Table 5.
Incidence | |||||
---|---|---|---|---|---|
| |||||
Canagliflozin 100 mg | Canagliflozin 300 mg | Placebo | Population | Study | |
| |||||
Renal-related AE | 2.60%a | 2.80%a | 2.80% | Pooled analysis of patients taking canagliflozin 100 mg or 300 mg up to 104 weeks | Desai et al, 201733 |
Fracture | 2.70%b | 2.70%c | 1.90% | Pooled analysis of patients taking canagliflozin 100 mg or 300 mg with a mean exposure of 116 weeks | Watts et al, 201628 |
DKA | 0.07%d | 0.11%d | 0.03% | Pooled analysis of patients taking canagliflozin 100 mg or 300 mg with a mean exposure of 72 weeks | Erondu et al, 201534 |
Amputation | 0.02%e,f | 0.02%e,f | 0.01% | Single study followed for a mean of 188 weeks | Neal et al, 201714 |
Note:
No statistical difference;
HR 1.28 (95% CI: 0.93–1.77);
HR 1.34 (CI: 0.98–1.84);
no P-value of HR reported;
P<0.001;
data unavailable regarding dosage of 100 mg or 300 mg of canagliflozin.
Abbreviations: AEs, adverse events; DKA, diabetic ketoacidosis.