대한트라넥사민산주사500mg 효능·효과
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광고
대한트라넥사민산주사500mg 복용법 (용법·용량)
대한트라넥사민산주사500mg 부작용·주의사항
전체 11개 항목 펼치기/접기
1. 경고
2. 다음 환자에는 투여하지 말 것.
3. 다음 환자에는 신중히 투여할 것.
4. 이상반응
5. 일반적 주의
6. 상호작용
7. 임부 및 수유부에 대한 투여
8. 고령자에 대한 투여
9. 과량투여
10. 적용상의 주의
11. 기타
대한트라넥사민산주사500mg 성분·함량
1mL 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 트라넥사민산 | Tranexamic Acid | 100 밀리그램 |
📍 대한트라넥사민산주사500mg 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 트라넥사민산
미국 FDA·NLM 자료 · 2026-10-01 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
Antifibrinolytic Agent [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Tranexamic acid injection is indicated in patients with hemophilia for short-term use (2 to 8 days) to reduce or prevent hemorrhage and reduce the need for replacement therapy during and following tooth extraction. Tranexamic acid injection is an antifibrinolytic indicated in patients with hemophilia for short-term use (2 to 8 days) to reduce or prevent hemorrhage and reduce the need for replacement therapy during and following tooth extraction.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
WARNING: RISK OF MEDICATION ERRORS DUE TO INCORRECT ROUTE OF ADMINISTRATION Tranexamic acid injection is for intravenous use only. Serious, including fatal, adverse reactions including seizures and cardiac arrythmias have occurred when tranexamic acid injection was inadvertently administered via the neuraxial route [see Warnings and Precautions (5.1) ] . WARNING: RISK OF MEDICATION ERRORS DUE TO INCORRECT ROUTE OF ADMINISTRATION See full prescribing information for complete boxed warning. Tranexamic acid injection is for intravenous use only. Serious, including fatal, adverse reactions including seizures and cardiac arrythmias have occurred when tranexamic acid injection was inadvertently administered intrathecally via the neuraxial route. (5.1)
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Tranexamic acid injection is contraindicated: As a neuraxial (i.e., intrathecal, epidural) injection [see Warnings and Precautions (5.1) ] . In patients with subarachnoid hemorrhage. Anecdotal experience indicates that cerebral edema and cerebral infarction may be caused by tranexamic acid in such patients. In patients with active intravascular clotting [see Warnings and Precautions (5.2) ] . In patients with hypersensitivity to tranexamic acid or any of the ingredients [see Warnings and Precautions (5.4) ] . As a neuraxial (i.e., intrathecal, epidural) injection. (4) In patients with subarachnoid hemorrhage, due to risk of cerebral edema and cerebral infarction. (4) In patients with active intravascular clotting. (4) In patients with severe hypersensitivity reactions to tranexamic acid or any of the ingredients. (4)
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Risk of Thrombosis with Concomitant Use of Factor IX: Avoid concomitant use. (5.2) Seizures: Inadvertent injection into neuraxial system may result in seizures. ( 5.3 ) Hypersensitivity Reactions: In case of severe reaction, discontinue use and seek immediate medical attention. ( 5.4 ) Visual Disturbances: Visual or ocular adverse effects may occur. Discontinue use if visual or ocular symptoms occur. ( 5.5 ) Dizziness: Advise patients not to drive if dizziness occurs. ( 5.6 ) 5.1 Risk of Medication Errors Due to Incorrect Route of Administration Tranexamic acid is for intravenous use only. Serious, including fatal, adverse reactions including seizures and cardiac arrythmias have occurred when tranexamic acid was inadvertently administered via the neuraxial route. Confirm the correct route of administration for tranexamic acid and avoid confusion with other injectable solutions that might be administered at the same time as tranexamic acid. Clearly label syringes containing tranexamic acid with the intravenous route of administration. 5.2 Thromboembolic Risk Tranexamic acid is contraindicated in patients with active intravascular clotting. Tranexamic acid is an antifibrinolytic and may increase the risk of thromboembolic events. Venous and arterial thrombosis or thromboembolism has been reported in patients treated with tranexamic acid. Avoid concomitant use of tranexamic acid and medical products that are pro-thrombotic, as the risk of thrombosis may be increased. These …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary Available data from published studies, case series and case reports with tranexamic acid use in pregnant women in the second and third trimester and at the time of delivery have not clarified whether there is a drug-associated risk of miscarriage or adverse maternal or fetal outcomes. There are 2 (0.02%) infant cases with structural abnormalities that resulted in death when tranexamic acid was used during conception or the first trimester of pregnancy; however, due to other confounding factors the risk of major birth defects with use of tranexamic acid during pregnancy is not clear. Tranexamic acid is known to pass the placenta and appears in cord blood at …
미국 제품명 Cyklokapron
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 8,842건 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 약효 없음drug ineffective642
- 2 적응증 외 사용off label use642
- 3 발열pyrexia366
- 4 오심nausea340
- 5 저혈압hypotension325
- 6 설사diarrhoea313
- 7 구토vomiting304
- 8 출혈haemorrhage302
- 9 호흡 곤란dyspnoea287
- 10 폐렴pneumonia274
- 11 발열성 호중구 감소증febrile neutropenia261
- 12 두통headache241
미국 리콜 기록
FDA 리콜(회수) 기록 4건 중 최근 4건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2023.06.21 · 3등급(경미) · Amring Pharmaceuticals Inc Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
- 2023.06.21 · 3등급(경미) · AVKARE LLC Failed Impurities/Degradation Specifications: Out of specification results obtained for conductivity.
- 2022.10.12 · 3등급(경미) · AuroMedics Pharma LLC Presence of Particulate Matter: Piece of metal found in a vial
- 2020.09.09 · 1등급(심각) · Mylan Institutional LLC Labeling: Label Mix-Up; potential for cartons labeled as Tranexamic Acid Injection, USP to contain vials of Amiodarone HCl Injection, USP and cartons labeled as Amiodarone HCl Injection, USP to contain vials of Tranexamic Acid Injection, USP.
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
- 200713361
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀봉용기, 실온(1~30℃)보관
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 5mL × 10 앰플
- ATC 코드
- B02AA02
- 표준코드
- 8806451028103, 8806451028110, 8806451028127
- 최근 변경
- 2026.09.21
허가 변경 이력
- · 용법용량변경, 2026-09-21
- · 사용상주의사항변경(부작용포함), 2026-09-21
- · 사용상주의사항변경(부작용포함), 2022-11-04
- · 사용상주의사항변경(부작용포함), 2015-01-28
원문: 식약처 의약품안전나라
