이르베사탄
Irbesartan
원료 코드 M255988 국내 제품 1개 (단일제 0 · 복합제 1) DUR 성분 D000046
🌐 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 2기 및 3기에 ACE 저해제 투여시 태아 위해 및 사망 보고.(정제)
- ⚖️ 용량주의 하루 최대 이르베사르탄 300밀리그램 이르베사르탄 300mg(정제)
- ⚖️ 용량주의 하루 최대 300밀리그램 (정제)
- 🔁 효능군중복 효능군: 혈압강하작용의약품 · ARB 안지오텐신 전환효소 억제제(Angiotensin-Converting-Enzyme inhibitor )와 안지오텐신수용체 차단제(Angiotensin Receptor Blocker)에 해당하는 성분이 2개 이상인 경우에도 효능군 중복에 해당
복합제·제형별 기준 1개 더 보기
- ⚖️ 용량주의 하루 최대 이르베사르탄 300밀리그램/히드로클로로티아지드 25밀리그램 이르베사탄 300mg, 히드로클로로티아지드 25mg(정제)
이 성분만 든 제품 (단일제 0)
다른 성분과 섞인 제품 (복합제 1)
🌐 해외(미국) 정보 — 이르베사탄
미국 FDA·NLM 자료 · 2026-10-01 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
Angiotensin 2 Receptor Blocker [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Irbesartan tablet is an angiotensin II receptor blocker (ARB) indicated for: • Treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. ( 1.1 ) Treatment of diabetic nephropathy in hypertensive patients with type 2 diabetes, an elevated serum creatinine, and proteinuria. ( 1.2 ) 1.1 Hypertension Irbesartan tablets are indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular (CV) events, primarily strokes and myocardial infarction. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including this drug. 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 …
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
WARNING: FETAL TOXICITY WARNING: FETAL TOXICITY When pregnancy is detected, discontinue irbesartan tablets as soon as possible [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ]. Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus [see Warnings and Precautions (5.1) and Use in Specific Populations (8.1) ]. WARNING: FETAL TOXICITY See full prescribing information for complete boxed warning. • When pregnancy is detected, discontinue irbesartan tablets as soon as possible. ( 5.1 , 8.1 ) • Drugs that act directly on the renin-angiotensin system can cause injury and death to the developing fetus. ( 5.1 , 8.1 )
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Irbesartan tablets are contraindicated in patients who are hypersensitive to any component of this product. Do not coadminister aliskiren with irbesartan tablets in patients with diabetes. • Hypersensitivity to any component of this product. ( 4 ) • Coadministration with aliskiren in patients with diabetes. ( 4 )
주요 경고·주의
영어 원문 (미국 FDA 라벨)
• Hypotension: Correct volume or salt depletion prior to administration. ( 5.2 ) • Monitor renal function and serum potassium. ( 5.3 ) 5.1 Fetal Toxicity Irbesartan 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 irbesartan tablets as soon as possible [see Use in Specific Populations ( 8.1 )]. 5.2 Hypotension in Volume or Salt-Depleted Patients In patients with an activated renin-angiotensin system, such as volume or salt-depleted patients (e.g., those being treated with high doses of diuretics), symptomatic hypotension may occur after initialization of treatment with irbesartan. Correct volume or salt depletion prior to administration of irbesartan or use a lower starting dose [see Dosage and Administration ( 2.4 )]. 5.3 Impaired Renal Function Changes in renal function including acute renal failure can be caused by drugs that inhibit the renin-angiotensin system. Patients whose renal function may depend in part on the activity of the renin-angiotensin system (e.g., patients with renal artery stenosis, chronic kidney disease, severe …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Risk Summary Irbesartan 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 [see Clinical Considerations]. 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 irbesartan as soon as possible. All pregnancies have a background risk of birth defect, loss or other adverse outcomes …
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 49,400건 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 피로fatigue2,818
- 2 오심nausea2,814
- 3 설사diarrhoea2,534
- 4 약효 없음drug ineffective2,474
- 5 어지러움dizziness2,346
- 6 호흡 곤란dyspnoea2,251
- 7 급성 신장 손상acute kidney injury2,216
- 8 두통headache2,164
- 9 낙상fall2,162
- 10 쇠약asthenia1,911
- 11 적응증 외 사용off label use1,835
- 12 권태감malaise1,822
미국 리콜 기록
FDA 리콜(회수) 기록 12건 중 최근 5건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2022.08.03 · 2등급 · Jubilant Cadista Pharmaceuticals, Inc. Failed Dissolution Specifications
- 2022.08.03 · 2등급 · Jubilant Cadista Pharmaceuticals, Inc. Failed dissolution specifications.
- 2021.11.10 · 2등급 · Lupin Pharmaceuticals Inc. CGMP Deviations: impurity N-nitrosoirbesartan detected in API
- 2021.11.10 · 2등급 · Lupin Pharmaceuticals Inc. CGMP Deviations: impurity N-nitrosoirbesartan detected in API
- 2021.11.10 · 2등급 · Lupin Pharmaceuticals Inc. CGMP Deviations: impurity N-nitrosoirbesartan detected in API
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.
