義大醫院藥品外觀辨識 暨 處方集 內容
藥品外觀
處方集
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藥品代碼:CDURVAL
廠商: Catalent
規格: 120mg/2.4ml/vial
顏色:
形狀:
劑型:
標記:
健保碼:無健保碼
ATC code:L01XC28
目前暫無圖片
藥品代碼:CDURVA2
廠商: 阿斯特捷利康
規格: 500mg/10ml/vial
顏色:
形狀:
劑型:
標記:
健保碼:無健保碼
ATC code:L01FF03
學名
Durvalumab
商品名
ImfinziImfinzi
中文名
抑癌寧注射劑抑癌寧注射劑
規格含量
120mg/2.4ml/vial500mg/10ml/vial
藥理分類
04. ANTINEOPLASTIC AGENTS; ;
04.05. MONOCLONAL ANTIBODIES;;
藥理作用
Anti-PD-L1 Monoclonal Antibody
適應症(藥袋)
標靶藥物
懷孕分級
D 已證實對人之胎兒有傷害,若是疾病對於孕婦有生命威脅或安全的藥品已無法治療的情況下,權衡利弊,仍可使用。
授乳安全性
Unknown
用法用量
IVF(rate: 60 minutes)
NSCLC
1.Non–small cell lung cancer, resectable, neoadjuvant and adjuvant therapy(Non-squamous or squamous tumor histologies)
≥30 kg:1500 mg once every 3 weeks (in combination with platinum-containing chemotherapy) for 4 cycles, followed by surgery, followed by 1500 mg once every 4 weeks (as a single agent) until disease progression that precludes definitive surgery, recurrence, or unacceptable toxicity or a maximum of 12 cycles after surgery
<30 kg: 20 mg/kg once every 3 weeks (in combination with platinum-containing chemotherapy) for 4 cycles, followed by surgery, followed by 20 mg/kg once every 4 weeks (as a single agent) until disease progression that precludes definitive surgery, recurrence, or unacceptable toxicity or a maximum of 12 cycles after surgery
2.Non–small cell lung cancer, stage 3, unresectable
≥30 kg: 10 mg/kg once every 2 weeks or 1500 mg once every 4 weeks; continue until disease progression or unacceptable toxicity or a maximum of 12 months
<30 kg: 10 mg/kg once every 2 weeks; continue until disease progression or unacceptable toxicity or a maximum of 12 months
ES-SCLC
Patients >30 kg: 1,500 mg once every 3 weeks (in combination with etoposide and either carboplatin or cisplatin) for 4 cycles, followed by 1,500 mg once every 4 weeks as a single agent; continue until disease progression or unacceptable toxicity
Patients ≤30 kg: 20 mg/kg once every 3 weeks (in combination with etoposide and either carboplatin or cisplatin) for 4 cycles, followed by 20 mg/kg once every 4 weeks as a single agent; continue until disease progression or unacceptable toxicity.
Biliary tract cancer, locally advanced or metastatic
≥30 kg: 1500 mg once every 3 weeks (in combination with gemcitabine and cisplatin) for up to 8 cycles, followed by 1500 mg once every 4 weeks as a single agent until disease progression or unacceptable toxicity
<30 kg: 20 mg/kg once every 3 weeks (in combination with gemcitabine and cisplatin) for up to 8 cycles, followed by 20 mg/kg once every 4 weeks as a single agent until disease progression or unacceptable toxicity.
副作用
Cough, fatigue, pneumonitis, upper respiratory tract infection, dyspnea
禁忌
注意事項
1.原瓶應儲存於2-8℃
2.藥品配製:
(1)配製時請勿搖晃小瓶,以0.9%NaCl或5%Destrose稀釋為濃度1-15mg/ml,輕柔翻轉混合稀釋溶液。
(2)稀釋後室溫應於8小時內使用完畢,或冷藏於2-8℃下可保存24小時。
3.輸液須以具有無菌、低蛋白結合率之0.2或0.22mm管內過濾器靜脈輸注管線輸注60分鐘,勿同時於同一管線給予其他藥物
4.建議婦女使用在治療期間即給予末次劑量後至少3個月不要哺餵母乳、並採取有效的避孕措施
藥品與食物交互作用
建立者
103617
建立時間
2019-10-31 14:02:06
維護者
103617
維護時間
2024-10-21 09:58:21

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