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Clinical pearls for initiating and utilizing liraglutide in patients with type 2 diabetes.

J Pharm Pract · 2013

Last updated 2026-05-28

Liraglutide is a once-daily medication approved to help lower blood sugar in adults with type 2 diabetes when used alongside diet and exercise. Studies show it can reduce blood sugar levels by 0.8% to 1.5% and may lead to weight loss of about 2% to 4% of a person's starting weight. Nausea is a common side effect but often improves over time, and the risk of low blood sugar is low.

AI summary of the abstract below.

JournalJ Pharm Pract, 2013
Citations3
Relative citation ratio0.12
NIH percentile8
Molecules liraglutide
Conditions studied Type 2 Diabetes

Abstract

This review presents clinical pearls for initiating liraglutide (Victoza®, Novo Nordisk Inc) therapy for the management of type 2 diabetes and selecting patients who will benefit from liraglutide therapy. Liraglutide, a once-daily glucagon-like peptide 1 receptor agonist, is Food and Drug Administration approved as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes. Liraglutide is effective for reducing hemoglobin A1c levels by 0.8% to 1.5% in patients with type 2 diabetes as monotherapy or in combination with other diabetic medications (such as metformin, sulfonylureas, rosiglitazone, or basal insulin) when compared with placebo and these other diabetic medications, including exenatide. Overweight or obese patients with type 2 diabetes or those with insulin resistance are good candidates for liraglutide therapy because liraglutide use is associated with weight loss (about 2%-4% of initial body weight) and improved β-cell function. The incidence of hypoglycemia with liraglutide is low; therefore, liraglutide would be a safe therapy choice for patients at risk or with a history of symptomatic or severe hypoglycemia. Nausea seems to be the most problematic adverse effect associated with liraglutide therapy, but it is usually transient and is minimized with dose titration.

Verbatim abstract via PubMed 23204146 ↗

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