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. 2009 Jun 30;6(6):e1000104. doi: 10.1371/journal.pmed.1000104

Table 4. Adverse effects reported in each arm after the pralidoxime chloride/placebo loading dose or during the first 3 d of the constant infusion.

Adverse Effect Loading dose (t = 20 min) Constant infusion (t = 20 min to 72 h)
Placebo Pralidoxime p-Value Placebo Pralidoxime p-Value
Tachycardia a , n (%) 30/110 (27.3) 61/115 (53.0) <0.0001 54/111 (48.6) 85/114 (74.6) <0.0001
Hypertension b , n (%) 2/110 (1.8) 27/115 (23.5) <0.0001 16/111 (14.4) 34/114 (29.8) 0.005
Headache, n (%) 5/110 (4.5) 7/115 (6.1) 0.61 33/111 (29.7) 36/114 (31.6) 0.76
Blurred vision, n (%) 3/110 (2.7) 8/115 (7.0) 0.14 26/111 (23.4) 40/114 (35.1) 0.06
Dizziness, n (%) 8/110 (7.3) 9/115 (7.8) 0.88 35/111 (31.5) 31/114 (27.2) 0.48
Nausea, n (%) 12/110 (10.9) 13/115 (11.3) 0.93 33/111 (29.7) 25/114 (21.9) 0.18
Vomiting, n (%) 8/110 (7.3) 21/115 (18.3) 0.01 24/111 (21.6) 26/114 (22.8) 0.83
Systolic BP, mmHg, mean (SD) 116 (15.3) 129 (27.6) <0.0001 ND ND
Diastolic BP, mmHg, mean (SD) 74 (13.5) 80 (20.2) 0.015 ND ND
Pulse, bpm, mean (SD) 99 (20.1) 113 (22.8) <0.0001 ND ND
a

Tachycardia, HR>100 bpm.

b

Hypertension, systolic BP>159 and/or diastolic>99 mmHg.

ND, not done.