Dose adjustment recommendations as per kidney functions | |||||
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SGLT2 inhibitor | Licensed indication | eGFR >60 | eGFR 45–59 | eGFR 30–44 | eGFR <30 |
Canagliflozin | Adults with insufficiently controlled T2D | Initiate 100 mg, titrate to 300 mg if needed | Initiate / continue with 100 mg only | Initiate / continue with 100 mg only if albuminuria >30 mg/mmol at initiation | Continue established treatment with 100 mg but do not initiate; stop if dialysis/transplant |
Dapagliflozin | Adults with insufficiently controlled T2D | Initiate 10 mg | Continue with 10 mg but do not initiate | Not recommended | Not recommended |
Dapagliflozin | HFrEF with or without T2D | Initiate 10 mg | Initiate 10 mg | Initiate 10 mg | Limited experience |
Empagliflozin | Adults with insufficiently controlled T2D | Initiate 10 mg, titrate to 25 mg if required | Continue with 10 mg only; do not initiate | Not recommended | Not recommended |
Ertugliflozin | Glycaemic control only | Initiate 5 mg, titrate to 15 mg if needed | Continue with 5 mg or 15 mg; do not initiate | Not recommended | Not recommended |
In appropriate high-risk patients, a decision to treat with an SGLT2 inhibitor to reduce risk of cardiovascular, kidney and/or heart failure events should be considered independent of HbA1c.
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Further trial results in areas of chronic kidney disease and heart failure are coming which may impact licensed indications in future. Please refer to current SmPC for individual drug for latest information on licenced indications and dose adjustment recommendations. |
CV = cardiovascular; eGFR = estimated glomerular filtration rate (mL/min/1.73 m2); HbA1c = glycated haemoglobin; HFrEF = heart failure with reduced ejection fraction; SGLT2 = sodium glucose co-transporter 2; SmPC = summary of product characteristics; T2D = type 2 diabetes. Box colours: green = initiate; yellow = can initiate in certain circumstances; orange = do not initiate but can continue established treatment; red = treatment not recommended.