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At any rate, this cluster of adverse events was experienced by 22.9% of the 7.2mg group versus 6% of the 2.4mg group (it was not an adverse event at all in the original STEP 1 trial at all.) The researchers claim that Dysaesthesia adverse events were mild for most participants who experienced them: and that Most participants recovered from the event by the end of the trial. Of course we dont know if they will come back and for those who hadnt recovered, we dont know how this impacts their life/quality of life

What we know about safety comes from extrapolating each compound's individual profile and applying first-principles pharmacology

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How you spread it across the day matters equally

Retrieved from Leehey, D

1 Retrospective case-control studies on cancer risk are susceptible to recall bias