Skip to main content
. 2021 Dec 20;45(1):45–64. doi: 10.1007/s40264-021-01127-2

Table 3.

Treatment-emergent adverse event-associated resource use in RELAY

Resource use RAM + ERL
(n = 221)
PBO + ERL
(n = 225)
Hospitalizations
 Patients hospitalized due to AEs 66 (29.9) 44 (19.6)
 Duration of hospitalization, days 12 (1–67) 11 (2–36)
Transfusions
 Any transfusion 8 (3.6) 0
 Packed red blood cells 7 (3.2) 0
 Platelets 2 (0.9) 0
Supportive care
 Dermatological products 195 (88.2) 202 (89.8)
  Topical steroids 176 (79.6) 187 (83.1)
  Emollients and protectives 133 (60.2) 128 (56.9)
  Antibiotics 92 (41.6) 77 (34.2)
 Systemic antimicrobials 194 (87.8) 192 (85.3)
  Antibiotics 191 (86.4) 190 (84.4)
  Antivirals 19 (8.6) 19 (8.4)
  Antifungals 7 (3.2) 4 (1.8)
 Analgesics 173 (78.3) 147 (65.3)
 Antihypertensives 153 (69.2) 95 (42.2)
  Calcium channel antagonists 110 (49.8) 56 (24.9)
  Angiotensin II inhibitors 108 (48.9) 60 (26.7)
  Diuretics 49 (22.2) 16 (7.1)
 H1 antagonists 135 (61.1) 123 (54.7)
 Antidiarrheals 130 (58.8) 126 (56.0)
 Acid suppressants/protectants 116 (52.5) 109 (48.4)
 Stomatological preparations 103 (46.6) 82 (36.4)
 Systemic corticosteroids 77 (34.8) 84 (37.3)
 Antiemetics 76 (34.4) 63 (28.0)
 Antihemorrhagics 30 (13.6) 13 (5.8)
 Bone modifiers 29 (13.1) 25 (11.1)
 Anticoagulants 19 (8.6) 12 (5.3)
 Antiplatelets 17 (7.7) 16 (7.1)
 Appetite stimulants 13 (5.9) 12 (5.3)
 Granulocyte colony-stimulating factors 2 (0.9) 1 (0.4)

Data are presented as n (%) or median (range)

AE treatment-emergent adverse event, ERL erlotinib, H1 histamine receptor 1, PBO placebo, RAM ramucirumab