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Description
Values presented as percentage of total Adverse events are presented for all participants who were randomised and took at least one dose of treatment, regardless of whether they discontinued * For the T2D trial, this was limited to supraventricular arrhythmias and cardiac conduction disorders ** For the obesity trial these are presented as hepatic disorder / biliary disorder separately NA : Not applicable In the obesity trial, serious adverse events (SAEs) occurred in 4% of participants with retatrutide use overall (06% across groups) vs
95% CI, 0.5-0.76)
Sarcopenia 9 , 7075 (2023)
The 2024 rules were designed to reduce exposure by requiring facilities to monitor emissions more closely and limit the release of the gas
To get started, all you need to do to request Wegovy treatments is complete an online assessment with one of our healthcare practitioners
Prevention: After drawing your dose, hold the syringe needle-up
