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Adding semaglutide to retatrutide would duplicate GLP-1 receptor activation, which could increase side effects without proportionally increasing efficacy
Why it was included in the FDA ban The FDA cites significant safety risks due to the potential for congestive heart failure in certain patients seen in a clinical trial that was terminated
(2023, August 28)
A complete COA quantifies these as part of the impurity profile
Consultation with a healthcare practitioner is recommended for personalized advice
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