토브라민점안액 효능·효과
토브라민점안액 복용법 (용법·용량)
토브라민점안액 부작용·주의사항
전체 16개 항목 펼치기/접기
1. 다음 환자에는 투여하지 말 것.
2. 이상반응
3. 일반적 주의
4. 상호작용
5. 임부 및 수유부에 대한 투여
6. 과량투여시의 처치
7. 적용상의 주의
8. 기타
1. 다음 환자에는 투여하지 말 것.
2. 이상반응
3. 일반적 주의
4. 상호작용
5. 임부 및 수유부에 대한 투여
6. 과량투여시의 처치
7. 적용상의 주의
8. 기타
토브라민점안액 성분·함량
1 밀리리터 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 토브라마이신 | Tobramycin | 3.0 밀리그램 |
📍 토브라민점안액 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 토브라마이신
미국 FDA·NLM 자료 · 2026-09-30 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)
Tobramycin injection is indicated for the treatment of serious bacterial infections caused by susceptible strains of the designated microorganisms in the diseases listed below: Septicemia in the neonate, child, and adult caused by P. aeruginosa , E. coli , and Klebsiella sp Lower respiratory tract infections caused by P. aeruginosa , Klebsiella sp, Enterobacter sp, Serratia sp, E. coli , and S. aureus (penicillinase- and non-penicillinase-producing strains) Serious central-nervous-system infections (meningitis) caused by susceptible organisms Intra-abdominal infections, including peritonitis, caused by E. coli , Klebsiella sp, and Enterobacter sp. Skin, bone, and skin structure infections caused by P. aeruginosa , Proteus sp, E. coli , Klebsiella sp, Enterobacter sp and S. aureus Complicated and recurrent urinary tract infections caused by P. aeruginosa, Proteus sp, (indole-positive and indole- negative), E. coli , Klebsiella sp, Enterobacter sp, Serratia sp, S. aureus , Providencia sp, and Citrobacte r sp. Aminoglycosides, including tobramycin, are not indicated in uncomplicated initial episodes of urinary tract infections unless the causative organisms are not susceptible to antibiotics having less potential toxicity. Tobramycin may be considered in serious staphylococcal infections when penicillin or other potentially less toxic drugs are contraindicated and when bacterial susceptibility testing and clinical judgment indicate its use. Bacterial cultures should be obtained …
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
Patients treated with Tobramycin Injection and other aminoglycosides should be under close clinical observation, because these drugs have an inherent potential for causing ototoxicity and nephrotoxicity. Neurotoxicity, manifested as both auditory and vestibular ototoxicity, can occur. The auditory changes are irreversible, are usually bilateral, and may be partial or total. Eighth-nerve impairment and nephrotoxicity may develop, primarily in patients having pre-existing renal damage and in those with normal renal function to whom aminoglycosides are administered for longer periods or in higher doses than those recommended. Other manifestations of neurotoxicity may include numbness, skin tingling, muscle twitching, and convulsions. The risk of aminoglycoside-induced hearing loss increases with the degree of exposure to either high peak or high trough serum concentrations. Patients who develop cochlear damage may not have symptoms during therapy to warn them of eighth-nerve toxicity, and partial or total irreversible bilateral deafness may continue to develop after the drug has been discontinued. Rarely, nephrotoxicity may not become apparent until the first few days after cessation of therapy. Aminoglycoside-induced nephrotoxicity usually is reversible. Renal and eighth-nerve function should be closely monitored in patients with known or suspected renal impairment and also in those whose renal function is initially normal but who develop signs of renal dysfunction during …
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
hypersensitivity to any aminoglycoside is a contraindication to the use of tobramycin. A history of hypersensitivity or serious toxic reactions to aminoglycosides may also contraindicate the use of any other aminoglycoside because of the known cross-sensitivity of patients to drugs in this class.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
See WARNINGS box above. This product contains sodium metabisulfite, a sulfite that may cause allergic-type reactions, including anaphylactic symptoms and life-threatening or less severe asthmatic episodes, in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in non-asthmatic people. Serious allergic reactions including anaphylaxis and dermatologic reactions including exfoliative dermatitis, toxic epidermal necrolysis, erythema multiforme, and Stevens-Johnson Syndrome have been reported rarely in patients on tobramycin therapy. Although rare, fatalities have been reported (see CONTRAINDICATIONS ). If an allergic reaction occurs, the drug should be discontinued and appropriate therapy instituted. Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Tobramycin, and may range in severity from mild diarrhea to fatal colitis. Treatment with antibacterial agents alters the normal flora of the colon leading to overgrowth of C. difficile. C. difficile produces toxins A and B which contribute to the development of CDAD. Hypertoxin producing strains of C. difficile cause increased morbidity and mortality, as these infections can be refractory to antimicrobial therapy and may require colectomy. CDAD must be considered in all patients who present with diarrhea following antibiotic …
미국 제품명 BETHKIS, Tobradex ST
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 28,041건 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 use2,242
- 2 사망death1,775
- 3 폐렴pneumonia1,621
- 4 INFECTIVE PULMONARY EXACERBATION OF CYSTIC FIBROSIS1,591
- 5 호흡 곤란dyspnoea1,543
- 6 기침cough1,369
- 7 CYSTIC FIBROSIS1,294
- 8 약효 없음drug ineffective1,098
- 9 HOSPITALISATION1,068
- 10 증상 악화condition aggravated1,066
- 11 감염infection924
- 12 급성 신장 손상acute kidney injury798
미국 리콜 기록
FDA 리콜(회수) 기록 3건 중 최근 3건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2024.03.20 · 2등급 · Eugia US LLC Failed Stability Specification: Water determination was found not complying with specification.
- 2023.08.23 · 3등급(경미) · ALEMBIC PHARMACEUTICALS, INC. Failed Impurities/Degradation Specifications
- 2022.06.15 · 2등급 · Mckesson Medical-Surgical Inc. Corporate Office cGMP deviations: Temperature abuse
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
- 201900664
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 위탁 제조
- 삼천당제약(주)
- 저장 방법
- 기밀용기, 실온보관
- 사용 기간
- 제조일로부터 24 개월
- 포장 단위
- 6mL/병
- ATC 코드
- S01AA12
- 표준코드
- 8806472054006, 8806472054013
- 최근 변경
- 2023.12.14
허가 변경 이력
- · 제품명, 2023-12-14
원문: 식약처 의약품안전나라
