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Instead, the FDA cited 'deficiencies in the manufacturing and chemistry documentation (CMC).' This means the issues are related to the paperwork and processes around how the drug is made, rather than how well it works or its side effects in patients

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8 Generally, these side-effects are self-limited, occur more commonly shortly after drug initiation or during dose escalation periods, and lessen after a few weeks of GLP-1 RA administration

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