루센비에스프리필드시린지 효능·효과
광고
루센비에스프리필드시린지 복용법 (용법·용량)
루센비에스프리필드시린지 부작용·주의사항
전체 15개 항목 펼치기/접기
1. 다음 환자에는 투여하지 말 것
2. 약물이상반응
3. 일반적 주의
4. 상호작용
5. 가임여성, 임주 및 수유부에 대한 투여
6. 소아에 대한 투여(18세 미만)
7. 고령자에 대한 투여(만 65세 이상)
8. 신장애 환자에 대한 투여
9. 간장애 환자에 대한 투여
10. 운전 및 기계 조작
11. 과량 투여시 처치
12. 적용상의 주의
13. 보관 및 취급상의 주의사항
14. 기타
루센비에스프리필드시린지 성분·함량
10.165 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 라니비주맙 | Ranibizumab | 밀리그램 |
📍 루센비에스프리필드시린지 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 라니비주맙
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).
Vascular Endothelial Growth Factor Inhibitor [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
(ranibizumab injection) is a vascular endothelial growth factor (VEGF) inhibitor indicated for the treatment of patients with: Neovascular (wet) Age-related Macular Degeneration (AMD) who have previously responded to at least two intravitreal injections of a VEGF inhibitor ( 1.1 ). Diabetic Macular Edema (DME) who have previously responded to at least two intravitreal injections of a VEGF inhibitor ( 1.2 ). Diabetic Retinopathy (DR) who have previously responded to at least two intravitreal injections of a VEGF inhibitor ( 1.3 ). 1.1 Neovascular (wet) Age-related Macular Degeneration (AMD) SUSVIMO (ranibizumab injection) is indicated for the treatment of patients with Neovascular (wet) Age-related Macular Degeneration (AMD) who have previously responded to at least two intravitreal injections of a Vascular Endothelial Growth Factor (VEGF) inhibitor medication. 1.2 Diabetic Macular Edema (DME) SUSVIMO (ranibizumab injection) is indicated for the treatment of patients with Diabetic Macular Edema (DME) who have previously responded to at least two intravitreal injections of a Vascular Endothelial Growth Factor (VEGF) inhibitor medication. 1.3 Diabetic Retinopathy (DR) SUSVIMO (ranibizumab injection) is indicated for the treatment of patients with Diabetic Retinopathy (DR) who have previously responded to at least two intravitreal injections of a Vascular Endothelial Growth Factor (VEGF) inhibitor medication.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
WARNING: ENDOPHTHALMITIS The SUSVIMO implant has been associated with an up to 3-fold higher rate of endophthalmitis than monthly intravitreal injections of ranibizumab. Many of these events were associated with conjunctival retractions or erosions. Appropriate conjunctiva management and early detection with surgical repair of conjunctival retractions or erosions may reduce the risk of endophthalmitis. [see Contraindications (4.1) , Warnings and Precautions (5.1) ] . WARNING: ENDOPHTHALMITIS See full prescribing information for complete boxed warning. The SUSVIMO implant has been associated with an up to 3-fold higher rate of endophthalmitis than monthly intravitreal injections of ranibizumab.
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Ocular or periocular infections ( 4.1 ) Active intraocular inflammation ( 4.2 ) Hypersensitivity ( 4.3 ) 4.1 Ocular or Periocular Infections SUSVIMO (ranibizumab injection) is contraindicated in patients with ocular or periocular infections. 4.2 Active Intraocular Inflammation SUSVIMO (ranibizumab injection) is contraindicated in patients with active intraocular inflammation. 4.3 Hypersensitivity SUSVIMO (ranibizumab injection) is contraindicated in patients with known hypersensitivity to ranibizumab products or any of the excipients in SUSVIMO (ranibizumab injection).
주요 경고·주의
영어 원문 (미국 FDA 라벨)
The SUSVIMO implant and/or implant-related procedures have been associated with endophthalmitis, rhegmatogenous retinal detachment, implant dislocation, septum dislodgement, vitreous hemorrhage, conjunctival erosion, conjunctival retraction, and conjunctival blebs. Patients should be instructed to report any signs or symptoms that could be associated with these events without delay. In some cases, these events can present asymptomatically. The implant and the tissue overlying the implant flange should be monitored routinely following the implant insertion, and refill-exchange procedures to permit early medical or surgical intervention as necessary. Special precautions need to be taken when handling SUSVIMO components [see How Supplied/Storage and Handling (16.3) ]. The SUSVIMO implant and/or implant-related procedures have been associated with endophthalmitis, rhegmatogenous retinal detachment, implant dislocation, septum dislodgement, vitreous hemorrhage, conjunctival retraction, conjunctival erosion, and conjunctival bleb. Patients should be instructed to report signs or symptoms that could be associated with these events without delay. Additional surgical and/or medical management may be required. ( 5.1 , 5.2 , 5.3 , 5.4 , 5.5 , 5.6 , 5.7 ) Vitreous Hemorrhage : Temporarily discontinue antithrombotic medication prior to the implant insertion procedure to reduce the risk of vitreous hemorrhage. Vitrectomy may be needed. ( 5.5 ) Postoperative Decrease in Visual Acuity : A …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary There are no adequate and well-controlled studies of SUSVIMO (ranibizumab injection) administration in pregnant women. Administration of ranibizumab to pregnant monkeys throughout the period of organogenesis resulted in a low incidence of skeletal abnormalities at intravitreal doses up to 41 times the human exposure (based on serum levels following the recommended clinical dose). No skeletal abnormalities were observed at serum trough levels similar to the human exposure after a single eye treatment at the recommended clinical dose ( see Data ) . Animal reproduction studies are not always predictive of human response, and it is not known whether ranibizumab can …
미국 제품명 Susvimo, NUFYMCO, Byooviz, LUCENTIS, CIMERLI
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 26,591건 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 사망death3,816
- 2 VISUAL ACUITY REDUCED2,905
- 3 적응증 외 사용off label use1,728
- 4 시력 저하visual impairment1,654
- 5 약효 없음drug ineffective1,271
- 6 뇌혈관 사고cerebrovascular accident1,238
- 7 이상반응 없음no adverse event1,053
- 8 BLINDNESS1,050
- 9 EYE HAEMORRHAGE1,047
- 10 시야 흐림vision blurred1,036
- 11 안구 통증eye pain965
- 12 RETINAL HAEMORRHAGE800
미국 리콜 기록
FDA 리콜(회수) 기록 1건 중 최근 1건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2022.11.09 · 3등급(경미) · Genentech Inc Defective Delivery System: Commercial implants do not meet the filed specification for the intended use, a few patients have experienced an issue with the implants that renders it non-functioning.
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
- 202301618
- 허가 구분
- 허가 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀봉용기, 2~8℃ 차광보관, 동결시키거나 진탕하지 말 것
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 1프리필드시린지/상자[프리필드시린지(0.165mL)]
- ATC 코드
- S01LA04
- 보험 코드
- 643309371
- 표준코드
- 8806433093709, 8806433093716
- 재심사
- 재심사대상(4년잔여),재심사대상(4년잔여),재심사대상(4년잔여),재심사대상(4년잔여),재심사대상(4년잔여),재심사대상(4년잔여) 2023-05-19~2026-10-19,2023-05-19~2026-10-19,2023-05-19~2026-10-19,2023-05-19~2026-10-19,2023-05-19~2026-10-19,2023-05-19~2026-10-19
- 최근 변경
- 2025.03.10
허가 변경 이력
- · 저장방법 및 사용(유효)기간, 2025-03-10
- · 저장방법 및 사용(유효)기간, 2024-04-11
- · 사용상의 주의사항, 2023-08-04
- · 저장방법 및 사용(유효)기간, 2023-07-10
원문: 식약처 의약품안전나라