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M.MukhopadhyaI
[1] [2] According to the Medicines and Healthcare products Regulatory Agency (MHRA) approved Summary of Product Characteristics (SmPC), dizziness is listed as an uncommon side effect, occurring in less than 1 in 100 but more than 1 in 1,000 patients
Oral semaglutide was subsequently evaluated in the PIONEER 6 trial, which confirmed a cardiovascular safety profile consistent with its injectable form
Liraglutide, in particular, has a half-life of only around 13 hours and requires a daily injection
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