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Pharmacokinetics of semaglutide and dose adjustments

They start you on the lowest possible dose even if youve taken GLPs before

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Excessive release of glutamate and its binding with NMDA, -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), or kainite (KA) receptors promotes excitotoxicity cell injury with a consequent activation of many molecular pathways, resulting in intracellular calcium (Ca 2+ ) overload 90,91 , reactive oxygen species (ROS) production, mPT, and cell swelling with brain edema 92

You might spend six weeks at 1.0 mg before moving to 1.5 mg