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Gastrointestinal Effects The most common side effects involve the digestive system, occurring in roughly 28% of participants at the 12mg dose

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Of those 15 cases, 12 were found to be possibly linked to use of GLP-1 RAs, while 3 could not be assessed due to missing clinical information

Its about the cause of the deficiency, what the patient prefers, and how well they absorb it

European Medicines Agency (EMA) Eli Lilly typically files for European approval (through the EMA's centralized procedure) around the same time as the FDA submission, sometimes within a few months

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