Table 3.
Predictors of Adverse Drug Reactions Among Patients Receiving Ceftaroline (n=96)
Patient Characteristics | ADR (n=20) | No ADR (n=76) | P value* |
---|---|---|---|
Age, Med [IQR] | 39 [32,65] | 60 [42,71] | 0.05 |
Female Sex, n (%) | 12 (60) | 40 (53) | 0.62 |
White Race, n (%) | 19 (95) | 69 (91) | 0.65 |
Comorbidities, n (%) | |||
Atopy | 2 (10) | 10 (13) | 1.00 |
Hypertension | 7 (35) | 43 (57) | 0.13 |
Diabetes Mellitus | 9 (45) | 23 (30) | 0.29 |
Coronary or peripheral vascular disease | 3 (15) | 24 (32) | 0.17 |
Chronic Kidney Disease, | 2 (10) | 18 (24) | 0.23 |
Hepatitis C Infection | 0 (0) | 11 (15) | 0.11 |
HIV Infection | 0 (0) | 4 (5) | 0.58 |
Intravenous Drug Use | 5 (25) | 12 (16) | 0.34 |
Any drug allergy | 12 (60) | 51 (67) | 0.60 |
Penicillin allergy | 3 (15) | 17 (23) | 0.55 |
Cephalosporin allergy | 2 (10) | 11 (15) | 1.00 |
| |||
Treatment Characteristics | |||
| |||
Doses of ceftaroline, Med [IQR] | 46 [21, 104] | 21 [6, 59] | 0.01 |
Off label indications, n (%) | 15 (75) | 42 (55) | 0.13 |
Wilcoxan rank sum test for continuous variables and Fisher’s Exact for binary variables