C01CA04 dopamine

CARDIOVASCULAR SYSTEM CARDIAC THERAPY CARDIAC STIMULANTS EXCL. CARDIAC GLYCOSIDES Adrenergic and dopaminergic agents

健保收載品項 TFDA 在效許可證 9 FDA 已核准

台灣藥品與外觀

台灣食藥署在效西藥許可證 9 張;以下列出 8 個品項。

健保收載品名:"中化"多巴命注射液、"優良"優瑞命注射液(杜帕明)、"南光" 吉利命注射液3毫克/毫升、"榮民"得保命注射液20毫克/毫升(杜帕明)、"瑞安" 保多命注射液40公絲/公撮(杜帕命)、"百特" 多保明注射液 1600微公克/毫升、"百特" 多保明注射液 3200微公克/毫升、"百特" 多保明注射液 800微公克/毫升、"菲尼斯"多巴胺注射液 200 毫克/5毫升、〝赫士睿〞多普明注射劑40公絲/公撮、加邦注射液、多博明注射液1600微克/公撮、多博明注射液800微毫克/公撮、多巴明注射液 40 毫克/毫升、多搏威注射液40公絲/公撮、多補命注射液40公絲/公撮

無外觀照
"優良"優瑞命注射液(杜帕明)
無外觀照
鹽酸杜帕明
無外觀照
得保命注射液40毫克/毫升
無外觀照
得保命注射液10公絲/公撮(杜帕明)
無外觀照
"榮民"得保命注射液20毫克/毫升(杜帕明)
無外觀照
多搏威注射液40公絲/公撮
無外觀照
"南光" 吉利命注射液3毫克/毫升
無外觀照
多巴明注射液 40 毫克/毫升

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. 休克症候群及心臟衰竭。
  2. 擬交感神經興奮藥。
  3. 擬交感神經劑。

美國 FDA 適應症(英文原文對照)

美國 FDA 核准成分 dopamine hydrochloride (商品名 Dopamine Hydrochloride / Dopamine Hydrochloride in Dextrose / Hormone Harmony) · 仿單更新 2025-11-03

INDICATIONS AND USAGE Dopamine Hydrochloride, USP is indicated for the correction of hemodynamic imbalances present in the shock syndrome due to myocardial infarction, trauma, endotoxic septicemia, open-heart surgery, renal failure, and chronic cardiac decompensation as in congestive failure. Patients most likely to respond adequately to Dopamine Hydrochloride, USP are those in whom physiological parameters, such as urine flow, myocardial function, and blood pressure, have not undergone profound deterioration. Multiclinic trials indicate that the shorter the time interval between onset of signs and symptoms and initiation of therapy with blood volume correction and Dopamine Hydrochloride, USP, the better the prognosis. Where appropriate, blood volume restoration with a suitable plasma expander or whole blood should be accomplished prior to administration of Dopamine Hydrochloride, USP. Poor Perfusion of Vital Organs – Urine flow appears to be one of the better diagnostic signs by which adequacy of vital organ perfusion can be monitored. Nevertheless, the physician should also observe the patient for signs of reversal of confusion or reversal of comatose condition. Loss of pallor, increase in toe temperature, and/or adequacy of nail bed capillary filling may also be used as indices of adequate dosage. Clinical studies have shown that when Dopamine Hydrochloride, USP is administered before urine flow has diminished to levels of approximately 0.3 mL/minute, prognosis is more favorable. Nevertheless, in a number of oliguric or anuric patients, administration of Dopamine Hydrochloride, USP has resulted in an increase in urine flow, which in some cases reached normal levels. Dopamine Hydrochloride, USP may also increase urine flow in patients whose output is within normal limits and thus may be of value in reducing the degree of pre-existing fluid accumulation. It should be noted that at doses above those optimal for the individual patient, urine flow may decrease, necessitating reduction of dosage. Low Cardiac Output – Increased cardiac output is related to dopamine’s direct inotropic effect on the myocardium. Increased cardiac output at low or moderate doses appears to be related to a favorable prognosis. Increase in cardiac output has been associated with either static or decreased systemic vascular resistance (SVR). Static or decreased SVR associated with low or moderate movements in cardiac output is believed to be a reflection of differential effects on specific vascular beds with increased resistance in peripheral beds (e.g., femoral) and concomitant decreases in mesenteric and renal vascular beds. Redistribution of blood flow parallels these changes so that an increase in cardiac output is accompanied by an increase in mesenteric and renal blood flow. In many instances the renal fraction of the total cardiac output has been found to increase. Increase in cardiac output produced by dopamine is not associated with substantial decreases in systemic vascular resistance as may occur with isoproterenol. Hypotension – Hypotension due to inadequate cardiac output can be managed by administration of low to moderate doses of Dopamine Hydrochloride, USP which have little effect on SVR. At high therapeutic doses, dopamine’s alpha-adrenergic activity becomes more prominent and thus may correct hypotension due to diminished SVR. As in the case of other circulatory decompensation states, prognosis is better in patients whose blood pressure and urine flow have not undergone profound deterioration. Therefore, it is suggested that the physician administer Dopamine Hydrochloride, USP as soon as a definite trend toward decreased systolic and diastolic pressure becomes evident.

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。