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Description
These findings have led the United States Food and Drug Administration (FDA) to issue a warning against the use of GLP-1RAs by individuals with a family or personal history of medullary thyroid cancer
The majority of nausea, vomiting, and/or diarrhea events occurred during a dose increase and decreased over time
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If tablets look wet, damaged, discolored, or different from what you expected, do not guess about use
This is therefore another key aspect that pharmaceutical companies will need to think about when developing new drugs for the AOM market
Adv Sci 12(4)
