C09DX01 valsartan, amlodipine and hydrochlorothiazide
CARDIOVASCULAR SYSTEM ›AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM ›ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS ›Angiotensin II receptor blockers (ARBs), other combinations
健保收載品項 FDA 已核准 TFDA 在效許可證 9 健保給付條款 1
健保收載品名:力安穩 膜衣錠 10/160/12.5毫克、力安穩 膜衣錠 10/160/25毫克、力安穩 膜衣錠 5/160/12.5毫克、力安穩 膜衣錠 5/160/25毫克、力脈樂10/160/12.5毫克膜衣錠、力脈樂10/160/25毫克膜衣錠、力脈樂5/160/12.5毫克膜衣錠、力脈樂5/160/25毫克膜衣錠、安壓三好膜衣錠 5/160/12.5 毫克
FDA 適應症
1 INDICATIONS AND USAGE Exforge HCT (amlodipine, valsartan, and hydrochlorothiazide) is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes, including amlodipine, hydrochlorothiazide, and the angiotensin II receptor blocker (ARB) class to which valsartan principally belongs. There are no controlled trials demonstrating risk reduction with Exforge HCT. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is blood pressure reduction, and not some other pharmacologic property of the drugs, that is largely responsible for those benefits. The largest and most consistent cardiovascular outcome benefit has been a reduction in the risk of stroke, but reductions in myocardial infarction and cardiovascular mortality also have been seen regularly. Elevated systolic or diastolic pressure causes increased cardiovascular risk, and the absolute risk increase per mmHg is greater at higher blood pressures, so that even modest reductions of severe hypertension can provide substantial benefit. Relative risk reduction from blood pressure reduction is similar across populations with varying absolute risk, so the absolute benefit is greater in patients who are at higher risk independent of their hypertension (e.g., patients with diabetes or hyperlipidemia), and such patients would be expected to benefit from more aggressive treatment to a lower blood pressure goal. Some antihypertensive drugs have smaller blood pressure effects (as monotherapy) in black patients, and many antihypertensive drugs have additional approved indications and effects (e.g., on angina, heart failure, or diabetic kidney disease). These considerations may guide selection of therapy. Limitations of Use Exforge HCT is not indicated for the initial therapy of hypertension [see Dosage and Administration (2)] . Exforge HCT is a combination tablet of amlodipine, a dihydropyridine calcium channel blocker (DHP CCB), valsartan, an angiotensin II receptor blocker (ARB), and hydrochlorothiazide, a thiazide diuretic. Exforge HCT is indicated for the treatment of hypertension to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes, and myocardial infarctions. ( 1 ) Limitations of Use Exforge HCT is not indicated for initial treatment of hypertension. ( 1 )
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):
- 治療高血壓。本品適用於以amlodipine、valsartan、hydrochlorothiazide其中兩種成分合併治療、仍無法有效控制血壓的高血壓患者。
許可證品項:藥品外觀與仿單(9 項)
| 品名 | 外觀 | 仿單/外盒 |
|---|---|---|
| 力安穩 膜衣錠 5/160/25毫克 | — | 仿單 · 外盒 |
| 力安穩 膜衣錠 5/160/12.5毫克 | 橢圓形 · 白 · 刻痕:無 · 標記:NVR / VCL · 13.4 外觀圖 | 仿單 · 外盒 |
| 力安穩 膜衣錠 10/160/12.5毫克 | — | 仿單 · 外盒 |
| 力安穩 膜衣錠 10/160/25毫克 | 橢圓形 · 黃 · 刻痕:無 · 標記:NVR / VHL · 13.4 外觀圖 | 仿單 · 外盒 |
| 力脈樂5/160/12.5毫克膜衣錠 | 橢圓形 · 白 · 刻痕:無 · 標記:NVR / VCL · 13.4 外觀圖 | 仿單 · 外盒 |
| 力脈樂5/160/25毫克膜衣錠 | — | 仿單 · 外盒 |
| 力脈樂10/160/12.5毫克膜衣錠 | — | 仿單 · 外盒 |
| 力脈樂10/160/25毫克膜衣錠 | 橢圓形 · 黃 · 刻痕:無 · 標記:NVR / VHL · 13.4 外觀圖 | 仿單 · 外盒 |
| 安壓三好膜衣錠 5/160/12.5 毫克 | — | 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
§ 2.14 Sacubitril+Valsartan (如Entresto):(106/3/1、109/6/1、110/7/1、111/5/1)
心臟血管及腎臟藥物 › Sacubitril+Valsartan (如Entresto):(106/3/1、109/6/1、110/7/1、111/5/1)
Sacubitril+Valsartan (如Entresto):(106/3/1、109/6/1、110/7/1、111/5/1) 1.限符合下列各項條件之慢性收縮性心衰竭患者使用: (1)依紐約心臟協會(NYHA)心衰竭功能分級為第二級至第四級。左心室收縮功能不全,左心室射出分率(LVEF)≦35% (初次使用者須檢附半年內心臟超音波、心導管左心室造影、核醫、電腦斷層或磁振造影等標準心臟功能檢查的左心室射出分率數值結果為參考依據;如果是急性心肌梗塞、急性心肌炎或初次裝置左心室再同步心律調節器或左心室再同步去顫復律器者,須經治療至少3個月並附上往後半年內之心臟超音波、心導管左心室造影、核醫、電腦斷層或磁振造影等標準心臟功能檢查的左心室射出分率數值結果為參考依據);或左心室射出分率(LVEF)介於36%至40%且對SGLT2抑制劑不耐受之病人(109/6/1、110/7/1、111/5/1)。 (2)經ACEI或ARB穩定劑量治療,及合併使用β-阻斷劑最大可耐受劑量已達4週(含)以上或使用β-阻斷劑有禁忌症而無法使用,且再併用SGLT-2抑制劑治療12週之後,LVEF仍≦35%,或對SGLT-2抑制劑無法耐受,仍有心衰竭症狀者。(109/6/1、111/5/1) 2.不應與ACEI或ARB合併使用,開始使用本藥,至少要和ACEI間隔36小時。(109/6/1) 3.曾有血管性水腫(angioedema)病史者,禁止使用。 4.每日限最多使用2粒。 5.111年5月1日前已依修訂前之給付規定使用本藥品之病人,得繼續使用本藥品至醫師更新其處方內容。(111/5/1)
歷史演變(4 次異動)
| 生效日 | 異動說明 |
|---|---|
| 106/3/1 | legacy_boan_parsed:ch02.txt |
| 109/6/1 | legacy_boan_parsed:ch02.txt |
| 110/7/1 | legacy_boan_parsed:ch02.txt |
| 111/5/1 | 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)。
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。