Surveillance of adverse events after the first trivalent inactivated influenza vaccine produced in mammalian cell culture (Flucelvax®) reported to the Vaccine Adverse Event Reporting System (VAERS), United States, 2013-2015

被引:11
|
作者
Moro, Pedro L. [1 ]
Winiecki, Scott [2 ]
Lewis, Paige [1 ]
Shimabukuro, Tom T. [1 ]
Cano, Maria [1 ]
机构
[1] Ctr Dis Control & Prevent, Immunizat Safety Off, Atlanta, GA 30333 USA
[2] US FDA, Ctr Biol Evaluat & Res, Rockville, MD 20857 USA
关键词
Adverse event; Cell culture; Surveillance; Trivalent inactivated influenza vaccine; Vaccine safety; GUILLAIN-BARRE-SYNDROME; SEASONAL INFLUENZA; IMMUNIZATION; GUIDELINES; COLLECTION;
D O I
10.1016/j.vaccine.2015.10.084
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: In November 2012, the first cell cultured influenza vaccine, a trivalent subunit inactivated influenza vaccine (Flucelvax (R), cclIV3), was approved in the US for adults aged >= 18 years. Objective: To assess adverse events (AEs) after ccIIV3 reported to the US Vaccine Adverse Event Reporting System (VAERS), a spontaneous reporting surveillance system. Methods: We searched VAERS for US reports after ccIIV3 among persons vaccinated from July 1, 2013-March 31, 2015. Medical records were requested for reports classified as serious (death, hospitalization, prolonged hospitalization, disability, life-threatening-illness), and those suggesting anaphylaxis and Guillain-Barre syndrome (GBS). Physicians reviewed available information and assigned a primary clinical category using MedDRA system organ classes (SOC) to each report. Empirical Bayesian data mining was used to identify disproportional AE reporting following cclIV3. Results: VAERS received 629 reports following ccIIV3 of which 313 were for administration of vaccine to persons <18 years. Among 309 reports with an AE documented, 19(6.1%) were serious and the most common categories were 152(49.2%) general disorders and administration site conditions (mostly injection site and systemic reactions) and 73 (23.6%) immune system disorders with two reports of anaphylaxis. Four reports of GBS were submitted. Disproportional reporting was identified for 'drug administered to patient of inappropriate age.' Conclusions: Review of VAERS reports did not identify any concerning pattern of AEs after ccIIV3. Injection site and systemic reactions were the most commonly reported AEs, similar to the pre-licensure clinical trials. Reports following ccIIV3 in persons <18 years highlight the need for education of healthcare providers regarding approved cclIV3 use. Published by Elsevier Ltd.
引用
收藏
页码:6684 / 6688
页数:5
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