멕실렌캡슐 효능·효과
광고
멕실렌캡슐 복용법 (용법·용량)
멕실렌캡슐 부작용·주의사항
전체 11개 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 수유뷰에 대한 투여
8. 소아에 대한 투여
9. 고령자에 대한 투여
10. 과량 투여시의 처치
11. 적용상의 주의
멕실렌캡슐 성분·함량
1캡슐(397밀리그램) 중 기준
| 성분 | 영문 | 분량 |
|---|---|---|
| 멕실레틴염산염 | Mexiletine Hydrochloride | 100.0 밀리그램 |
멕실렌캡슐 낱알 모양 (식별 표시)
- 모양
- 장방형 · 경질캡슐제, 산제
- 색
- 갈색 / 갈색
- 표시(앞/뒤)
- H.Krs H.Krs / -
- 크기
- 19.1 × 6.6 mm, 두께 6.9mm
📍 멕실렌캡슐 살 수 있는 내 주변 약국
전문의약품은 의사 처방전이 있어야 약국에서 받을 수 있습니다. 재고는 약국에 전화로 확인하세요.
🗺️ 지도에서 찾기🌐 해외(미국) 정보 — 멕실레틴염산염
미국 FDA·NLM 자료 · 2026-10-04 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)
Mexiletine hydrochloride capsules, USP are indicated for the treatment of documented ventricular arrhythmias, such as sustained ventricular tachycardia, that, in the judgment of the physician, are life-threatening. Because of the proarrhythmic effects of mexiletine, its use with lesser arrhythmias is generally not recommended. Treatment of patients with asymptomatic ventricular premature contractions should be avoided. Initiation of mexiletine treatment, as with other antiarrhythmic agents used to treat life-threatening arrhythmias, should be carried out in the hospital. Antiarrhythmic drugs have not been shown to enhance survival in patients with ventricular arrhythmias.
⚠️ 박스 경고(가장 강한 경고)
영어 원문 (미국 FDA 라벨)
Mortality In the National Heart, Lung and Blood Institute's Cardiac Arrhythmia Suppression Trial (CAST), a long-term, multicentered, randomized, double-blind study in patients with asymptomatic non-life-threatening ventricular arrhythmias who had a myocardial infarction more than six days but less than two years previously, an excessive mortality or non-fatal cardiac arrest rate (7.7%) was seen in patients treated with encainide or flecainide compared with that seen in patients assigned to carefully matched placebo-treated groups (3%). The average duration of treatment with encainide or flecainide in this study was ten months. The applicability of the CAST results to other populations (e.g., those without recent myocardial infarction) is uncertain. Considering the known proarrhythmic properties of mexiletine and the lack of evidence of improved survival for any antiarrhythmic drug in patients without life-threatening arrhythmias, the use of mexiletine as well as other antiarrhythmic agents should be reserved for patients with life-threatening ventricular arrhythmia. Acute Liver Injury In postmarketing experience abnormal liver function tests have been reported, some in the first few weeks of therapy with mexiletine hydrochloride. Most of these have been observed in the setting of congestive heart failure or ischemia and their relationship to mexiletine hydrochloride has not been established.
쓰면 안 되는 경우
영어 원문 (미국 FDA 라벨)
Mexiletine hydrochloride capsules are contraindicated in the presence of cardiogenic shock or preexisting second- or third-degree AV block (if no pacemaker is present).
주요 경고·주의
영어 원문 (미국 FDA 라벨)
Mortality In the National Heart, Lung and Blood Institute's Cardiac Arrhythmia Suppression Trial (CAST), a long-term, multicentered, randomized, double-blind study in patients with asymptomatic non-life-threatening ventricular arrhythmias who had a myocardial infarction more than six days but less than two years previously, an excessive mortality or non-fatal cardiac arrest rate (7.7%) was seen in patients treated with encainide or flecainide compared with that seen in patients assigned to carefully matched placebo-treated groups (3%). The average duration of treatment with encainide or flecainide in this study was ten months. The applicability of the CAST results to other populations (e.g., those without recent myocardial infarction) is uncertain. Considering the known proarrhythmic properties of mexiletine and the lack of evidence of improved survival for any antiarrhythmic drug in patients without life-threatening arrhythmias, the use of mexiletine as well as other antiarrhythmic agents should be reserved for patients with life-threatening ventricular arrhythmia. Acute Liver Injury In postmarketing experience abnormal liver function tests have been reported, some in the first few weeks of therapy with mexiletine hydrochloride. Most of these have been observed in the setting of congestive heart failure or ischemia and their relationship to mexiletine hydrochloride has not been established. Drug Reactions with Eosinophilia and Systemic Symptoms (DRESS) Drug reactions with …
미국 부작용 보고(FAERS)에 많이 나온 증상
미국 FDA에 접수된 이 성분 관련 보고 420건 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 ineffective43
- 2 피로fatigue32
- 3 VENTRICULAR TACHYCARDIA31
- 4 호흡 곤란dyspnoea27
- 5 오심nausea24
- 6 POOR QUALITY SLEEP24
- 7 IMPAIRED WORK ABILITY23
- 8 IMPAIRED QUALITY OF LIFE22
- 9 발열pyrexia22
- 10 심부전cardiac failure19
- 11 고혈압hypertension18
- 12 폐렴pneumonia18
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
- 201801269
- 허가 구분
- 허가 · 완제의약품
- 상태
- 정상
- 저장 방법
- 차광기밀용기, 실온(1~30℃)보관
- 사용 기간
- 제조일로부터 36 개월
- 포장 단위
- 10캡슐/병,30캡슐/병,50캡슐/병,100캡슐/병,500캡슐/병,1000캡슐/병
- ATC 코드
- C01BB02
- 표준코드
- 8806472050701, 8806472050718, 8806472050725
- 최근 변경
- 2026.07.23
허가 변경 이력
- · 사용상주의사항변경(부작용포함), 2026-07-23
원문: 식약처 의약품안전나라
