Table II.
Rates of adverse events occurring within 72 hours after LAIV administration in this study compared with published rates in the literature
Symptoms within 72 h | Current study | Reported | |
---|---|---|---|
Allergic reaction (mild symptoms) only | 9/433 | 2.1% | 0.02% |
Allergic reaction: anaphylaxis | 0/433 | 0% | 0% |
Fever | 25/426 | 5.9% | 5.4% |
Nasal symptoms | 65/426 | 15.3% | 31% |
Wheeze (parent reported) | 13/426 | 3.1% | Not reported |
Wheeze requiring treatment by physician | 0/426 | 0% | 0.2% |
Lower respiratory symptoms | 26/426 | 6.1% | Not reported |
Eczema flare | 13/426 | 3.1% | Not reported |
Rates are reported as a proportion of the total number of doses given to be consistent with the method of reporting used in the existing literature.10