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angiotensin receptors. In individuals with prevalent kidney disease at baseline, empagliflozin reduced the risk of cardiovascular death by 29 compared with placebo hazard ratio HR, 0. 71; 95 CI, 0. 52-0. 98, the risk of all-cause mortality by 24 HR, 0. 76; 0. 59 to 0. 99, the risk of hospitalization for heart failure by 39 HR, 0. 61; 0. 42 to 0. 87 and the risk of hospitalization for general causes by 19 RR, 0. 81; 95 CI, 0. 72 to 0. The effects of the drug on these outcomes were consistent between categories of eGFR and urinary albumin-creatinine ratio glibenese baseline and between the two doses studied. Finally, the adverse event profile in people with eGFR 60 mL-min-1 1. 73 m-2 was consistent with the overall trial population. But most of the time, contact with CIMADE allowed MSF to report ongoing treatment and to alert people to psychological fragility linked to glibenese past of traumatic events.

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