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Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir
BACKGROUND: Interferon and ribavirin have been used as therapeutic agents for chronic hepatitis C infection or C-compensated cirrhosis in the conventional treatment. Hepatitis C virus (HCV) -specific direct-acting antiviral agents that directly inhibit the growth process of HCV have been approved si...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114806/ https://www.ncbi.nlm.nih.gov/pubmed/32266075 http://dx.doi.org/10.1186/s40780-020-00162-y |
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author | Omotani, Sachiko Ishizaka, Toshihiko Inoue, Miki Nishida, Koji Yasui, Yukako Hatsuda, Yasutoshi Mukai, Junji Myotoku, Michiaki |
author_facet | Omotani, Sachiko Ishizaka, Toshihiko Inoue, Miki Nishida, Koji Yasui, Yukako Hatsuda, Yasutoshi Mukai, Junji Myotoku, Michiaki |
author_sort | Omotani, Sachiko |
collection | PubMed |
description | BACKGROUND: Interferon and ribavirin have been used as therapeutic agents for chronic hepatitis C infection or C-compensated cirrhosis in the conventional treatment. Hepatitis C virus (HCV) -specific direct-acting antiviral agents that directly inhibit the growth process of HCV have been approved since 2011. However, in the early post-marketing vigilance phase of ledipasvir acetonate/sofosbuvir (LDV/SOF), there were reports of interstitial lung disease in 4 out of 32,700 cases with death in 1 case; the onset mechanism is unknown. CASE PRESENTATION: Treatment for hepatitis C was deemed to be necessary, and the patient was referred to our hospital. Oral administration of LDV/SOF was started. On day 8 of administration, a fever of 38–39 °C and coughing were observed followed by the gradual appearance of shortness of breath. As there was no improvement, the patient visited her primary care physician on day 16 of administration and the patient was brought urgently to our hospital on the same day. Blood tests and imaging tests were conducted at our hospital on the day of emergency transport; inflammatory response markers showed abnormal values, and sialylated carbohydrate antigen Krebs von den Lungen-6 was within the normal value range at 303 U/mL. Because the possibility of infection was low based on results of imaging and bronchoalveolar lavage, drug-induced lung disease was suspected, LDV/SOF administration was discontinued, and steroid administration was started. Following steroid pulse therapy, treatment with oral prednisolone tablets was gradually tapered. The patient’s symptoms were relieved and she was discharged. CONCLUSIONS: The patient’s medication history in this case indicated that there were no drugs taken before or after administration of LDV/SOF until the adverse reaction occurred, and there were no supplements or dietary supplements taken. Therefore, LDV/SOF has been proposed as the cause of the suspected adverse effect. Pharmacists should try to collect adverse effect reports to identify adverse effects early. |
format | Online Article Text |
id | pubmed-7114806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71148062020-04-07 Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir Omotani, Sachiko Ishizaka, Toshihiko Inoue, Miki Nishida, Koji Yasui, Yukako Hatsuda, Yasutoshi Mukai, Junji Myotoku, Michiaki J Pharm Health Care Sci Case Report BACKGROUND: Interferon and ribavirin have been used as therapeutic agents for chronic hepatitis C infection or C-compensated cirrhosis in the conventional treatment. Hepatitis C virus (HCV) -specific direct-acting antiviral agents that directly inhibit the growth process of HCV have been approved since 2011. However, in the early post-marketing vigilance phase of ledipasvir acetonate/sofosbuvir (LDV/SOF), there were reports of interstitial lung disease in 4 out of 32,700 cases with death in 1 case; the onset mechanism is unknown. CASE PRESENTATION: Treatment for hepatitis C was deemed to be necessary, and the patient was referred to our hospital. Oral administration of LDV/SOF was started. On day 8 of administration, a fever of 38–39 °C and coughing were observed followed by the gradual appearance of shortness of breath. As there was no improvement, the patient visited her primary care physician on day 16 of administration and the patient was brought urgently to our hospital on the same day. Blood tests and imaging tests were conducted at our hospital on the day of emergency transport; inflammatory response markers showed abnormal values, and sialylated carbohydrate antigen Krebs von den Lungen-6 was within the normal value range at 303 U/mL. Because the possibility of infection was low based on results of imaging and bronchoalveolar lavage, drug-induced lung disease was suspected, LDV/SOF administration was discontinued, and steroid administration was started. Following steroid pulse therapy, treatment with oral prednisolone tablets was gradually tapered. The patient’s symptoms were relieved and she was discharged. CONCLUSIONS: The patient’s medication history in this case indicated that there were no drugs taken before or after administration of LDV/SOF until the adverse reaction occurred, and there were no supplements or dietary supplements taken. Therefore, LDV/SOF has been proposed as the cause of the suspected adverse effect. Pharmacists should try to collect adverse effect reports to identify adverse effects early. BioMed Central 2020-04-02 /pmc/articles/PMC7114806/ /pubmed/32266075 http://dx.doi.org/10.1186/s40780-020-00162-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Omotani, Sachiko Ishizaka, Toshihiko Inoue, Miki Nishida, Koji Yasui, Yukako Hatsuda, Yasutoshi Mukai, Junji Myotoku, Michiaki Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title | Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title_full | Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title_fullStr | Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title_full_unstemmed | Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title_short | Drug-induced lung disease adverse effect with Ledipasvir Acetonate/Sofosbuvir |
title_sort | drug-induced lung disease adverse effect with ledipasvir acetonate/sofosbuvir |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114806/ https://www.ncbi.nlm.nih.gov/pubmed/32266075 http://dx.doi.org/10.1186/s40780-020-00162-y |
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