종근당황산스트렙토마이신주 효능·효과
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광고
종근당황산스트렙토마이신주 복용법 (용법·용량)
1. 결핵
2. 기타질환
종근당황산스트렙토마이신주 부작용·주의사항
전체 12개 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. 소아에 대한 투여
9. 고령자에 대한 투여
10. 과량투여시의 처치
11. 적용상의 주의
12. 기타
종근당황산스트렙토마이신주 성분·함량
매 바이알 당 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 스트렙토마이신황산염 | Streptomycin Sulfate | 1 그램 |
📍 종근당황산스트렙토마이신주 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 스트렙토마이신황산염
미국 FDA·NLM 자료 · 2026-10-04 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)
Streptomycin is indicated for the treatment of individuals with moderate to severe infections caused by susceptibile strains of microorganisms in the specific conditions listed below: 1. Mycobacterium tuberculosis: The Advisory Council for the Elimination of Tuberculosis, the American Thoracic Society, and the Center for Disease Control recommend that either streptomycin or ethambutol be added as a fourth drug in a regimen containing isoniazid (INH), rifampin and pyrazinamide for initial treatment of tuberculosis unless the likelihood of INH or rifampin resistance is very low. The need for a fourth drug should be reassessed when the results of susceptibility testing are known. In the past when the national rate of primary drug resistance to isoniazid was known to be less than 4% and was either stable or declining, therapy with two and three drug regimens was considered adequate. If community rates of INH resistance are currently less than 4%, an initial treatment regimen with less than four drugs may be considered. Streptomycin is also indicated for therapy of tuberculosis when one or more of the above drugs is contraindicated because of toxicity or intolerance. The management of tuberculosis has become more complex as a consequence of increasing rates of drug resistance and concomitant HIV infection. Additional consultation from experts in the treatment of tuberculosis may be desirable in those settings. 2. Non-tuberculosis infections: The use of streptomycin should be …
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
AZOTEMIA. THESE INCLUDE DISTURBANCES OF VESTIBULAR AND COCHLEAR FUNCTION, OPTIC NERVE DYSFUNCTION, PERIPHERAL NEURITIS, ARACHNOIDITIS, AND ENCEPHALOPATHY MAY ALSO OCCUR. THE INCIDENCE OF CLINICALLY DETECTABLE, IRREVERSIBLE VESTIBULAR DAMAGE IS PARTICULARLY HIGH IN PATIENTS TREATED WITH STREPTOMYCIN. RENAL FUNCTION SHOULD BE MONITORED CAREFULLY; PATIENTS WITH RENAL IMPAIRMENT AND/OR NITROGEN RETENTION SHOULD RECEIVE REDUCED DOSES. THE PEAK SERUM CONCENTRATION IN INDIVIDUALS WITH KIDNEY DAMAGE SHOULD NOT EXCEED 20 TO 25 MCG/ML. THE CONCURRENT OR SEQUENTIAL USE OF OTHER NEUROTOXIC AND/OR NEPHROTOXIC DRUGS WITH STREPTOMYCIN SULFATE, INCLUDING NEOMYCIN, KANAMYCIN, GENTAMICIN, CEPHALORIDINE, PAROMOMYCIN, VIOMYCIN, POLYMYXIN B, COLISTIN, TOBRAMYCIN AND CYCLOSPORINE SHOULD BE AVOIDED. THE NEUROTOXICITY OF STREPTOMYCIN CAN RESULT IN RESPIRATORY PARALYSIS FROM NEUROMUSCULAR BLOCKAGE, ESPECIALLY WHEN THE DRUG IS GIVEN SOON AFTER THE USE OF ANESTHESIA OR MUSCLE RELAXANTS. THE ADMINISTRATION OF STREPTOMYCIN IN PARENTERAL FORM SHOULD BE RESERVED FOR PATIENTS WHERE ADEQUATE LABORATORY AND AUDIOMETRIC TESTING FACILITIES ARE AVAILABLE DURING THERAPY.
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
history of clinically significant hypersensitivity to streptomycin is a contraindication to its use. Clinically significant hypersensitivity to other aminoglycosides may contraindicate the use of streptomycin because of the known cross-sensitivity of patients to drugs in this class.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Ototoxicity Both vestibular and auditory dysfunction can follow the administration of streptomycin. The degree of impairment is directly proportional to the dose and duration of streptomycin administration, to the age of the patient, to the level of renal function and to the amount of underlying existing auditory dysfunction. The ototoxic effects of the aminoglycosides, including streptomycin, are potentiated by the co-administration of ethacrynic acid, mannitol, furosemide and possibly other diuretics. The vestibulotoxic potential of streptomycin exceeds that of its capacity for cochlear toxicity. Vestibular damage is heralded by headache, nausea, vomiting and disequilibrium. Early cochlear injury is demonstrated by the loss of high frequency hearing. Appropriate monitoring and early discontinuation of the drug may permit recovery prior to irreversible damage to the sensorineural cells. Pregnancy Streptomycin can cause fetal harm when administered to a pregnant woman. Because streptomycin readily crosses the placental barrier, caution in use of the drug is important to prevent ototoxicity in the fetus. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to the fetus. Clostridium difficile associated diarrhea Clostridium difficile associated diarrhea (CDAD) has been reported with use of nearly all antibacterial agents, including Streptomycin for Injection, and may range in …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
Pregnancy See WARNINGS section.
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 1,145건 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 DRUG RESISTANCE147
- 2 발열pyrexia97
- 3 약효 없음drug ineffective62
- 4 PARADOXICAL DRUG REACTION59
- 5 약물 과민반응drug hypersensitivity56
- 6 호산구 증가를 동반한 전신 증상 약물 반응drug reaction with eosinophilia and systemic symptoms55
- 7 TUBERCULOSIS54
- 8 오심nausea49
- 9 DRUG-INDUCED LIVER INJURY47
- 10 적응증 외 사용off label use41
- 11 발진rash40
- 12 구토vomiting39
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
- 196100002
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀봉용기에 넣어 건냉암소에 보관
- 사용 기간
- 제조일로부터 48 개월
- 포장 단위
- 10바이알/상자[1바이알 X 10]
- ATC 코드
- J01GA01
- 보험 코드
- 643303331
- 표준코드
- 8806433033309, 8806433033316, 8806433033323
- 최근 변경
- 2015.11.03
허가 변경 이력
- · 용법용량변경, 2015-11-03
- · 성상변경, 2013-03-11
- · 제품명칭변경, 2013-03-11
- · 사용상의 주의사항, 2005-01-23
- · 용법·용량, 2005-01-23
- · 효능·효과, 2005-01-23
- · 사용상의 주의사항, 2002-11-24
- · 사용상주의사항변경(부작용포함), 1994-04-18
- · 용법용량변경, 1994-04-18
- · 효능효과변경, 1994-04-18
- · 사용상주의사항변경(부작용포함), 1993-01-01
- · 용법용량변경, 1993-01-01
- · 효능효과변경, 1993-01-01
- · 사용상주의사항변경(부작용포함), 1992-11-16
- · 저장방법 및 유효기간(사용기간)변경, 1985-12-06
- · 사용상주의사항변경(부작용포함), 1977-10-13
- · 용법용량변경, 1977-10-13
- · 효능효과변경, 1977-10-13
원문: 식약처 의약품안전나라