세파메칠정 효능·효과
○ 유효균종
○ 적응증
광고
세파메칠정 복용법 (용법·용량)
1. 성인
세파메칠정 부작용·주의사항
전체 9개 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. 임부에 대한 투여
8. 임상검사치에 대한 영향
9. 적용상의 주의
세파메칠정 성분·함량
1정(604.2mg) 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 메틸올세팔렉신리시네이트 | Methylolcefalexin Lysinate | 500 밀리그램 |
세파메칠정 낱알 모양 (식별 표시)
- 모양
- 장방형 · 필름코팅정
- 색
- 주황
- 표시(앞/뒤)
- 마크 / MCL
- 마크

- 크기
- 15.1 × 8.3 mm, 두께 6.35mm
📍 세파메칠정 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 메틸올세팔렉신리시네이트
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).
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Ibuprofen Lysine is indicated to close a clinically significant patent ductus arteriosus (PDA) in premature infants weighing between 500 and 1500 g, who are no more than 32 weeks gestational age when usual medical management (e.g., fluid restriction, diuretics, respiratory support, etc.) is ineffective. The clinical trial was conducted among infants with an asymptomatic PDA. However, the consequences beyond 8 weeks after treatment have not been evaluated; therefore, treatment should be reserved for infants with clear evidence of a clinically significant PDA. Ibuprofen Lysine is a nonsteroidal anti-inflammatory drug indicated to close a clinically significant patent ductus arteriosus (PDA) in premature infants weighing between 500 and 1500 g, who are no more than 32 weeks gestational age when usual medical management is ineffective. The clinical trial was conducted among infants with an asymptomatic PDA. However, the consequences beyond 8 weeks after treatment have not been evaluated; therefore, treatment should be reserved for infants with clear evidence of a clinically significant PDA. (1)
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Ibuprofen Lysine is contraindicated in: Preterm infants with proven or suspected infection that is untreated; Preterm infants with congenital heart disease in whom patency of the PDA is necessary for satisfactory pulmonary or systemic blood flow (e.g., pulmonary atresia, severe tetralogy of Fallot, severe coarctation of the aorta); Preterm infants who are bleeding, especially those with active intracranial hemorrhage or gastrointestinal bleeding; Preterm infants with thrombocytopenia; Preterm infants with coagulation defects; Preterm infants with or who are suspected of having necrotizing enterocolitis; Preterm infants with significant impairment of renal function. Ibuprofen Lysine is contraindicated in preterm infants: With proven or suspected infection that is untreated (4) With congenital heart disease in whom patency of the PDA is necessary for satisfactory pulmonary or systemic blood flow (4) With impaired renal function (4) With thrombocytopenia, coagulation defects or who are …
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Ibuprofen Lysine has not been assessed for neurodevelopmental outcome and growth (5.1) Ibuprofen Lysine may alter the usual signs of infection (5.2) Ibuprofen Lysine can inhibit platelet aggregation, and has been shown to prolong bleeding time in normal adult subjects (5.3) Ibuprofen has been shown to displace bilirubin from albumin binding-sites (5.4) Ibuprofen Lysine should be administered carefully to avoid extravascular injection or leakage (5.5) Ibuprofen Lysine may cause serious skin reactions ( 5.6 ) 5.1 General There are no long-term evaluations of the infants treated with ibuprofen at durations greater than the 36 weeks post-conceptual age observation period. Ibuprofen's effects on neurodevelopmental outcome and growth as well as disease processes associated with prematurity (such as retinopathy of prematurity and chronic lung disease) have not been assessed. 5.2 Infection Ibuprofen Lysine may alter the usual signs of infection. The physician must be continually on the alert and should use the drug with extra care in the presence of controlled infection and in infants at risk of infection. 5.3 Platelet Aggregation Ibuprofen Lysine, like other non-steroidal anti-inflammatory agents, can inhibit platelet aggregation. Preterm infants should be observed for signs of bleeding. Ibuprofen has been shown to prolong bleeding time (but within the normal range) in normal adult subjects. This effect may be exaggerated in patients with underlying hemostatic defects (see …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.4 Pediatric Use Safety and effectiveness have only been established in premature infants.
미국 제품명 Ibuprofen Lysine, Livdelzi, NEOPROFEN, L-Lysine 7415, L-Lysine High 7416, OSTEOBIOS
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 2,218건 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 오심nausea121
- 2 BRONCHOPULMONARY DYSPLASIA115
- 3 두통headache110
- 4 피로fatigue101
- 5 어지러움dizziness99
- 6 설사diarrhoea97
- 7 약효 없음drug ineffective74
- 8 통증pain73
- 9 구토vomiting72
- 10 발열pyrexia69
- 11 호흡 곤란dyspnoea60
- 12 발진rash59
미국 리콜 기록
FDA 리콜(회수) 기록 10건 중 최근 5건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2017.04.12 · 1등급(심각) · X-Gen Pharmaceuticals Inc. Presence of Particulate Matter
- 2017.01.18 · 2등급 · Baxter Healthcare Corporation Discoloration: there were customer reports of yellow discolored solution. The yellow coloration is the result of oxidation of the amino acid tryptophan due to a damaged overpouch.
- 2016.06.01 · 1등급(심각) · Baxter Healthcare Corp. Presence of Particulate Matter: identified as dried skin.
- 2015.06.10 · 2등급 · Fresenius Kabi USA, LLC Labeling: Label Error on Declared Strength: Labeled 3.1% Amino Acids but contains 3.3% Amino Acids
- 2015.04.08 · 2등급 · Baxter Healthcare Corp Lack of Assurance of Sterility; increased complaints received for leaks
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
- 199501552
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 위탁 제조
- (주)경보제약
- 저장 방법
- 기밀용기, 실온보관
- 사용 기간
- 제조일로부터 18 개월
- 포장 단위
- 30정/병, 100정/병, 500정/병
- ATC 코드
- J01DB01
- 보험 코드
- 645601100
- 표준코드
- 8806456011001, 8806456011018, 8806456011025, 8806456011032
- 최근 변경
- 2011.11.27
허가 변경 이력
- · 사용상주의사항변경(부작용포함), 2011-11-27
- · 제품명칭변경, 2011-06-07
- · 사용상주의사항변경(부작용포함), 2010-07-08
- · 용법용량변경, 2010-07-08
- · 효능효과변경, 2010-07-08
- · 제품명칭변경, 2010-03-31
- · 사용상주의사항변경(부작용포함), 2005-01-22
- · 용법용량변경, 2005-01-22
- · 효능효과변경, 2005-01-22
- · 성상변경, 1997-07-01
원문: 식약처 의약품안전나라
