페로친주 효능·효과
페로친주 복용법 (용법·용량)
페로친주 부작용·주의사항
전체 13개 항목 펼치기/접기
1. 경고
2. 다음 환자에는 투여하지 말 것.
3. 다음 환자에는 신중히 투여할 것.
4. 이상반응
5. 일반적 주의
6. 상호작용
7. 임부 및 수유부에 대한 투여
8. 소아에 대한 투여
9. 고령자에 대한 투여
10. 적용상의 주의
11. 과량투여시의 처치
12. 보관 및 취급상의 주의사항
13. 기타
페로친주 성분·함량
1 mL 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 페르페나진염산염 | Perphenazine Hydrochloride | 3 밀리그램 |
병용금기 — 함께 쓰면 안 되는 성분 (3)
이 약의 성분과 같이 처방·복용하면 안 되는 성분입니다(식약처 DUR 병용금기). 해당 성분이 든 약을 먹고 있다면 의사·약사에게 알리세요.
📍 페로친주 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 페르페나진염산염
미국 FDA·NLM 자료 · 2026-10-05 기준이 성분은 한국어 번역이 없습니다(검수 전 자동 번역 게시는 멈춰 두었습니다). 아래는 미국 FDA 원문입니다 — 원문 라벨(DailyMed).
Phenothiazine [EPC]
미국에서 쓰이는 곳(적응증)
영어 원문 (미국 FDA 라벨)
Perphenazine is indicated for use in the treatment of schizophrenia and for the control of severe nausea and vomiting in adults. Perphenazine has not been shown effective for the management of behavioral complications in patients with mental retardation.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
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. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in the placebo group. Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. Observational studies suggest that, similar to atypical antipsychotic drugs, treatment with conventional antipsychotic drugs may increase mortality. The extent to which the findings of increased mortality in observational studies may be attributed to the antipsychotic drug as opposed to some characteristic(s) of the patients is not clear. Perphenazine is not approved for the treatment of patients with dementia-related psychosis (see WARNINGS ).
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Perphenazine products are contraindicated in comatose or greatly obtunded patients and in patients receiving large doses of central nervous system depressants (barbiturates, alcohol, narcotics, analgesics, or antihistamines); in the presence of existing blood dyscrasias, bone marrow depression, or liver damage; and in patients who have shown hypersensitivity to perphenazine products, their components, or related compounds. Perphenazine products are also contraindicated in patients with suspected or established subcortical brain damage, with or without hypothalamic damage, since a hyperthermic reaction with temperatures in excess of 104°F may occur in such patients, sometimes not until 14 to 16 hours after drug administration. Total body ice-packing is recommended for such a reaction; antipyretics may also be useful.
주요 경고·주의
영어 원문 (미국 FDA 라벨)
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. Perphenazine is not approved for the treatment of patients with dementia-related psychosis (see BOXED WARNING ). Tardive dyskinesia, a syndrome consisting of potentially irreversible, involuntary, dyskinetic movements, may develop in patients treated with antipsychotic drugs. Older patients are at increased risk for development of tardive dyskinesia. Although the prevalence of the syndrome appears to be highest among the elderly, especially elderly women, it is impossible to rely upon prevalence estimates to predict, at the inception of antipsychotic treatment, which patients are likely to develop the syndrome. Whether antipsychotic drug products differ in their potential to cause tardive dyskinesia is unknown. Both the risk of developing the syndrome and the likelihood that it will become irreversible are believed to increase as the duration of treatment and the total cumulative dose of antipsychotic drugs administered to the patient increase. However, the syndrome can develop, although much less commonly, after relatively brief treatment periods at low doses. There is no known treatment for established cases of tardive dyskinesia, although the syndrome may remit, partially or completely, if antipsychotic treatment is withdrawn. Antipsychotic treatment itself, however, may suppress (or …
임신·특수 환자
영어 원문 (미국 FDA 라벨)
Pregnancy Non-teratogenic Effects: Neonates exposed to antipsychotic drugs, during the third trimester of pregnancy are at risk for extrapyramidal and/or withdrawal symptoms following delivery. There have been reports of agitation, hypertonia, hypotonia, tremor, somnolence, respiratory distress and feeding disorder in these neonates. These complications have varied in severity; while in some cases symptoms have been self-limited, in other cases neonates have required intensive care unit support and prolonged hospitalization. Perphenazine should be used during pregnancy only if the potential benefit justifies the potential risk to the fetus.
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 2,104건 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 ineffective370
- 2 다양한 물질 독성toxicity to various agents293
- 3 체중 증가weight increased226
- 4 AKATHISIA186
- 5 적응증 외 사용off label use186
- 6 SUICIDE ATTEMPT181
- 7 OBSESSIVE-COMPULSIVE DISORDER164
- 8 INCREASED APPETITE157
- 9 미승인 적응증 사용product use in unapproved indication157
- 10 EUPHORIC MOOD154
- 11 ANTIPSYCHOTIC DRUG LEVEL BELOW THERAPEUTIC150
- 12 DISINHIBITION149
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
- 199600631
- 허가 구분
- 신고 · 완제의약품
- 상태
- 정상
- 저장 방법
- 차광한 밀봉용기
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 1밀리리터x10, 20, 50, 100앰플
- ATC 코드
- N05AB03
- 표준코드
- 8806505009607, 8806505009614, 8806505009621
- 최근 변경
- 2018.03.02
허가 변경 이력
- · 제품명칭변경, 2018-03-02
- · 사용상주의사항변경(부작용포함), 2012-01-28
- · 용법용량변경, 2012-01-28
- · 효능효과변경, 2012-01-28
- · 사용상주의사항변경(부작용포함), 2010-07-29
- · 사용상주의사항변경(부작용포함), 2010-04-09
- · 사용상주의사항변경(부작용포함), 2009-04-19
- · 사용상주의사항변경(부작용포함), 2008-05-06
- · 용법용량변경, 2008-05-06
- · 성상변경, 2008-05-06
- · 제품명칭변경, 2008-05-06
- · 사용상주의사항변경(부작용포함), 1997-01-08
- · 사용상주의사항변경(부작용포함), 1997-01-01
- · 용법용량변경, 1997-01-01
- · 효능효과변경, 1997-01-01
원문: 식약처 의약품안전나라
