니카르디핀염산염
Nicardipine Hydrochloride
원료 코드 M222948 국내 제품 4개 (단일제 4 · 복합제 0) DUR 성분 D000497
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이 성분만 든 제품 (단일제 4)
광고
병용금기 성분 (1)
아래 성분이 든 약과 함께 쓰면 안 됩니다 (식약처 DUR).
| 상대 성분 | 이유 |
|---|---|
| 아바나필 | 기절의 효과감소 |
🌐 해외(미국) 정보 — 니카르디핀염산염
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)
Nicardipine Hydrochloride Injection is a calcium channel blocker indicated for the short-term treatment of hypertension in adults when oral therapy is not feasible. (1.1) 1.1 Hypertension Nicardipine Hydrochloride Injection is indicated in adults for the short-term treatment of hypertension when oral therapy is not feasible or not desirable. For prolonged control of blood pressure, transfer patients to oral medication as soon as their clinical condition permits [see Dosage and Administration (2.1)].
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Do not use in patients with advanced aortic stenosis ( 4.1 ). 4.1 Advanced Aortic Stenosis Nicardipine hydrochloride injection is contraindicated in patients with advanced aortic stenosis because part of the effect of nicardipine hydrochloride injection is secondary to reduced afterload. Reduction of diastolic pressure in these patients may worsen rather than improve myocardial oxygen balance.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Closely monitor response in patients with angina, heart failure, impaired hepatic function, or renal impairment. ( 5.1, 5.2, 5.3, 5.4 ) To reduce the possibility of venous thrombosis, phlebitis, and vascular impairment, do not use small veins, such as those on the dorsum of the hand or wrist. Exercise extreme care to avoid intra-arterial administration or extravasation. ( 5.5 ) To minimize the risk of peripheral venous irritation, change the site of infusion of nicardipine hydrochloride injection every 12 hours. ( 5.5 ) 5.1 Exacerbation of Angina Increases in frequency, duration, or severity of angina have been seen in chronic therapy with oral nicardipine. Induction or exacerbation of angina has been seen in less than 1% of coronary artery disease patients treated with nicardipine hydrochloride injection. The mechanism of this effect has not been established. 5.2 Exacerbation of Heart Failure Titrate slowly when using nicardipine hydrochloride injection, particularly in combination with a beta-blocker, in patients with heart failure or significant left ventricular dysfunction because of possible negative inotropic effects. 5.3 Increased Effect with Impaired Hepatic Function Since nicardipine is metabolized in the liver, consider lower dosages and closely monitor responses in patients with impaired liver function or reduced hepatic blood flow. 5.4 Prolonged Effect with Impaired Renal Function When nicardipine hydrochloride injection was given to mild to moderate hypertensive …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary Available data from published literature (clinical trials and case series) over decades of use of intravenous nicardipine during pregnancy have not identified a drug-associated risk of major birth defects or miscarriage. However, nicardipine is predominantly used in pregnancy after 20 gestational weeks. Use of nicardipine in women with preeclampsia or pre-term labor is associated with maternal and fetal/neonatal adverse events. Maternal adverse events included pulmonary edema, dyspnea, hypoxia, hypotension, reflex tachycardia, postpartum hemorrhage, tocolysis, headache, nausea, dizziness, flushing, and phlebitis at site of injection. Fetal/neonatal adverse events …
미국 제품명 Cardene IV
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 4,340건 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 급성 신장 손상acute kidney injury243
- 2 적응증 외 사용off label use211
- 3 PREMATURE BABY205
- 4 FOETAL EXPOSURE DURING PREGNANCY195
- 5 약효 없음drug ineffective192
- 6 MATERNAL EXPOSURE DURING PREGNANCY183
- 7 저혈압hypotension172
- 8 약물 상호작용drug interaction167
- 9 고혈압hypertension165
- 10 발열pyrexia123
- 11 PREMATURE DELIVERY108
- 12 구토vomiting105
미국 리콜 기록
FDA 리콜(회수) 기록 8건 중 최근 5건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2026.09.09 · 2등급 · Baxter Healthcare Corporation CGMP Deviations
- 2026.08.26 · 2등급 · American Regent, Inc. Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
- 2025.05.07 · 2등급 · American Regent, Inc. Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- 2025.05.07 · 2등급 · American Regent, Inc. Lack of sterility assurance: Product leakage around the vial neck, which could potentially result in a lack of sterility assurance.
- 2024.05.29 · 2등급 · American Regent, Inc. Lack of Assurance of Sterility.
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.
