Publication

Compounded GLP-1 and Dual GIP/GLP-1 Receptor Agonists: A Statement from the American Diabetes Association

Joshua J. Neumiller, Mandeep Singh Bajaj, Raveendhara R. Bannuru, Rozalina Grubina McCoy, Elizabeth J. Pekas, Alissa R. Segal, Nuha A. ElSayed

Diabetes CareDec 2, 2024
Abstract

The use of glucagon-like peptide 1 receptor agonist (GLP-1 RA) and dual glucose-dependent insulinotropic polypeptide (GIP) and GLP-1 RA (GIP/GLP-1 RA) classes has increased substantially over the past several years for treating type 2 diabetes and obesity. Increased demand for these pharmacotherapies has resulted in temporary product shortages for both GLP-1 RA and dual GIP/GLP-1 RA medications. These shortages, in part, have led to entities producing and marketing compounded formulations that bypass regulatory measures, raising safety, quality, and efficacy concerns. Even as shortages resolve, compounded GLP-1 RA and GIP/GLP-1 RA products continue to be heavily marketed to people with diabetes and obesity. The purpose of this statement by the American Diabetes Association is to guide health care professionals and people with diabetes and/or obesity in these circumstances of medication unavailability to promote optimal care and medication use safety.

1Authors

AuthorAffiliationh-indexCitations
Joshua J. NeumillerWashington State University Spokane4611,422
Mandeep Singh BajajBaylor College of Medicine355,026
Raveendhara R. BannuruAmerican Diabetes Association9042,271
Rozalina Grubina McCoyUniversity of Maryland, Baltimore7221,596
Elizabeth J. PekasAmerican Diabetes Association418,422
Alissa R. SegalMassachusetts College of Pharmacy and Health Sciences5414,785
Nuha A. ElSayedAmerican Diabetes Association7023,834

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