화이자카보플라틴주10mg 효능·효과
1. 진행성 상피성 난소암
광고
화이자카보플라틴주10mg 복용법 (용법·용량)
화이자카보플라틴주10mg 부작용·주의사항
전체 11개 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. 고령자에 대한 투여
9. 과량투여시의 처치
10. 적용상의 주의
바이알역가
희석액분량
10 mg
1 mL
50 mg
5 mL
150 mg
15 mL
450 mg
45 mL
11. 기타
화이자카보플라틴주10mg 성분·함량
1mL 중, 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 카보플라틴 | Carboplatin | 10 밀리그램 |
📍 화이자카보플라틴주10mg 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 카보플라틴
미국 FDA·NLM 자료 · 2026-10-03 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
Platinum-based Drug [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Initial Treatment of Advanced Ovarian Carcinoma Carboplatin injection is indicated for the initial treatment of advanced ovarian carcinoma in established combination with other approved chemotherapeutic agents. One established combination regimen consists of carboplatin and cyclophosphamide. Two randomized controlled studies conducted by the NCIC and SWOG with carboplatin versus cisplatin, both in combination with cyclophosphamide, have demonstrated equivalent overall survival between the two groups (see CLINICAL STUDIES ). There is limited statistical power to demonstrate equivalence in overall pathologic complete response rates and long-term survival (≥ 3 years) because of the small number of patients with these outcomes: the small number of patients with residual tumor < 2 cm after initial surgery also limits the statistical power to demonstrate equivalence in this subgroup. Secondary Treatment of Advanced Ovarian Carcinoma Carboplatin injection is indicated for the palliative treatment of patients with ovarian carcinoma recurrent after prior chemotherapy, including patients who have been previously treated with cisplatin. Within the group of patients previously treated with cisplatin, those who have developed progressive disease while receiving cisplatin therapy may have a decreased response rate.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
Carboplatin injection should be administered under the supervision of a qualified physician experienced in the use of cancer chemotherapeutic agents. Appropriate management of therapy and complications is possible only when adequate treatment facilities are readily available. Bone marrow suppression is dose related and may be severe, resulting in infection and/or bleeding. Anemia may be cumulative and may require transfusion support. Vomiting is another frequent drug related side effect. Anaphylactic-like reactions to carboplatin have been reported and may occur within minutes of carboplatin injection administration. Epinephrine, corticosteroids, and antihistamines have been employed to alleviate symptoms.
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Carboplatin injection is contraindicated in patients with a history of severe allergic reactions to cisplatin or other platinum-containing compounds. Carboplatin injection should not be employed in patients with severe bone marrow depression or significant bleeding.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Bone marrow suppression (leukopenia, neutropenia, and thrombocytopenia) is dose-dependent and is also the dose-limiting toxicity. Peripheral blood counts should be frequently monitored during carboplatin injection treatment and, when appropriate, until recovery is achieved. Median nadir occurs at day 21 in patients receiving single agent carboplatin. In general, single intermittent courses of carboplatin should not be repeated until leukocyte, neutrophil, and platelet counts have recovered. Since anemia is cumulative, transfusions may be needed during treatment with carboplatin, particularly in patients receiving prolonged therapy. Bone marrow suppression is increased in patients who have received prior therapy, especially regimens including cisplatin. Marrow suppression is also increased in patients with impaired kidney function. Initial carboplatin injection dosages in these patients should be appropriately reduced (see DOSAGE AND ADMINISTRATION) and blood counts should be carefully monitored between courses. The use of carboplatin in combination with other bone marrow suppressing therapies must be carefully managed with respect to dosage and timing in order to minimize additive effects. Carboplatin has limited nephrotoxic potential, but concomitant treatment with aminoglycosides has resulted in increased renal and/or audiologic toxicity, and caution must be exercised when a patient receives both drugs. Clinically significant hearing loss has been reported to occur in …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
Pregnancy Pregnancy Category D See WARNINGS.
미국 제품명 KYXATA
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 126,274건 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 적응증 외 사용off label use8,564
- 2 호중구 감소증neutropenia7,435
- 3 빈혈anaemia7,235
- 4 오심nausea7,052
- 5 발열성 호중구 감소증febrile neutropenia6,609
- 6 설사diarrhoea6,243
- 7 MALIGNANT NEOPLASM PROGRESSION6,115
- 8 DISEASE PROGRESSION6,076
- 9 THROMBOCYTOPENIA5,938
- 10 호흡 곤란dyspnoea5,431
- 11 구토vomiting5,151
- 12 발열pyrexia4,847
미국 리콜 기록
FDA 리콜(회수) 기록 4건 중 최근 4건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2013.02.13 · 1등급(심각) · Hospira Inc. Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.
- 2013.02.13 · 1등급(심각) · Hospira Inc. Crystallization: Product is being recalled due to visible particulates identified during a retain sample inspection. Findings have identified the particles as Carboplatin crystals.
- 2012.09.26 · 2등급 · Hospira Inc. The affected lots of Carboplatin Injection, Cytarabine Injection, Methotrexate Injection, USP, and Paclitaxel Injection are beig recalled due to visible particles embedded in the glass located at the neck of the vial. There may be the potential for product to come into contact with the embedded particles and the particles may become dislodged into the solution.
- 2012.08.22 · 3등급(경미) · Hospira Inc. Failed PH specification: The lots of Carboplatin Injection were manufactured from Carboplatin API lots which trended out of specification low pH.
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
- 200210228
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 위탁 제조
- Hospira Australia Pty Ltd.
- 저장 방법
- 밀봉용기 2-25℃, 차광보관
- 사용 기간
- 제조일로부터 18 개월
- 포장 단위
- 150mg/15ml*1바이알, 450mg/45ml*1바이알, 600mg/60ml*1바이알
- ATC 코드
- L01XA02
- 보험 코드
- 648903231,648903232,648903233
- 표준코드
- 8806489032301, 8806489032318, 8806489032325, 8806489032332, 8806489032349, 8806767001005 외 15개
- 최근 변경
- 2024.03.27
허가 변경 이력
- · 사용상주의사항변경(부작용포함), 2024-03-27
- · 사용상주의사항변경(부작용포함), 2023-05-10
- · 사용상주의사항변경(부작용포함), 2019-12-18
- · 사용상주의사항변경(부작용포함), 2018-07-29
- · 제품명칭변경, 2016-11-07
- · 제품명칭변경, 2009-07-01
- · 사용상주의사항변경(부작용포함), 2008-02-02
- · 용법용량변경, 2008-02-02
- · 효능효과변경, 2008-02-02
- · 저장방법 및 유효기간(사용기간)변경, 2007-05-14
원문: 식약처 의약품안전나라
