Sharrar R G, LaRussa P, Galea S A, Steinberg S P, Sweet A R, Keatley R M, Wells M E, Stephenson W P, Gershon A A
Worldwide Product Safety and Epidemiology, Merck Research Laboratories, BLB-30, PO Box 4, West Point, PA 19486, USA.
Vaccine. 2000 Nov 22;19(7-8):916-23. doi: 10.1016/s0264-410x(00)00297-8.
The postmarketing safety profile of varicella vaccine was evaluated by analyzing selected adverse experience reports temporally associated with the administration of the vaccine. There were 7963 reports voluntarily submitted to Merck for an overall reporting rate of 5.0 per 10000 doses of vaccine distributed. A varicella zoster virus (VZV) identification program detected the presence of the Oka vaccine strain in three individuals with an immune deficiency - two with pneumonia and one with hepatitis - and in three instances of secondary transmission from vaccinees with vesicular lesions to susceptible household contacts. The Oka vaccine strain was present in 23 patients and wild-type VZV was present in 15 patients with herpes zoster. Vesicular rashes that occurred within 2 weeks of vaccination were more likely to contain the presence of wild-type VZV, while vesicular rashes that occurred more than 2 weeks post-vaccination were more likely to contain the Oka vaccine strain. Eleven patients were hospitalized with complications of breakthrough varicella infection.
通过分析与水痘疫苗接种在时间上相关的特定不良事件报告,对水痘疫苗上市后的安全性进行了评估。共有7963份报告自愿提交给默克公司,疫苗总体报告率为每10000剂分发量中有5.0例。一项水痘带状疱疹病毒(VZV)鉴定程序在3名免疫缺陷个体中检测到了Oka疫苗株的存在——2例肺炎患者和1例肝炎患者——以及在3起从有水泡疹病变的疫苗接种者向易感家庭接触者的二次传播事件中检测到该疫苗株。23例患者中存在Oka疫苗株,15例带状疱疹患者中存在野生型VZV。接种疫苗后2周内出现的水泡疹更有可能含有野生型VZV,而接种疫苗2周后出现的水泡疹更有可能含有Oka疫苗株。11名患者因突破性水痘感染并发症住院。