루파핀정 효능·효과
광고
루파핀정 복용법 (용법·용량)
루파핀정 부작용·주의사항
전체 11개 항목 펼치기/접기
1. 다음 환자에는 투여하지 말 것
2. 다음 환자에는 신중히 투여할 것
3. 이상반응
신체부위
흔하게
흔하지 않게
드물게
감염
인두염, 비염
대사 및 영양
식욕증가
신경계
졸림, 두통, 어지러움
주의력 장애
심혈관계
빈맥, 두근거림
호흡기, 흉부 및 종격동
코피, 코마름, 기침, 인후부건조, 구인두 통증
위장관계
입 마름
오심, 상복부통, 설사, 소화불량, 구토, 복통, 변비
피부 및 피하조직
발진
전신이상 및 투여부위
피로, 무력증
목마름, 권태감, 발열, 과민성
임상실험실 검사
혈중크레아틴인산활성효소증가, 알라닌아미노전이효소증가, 아스파르테이트아미노전이효소 증가, 간기능 검사 이상, 체중 증가
신체부위
흔하게
흔하지 않게
드물게
감염
비인두염
신경계
졸림, 두통
어지러움, 기면증, 진전
호흡기, 흉부 및
종격동
구인두염
코마름, 기침, 젖은 기침
위장관계
설사, 소화불량
복통, 변비, 복부팽만, 충치
피부 및 피하조직
두드러기
간담도계
간지방증
임상실험실 검사
알라닌아미노전이효소증가, 아스파르테이트아미노전이효소 증가, 혈중 빌리루빈 상승
생식기계 및 유방
월경통
눈
눈 가려움
근골격계 및
결합조직
근육통
발현빈도
기관계명
예상하지 못한 약물이상반응
0.86%(6/698명, 7건)
흔하지 않게
(0.1~1%미만)
전신 장애 및 투여 부위 병태
안면 부종, 열감, 체온이 변한 느낌, 부종
혈액 및 림프계 장애
빈혈
각종 정신 장애
불안
4. 일반적 주의
5. 상호작용
6. 임부 및 수유부에 대한 투여
7. 소아에 대한 투여
8. 고령자에 대한 투여
9. 신장애 및 간장애 환자
10. 과량투여시의 처치
11. 보관 및 취급상의 주의사항
루파핀정 성분·함량
이 약 1정(100mg) 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 루파타딘푸마르산염 | Rupatadine Fumarate | 12.8 밀리그램 |
루파핀정 낱알 모양 (식별 표시)
- 모양
- 원형 · 나정
- 색
- 주황
- 표시(앞/뒤)
- RUP / -
- 크기
- 6.3 × 6.3 mm, 두께 3mm
📍 루파핀정 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 루파타딘푸마르산염
미국 FDA·NLM 자료 · 2026-10-07 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)
Quetiapine tablet is an atypical antipsychotic indicated for the treatment of: Schizophrenia ( 1.1 ) Bipolar I disorder manic episodes ( 1.2 ) Bipolar disorder, depressive episodes ( 1.2 ) 1.1 Schizophrenia Quetiapine tablets are indicated for the treatment of schizophrenia. The efficacy of quetiapine tablets in schizophrenia was established in three 6-week trials in adults and one 6-week trial in adolescents (13 to 17 years). The effectiveness of quetiapine tablets for the maintenance treatment of schizophrenia has not been systematically evaluated in controlled clinical trials [see CLINICAL STUDIES ( 14.1 )]. 1.2 Bipolar Disorder Quetiapine tablets are indicated for the acute treatment of manic episodes associated with bipolar I disorder, both as monotherapy and as an adjunct to lithium or divalproex. Efficacy was established in two 12-week monotherapy trials in adults, in one 3-week adjunctive trial in adults, and in one 3-week monotherapy trial in pediatric patients (10 to 17 years) [see CLINICAL STUDIES ( 14.2 )]. Quetiapine tablets are indicated as monotherapy for the acute treatment of depressive episodes associated with bipolar disorder. Efficacy was established in two 8-week monotherapy trials in adult patients with bipolar I and bipolar II disorder [see CLINICAL STUDIES ( 14.2 )]. Quetiapine tablets are indicated for the maintenance treatment of bipolar I disorder, as an adjunct to lithium or divalproex. Efficacy was established in two maintenance trials in adults. …
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS See full prescribing information for complete boxed warning. Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Quetiapine is not approved for elderly patients with dementia-related psychosis ( 5.1 ) Suicidal Thoughts and Behaviors Increased risk of suicidal thoughts and behavior in children, adolescents and young adults taking antidepressants ( 5.2 ) Monitor for worsening and emergence of suicidal thoughts and behaviors ( 5.2 ) WARNING: INCREASED MORTALITY IN ELDERLY PATIENTS WITH DEMENTIA-RELATED PSYCHOSIS; and SUICIDAL THOUGHTS AND BEHAVIORS Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death [see WARNINGS AND PRECAUTIONS ( 5.1 )]. Quetiapine is not approved for the treatment of patients with dementia-related psychosis [see WARNINGS AND PRECAUTIONS ( 5.1 )]. Suicidal Thoughts and Behaviors Antidepressants increased the risk of suicidal thoughts and behavior in children, adolescents, and young adults in short-term studies. These studies did not show an increase in the risk of suicidal thoughts and behavior with antidepressant use in patients over age 24; there was a reduction in risk with …
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Known hypersensitivity to quetiapine or any components in the formulation. ( 4 ) Hypersensitivity to quetiapine or to any excipients in the quetiapine tablets formulation. Anaphylactic reactions have been reported in patients treated with quetiapine tablets.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Cerebrovascular Adverse Reactions: Increased incidence of cerebrovascular adverse reactions (e.g., stroke, transient ischemic attack) has been seen in elderly patients with dementia-related psychoses treated with atypical antipsychotic drugs ( 5.3 ) Neuroleptic Malignant Syndrome (NMS): Manage with immediate discontinuation and close monitoring ( 5.4 ) Metabolic Changes: Atypical antipsychotics have been associated with metabolic changes. These metabolic changes include hyperglycemia, dyslipidemia, and weight gain ( 5.5 ) Hyperglycemia and Diabetes Mellitus: Monitor patients for symptoms of hyperglycemia including polydipsia, polyuria, polyphagia, and weakness. Monitor glucose regularly in patients with diabetes or at risk for diabetes Dyslipidemia: Undesirable alterations have been observed in patients treated with atypical antipsychotics. Appropriate clinical monitoring is recommended, including fasting blood lipid testing at the beginning of, and periodically, during treatment Weight Gain: Gain in body weight has been observed; clinical monitoring of weight is recommended Tardive Dyskinesia: Discontinue if clinically appropriate ( 5.6 ) Hypotension: Use with caution in patients with known cardiovascular or cerebrovascular disease ( 5.7 ) Increased Blood Pressure in Children and Adolescents: Monitor blood pressure at the beginning of, and periodically during treatment in children and adolescents ( 5.9 ) Leukopenia, Neutropenia and Agranulocytosis: Monitor complete blood …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
8.1 Pregnancy Pregnancy Exposure Registry There is a pregnancy exposure registry that monitors pregnancy outcomes in women exposed to atypical antipsychotics, including quetiapine, during pregnancy. Healthcare providers are encouraged to register patients by contacting the National Pregnancy Registry for Atypical Antipsychotics at 1-866-961-2388 or online at http://womensmentalhealth.org/clinical-and-research-programs/pregnancyregistry/. Risk Summary Neonates exposed to antipsychotic drugs (including quetiapine) during the third trimester are at risk for extrapyramidal and/or withdrawal symptoms following delivery (see CLINICAL CONSIDERATIONS ). Overall available data from published …
미국 제품명 Quetiapine fumarate, Tenofovir Disoproxil Fumarate, VOQUEZNA, Formoterol Fumarate, Ibutilide Fumarate, Bisoprolol Fumarate, Dimethyl Fumarate, KETOTIFEN FUMARATE
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 527,586건 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 호흡 곤란dyspnoea35,942
- 2 약효 없음drug ineffective27,528
- 3 피로fatigue26,883
- 4 오심nausea26,145
- 5 설사diarrhoea24,049
- 6 통증pain23,287
- 7 BONE DENSITY DECREASED20,427
- 8 두통headache20,273
- 9 FLUSHING20,067
- 10 적응증 외 사용off label use19,635
- 11 구토vomiting17,751
- 12 어지러움dizziness17,525
미국 리콜 기록
FDA 리콜(회수) 기록 12건 중 최근 5건 — 특정 회사·제조번호 제품의 회수로, 국내 제품과는 관계없을 수 있습니다.
- 2026.02.11 · 2등급 · Unichem Pharmaceuticals USA Inc. cGMP Deviations: recall due to not meeting the N-Nitroso Bisoprolol impurity specification limits.
- 2026.01.14 · 3등급(경미) · Alembic Pharmaceuticals Limited Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- 2025.11.26 · 3등급(경미) · Alembic Pharmaceuticals Limited Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
- 2022.08.17 · 2등급 · Mckesson Medical-Surgical Inc. Corporate Office CGMP Deviations: products were stored outside the drug label specifications.
- 2021.06.02 · 2등급 · Cardinal Health Inc. CGMP Deviations: Intermittent exposure to temperature excursion during storage.
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
- 201702246
- 허가 구분
- 허가 · 완제의약품
- 상태
- 정상
- 저장 방법
- 기밀용기, 차광하여 실온(1∼30℃)보관
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 10정, 30정, 100정/박스
- ATC 코드
- R06AX28
- 보험 코드
- 650204770
- 표준코드
- 8806502047701, 8806502047718, 8806502047725, 8806502047732
- 최근 변경
- 2024.04.04
허가 변경 이력
- · 사용상주의사항변경(부작용포함), 2024-04-04
- · 사용상의 주의사항, 2023-03-09
원문: 식약처 의약품안전나라
