녹십자-파이브리노겐주 효능·효과
광고
녹십자-파이브리노겐주 복용법 (용법·용량)
녹십자-파이브리노겐주 부작용·주의사항
전체 8개 항목 펼치기/접기
1. 경고
2. 다음 환자에는 투여하지 말 것.
3. 다음 환자에게는 신중히 투여할 것.
4. 약물이상반응
5. 일반적 주의
6. 임부에 대한 투여
7. 고령자에 대한 투여
8. 적용상의 주의
녹십자-파이브리노겐주 성분·함량
1 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 사람 피브리노겐 | Human Fibrinogen | 1 그램 |
📍 녹십자-파이브리노겐주 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 사람 피브리노겐
미국 FDA·NLM 자료 · 2026-10-07 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
Human Blood Coagulation Factor [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
TachoSil is a fibrin sealant patch indicated for use with manual compression in adult and pediatric patients as an adjunct to hemostasis in cardiovascular and hepatic surgery when control of bleeding by standard surgical techniques (such as suture, ligature or cautery) is ineffective or impractical. Limitations for Use TachoSil cannot safely or effectively be used in place of sutures or other form of mechanical ligation for the treatment of major arterial or venous bleeding. Not for use in children under one month of age. TachoSil is a fibrin sealant patch indicated for use with manual compression in adult and pediatric patients as an adjunct to hemostasis in cardiovascular and hepatic surgery, when control of bleeding by standard surgical techniques (such as suture, ligature or cautery) is ineffective or impractical. ( 1 ) Limitations for Use Not for use in place of sutures or other forms of mechanical ligation in treatment of major arterial or venous bleeding. ( 1 ) Not for use in children under one month of age. ( 8.4 )
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Do not use TachoSil for: • Intravascular application. Bleeding from large defects in visible arteries or veins where the injured vascular wall requires repair and maintenance of vessel patency or where there would be persistent exposure of TachoSil to blood flow during absorption of the product. This can result in life-threatening thromboembolic events [see Warnings and Precautions (5.1) ] . • Individuals known to have anaphylactic or severe systemic reaction to human blood products or horse proteins [see Warnings and Precautions (5.2) ] . Do not apply TachoSil intravascularly. Intravascular application of TachoSil may result in life-threatening thromboembolic events. ( 4 ) Do not use TachoSil in individuals with known hypersensitivity to human blood products or horse proteins. ( 4 )
주요 경고·주의
영어 원문 (미국 FDA 라벨)
• Thrombosis can occur if TachoSil is applied intravascularly. Ensure that TachoSil is applied to the surface of cardiac, vascular or hepatic tissue only. ( 5.1 ) • Can cause hypersensitivity or allergic/anaphylactoid reactions with first time or repetitive application. ( 5.2 ) • Avoid use in contaminated areas of the body or in the presence of an active infection. ( 5.3 ) • TachoSil contains collagen, which may adhere to bleeding surfaces. May carry a risk of gastrointestinal obstruction in abdominal surgery due to tissue adhesions. To prevent the development of tissue adhesions at undesired sites, ensure tissue areas outside the application area are adequately cleansed before administration of TachoSil. ( 5.4 ) • Avoid packing in cavities or closed spaces, because this may cause compression of underlying tissue. ( 5.5 ) • Use the least number of patches required to cover the entire bleeding area. Do not pack. Remove any unattached pieces of TachoSil. ( 5.6 ) • May carry a risk of transmitting infectious agents, such as viruses, and theoretically, the variant Creutzfeldt-Jakob disease (vCJD) agent, and the Creutzfeldt-Jakob disease (CJD) agents, despite manufacturing steps designed to reduce the risk of viral transmission. ( 5.7 ) 5.1 Thrombosis Thrombosis can occur if TachoSil is applied intravascularly. Ensure that TachoSil is applied to the surface of cardiac, vascular, or hepatic tissue only. 5.2 Hypersensitivity Reactions Hypersensitivity or allergic/anaphylactoid …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary A review of available data suggests that major birth defects occur in 2-4% of the U.S. general population and that miscarriage occurs in 15-20% of clinically recognized pregnancies, regardless of drug exposure. Animal reproduction studies have not been conducted with TachoSil. There are no adequate and well-controlled studies in pregnant women. It is also not known whether TachoSil can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. TachoSil should be administered to pregnant women only if clearly needed.
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 334건 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 use43
- 2 약효 없음drug ineffective28
- 3 CEREBROSPINAL FLUID LEAKAGE15
- 4 INTESTINAL OBSTRUCTION11
- 5 POST PROCEDURAL HAEMORRHAGE11
- 6 제품 부착 문제product adhesion issue11
- 7 발열pyrexia11
- 8 ABDOMINAL ABSCESS10
- 9 오심nausea10
- 10 복통abdominal pain8
- 11 HAEMATOMA8
- 12 두통headache8
미국 리콜 기록
FDA 리콜 기록이 없습니다.
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
- 200403354
- 허가 구분
- 허가 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀봉용기, 10℃이하에서 보관
- 사용 기간
- 제조일로부터 38 개월
- 포장 단위
- 1세트/상자[1동결건조바이알(1그램) + 1첨부용제바이알(50밀리리터)]
- ATC 코드
- B02BB01
- 보험 코드
- 643600821
- 표준코드
- 8806436008205, 8806436008212
- 최근 변경
- 2026.08.04
허가 변경 이력
- · 사용상의 주의사항, 2026-08-04
- · 성상변경, 2021-11-02
- · 사용상주의사항변경(부작용포함), 2018-10-05
- · 사용상주의사항변경(부작용포함), 2017-09-16
- · 용법용량변경, 2017-09-16
- · 효능효과변경, 2017-09-16
- · 사용상주의사항변경(부작용포함), 2012-02-21
- · 성상변경, 2008-10-21
- · 사용상주의사항변경(부작용포함), 2007-02-03
- · 용법용량변경, 2007-02-03
- · 효능효과변경, 2007-02-03
- · 제품명칭변경, 2004-03-09
원문: 식약처 의약품안전나라
