Surveillance of adverse events following immunisation in Australia annual report, 2014.

Aditi Dey, Han Wang, Helen E Quinn, Richard Hill, Kristine K Macartney
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Abstract

This report summarises Australian passive surveillance data for adverse events following immunisation (AEFI) for 2014 reported to the Therapeutic Goods Administration for 2014 and describes reporting trends over the 15-year period 1 January 2000 to 31 December 2014. There were 3,087 AEFI records for vaccines administered in 2014; an annual AEFI reporting rate of 13.2 per 100,000 population. There was a decline of 5% in the overall AEFI reporting rate in 2014 compared with 2013. This decline in reported adverse events in 2014 compared with the previous year was mainly attributable to fewer reports following the human papillomavirus (HPV) vaccine as it was the 2nd year of the extension of the National HPV Vaccination Program to males. AEFI reporting rates for most vaccines were lower in 2014 compared with 2013. The most commonly reported reactions were injection site reaction (27%), pyrexia (18%), rash (16%), vomiting (9%), headache (7%), and syncope (5%). The majority of AEFI reports described non-serious events while 7% (n=211) were classified as serious. There were 5 deaths reported with no clear causal relationship with vaccination found.

2014年澳大利亚年度报告中免疫接种后不良事件监测。
本报告总结了2014年澳大利亚向药品管理局报告的2014年免疫不良事件(AEFI)被动监测数据,并描述了2000年1月1日至2014年12月31日15年期间的报告趋势。2014年接种的疫苗有3087份AEFI记录;每年的AEFI报告率为每10万人13.2人。与2013年相比,2014年整体AEFI报告率下降了5%。与前一年相比,2014年报告的不良事件减少主要是由于人乳头瘤病毒(HPV)疫苗接种后的报告减少,因为这是国家HPV疫苗接种计划扩展到男性的第二年。与2013年相比,2014年大多数疫苗的AEFI报告率较低。最常见的反应是注射部位反应(27%)、发热(18%)、皮疹(16%)、呕吐(9%)、头痛(7%)和晕厥(5%)。大多数AEFI报告描述了非严重事件,而7% (n=211)被归类为严重事件。报告了5例死亡病例,未发现与接种疫苗有明确的因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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