G04BE03 sildenafil
GENITO URINARY SYSTEM AND SEX HORMONES ›UROLOGICALS ›UROLOGICALS ›Drugs used in erectile dysfunction
健保收載品項 TFDA 在效許可證 67 FDA 已核准 健保給付條款 1
台灣藥品與外觀
健保收載品名:"信東"欣格膜衣錠20毫克、瑞肺得膜衣錠20毫克、肺活膜衣錠20毫克、肺紓解膜衣錠20毫克
無外觀照
檸檬酸思登那菲
無外觀照
檸檬酸思登那菲
無外觀照
檸檬酸思登那菲
無外觀照
檸檬酸思登那菲
無外觀照
檸檬酸思登那菲
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
- 成人肺動脈高血壓(WHOGroupI)之治療以改善運動能力。
- 肺動脈高血壓(WHOGroupI)之治療以改善運動能力。
- 成年男性勃起功能障礙。
- 男性勃起障礙治療。
美國 FDA 適應症(英文原文對照)
1 INDICATIONS & USAGE Sildenafil tablets are indicated for the treatment of pulmonary arterial hypertension (WHO Group I) in adults to improve exercise ability and delay clinical worsening. The delay in clinical worsening was demonstrated when sildenafil tablets were added to background epoprostenol therapy [ see Clinical Studies (14) ]. Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with New York Heart Association (NYHA) Functional Class II-III symptoms and idiopathic etiology (71%) or associated with connective tissue disease (CTD) (25%). Limitation of Use: Adding sildenafil to bosentan therapy does not result in any beneficial effect on exercise capacity [ see Clinical Studies ( 14 ) ]. Sildenafil is a phosphodiesterase-5 (PDE-5) inhibitor indicated for the treatment of pulmonary arterial hypertension (PAH) (WHO Group I) in adults to improve exercise ability and delay clinical worsening. Studies establishing effectiveness were short-term (12 to 16 weeks), and included predominately patients with NYHA Functional Class II-III symptoms. Etiologies were idiopathic (71%) or associated with connective tissue disease (25%). ( 1 ) Limitation of Use : Adding sildenafil to bosentan therapy does not result in any beneficial effect on exercise capacity. ( 1 , 14 )
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
直接適用條款
§ 2.8.2.2 Sildenafil (如Revatio):(97/6/1、100/4/1、102/8/1)
心臟血管及腎臟藥物 › 其他
Sildenafil (如Revatio):(97/6/1、100/4/1、102/8/1) 1.用於原發性肺動脈高血壓、結締組織病變導致之肺動脈高血壓或先天性心臟病併發之肺動脈高血壓(Eisenmenger 症候群)運動能力差 (WHO Functional Class III及IV) 患者。(102/8/1)。 2.不得與任何有機硝酸鹽藥物合併使用。
歷史演變(3 次異動)
| 生效日 | 異動說明 |
|---|---|
| 97/6/1 | legacy_boan_parsed:ch02.txt |
| 100/4/1 | legacy_boan_parsed:ch02.txt |
| 102/8/1 | legacy_boan_parsed:ch02.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)。
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。