMACOLOGY ). Obsessive-Compulsive Disorder – Sertraline hydrochloride is indicated for the treatment of obsessions and compulsions in patients with obsessive-compulsive disorder (OCD), as defined in the DSM-III-R; i.e., the obsessions or compulsions cause marked distress, are time-consuming, or significantly interfere with social or occupational functioning. The efficacy of Sertraline hydrochloride was established in 12-week trials with obsessive-compulsive outpatients having diagnoses of obsessive-compulsive disorder as defined according to DSM-III or DSM-III-R criteria (see Clinical Trials under CLINICAL PHARMACOLOGY ). Obsessive-compulsive disorder is characterized by recurrent and persistent ideas, thoughts, impulses, or images (obsessions) that are ego-dystonic and/or repetitive, purposeful, and intentional behaviors (compulsions) that are recognized by the person as excessive or unreasonable. The efficacy of Sertraline hydrochloride in maintaining a response, in patients with OCD who responded during a 52-week treatment phase while taking Sertraline hydrochloride and were then observed for relapse during a period of up to 28 weeks, was demonstrated in a placebo-controlled trial (see Clinical Trials under CLINICAL PHARMACOLOGY ). Nevertheless, the physician who elects to use Sertraline hydrochloride for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION ). Panic Disorder – Sertraline hydrochloride is indicated for the treatment of panic disorder in adults, with or without agoraphobia, as defined in DSM-IV. Panic disorder is characterized by the occurrence of unexpected panic attacks and associated concern about having additional attacks, worry about the implications or consequences of the attacks, and/or a significant change in behavior related to the attacks. The efficacy of Sertraline hydrochloride was established in three 10-12 week trials in adult panic disorder patients whose diagnoses corresponded to the DSM-III-R category of panic disorder (see Clinical Trials under CLINICAL PHARMACOLOGY ). Panic disorder (DSM-IV) is characterized by recurrent unexpected panic attacks, i.e., a discrete period of intense fear or discomfort in which four (or more) of the following symptoms develop abruptly and reach a peak within 10 minutes: (1) palpitations, pounding heart, or accelerated heart rate; (2) sweating; (3) trembling or shaking; (4) sensations of shortness of breath or smothering; (5) feeling of choking; (6) chest pain or discomfort; (7) nausea or abdominal distress; (8) feeling dizzy, unsteady, lightheaded, or faint; (9) derealization (feelings of unreality) or depersonalization (being detached from oneself); (10) fear of losing control; (11) fear of dying; (12) paresthesias (numbness or tingling sensations); (13) chills or hot flushes. The efficacy of Sertraline hydrochloride in maintaining a response, in adult patients with panic disorder who responded during a 52-week treatment phase while taking Sertraline hydrochloride and were then observed for relapse during a period of up to 28 weeks, was demonstrated in a placebo-controlled trial (see Clinical Trials under CLINICAL PHARMACOLOGY ). Nevertheless, the physician who elects to use Sertraline hydrochloride for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION ). Posttraumatic Stress Disorder (PTSD) – Sertraline hydrochloride (sertraline hydrochloride) is indicated for the treatment of posttraumatic stress disorder in adults. The efficacy of Sertraline hydrochloride in the treatment of PTSD was established in two 12-week placebo-controlled trials of adult outpatients whose diagnosis met criteria for the DSM-III-R category of PTSD (see Clinical Trials under CLINICAL PHARMACOLOGY ). PTSD, as defined by DSM-III-R/IV, requires exposure to a traumatic event that involved actual or threatened death or serious injury, or threat to the physical integrity of self or others, and a response which involves intense fear, helplessness, or horror. Symptoms that occur as a result of exposure to the traumatic event include reexperiencing of the event in the form of intrusive thoughts, flashbacks or dreams, and intense psychological distress and physiological reactivity on exposure to cues to the event; avoidance of situations reminiscent of the traumatic event, inability to recall details of the event, and/or numbing of general responsiveness manifested as diminished interest in significant activities, estrangement from others, restricted range of affect, or sense of foreshortened future; and symptoms of autonomic arousal including hypervigilance, exaggerated startle response, sleep disturbance, impaired concentration, and irritability or outbursts of anger. A PTSD diagnosis requires that the symptoms are present for at least a month and that they cause clinically significant distress or impairment in social, occupational, or other important areas of functioning. The efficacy of Sertraline hydrochloride in maintaining a response in adult patients with PTSD for up to 28 weeks following 24 weeks of open-label treatment was demonstrated in a placebo-controlled trial. Nevertheless, the physician who elects to use Sertraline hydrochloride for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION ). Premenstrual Dysphoric Disorder (PMDD) – Sertraline hydrochloride is indicated for the treatment of premenstrual dysphoric disorder (PMDD) in adults. The efficacy of sertraline hydrochloride in the treatment of PMDD was established in 2 placebo-controlled trials of female adult outpatients treated for 3 menstrual cycles who met criteria for the DSM-IIIR/IV category of PMDD (see Clinical Trials under CLINICAL PHARMACOLOGY ). The essential features of PMDD include markedly depressed mood, anxiety or tension, affective lability, and persistent anger or irritability. Other features include decreased interest in activities, difficulty concentrating, lack of energy, change in appetite or sleep, and feeling out of control. Physical symptoms associated with PMDD include breast tenderness, headache, joint and muscle pain, bloating and weight gain. These symptoms occur regularly during the luteal phase and remit within a few days following onset of menses; the disturbance markedly interferes with work or school or with usual social activities and relationships with others. In making the diagnosis, care should be taken to rule out other cyclical mood disorders that may be exacerbated by treatment with an antidepressant. The effectiveness of Sertraline hydrochloride in long-term use, that is, for more than 3 menstrual cycles, has not been systematically evaluated in controlled trials. Therefore, the physician who elects to use Sertraline hydrochloride for extended periods should periodically re-evaluate the long-term usefulness of the drug for the individual patient (see DOSAGE AND ADMINISTRATION ). Social Anxiety Disorder – Sertraline hydrochloride is indicated for the treatment of social anxiety disorder, also known as social phobia in adults. The efficacy of Sertraline hydrochloride in the treatment of social anxiety disorder was established in two placebo-controlled trials of adult outpatients with a diagnosis of social anxiety disorder as defined by DSM-IV criteria (see Clinical Trials under CLINICAL PHARMACOLOGY ). Social anxiety disorder, as defined by DSM-IV, is characterized by marked and persistent fear of social or performance situations involving exposure to unfamiliar people or possible scrutiny by others and by fears of acting in a humiliating or embarrassing way. Exposure to the feared social situation almost always provokes anxiety and feared social or performance situations are avoided or else are endured with intense anxiety or distress. In addition, patients recognize that the fear is excessive or unreasonable and the avoidance and anticipatory anxiety of the feared situation is associated with functional impairment or marked distress. The efficacy of Sertraline hydrochloride in maintaining a response in adult patients with social anxiety disorder for up to 24 weeks following 20 weeks of Sertraline hydrochloride treatment was demonstrated in a placebo-controlled trial. Physicians who prescribe Sertraline hydrochloride for extended periods should periodically reevaluate the long-term usefulness of the drug for the individual patient (see Clinical Trials under CLINICAL PHARMACOLOGY ).

資料來源:食藥署西藥許可證適應症(中文)、openFDA US SPL(英文,僅供對照)。

健保給付規定

上層 ATC 繼承條款

下列條款掛在較上層的 ATC 分類,依 ATC 階層也適用於本代碼。

繼承自 ATC N06AB

§ 1.2.1 戒菸治療藥品 — narrative parent
神經系統藥物 › 精神治療劑
選擇性血清促進素再吸收抑制劑(SSRI)、血清促進素及正腎上腺素再吸收抑制劑(SNRI)及其他抗憂鬱劑(fluvoxamine maleate、fluoxetine、paroxetine、sertraline、venlafaxine、milnacipran、mirtazapine、citalopram、escitalopram、duloxetine、agomelatine、vortioxetine等製劑):(88/12/1、89/10/1、91/5/1、92/6/1、93/5/1、94/2/1、94/12/1、99/10/1、101/7/1、107/3/1)

使用時病歷上應詳細註明診斷依據及使用理由。

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)。


台灣藥品與適應症:食藥署西藥許可證+ATC+外觀+仿單開放資料 · FDA:openFDA US SPL · 健保給付:健保署「全民健康保險藥品給付規定」(更新日 2026-06-09)· 實證補充: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。