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Levosulpiride 복용 이후 발생한 고프로락틴혈증 및 그 인과성 분석: 지역약국에서 보고된 부작용 증례Hyperprolactinemia after taking Levosulpiride and its Causality Assessment: An Adverse Event Reported by a Community Pharmacy

Other Titles
Hyperprolactinemia after taking Levosulpiride and its Causality Assessment: An Adverse Event Reported by a Community Pharmacy
Authors
이희영조유진윤중식지은희
Issue Date
Jun-2018
Publisher
한국임상약학회
Keywords
Levosulpiride; adverse drug reaction; hyperprolactinemia; causality assessment; community pharmacy
Citation
한국임상약학회지, v.28, no.2, pp.154 - 157
Journal Title
한국임상약학회지
Volume
28
Number
2
Start Page
154
End Page
157
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4983
DOI
10.24304/kjcp.2018.28.2.154
ISSN
1226-6051
Abstract
Levosulpiride is one of the most frequently prescribed medicines in Korea. An adverse drug reaction (ADR) after takinglevosulpiride was reported at a community pharmacy in Korea. A 31-year-old woman reported the symptoms of lactation andamenorrhea after taking levosulpiride; an evaluation of whether these symptoms were caused by the medication was thereforenecessary. Several tools can be used to determine if the ADR resulted from the administered drug or other factors, including theWorld Health Organization-Uppsala Monitoring Centre (WHO-UMC) criteria, the Naranjo scale, and the Korean causality assessmentalgorithm (Ver. 2). The causality was evaluated as “possible” by the WHO-UMC and Naranjo scales, but as “probable” by theKorean causality assessment algorithm (Ver. 2). In conclusion, the information provided did not indicate definite causality and therewere slight differences in the results obtained from each assessment method.
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