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Long-term clinical trial safety experience with the inactivated split influenza vaccine, Vaxigrip super([registered])
Safety data on the inactivated split influenza vaccine, Vaxigrip super([registered]), were compiled and analysed from 28 clinical trials (total: 4599 subjects aged 6 months to 99 years) to provide a robust estimate of the reactogenicity profile. The most frequent solicited reactions were non- severe...
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Published in: | Vaccine 2006-03, Vol.24 (10), p.1586-1592 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | Safety data on the inactivated split influenza vaccine, Vaxigrip super([registered]), were compiled and analysed from 28 clinical trials (total: 4599 subjects aged 6 months to 99 years) to provide a robust estimate of the reactogenicity profile. The most frequent solicited reactions were non- severe injection site pain and erythema in children, adults, and elderly. Mild or moderate fever was the most frequent reaction in 6-36 months olds; few systemic reactions were reported in older groups. Reactogenicity was comparable in healthy and high-risk children. The long-term experience with the world's most widely used influenza vaccine, Vaxigrip super([registered]), confirms its excellent tolerability, and supports its continued use in clinical practice worldwide. |
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ISSN: | 0264-410X |
DOI: | 10.1016/j.vaccine.2005.10.008 |