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Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database

Background: Cyclosporine is widely used to prevent allograft rejection after transplantation. The purpose of this study was to clarify the adverse events profiles associated with cyclosporine in transplant patients using a spontaneous reporting system database. Methods: Retrospective pharmacovigilan...

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Autores principales: Niinomi, Iku, Oyama, Saki, Inada, Ayaka, Wakabayashi, Tomohito, Iida, Tatsuya, Kambara, Hiroko, Uchida, Mayako, Sano, Yukako, Hosohata, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490292/
https://www.ncbi.nlm.nih.gov/pubmed/36159360
http://dx.doi.org/10.7759/cureus.29383
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author Niinomi, Iku
Oyama, Saki
Inada, Ayaka
Wakabayashi, Tomohito
Iida, Tatsuya
Kambara, Hiroko
Uchida, Mayako
Sano, Yukako
Hosohata, Keiko
author_facet Niinomi, Iku
Oyama, Saki
Inada, Ayaka
Wakabayashi, Tomohito
Iida, Tatsuya
Kambara, Hiroko
Uchida, Mayako
Sano, Yukako
Hosohata, Keiko
author_sort Niinomi, Iku
collection PubMed
description Background: Cyclosporine is widely used to prevent allograft rejection after transplantation. The purpose of this study was to clarify the adverse events profiles associated with cyclosporine in transplant patients using a spontaneous reporting system database. Methods: Retrospective pharmacovigilance disproportionality analysis was conducted using the Japanese Adverse Drug Event Report (JADER) database, with the reporting odds ratio (ROR) and 95% confidence interval (CI) for each adverse event. Results: The database comprised 3,327, 958, and 956 reports associated with cyclosporine in the kidney, stem cell, and heart transplant patients, respectively. Infectious and renal disorders were commonly detected in these transplant patients. The signal scores of cyclosporine for toxic nephropathy were noteworthy in the kidney (ROR: 15.1, 95% CI: 11-20.8) and stem cell (ROR, 216; 95% CI, 29.3-1593) transplantation. Cyclosporine in heart transplantation was strongly associated with gastric cancer (ROR, 39.4; 95% CI, 16.7-93.2), but not kidney or stem cell transplantation. Conclusion: It was suggested that there is a diversity in the strength of the association between cyclosporine and adverse events in the kidney, stem cell, and heart transplantation. Our results may provide useful information for treatment with cyclosporine, although further research with more data is needed.
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spelling pubmed-94902922022-09-23 Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database Niinomi, Iku Oyama, Saki Inada, Ayaka Wakabayashi, Tomohito Iida, Tatsuya Kambara, Hiroko Uchida, Mayako Sano, Yukako Hosohata, Keiko Cureus Transplantation Background: Cyclosporine is widely used to prevent allograft rejection after transplantation. The purpose of this study was to clarify the adverse events profiles associated with cyclosporine in transplant patients using a spontaneous reporting system database. Methods: Retrospective pharmacovigilance disproportionality analysis was conducted using the Japanese Adverse Drug Event Report (JADER) database, with the reporting odds ratio (ROR) and 95% confidence interval (CI) for each adverse event. Results: The database comprised 3,327, 958, and 956 reports associated with cyclosporine in the kidney, stem cell, and heart transplant patients, respectively. Infectious and renal disorders were commonly detected in these transplant patients. The signal scores of cyclosporine for toxic nephropathy were noteworthy in the kidney (ROR: 15.1, 95% CI: 11-20.8) and stem cell (ROR, 216; 95% CI, 29.3-1593) transplantation. Cyclosporine in heart transplantation was strongly associated with gastric cancer (ROR, 39.4; 95% CI, 16.7-93.2), but not kidney or stem cell transplantation. Conclusion: It was suggested that there is a diversity in the strength of the association between cyclosporine and adverse events in the kidney, stem cell, and heart transplantation. Our results may provide useful information for treatment with cyclosporine, although further research with more data is needed. Cureus 2022-09-20 /pmc/articles/PMC9490292/ /pubmed/36159360 http://dx.doi.org/10.7759/cureus.29383 Text en Copyright © 2022, Niinomi et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Transplantation
Niinomi, Iku
Oyama, Saki
Inada, Ayaka
Wakabayashi, Tomohito
Iida, Tatsuya
Kambara, Hiroko
Uchida, Mayako
Sano, Yukako
Hosohata, Keiko
Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title_full Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title_fullStr Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title_full_unstemmed Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title_short Current Status of Adverse Event Profile of Cyclosporine in Kidney, Stem Cell, and Heart Transplantations Using the Japanese Pharmacovigilance Database
title_sort current status of adverse event profile of cyclosporine in kidney, stem cell, and heart transplantations using the japanese pharmacovigilance database
topic Transplantation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490292/
https://www.ncbi.nlm.nih.gov/pubmed/36159360
http://dx.doi.org/10.7759/cureus.29383
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