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. 2016 May;16(5):546–555. doi: 10.1016/S1473-3099(15)00484-3

Table 2.

Number of women reporting local and systemic adverse reactions during the first 7 days after vaccination

HIV-infected, low CD4 cell count (n=87) HIV-infected, high CD4 cell count (n=88) HIV-uninfected (n=90)
Local
Any local 16 (18%) 26 (30%) 35 (39%)
Ecchymosis 0 0 1 (1%)
Erythema 0 1 (1%) 1 (1%); n=89
Induration 0 1 (1%) 0
Swelling 0 0 2 (2%)
Pain
Any 16 (18%) 26 (30%) 35 (39%)
Severe 2 (2%) 0 4 (4%)
Systemic
Any systemic 35 (40%) 48 (55%) 53 (59%)
Chills
Any 8 (9%) 12 (14%) 20 (22%)
Severe 1 (1%) 1 (1%) 0
Nausea
Any 11 (13%) 15 (17%) 20 (22%); n=89
Severe 1 (1%) 0 2 (2%); n=89
Malaise
Any 9 (10%) 17 (19%) 21 (23%)
Severe 1 (1%) 0 1 (1%)
Myalgia 7 (8%) 15 (17%) 21 (23%)
Arthralgia
Any 11 (13%) 20 (23%) 26 (29%)
Severe 0 0 1 (1%)
Headache
Any 21 (24%) 28 (32%) 39 (43%)
Severe 1 (1%) 1 (1%) 2 (2%)
Fatigue
Any 21 (24%) 27 (31%) 42 (47%)
Severe 2 (2%) 1 (1%) 3 (3%)
Rash 3 (3%) 1 (1%) 1 (1%)
Fever (≥38°C) 3 (3%) 0 0

For local adverse reactions, no participants reported severe reactions (>100 mm), with the exception of pain. Data are given for local reactions (≥25 mm).