Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital

Abstract Background The anticoagulant edoxaban is used clinically at doses of 30–60 mg/day; however, we experienced a patient who had taken an overdose of edoxaban of 750 mg. We investigated the pharmacokinetics of edoxaban in this patient by using liquid chromatography–tandem spectrometry to estima...

Full description

Bibliographic Details
Main Authors: Koichiro Adachi, Jumpei Tuchiya, Satoru Beppu, Kei Nishiyama, Makiko Shimizu, Hiroshi Yamazaki
Format: Article
Language:English
Published: BMC 2020-09-01
Series:Journal of Pharmaceutical Health Care and Sciences
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40780-020-00176-6
id doaj-9eaea91374c64c85ac3b1d428a6503ae
record_format Article
spelling doaj-9eaea91374c64c85ac3b1d428a6503ae2020-11-25T03:12:44ZengBMCJournal of Pharmaceutical Health Care and Sciences2055-02942020-09-01611410.1186/s40780-020-00176-6Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospitalKoichiro Adachi0Jumpei Tuchiya1Satoru Beppu2Kei Nishiyama3Makiko Shimizu4Hiroshi Yamazaki5Laboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical UniversityKyoto Medical CenterKyoto Medical CenterKyoto Medical CenterLaboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical UniversityLaboratory of Drug Metabolism and Pharmacokinetics, Showa Pharmaceutical UniversityAbstract Background The anticoagulant edoxaban is used clinically at doses of 30–60 mg/day; however, we experienced a patient who had taken an overdose of edoxaban of 750 mg. We investigated the pharmacokinetics of edoxaban in this patient by using liquid chromatography–tandem spectrometry to estimate the follow-up period in emergency clinical practice with this medicine. Case presentation The patient was a 57-year-old woman (body weight, 69 kg) who had taken a single oral dose of 750 mg of edoxaban in a suicide attempt. She was emergently admitted to Kyoto Medical Center. The patient’s edoxaban plasma concentrations during ambulance transport (8 h after oral administration) were ~ 4900 ng/ml, and the concentration gradually decreased to ~ 10 ng/mL and to detectable but unmeasurable levels of ~ 1.0 ng/mL at 60 h and 100 h, respectively. The linear range of the relationship between the dose and plasma concentration was assumed to have been exceeded during the first 8 h; however, the measured elimination rate of edoxaban was similar to that visualized curves predicted by a simplified physiologically based pharmacokinetic model previously established. Conclusion Simplified physiologically based pharmacokinetic models for creating visualized curves have proven to be useful not only during drug discovery or chemical risk assessment but also in cases of medical poisoning. We used a physiologically based pharmacokinetic model previously established for edoxaban to predict the pharmacokinetics in the current case. It is hoped that the results of this study, which encompass drug monitoring data in the patient and visualized pharmacokinetic prediction, will serve as an index when setting the treatment and follow-up period in cases of drug overdose for medicines such as edoxaban in emergency clinical practice.http://link.springer.com/article/10.1186/s40780-020-00176-6AnticoagulantsPharmacokinetic modelingOverdose
collection DOAJ
language English
format Article
sources DOAJ
author Koichiro Adachi
Jumpei Tuchiya
Satoru Beppu
Kei Nishiyama
Makiko Shimizu
Hiroshi Yamazaki
spellingShingle Koichiro Adachi
Jumpei Tuchiya
Satoru Beppu
Kei Nishiyama
Makiko Shimizu
Hiroshi Yamazaki
Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
Journal of Pharmaceutical Health Care and Sciences
Anticoagulants
Pharmacokinetic modeling
Overdose
author_facet Koichiro Adachi
Jumpei Tuchiya
Satoru Beppu
Kei Nishiyama
Makiko Shimizu
Hiroshi Yamazaki
author_sort Koichiro Adachi
title Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
title_short Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
title_full Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
title_fullStr Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
title_full_unstemmed Pharmacokinetics of anticoagulant edoxaban in overdose in a Japanese patient transported to hospital
title_sort pharmacokinetics of anticoagulant edoxaban in overdose in a japanese patient transported to hospital
publisher BMC
series Journal of Pharmaceutical Health Care and Sciences
issn 2055-0294
publishDate 2020-09-01
description Abstract Background The anticoagulant edoxaban is used clinically at doses of 30–60 mg/day; however, we experienced a patient who had taken an overdose of edoxaban of 750 mg. We investigated the pharmacokinetics of edoxaban in this patient by using liquid chromatography–tandem spectrometry to estimate the follow-up period in emergency clinical practice with this medicine. Case presentation The patient was a 57-year-old woman (body weight, 69 kg) who had taken a single oral dose of 750 mg of edoxaban in a suicide attempt. She was emergently admitted to Kyoto Medical Center. The patient’s edoxaban plasma concentrations during ambulance transport (8 h after oral administration) were ~ 4900 ng/ml, and the concentration gradually decreased to ~ 10 ng/mL and to detectable but unmeasurable levels of ~ 1.0 ng/mL at 60 h and 100 h, respectively. The linear range of the relationship between the dose and plasma concentration was assumed to have been exceeded during the first 8 h; however, the measured elimination rate of edoxaban was similar to that visualized curves predicted by a simplified physiologically based pharmacokinetic model previously established. Conclusion Simplified physiologically based pharmacokinetic models for creating visualized curves have proven to be useful not only during drug discovery or chemical risk assessment but also in cases of medical poisoning. We used a physiologically based pharmacokinetic model previously established for edoxaban to predict the pharmacokinetics in the current case. It is hoped that the results of this study, which encompass drug monitoring data in the patient and visualized pharmacokinetic prediction, will serve as an index when setting the treatment and follow-up period in cases of drug overdose for medicines such as edoxaban in emergency clinical practice.
topic Anticoagulants
Pharmacokinetic modeling
Overdose
url http://link.springer.com/article/10.1186/s40780-020-00176-6
work_keys_str_mv AT koichiroadachi pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
AT jumpeituchiya pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
AT satorubeppu pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
AT keinishiyama pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
AT makikoshimizu pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
AT hiroshiyamazaki pharmacokineticsofanticoagulantedoxabaninoverdoseinajapanesepatienttransportedtohospital
_version_ 1724648865401929728