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Firstly, not all patients respond well to oral tablets and, secondly, the tablets prescribed are not guaranteed to be pharmaceutical standard and are instead regulated by the Food Standards Agency
Gastrointestinal adverse events, predominantly mild-to-moderate in severity, were more frequently reported with semaglutide compared to placebo (82.2% versus 53.9%)
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doi: 10.3390/jcm11206102 145 PatelVPauliNBiggsEBarbourLBoruffB
That is precisely when errors happen
Oral protocols use tablet-based dosing rather than reconstitution-based dosing, simplifying the protocol logistics considerably
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