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. 2008 Apr 23;3(4):e1993. doi: 10.1371/journal.pone.0001993

Table 2. Solicited adverse events after primary and booster YF-17D vaccination.

Adverse event Primary vaccination (N = 155) Booster vaccination (N = 20)
Intradermal Subcutaneous Intradermal Subcutaneous
Local Erythema N yes (%) 63 (82) 25 (32) 6 (60) 1 (10)
Mean N days (s.e.m.) 4·3 (±0·5) 1·1 (±0·2) 3·2 (±1·0) 1·0 (±0·9)
Swelling N yes (%) 52 (68) 9 (12) 6 (60) 0 (0)
Mean N days (s.e.m.) 2·6 (±0·4) 0·3 (±0·1) 2·6 (±0·9) -
Pain N yes (%) 6 (8) 15 (19) 2 (20) 0 (0)
Mean N days (s.e.m.) 0·1 (±0·06) 0·6 (±0·2) 0·2 (±0·1) -
Severity N +/− (mild) 39 15 3 -
N + (moderate) 24 9 2 2
N ++ (severe) - 1 -
Systemic Myalgia N yes (%) 12 (16) 27 (22) 1 (10) 1 (10)
Mean N days (s.e.m.) 0·4 (±0·1) 0·7 (±0·1) 0·1 (±0·1) 0·7 (±0·7)
Fever N yes (%) 4 (5) 8 (10) 0 (0) 0 (0)
Mean N days (s.e.m.) 0·1 (±0·03) 0·2 (±0·06) - -
Severity N +/− (mild) 9 17 - -
N + (moderate) 3 8 1 1
N ++ (severe) - 2 - -

Safety of vaccination expressed in various parameters. Severity of adverse events could be graded with - (absent), +/− (mild), + (moderate) and ++ (severe). S.e.m. = standard error of the mean.