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The route of administration doesn't determine the code
doi: 10.1007/s10585-010-9305-4
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Subcutaneous administration bypasses intestinal conversion to trimethylamine-N-oxide (TMAO), a metabolite associated with cardiovascular concerns [4] , while providing 100% bioavailability compared to 518% for large oral doses [3]
Relationship of C-reactive protein reduction to cardiovascular event reduction following treatment with canakinumab: a secondary analysis from the CANTOS randomised controlled trial
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