독소신주사 효능·효과
광고
독소신주사 복용법 (용법·용량)
1. 체표면적 기준(m2)
2. 체중기준(Kg)
3. 다른 항암제와 병용요법시
4. 간장애 환자
5. 투여방법
독소신주사 부작용·주의사항
전체 10개 항목 펼치기/접기
1. 다음 환자에는 투여하지 말 것.
2. 다음 환자에는 신중히 투여할 것.
3. 이상반응
4. 일반적 주의
5. 상호작용
6. 임부 및 수유부에 대한 투여
7. 소아에 대한 투여
8. 과량투여시의 처치
9. 적용상의 주의
10. 기타
독소신주사 성분·함량
1밀리리터 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 독소루비신염산염 | Doxorubicin Hydrochloride | 2.0 밀리그램 |
📍 독소신주사 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 독소루비신염산염
미국 FDA·NLM 자료 · 2026-10-02 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Doxorubicin hydrochloride liposome injection is an anthracycline topoisomerase inhibitor indicated for: Ovarian cancer : After failure of platinum-based chemotherapy ( 1.1 ) AIDS-related Kaposi’s Sarcoma : After failure of prior systemic chemotherapy or intolerance to such therapy ( 1.2 ) Multiple Myeloma : In combination with bortezomib in patients who have not previously received bortezomib and have received at least one prior therapy ( 1.3 ) 1.1 Ovarian Cancer Doxorubicin hydrochloride liposome injection is indicated for the treatment of patients with ovarian cancer whose disease has progressed or recurred after platinum-based chemotherapy. 1.2 AIDS-Related Kaposi’s Sarcoma Doxorubicin hydrochloride liposome injection is indicated for the treatment of AIDS-related Kaposi’s sarcoma in patients after failure of prior systemic chemotherapy or intolerance to such therapy. 1.3 Multiple Myeloma Doxorubicin hydrochloride liposome injection, in combination with bortezomib, is indicated for the treatment of patients with multiple myeloma who have not previously received bortezomib and have received at least one prior therapy.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
WARNING: CARDIOMYOPATHY and INFUSION-RELATED REACTIONS Doxorubicin hydrochloride liposome injection can cause myocardial damage, including acute left ventricular failure. The risk of cardiomyopathy was 11% when the cumulative anthracycline dose was between 450 mg/m 2 to 550 mg/m 2 . Assess left ventricular cardiac function prior to initiation of doxorubicin hydrochloride liposome injection and during and after treatment [see Warnings and Precautions ( 5.1 )]. Serious, life-threatening, and fatal infusion-related reactions can occur with doxorubicin hydrochloride liposome injection. Acute infusion-related reactions occurred in 11% of patients with solid tumors. Withhold doxorubicin hydrochloride liposome injection for infusion-related reactions and resume at a reduced rate. Discontinue doxorubicin hydrochloride liposome injection for serious or life-threatening infusion-related reactions [see Warnings and Precautions ( 5.2 )]. WARNING: CARDIOMYOPATHY and INFUSION-RELATED REACTIONS See full prescribing information for complete boxed warning. Doxorubicin hydrochloride liposome injection can cause myocardial damage, including acute left ventricular failure. The risk of cardiomyopathy was 11% when the cumulative anthracycline dose was between 450 mg/m 2 to 550 mg/m 2 . Assess left ventricular cardiac function prior to initiation of doxorubicin hydrochloride liposome injection, during treatment, and after treatment ( 5.1 ). Serious, life-threatening, and fatal infusion-related …
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Doxorubicin hydrochloride liposome injection is contraindicated in patients who have a history of severe hypersensitivity reactions, including anaphylaxis, to doxorubicin hydrochloride [see Warnings and Precautions ( 5.2 )] . Hypersensitivity reactions to doxorubicin hydrochloride or the components of doxorubicin hydrochloride liposome injection (4, 5.2)
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Hand-Foot Syndrome may occur. Dose modification or discontinuation may be required ( 5.3 ) Embryo-Fetal Toxicity: Can cause fetal harm. Advise of potential risk to a fetus. Use effective contraception ( 5.5 , 8.1 , 8.3 ) 5.1 Cardiomyopathy Doxorubicin hydrochloride can cause myocardial damage, including acute left ventricular failure. The risk of cardiomyopathy with doxorubicin hydrochloride is generally proportional to the cumulative exposure. Include prior use of other anthracyclines or anthracenediones in calculations of cumulative dose. The risk of cardiomyopathy may be increased at lower cumulative doses in patients with prior mediastinal irradiation. In a clinical study in 250 patients with advanced cancer who were treated with doxorubicin hydrochloride liposome injection, the risk of cardiomyopathy was 11% when the cumulative anthracycline dose was between 450 mg/m 2 to 550 mg/m 2 . Cardiomyopathy was defined as >20% decrease in resting left ventricular ejection fraction (LVEF) from baseline where LVEF remained in the normal range or a >10% decrease in LVEF from baseline where LVEF was less than the institutional lower limit of normal. Two percent of patients developed signs and symptoms of congestive heart failure without documented evidence of cardiomyopathy. Assess left ventricular cardiac function (e.g. MUGA or echocardiogram) prior to initiation of doxorubicin hydrochloride liposome injection, during treatment to detect acute changes, and after treatment to …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary Based on findings in animals and its mechanism of action, doxorubicin hydrochloride liposome injection can cause fetal harm when administered to a pregnant woman; avoid the use of doxorubicin hydrochloride liposome injection during the 1 st trimester. In animal reproduction studies, doxorubicin hydrochloride liposome injection was embryotoxic in rats and abortifacient in rabbits following intravenous administration during organogenesis at doses approximately 0.12 times the recommended clinical dose (see Data). Available human data do not establish the presence or absence of major birth defects and miscarriage related to the use of doxorubicin hydrochloride during …
미국 제품명 DOXIL
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 95,403건 가운데 많이 적힌 증상입니다. 보고 수는 약 때문이라는 증거가 아니며, 많이 쓰는 약일수록 많아집니다. 증상 이름의 한국어는 AI 번역(참고용)이라 영어 원어를 함께 적었습니다.
- 1 발열성 호중구 감소증febrile neutropenia9,530
- 2 적응증 외 사용off label use9,169
- 3 DISEASE PROGRESSION6,748
- 4 호중구 감소증neutropenia6,687
- 5 약효 없음drug ineffective5,347
- 6 발열pyrexia4,361
- 7 빈혈anaemia4,096
- 8 THROMBOCYTOPENIA3,987
- 9 오심nausea3,568
- 10 사망death3,402
- 11 미승인 적응증 사용product use in unapproved indication3,146
- 12 폐렴pneumonia3,095
미국 리콜 기록
FDA 리콜(회수) 기록 4건 중 최근 4건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2026.06.17 · 1등급(심각) · SUN PHARMACEUTICAL INDUSTRIES INC Presence of Particulate matter: Particulate matter identified as glass.
- 2023.10.25 · 2등급 · Baxter Healthcare Corporation CGMP Deviations: Product was exposed to temperatures exceeding the labeled storage conditions during transportation were released by mistake.
- 2020.12.02 · 3등급(경미) · Fresenius Kabi USA, LLC Cross Contamination with Other Products: trace amounts of octreotide found during testing
- 2018.01.31 · 2등급 · Sun Pharmaceutical Industries, Inc. Lack Of Assurance Of Sterility
출처: 미국 FDA openFDA(라벨·FAERS·리콜), 미국 국립의학도서관 RxNorm · DailyMed 원문 라벨. 한국어는 오픈드럭 서버 AI(gemma)가 자동 번역한 참고용(사람 검수 전)으로 오역이 있을 수 있으니 반드시 원문을 확인하세요.
허가 정보
- 품목기준코드
- 200101715
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀봉용기, 냉암소(2~8℃)보관
- 사용 기간
- 제조일로부터 18 개월,제조일로부터 24 개월
- 포장 단위
- 5㎖/바이알, 25㎖/바이알, 50㎖/바이알
- ATC 코드
- L01DB01
- 보험 코드
- 644300521,644309061
- 표준코드
- 8806443005204, 8806443005211, 8806443061804, 8806443061811, 8806443090606, 8806443090613
- 최근 변경
- 2022.09.14
허가 변경 이력
- · 저장방법 및 사용(유효)기간, 2022-09-14
- · 사용상주의사항변경(부작용포함), 2021-03-04
- · 사용상주의사항변경(부작용포함), 2020-03-17
- · 사용상주의사항변경(부작용포함), 2018-07-29
- · 사용상주의사항변경(부작용포함), 2018-01-20
- · 사용상주의사항변경(부작용포함), 2017-01-19
- · 제품명칭변경, 2010-09-01
- · 사용상주의사항변경(부작용포함), 2005-01-22
- · 용법용량변경, 2005-01-22
- · 효능효과변경, 2005-01-22
- · 제품명칭변경, 2004-07-16
원문: 식약처 의약품안전나라