Table 4

Serious adverse events by treatment group

AmoxicillinPlaceboOverall
Serious adverse events per group4656102
Serious adverse events (can be multiple events per child)
Pneumonia-related, n (%)*34 (73.9)43 (76.8)77 (75.5)
 Chest indrawing pneumonia17 (50.0)18 (41.9)35 (45.5)
 Fast breathing pneumonia7 (20.6)12 (27.9)19 (24.7)
 Pneumonia with respiratory distress or WHO general danger signs5 (14.7)9 (20.9)14 (18.1)
 Chest radiograph confirmed pneumonia†4 (11.8)4 (9.3)8 (10.4)
 Pneumonia‡1 (3.0)0 (0.0)1 (1.3)
Non-pneumonia related, n (%)*12 (26.0)13 (23.2)25 (24.5)
 Acute gastroenteritis4 (33.3)4 (30.8)8 (32.0)
 Fever1 (8.3)4 (30.8)5 (20.0)
 Malaria2 (16.7)1 (7.7)3 (12.0)
 Convulsion1 (8.3)1 (7.7)2 (8.0)
 Urinary tract infection0 (0.0)2 (15.4)2 (8.0)
 Vomiting2 (16.7)0 (0.0)2 (8.0)
 Anaemia0 (0.0)1 (7.7)1 (4.0)
 Epistaxis1 (8.3)0 (0.0)1 (4.0)
 Febrile convulsion1 (8.3)0 (0.0)1 (4.0)
  • *Percentages for ‘Amoxicillin’ and ‘Placebo’ columns reflect total number of children within each category by treatment group. Percentages for ‘Overall’ column reflect total number of serious adverse event cases.

  • †Chest radiograph performed due to persistent fever leading to identification of pneumonia.

  • ‡Event reported from an outside hospital and hospital records did not specify type of pneumonia.