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, (i) 0.1% 10% GLP-1 (ii) 15% 25% , (iii) 30% 50% .In certain embodiments, the pharmaceutical composition for oral administration comprises (i) from about 0.1% to about 10% of a lipidized GLP-1 peptide analog (ii) from about 15% to about 25% of sodium kenodeoxycholate, and ( iii) about 30% to about 50% propyl gallate

When both occur during one encounter, both codes bill with appropriate modifiers indicating distinct services at separate anatomical targets

Those patients should not experiment with immune-active compounds without medical review