아자설판장용정250mg 효능·효과
아자설판장용정250mg 복용법 (용법·용량)
1. 류마티스성 관절염
2. 궤양성 대장염
아자설판장용정250mg 부작용·주의사항
전체 7개 항목 펼치기/접기
1. 다음 환자에는 투여하지 말 것.
2. 다음 환자에는 신중히 투여할 것.
3. 부작용
4. 일반적 주의
5. 상호작용
6. 임부 및 수유부에 대한 투여
7. 기타
아자설판장용정250mg 성분·함량
1정(340.5mg) 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 설파살라진 | Sulfasalazine | 250.0 밀리그램 |
📍 아자설판장용정250mg 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 설파살라진
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).
Aminosalicylate [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Sulfasalazine delayed release tablets are indicated: a) in the treatment of mild to moderate ulcerative colitis, and as adjunctive therapy in severe ulcerative colitis; b) for the prolongation of the remission period between acute attacks of ulcerative colitis; c) in the treatment of patients with rheumatoid arthritis who have responded inadequately to salicylates or other nonsteroidal anti-inflammatory drugs (e.g., an insufficient therapeutic response to, or intolerance of, an adequate trial of full doses of one or more nonsteroidal anti-inflammatory drugs); and d) in the treatment of pediatric patients with polyarticular-course 1 juvenile rheumatoid arthritis who have responded inadequately to salicylates or other nonsteroidal anti-inflammatory drugs. Sulfasalazine delayed release tablets are particularly indicated in patients with ulcerative colitis who cannot take uncoated sulfasalazine tablets because of gastrointestinal intolerance, and in whom there is evidence that this intolerance is not primarily the result of high blood levels of sulfapyridine and its metabolites, e.g., patients experiencing nausea and vomiting with the first few doses of the drug, or patients in whom a reduction in dosage does not alleviate the adverse gastrointestinal effects. In patients with rheumatoid arthritis or juvenile rheumatoid arthritis, rest and physiotherapy as indicated should be continued. Unlike anti-inflammatory drugs, sulfasalazine delayed release tablets do not produce an …
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Sulfasalazine delayed release tablets are contraindicated in: Hypersensitivity to sulfasalazine, its metabolites, sulfonamides or salicylates, Patients with intestinal or urinary obstruction, Patients with porphyria, as the sulfonamides have been reported to precipitate an acute attack.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Hepatic, Renal, and Hematologic Toxicity or Other Conditions Only after critical appraisal should sulfasalazine delayed release tablets be given to patients with hepatic or renal damage or blood dyscrasias. Deaths associated with the administration of sulfasalazine have been reported from hypersensitivity reactions, agranulocytosis, aplastic anemia, other blood dyscrasias, renal and liver damage, irreversible neuromuscular and central nervous system changes, and fibrosing alveolitis. The presence of clinical signs such as sore throat, fever, pallor, purpura, or jaundice may be indications of serious blood disorders or hepatotoxicity. Complete blood counts, as well as urinalysis with careful microscopic examination, should be done frequently in patients receiving sulfasalazine delayed release tablets (see PRECAUTIONS, Laboratory Tests ). Discontinue treatment with sulfasalazine while awaiting the results of blood tests. Discontinue sulfasalazine delayed release tablets if renal function deteriorates while on therapy. Oligospermia and Infertility Oligospermia and infertility have been observed in men treated with sulfasalazine; however, withdrawal of the drug appears to reverse these effects. Serious Infections Serious infections, including fatal sepsis and pneumonia, have been reported. Some infections were associated with agranulocytosis, neutropenia, or myelosuppression. Discontinue sulfasalazine delayed release tablets if a patient develops a serious infection. Closely …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
Pregnancy: There are no adequate and well-controlled studies of sulfasalazine in pregnant women. Reproduction studies have been performed in rats and rabbits at doses up to 6 times the human maintenance dose of 2 g/day based on body surface area and have revealed no evidence of impaired female fertility or harm to the fetus due to sulfasalazine. Because animal reproduction studies are not always predictive of human response, this drug should be used during pregnancy only if clearly needed. There have been case reports of neural tube defects (NTDs) in infants born to mothers who were exposed to sulfasalazine during pregnancy, but the role of sulfasalazine in these defects has not been …
미국 제품명 Azulfidine EN-tabs, Azulfidine
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 77,785건 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 약효 없음drug ineffective29,355
- 2 류마티스 관절염rheumatoid arthritis19,529
- 3 통증pain15,948
- 4 약물 불내성drug intolerance13,762
- 5 관절통arthralgia13,481
- 6 피로fatigue13,318
- 7 관절 부종joint swelling12,744
- 8 적응증 외 사용off label use11,129
- 9 발진rash10,987
- 10 복부 불편감abdominal discomfort10,045
- 11 CONTRAINDICATED PRODUCT ADMINISTERED9,681
- 12 증상 악화condition aggravated9,593
미국 리콜 기록
FDA 리콜 기록이 없습니다.
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
- 201110251
- 허가 구분
- 허가 · 완제의약품
- 상태
- 정상
- 저장 방법
- 밀폐용기, 실온(1-30℃)보관
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 100정(10정/PTP포장 X 10)
- ATC 코드
- A07EC01
- 표준코드
- 8806482035309, 8806482035316
- 최근 변경
- 2022.10.11
허가 변경 이력
- · 사용상주의사항변경(부작용포함), 2022-10-11
- · 사용상주의사항변경(부작용포함), 2021-06-30
- · 사용상주의사항변경(부작용포함), 2018-04-30
원문: 식약처 의약품안전나라