دورية أكاديمية

Safety evaluation on concomitant immunization with inactivated poliomyelitis vaccine produced from Sabin strains and other vaccines (from 2015 to 2020)

التفاصيل البيبلوغرافية
العنوان: Safety evaluation on concomitant immunization with inactivated poliomyelitis vaccine produced from Sabin strains and other vaccines (from 2015 to 2020)
المؤلفون: Yan Deng, Li Yi, Ying Li, Zhimei Zhao, Zhilei Zhong, Haoyu Shi, Jiarong Li, Yan Liang, Jingsi Yang
المصدر: Human Vaccines & Immunotherapeutics, Vol 18, Iss 1 (2022)
بيانات النشر: Taylor & Francis Group, 2022.
سنة النشر: 2022
المجموعة: LCC:Immunologic diseases. Allergy
LCC:Therapeutics. Pharmacology
مصطلحات موضوعية: inactivated poliomyelitis vaccine made from the sabin strain, adverse events following immunization, concomitant immunization, safety, medical dictionary for regulatory activities, Immunologic diseases. Allergy, RC581-607, Therapeutics. Pharmacology, RM1-950
الوصف: Objective To evaluate the safety of concomitantly administering inactivated poliomyelitis vaccine produced from Sabin strains (sIPVs) with other vaccines. Methods A descriptive analysis was carried out on adverse events following immunization (AEFI) based on the administration of sIPV alone or concomitant with other vaccines (from 2015 to 2020) using data from the national AEFI surveillance system of China (CNAEFIS). All adverse reactions (ADRs) of the concomitant immunization were coded using a medical dictionary for regulatory activities (MedDRA) before comparison. Results The CNAEFIS reported a total of 9130 sIPV-related AEFI cases, including 6842 AEFI cases collected after immunization with sIPV alone and 2288 AEFI cases collected after immunization of sIPV concomitant with other vaccines. The combination of sIPV with diphtheria, tetanus and pertussis vaccine (DTaP) was correlated with the highest frequency of AEFI, which accounted for 53.50% of all 2288 AEFI cases. After MedDRA-based coding, the most frequent ADR was fever (70.18%), followed by erythema and swelling at the injection site (6.95%), induration at the injection site (3.85%), dermatitis allergy (3.56%) and urticaria (1.55%). A statistically significant difference (P
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2164-5515
2164-554X
21645515
Relation: https://doaj.org/toc/2164-5515; https://doaj.org/toc/2164-554X
DOI: 10.1080/21645515.2022.2041944
URL الوصول: https://doaj.org/article/699efae8520e44df83a3835d38a9e1e7
رقم الأكسشن: edsdoj.699efae8520e44df83a3835d38a9e1e7
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21645515
2164554X
DOI:10.1080/21645515.2022.2041944