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In response to these findings, the European Medicines Agency (EMA) conducted a review and concluded that NAION is a very rare adverse reaction to semaglutide-containing products, potentially affecting up to 1 in 10,000 users

Six GLP-1 RAs, each utilizing a unique drug delivery strategy, are now approved by the Food and Drug Administration (FDA) and additional, novel GLP-1 RAs are still under development, making for a crowded marketplace and fierce competition among the manufacturers of these products

Nowicki, M., Kosacka, J., Serke, H., Blher, M