Table 3.
Adverse events | Overall SGLT2i [100] | Empagliflozin [58] | Canagliflozin [98] | Dapagliflozin [99] |
---|---|---|---|---|
Acute kidney injury | RR 0.59 (95% CI 0.39–0.89; I2 = 0.0%) | Not analyzed | Not analyzed | Not analyzed |
Diabetic ketoacidosis | RR 0.66 (95% CI 0.30–1.45, I2 = 0.0%) | Not analyzed | Not analyzed | Not analyzed |
Urinary tract infections | RR 1.02 (95% CI 0.95–1.09, I2 = 0.0%) | OR 1.119 (95% CI 0.886–1.411) |
Cana 100 mg: RR 1.45 (95% CI 0.91–2.29, p = 0.12) Cana 300 mg: RR 1.18 (95% CI 0.73–1.91, p = 0.49) |
RR 1.74 (95% CI 1.21–2.49, p = 0.003) |
Genital tract infections | Not analyzed | OR 2.814 (95% CI 1.712–4.625) |
Cana 100 mg: RR 3.79 (95% CI 2.05–7.01, p < 0.01) Cana 300 mg: RR 3.99 (95% CI 2.16–7.35, p < 0.01) |
RR: 3.52 (95% CI 2.06–6.03, p < 0.00001) |
Bone fractures | RR 0.87 (95% CI 0.69–1.09, I2 = 1.3%) | Not analyzed | Not analyzed | Not analyzed |
Osmotic diuresis-related AE/hypovolemia | Not analyzed | Not analyzed |
Cana 100 mg: RR 5.35 (95% CI 2.43–11.77, p < 0.01) Cana 300 mg: RR 5.35 (95% CI 2.43–11.77, p < 0.01) |
RR: 0.74 (95% CI 0.32–1.71, p = 0.47) |
AE Adverse events, OR odds ratio, RR relative risk, SGLT2i sodium-glucose cotransporter 2 inhibitors