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Safety of injectable semaglutide for type 2 diabetes.

Expert Opin Drug Saf · 2020

Last updated 2026-05-28

A review of injectable semaglutide, a once-weekly GLP-1 drug for type 2 diabetes, found its side effects were mostly mild gastrointestinal issues, like nausea or vomiting. The drug did not show harm to the thyroid, pancreas, kidneys, or liver, and may even protect the kidneys and liver. However, it was linked to a higher chance of gallbladder problems and a modest increase in eye-related issues called diabetic retinopathy.

AI summary of the abstract below.

JournalExpert Opin Drug Saf, 2020
Citations11
Relative citation ratio0.50
NIH percentile29
Molecules semaglutide
Conditions studied Type 2 Diabetes

Abstract

INTRODUCTION: Semaglutide is the most recently approved injectable glucagon-like peptide-1 receptor agonist (GLP-1RA) for people with type 2 diabetes (T2DM). It is one of the three currently marketed GLP-1RAs that can be administered once weekly. AREAS COVERED: This review focusses on the safety of injectable semaglutide. Semaglutide has been assessed in the SUSTAIN phase 3 clinical trial programme, which included patients across the disease spectrum, i.e. treatment-naïve to those receiving insulin. The authors have looked at all published literature on safety considerations of once weekly GLP-1RA with particular reference to semaglutide. EXPERT OPINION: Semaglutide is the most powerful injectable GLP-1RA. The cardiovascular (CV) outcome trial (SUSTAIN 6) showed CV superiority and its adverse event profile is as expected for the GLP-1RA class with predominantly gastrointestinal side-effects. Concerns about the thyroid and pancreatic safety have not been substantiated. There is no indication of renal or liver harm for semaglutide. Data consistent with reno-protection and benefit in liver disease is presented. There is a modest signal for increased gall bladder adverse events. An increase in diabetic retinopathy (DR) events in the SUSTAIN 6 trial is the most concerning safety signal. Caution regarding DR is needed when initiating semaglutide and recommendations are suggested.

Verbatim abstract via PubMed 32428416 ↗

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