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An ideal 3-month InBody result on semaglutide with appropriate support shows: body fat mass reduced by 24 kg, skeletal muscle mass stable or minimally changed (within 0.3 kg of baseline), visceral fat level reduced by at least 1 level, BMR within 75100 kcal of baseline, and phase angle stable or improved
[309] [310] In other nations, such as Brazil (class A3), [311] Canada (schedule I drug), [312] the Netherlands (List I drug), [313] the United States (schedule II drug), [7] Australia (schedule 8), [314] Thailand (category 1 narcotic), [315] and United Kingdom (class B drug), [316] amphetamine is in a restrictive national drug schedule that allows for its use as a medical treatment
Half of the patients received the GLP-1 agonist medication, and the other half received a placebo, with a mix of those also taking buprenorphine and not taking it in each group
Ophthalmologists evaluating new NAION cases should inquire about semaglutide exposure, and patients diagnosed while on therapy should inform their prescribing clinicians. Consideration of baseline ocular risk factors, including prior NAION or existing optic nerve disease, may also inform treatment discussions. READ MORE: Regaining Vision with Optic Nerve Cell Regeneration Understanding the mechanism The biologic mechanism underlying the association remains uncertain
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