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

被引:2
|
作者
Neumiller, Joshua J. [1 ]
Bajaj, Mandeep [2 ]
Bannuru, Raveendhara R. [3 ]
Mccoy, Rozalina G. [4 ]
Pekas, Elizabeth J. [3 ]
Segal, Alissa R. [5 ]
Elsayed, Nuha A. [3 ,6 ]
机构
[1] Washington State Univ, Dept Pharmacotherapy, Spokane, WA USA
[2] Baylor Coll Med, Dept Med, Houston, TX USA
[3] Amer Diabet Assoc, Arlington, VA 22202 USA
[4] Univ Maryland, Sch Med, Dept Med, Div Endocrinol Diabet & Nutr, Baltimore, MD USA
[5] Massachusetts Coll Pharm & Hlth Sci, Boston, MA USA
[6] Harvard Med Sch, Boston, MA 02115 USA
关键词
D O I
10.2337/dci24-0091
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:177 / 181
页数:5
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