Pramlintide in the treatment of type 1 and type 2 diabetes mellitus
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TL;DR
Use of pramlintide in addition to insulin in patients with type 1 and type 2 diabetes was associated with modest reductions in HbA(1c) and the incidence of hypoglycemia in the first 4 weeks of therapy was 2 to 4 times greater with pramsintide compared with placebo; thus, the manufacturer recommends reducing the dose of premeal insulin by 50% when starting pramlintide.
Abstract
Use of pramlintide in addition to insulin in patients with type 1 and type 2 diabetes was associated with modest reductions in HbA(1c). The primary adverse effects of pramlintide therapy were nausea and hypoglycemia.
