Cargando…
A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan
The universal health care system in Japan is facing a historical turning point as a result of the increasing fiscal burden, rapidly aging society, and a decreasing population. To understand the challenges and opportunities in the Japanese pharmaceutical market, which occupies one tenth of the global...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386774/ https://www.ncbi.nlm.nih.gov/pubmed/25848223 http://dx.doi.org/10.2147/DDDT.S62636 |
_version_ | 1782365205886402560 |
---|---|
author | Tanimoto, Tetsuya |
author_facet | Tanimoto, Tetsuya |
author_sort | Tanimoto, Tetsuya |
collection | PubMed |
description | The universal health care system in Japan is facing a historical turning point as a result of the increasing fiscal burden, rapidly aging society, and a decreasing population. To understand the challenges and opportunities in the Japanese pharmaceutical market, which occupies one tenth of the global share, this review highlights several issues related to the benefit-risk assessment that is unique to the modern Japanese society: 1) regulatory system for new drug development; 2) health hazards related to pharmaceuticals (“Yakugai” in Japanese); 3) drug lag; 4) problems and controversies in the vaccination policy; and 5) clinical study misconduct. The regulatory process places a significant importance on Japanese data collection regardless of data accumulation from other countries. Because Yakugai has repeatedly caused tragedies and social disputes historically, the regulatory judgments generally tend to be more prudential when safety concerns are raised for new and emerging pharmaceuticals. Such a regulatory system has caused more than several years of approval delays compared to delays in other countries. The problem of drug lag still lingers on despite several regulatory system revisions, while the solution is incompatible with the elimination of Yakugai because the lag potentially reduces the risk of unpredictable adverse events. The Japanese vaccination policy has also received a lot of criticism, and needs improvements so that the decision-making process can be more transparent and scientifically based. Additionally, repeated clinical study misconduct damaged the reputation of Japanese clinical studies with unnecessary defrayment in health insurance; therefore, the medical community must change its inappropriate relationship with the industry. The problems surrounding pharmaceuticals are related to centralized, strict drug pricing control under the universal health coverage. Although the current government attempts to facilitate innovative research and development of novel therapeutics in Japan, further reforms should be explored for patients who need new and emerging pharmaceuticals. |
format | Online Article Text |
id | pubmed-4386774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43867742015-04-06 A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan Tanimoto, Tetsuya Drug Des Devel Ther Review The universal health care system in Japan is facing a historical turning point as a result of the increasing fiscal burden, rapidly aging society, and a decreasing population. To understand the challenges and opportunities in the Japanese pharmaceutical market, which occupies one tenth of the global share, this review highlights several issues related to the benefit-risk assessment that is unique to the modern Japanese society: 1) regulatory system for new drug development; 2) health hazards related to pharmaceuticals (“Yakugai” in Japanese); 3) drug lag; 4) problems and controversies in the vaccination policy; and 5) clinical study misconduct. The regulatory process places a significant importance on Japanese data collection regardless of data accumulation from other countries. Because Yakugai has repeatedly caused tragedies and social disputes historically, the regulatory judgments generally tend to be more prudential when safety concerns are raised for new and emerging pharmaceuticals. Such a regulatory system has caused more than several years of approval delays compared to delays in other countries. The problem of drug lag still lingers on despite several regulatory system revisions, while the solution is incompatible with the elimination of Yakugai because the lag potentially reduces the risk of unpredictable adverse events. The Japanese vaccination policy has also received a lot of criticism, and needs improvements so that the decision-making process can be more transparent and scientifically based. Additionally, repeated clinical study misconduct damaged the reputation of Japanese clinical studies with unnecessary defrayment in health insurance; therefore, the medical community must change its inappropriate relationship with the industry. The problems surrounding pharmaceuticals are related to centralized, strict drug pricing control under the universal health coverage. Although the current government attempts to facilitate innovative research and development of novel therapeutics in Japan, further reforms should be explored for patients who need new and emerging pharmaceuticals. Dove Medical Press 2015-03-31 /pmc/articles/PMC4386774/ /pubmed/25848223 http://dx.doi.org/10.2147/DDDT.S62636 Text en © 2015 Tanimoto. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Tanimoto, Tetsuya A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title | A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title_full | A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title_fullStr | A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title_full_unstemmed | A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title_short | A perspective on the benefit-risk assessment for new and emerging pharmaceuticals in Japan |
title_sort | perspective on the benefit-risk assessment for new and emerging pharmaceuticals in japan |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4386774/ https://www.ncbi.nlm.nih.gov/pubmed/25848223 http://dx.doi.org/10.2147/DDDT.S62636 |
work_keys_str_mv | AT tanimototetsuya aperspectiveonthebenefitriskassessmentfornewandemergingpharmaceuticalsinjapan AT tanimototetsuya perspectiveonthebenefitriskassessmentfornewandemergingpharmaceuticalsinjapan |