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Discontinuation rates due to adverse events were 4.1% (4 mg), 6.9% (9 mg), and 11.3% (12 mg), compared with 4.9% for placebo
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doi: 10.1124/jpet.103.051987 [DOI] [PubMed] [Google Scholar] 89
[DOI] [PubMed] [Google Scholar] 68.Fridley J, Foroozan R, Sherman V, Brandt ML, Yoshor D
Subcutaneous semaglutide treatment led to an increased number of retinopathy complications in the SUSTAIN-6 cardiovascular outcomes trial (81)
