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After a 2 week screening period all eligible participants were randomly assigned to treatment groups receiving either a subcutaneous injection of 2.4 mg of semaglutide, 2.4 mg of cagrilintide, a combination of cagrilintide and semaglutide, a semaglutide placebo, or a cagrilintide placebo [2]
10.1016/j.reprotox.2022.08.010 12 BassiounyY
Fever, chills, and redness, pus or spreading warmth at the site can indicate cellulitis or a bloodstream infection and need medical attention
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