C09DB02 olmesartan medoxomil and amlodipine

CARDIOVASCULAR SYSTEM AGENTS ACTING ON THE RENIN-ANGIOTENSIN SYSTEM ANGIOTENSIN II RECEPTOR BLOCKERS (ARBs), COMBINATIONS Angiotensin II receptor blockers (ARBs) and calcium channel blockers

健保收載品項 TFDA 在效許可證 15 FDA 已核准

台灣藥品與外觀

台灣食藥署在效西藥許可證 15 張;以下列出 15 個品項(14 項有外觀照)。

健保收載品名:?優惠脈錠5/20毫克、?優惠脈錠5/40毫克、歐舒卡膜衣錠10/40毫克、歐舒卡膜衣錠5/20毫克、歐舒卡膜衣錠5/40毫克、歐舒脈膜衣錠5/20毫克、歐舒脈膜衣錠5/40毫克、舒脈康膜衣錠 5/20 毫克、舒脈康膜衣錠10/40毫克、舒脈康膜衣錠5/40毫克、迪高平膜衣錠10/40毫克、迪高平膜衣錠5/20毫克、迪高平膜衣錠5/40毫克、降壓安錠5/40毫克

舒脈康膜衣錠 5/20 毫克 外觀
舒脈康膜衣錠 5/20 毫克
圓形 · 白 · 刻痕:無 · 標記:C73 · 7 mm
舒脈康膜衣錠5/40毫克 外觀
舒脈康膜衣錠5/40毫克
圓形 · 黃 · 刻痕:無 · 標記:C75 · 8 mm
無外觀照
舒脈康膜衣錠10/40毫克
歐舒卡膜衣錠5/40毫克 外觀
歐舒卡膜衣錠5/40毫克
圓形 · 白 · 刻痕:無 · 標記:A11 / H · 10 mm
歐舒卡膜衣錠10/40毫克 外觀
歐舒卡膜衣錠10/40毫克
圓形 · 棕 · 刻痕:無 · 標記:A 1 2 / H · 10 mm
歐舒卡膜衣錠5/20毫克 外觀
歐舒卡膜衣錠5/20毫克
圓形 · 白 · 刻痕:無 · 標記:A9 / H · 10 mm
迪高平膜衣錠5/40毫克 外觀
迪高平膜衣錠5/40毫克
圓形 · 黃 · 刻痕:無 · 標記:L77 · 8 mm
迪高平膜衣錠5/20毫克 外觀
迪高平膜衣錠5/20毫克
圓形 · 白 · 刻痕:無 · 標記:L75 · 6 mm
迪高平膜衣錠10/40毫克 外觀
迪高平膜衣錠10/40毫克
圓形 · 棕 · 刻痕:無 · 標記:L78 · 9 mm
双優惠脈錠5/40毫克 外觀
双優惠脈錠5/40毫克
圓形 · 黃 · 刻痕:無 · 標記:131 · 8.1 mm
歐舒脈膜衣錠5/40毫克 外觀
歐舒脈膜衣錠5/40毫克
圓形 · 黃 · 刻痕:無 · 標記:SYN 067 · 7 mm
双優惠脈錠5/20毫克 外觀
双優惠脈錠5/20毫克
圓形 · 白 · 刻痕:無 · 標記:251 · 6 mm
降壓安錠5/40毫克 外觀
降壓安錠5/40毫克
圓形 · 黃 · 刻痕:無 · 標記:73 / S · 8.0 mm
歐舒脈膜衣錠5/20毫克 外觀
歐舒脈膜衣錠5/20毫克
圓形 · 白 · 刻痕:無 · 標記:SYN 111 · 6 mm
釋壓膜衣錠 5/40 毫克 外觀
釋壓膜衣錠 5/40 毫克
圓形 · 黃 · 刻痕:無 · 標記:40 · 8 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. 治療高血壓、此複方Amlodipine/Olmesartanmedoxomil不適合用於起始治療。
  2. 治療高血壓、此複方藥品不適合用於起始治療。

美國 FDA 適應症(英文原文對照)

美國 FDA 核准成分 amlodipine and olmesartan medoxomil (商品名 Amlodipine and Olmesartan Medoxomil / amlodipine besylate and olmesartan medoxomil) · 仿單更新 2026-04-28

1 INDICATIONS AND USAGE Amlodipine and olmesartan medoxomil tablets are indicated for the treatment of hypertension, alone or with other antihypertensive agents, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular (CV) 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 the class to which this drug principally belongs. There are no controlled trials demonstrating risk reduction with amlodipine and olmesartan medoxomil tablets. 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 one 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 (for example, 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. Amlodipine and olmesartan medoxomil tablets may also be used as initial therapy in patients who are likely to need multiple antihypertensive agents to achieve their blood pressure goals. Patients with moderate or severe hypertension are at relatively high risk for cardiovascular events (such as strokes, heart attacks, and heart failure), kidney failure, and vision problems, so prompt treatment is clinically relevant. The decision to use a combination as initial therapy should be individualized and should be shaped by considerations such as baseline blood pressure, the target goal, and the incremental likelihood of achieving goal with a combination compared to monotherapy. Individual blood pressure goals may vary based upon the patient’s risk. Data from an 8-week, placebo-controlled, parallel-group factorial study [ see Clinical Studies (14.1) ] provide estimates of the probability of reaching a blood pressure goal with amlodipine and olmesartan medoxomil tablets compared to amlodipine or olmesartan medoxomil monotherapy. The figures below provide estimates of the likelihood of achieving the targeted systolic or diastolic blood pressure goals with amlodipine and olmesartan medoxomil tablets 10/40 mg compared with amlodipine or olmesartan medoxomil monotherapy, based upon baseline systolic or diastolic blood pressure. The curve of each treatment group was estimated by logistic regression modeling from all available data of that treatment group. The right tail of each curve is less reliable because of small numbers of subjects with high baseline blood pressures. Figure 1: Probability of Achieving Systolic Blood Pressure (SBP) < 140 mmHg at Week 8 With LOCF Figure 2: Probability of Achieving Diastolic Blood Pressure (DBP) < 90 mmHg at Week 8 With LOCF Figure 3: Probability of Achieving Systolic Blood Pressure (SBP) < 130 mmHg at Week 8 With LOCF Figure 4: Probability of Achieving Diastolic Blood Pressure (DBP) < 80 mmHg at Week 8 With LOCF The figures above provide an approximation of the likelihood of reaching a targeted blood pressure goal (e.g., Week 8 SBP < 140 mmHg or < 130 mmHg or a DBP < 90 mmHg or <80 mmHg) for the high-dose treatment groups evaluated in the study. Amlodipine and olmesartan medoxomil tablets 5/20 mg, the lowest dose combination treatment group, increases the probability of reaching blood pressure goal compared with the highest dose monotherapies, amlodipine 10 mg and olmesartan medoxomil 40 mg. For example, a patient with a baseline blood pressure of 160/100 mmHg has about a 48% likelihood of achieving a goal of < 140 mmHg (systolic) and a 51% likelihood of achieving a goal of < 90 mmHg (diastolic) on monotherapy with olmesartan medoxomil 40 mg, and about a 46% likelihood of achieving a goal of < 140 mmHg (systolic) and a 60% likelihood of achieving a goal of < 90 mmHg (diastolic) on monotherapy with amlodipine 10 mg. The likelihood of achieving these same goals increases to 63% (systolic) and 71% (diastolic) on amlodipine and olmesartan medoxomil tablets 5/20 mg, and to 68% (systolic) and 85% (diastolic) on amlodipine and olmesartan medoxomil tablets 10/40 mg. Amlodipine and olmesartan medoxomil tablets are a combination of amlodipine besylate, a dihydropyridine calcium channel blocker, and olmesartan medoxomil, an angiotensin II receptor blocker, indicated for the treatment of hypertension, alone or with other antihypertensive agents, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions ( 1 ). Amlodipine and olmesartan medoxomil tablets may also be used as initial therapy in patients likely to need multiple antihypertensive agents to achieve their blood pressure goals (1) . Figures 1 & 2 Figures 1 & 2 Figures 3 & 4 Figures 3 & 4

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

查無健保特殊給付規定條款;本藥品依一般健保藥品支付規定給付。

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。