리시노프릴

Lisinopril

원료 코드 M023167 국내 제품 1개 (단일제 1 · 복합제 0) DUR 성분 D000528

🌐 미국 FDA 자료(영문 라벨·부작용 보고·리콜)가 있습니다. 한국어는 AI 번역 참고용이니 원문을 함께 확인하세요. 해외 정보 보기

⚠️ DUR 안전사용 기준

  • 🤰 임부금기 2등급 "임신 제2 및 3기에 ACE 저해제 투여시 태아 및 신생아에 저혈압, 고칼륨혈증, 신생아 두골형성부전, 양수과소증(태아사지경축, 두개안면변형, 폐발육형성부전과 관련), 무뇨, 신부전 및 사망 가능성. 임신 제1기에 임부에 대한 안전성 미확립."(정제)
  • 🤰 임부금기 2등급 ACE억제제는 태아에 손상 및 사망을 초래할 수 있다 (리시노프릴에 한함)(정제)
  • 🔁 효능군중복 효능군: 혈압강하작용의약품 · ACE inhibitors 안지오텐신 전환효소 억제제(Angiotensin-Converting-Enzyme inhibitor )와 안지오텐신수용체 차단제(Angiotensin Receptor Blocker)에 해당하는 성분이 2개 이상인 경우에도 효능군 중복에 해당

이 성분만 든 제품 (단일제 1)

🌐 해외(미국) 정보 — 리시노프릴

미국 FDA·NLM 자료 · 2026-10-07 기준

이 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)

Lisinopril is an angiotensin converting enzyme (ACE) inhibitor indicated for: Treatment of hypertension in adults and pediatric patients 6 years of age and older (1.1) Adjunct therapy for heart failure (1.2) Treatment of Acute Myocardial Infarction (1.3) 1.1 Hypertension Lisinopril tablets are indicated for the treatment of hypertension in adult patients and pediatric patients 6 years of age and older to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blood pressure goals. For specific advice on goals and management, see published guidelines, such as those of the National High Blood Pressure Education Program’s Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure (JNC). Numerous antihypertensive drugs, from a variety of pharmacologic classes and with different mechanisms of action, have been shown in randomized controlled trials to reduce cardiovascular morbidity and mortality, and it can be concluded that it is …

⚠️ 박스 경고(가장 강한 경고)

영어 원문 (미국 FDA 라벨)

WARNING: FETAL TOXICITY When pregnancy is detected, discontinue lisinopril as soon as possible [see Warnings and Precautions (5.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) ]. WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. When pregnancy is detected, discontinue lisinopril as soon as possible. (5.1) Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. (5.1)

쓰면 안 되는 경우

영어 원문 (미국 FDA 라벨)

Lisinopril tablets are contraindicated in combination with a neprilysin inhibitor (e.g., sacubitril). Do not administer lisinopril tablets within 36 hours of switching to or from sacubitril/valsartan, a neprilysin inhibitor [see Warnings and Precautions (5.2) ]. Lisinopril tablets are contraindicated in patients with: a history of angioedema or hypersensitivity related to previous treatment with an angiotensin converting enzyme inhibitor hereditary or idiopathic angioedema Do not co-administer aliskiren with lisinopril tablets in patients with diabetes [see Drug Interactions (7.4) ] . Angioedema or a history of hereditary or idiopathic angioedema (4) Hypersensitivity (4) Co-administration of aliskiren with lisinopril in patients with diabetes (4 , 7.4)

주요 경고·주의

영어 원문 (미국 FDA 라벨)

Angioedema: Discontinue lisinopril, provide appropriate therapy and monitor until resolved (5.2) Renal impairment: Monitor renal function periodically (5.3) Hypotension: Patients with other heart or renal diseases have increased risk, monitor blood pressure after initiation (5.4) Hyperkalemia: Monitor serum potassium periodically (5.5) Cholestatic jaundice and hepatic failure: Monitor for jaundice or signs of liver failure (5.6) 5.1 Fetal Toxicity Lisinopril can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. Resulting oligohydramnios can be associated with fetal lung hypoplasia and skeletal deformations. Potential neonatal adverse effects include skull hypoplasia, anuria, hypotension, renal failure, and death. When pregnancy is detected, discontinue lisinopril as soon as possible [see Use in specific Populations (8.1) ]. 5.2 Angioedema and Anaphylactoid Reactions Patients taking concomitant mTOR inhibitor (e.g. temsirolimus, sirolimus, everolimus) therapy or a neprilysin inhibitor may be at increased risk for angioedema [see Drug Interactions (7.7 , 7.8) ]. Angioedema Head and Neck Angioedema Angioedema of the face, extremities, lips, tongue, glottis and/or larynx, including some fatal reactions, have occurred in patients treated with angiotensin converting enzyme inhibitors, …

임신·특수 환자

영어 원문 (미국 FDA 라벨)

8.1 Pregnancy Risk Summary Lisinopril can cause fetal harm when administered to a pregnant woman. Use of drugs that act on the renin-angiotensin system during the second and third trimesters of pregnancy reduces fetal renal function and increases fetal and neonatal morbidity and death. Most epidemiologic studies examining fetal abnormalities after exposure to antihypertensive use in the first trimester have not distinguished drugs affecting the renin-angiotensin system from other antihypertensive agents. When pregnancy is detected, discontinue lisinopril as soon as possible. The estimated background risk of major birth defects and miscarriage for the indicated population(s) are unknown. In …

미국 부작용 보고(FAERS)에 많이 나온 증상

미국 FDA에 접수된 이 성분 관련 보고 313,738건 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. 1 피로fatigue20,509
  2. 2 오심nausea19,122
  3. 3 약효 없음drug ineffective18,150
  4. 4 설사diarrhoea17,854
  5. 5 호흡 곤란dyspnoea14,364
  6. 6 통증pain14,063
  7. 7 어지러움dizziness13,969
  8. 8 두통headache13,418
  9. 9 구토vomiting11,368
  10. 10 쇠약asthenia11,282
  11. 11 적응증 외 사용off label use11,255
  12. 12 관절통arthralgia9,943

미국 리콜 기록

FDA 리콜(회수) 기록 15건 중 최근 5건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.

  • 2025.07.23 · 2등급 · Lupin Pharmaceuticals Inc. Product Mix Up: This product is being recalled because of a complaint received that a sealed bottle of lisinopril and hydrochlorothiazide tablets 20mg/12.5 mg had a foreign tablet identified as atazanavir and ritonavir tablet 300mg/100mg.
  • 2024.11.27 · 2등급 · Evaric Pharmaceuticals Inc. Presence of Foreign Object: A pharmacist discovered a metal fragment embedded in a lisinopril 10 mg tablet.
  • 2024.01.03 · 2등급 · CARDINAL HEALTHCARE CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
  • 2023.11.29 · 3등급(경미) · NCS Healthcare of Kentucky Inc Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots
  • 2022.09.21 · 2등급 · Lupin Pharmaceuticals Inc. Presence of Foreign Substance: Foreign material (metal piece) embedded in one tablet.

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.