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Clinical trial data from the STEP programme found no increase in anxiety-related adverse events with semaglutide compared to placebo
Eligible participants were men or women aged 5585 years with mild cognitive impairment or mild dementia due to AD with confirmed amyloid abnormalities (assessed by positron emission tomography or cerebrospinal fluid [CSF] analysis)
Monitor renal function in patients reporting adverse reactions to RYBELSUS that could lead to volume depletion, especially during initiation and escalation of RYBELSUS Severe Gastrointestinal Adverse Reactions: Use of RYBELSUS has been associated with gastrointestinal adverse reactions, sometimes severe
Curious about how compounded semaglutide compares to the standard version
Abeer MM, Meka AK, Pujara N, Kumeria T, Strounina E, Nunes R, et al
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