Bias in spontaneous reporting of adverse drug reactions in Japan.
PLoS One
; 10(5): e0126413, 2015.
Article
em En
| MEDLINE
| ID: mdl-25933226
ABSTRACT
BACKGROUND:
Attitudes of healthcare professionals regarding spontaneous reporting of adverse drug reactions (ADRs) in Japan are not well known, and Japan's unique system of surveillance, called early post-marketing phase vigilance (EPPV), may affect these reporting attitudes. Our objectives were to describe potential effects of EPPV and to test whether ADR seriousness, prominence, and frequency are related to changes in reporting over time.METHODS:
A manufacturer's database of spontaneous ADR reports was used to extract data from individual case safety reports for 5 drugs subject to EPPV. The trend of reporting and the time lag between ADR onset and reporting to the manufacturer were examined. The following indices for ADRs occurring with each drug were calculated and analyzed to assess reporting trends SeriousNon-serious ratio, High prominenceLow prominence ratio, and High frequencyLow frequency ratio.RESULTS:
For all 5 drugs, the time lag between ADR onset and reporting to the manufacturer was shorter in the EPPV period than in the post-EPPV period. All drugs showed higher SeriousNon-serious ratios in the post-EPPV period. No specific patterns were observed for the High prominenceLow prominence ratio. The High frequencyLow frequency ratio for peginterferon alpha-2a and sevelamer hydrochloride decreased steadily throughout the study period.CONCLUSIONS:
Healthcare professionals may be more likely to report serious ADRs than to report non-serious ADRs, but the effect of event prominence on reporting trends is still unclear. Factors associated with ADR reporting attitude in Japan might be different from those in other countries because of EPPV and the involvement of medical representatives in the spontaneous reporting process. Pharmacovigilance specialists should therefore be cautious when comparing data between different time periods or different countries. Further studies are needed to elucidate the underlying mechanism of spontaneous ADR reporting in Japan.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Viés
/
Sistemas de Notificação de Reações Adversas a Medicamentos
País/Região como assunto:
Asia
Idioma:
En
Ano de publicação:
2015
Tipo de documento:
Article
País de afiliação:
Japão