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Eventually, the optic disc edema resolved, leaving residual structural damage i.e., GCL atrophy, consistent with the typical presentation of NAION
In September 2019 , the FDA approved Rybelsus , the first oral GLP-1 receptor agonist, available in 3 mg (starter dose), 7 mg, and 14 mg daily tablets
Further studies should explore if prokinetics can be given to patients who are shown to have RGC on ultrasound and then be re-scanned to see if sedation can proceed
Foundayo is not yet approved in the UK
Alzheimers disease is type 3 diabetesEvidence reviewed
The five-day half-life means that after seven days, approximately 75% of the previous dose remains active in the bloodstream before the next injection
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