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This includes the following 2 : Dose The amount of drug administered, denoted by the symbol D Dosing Interval The time between drug dose administrations, denoted by the symbol T C max The peak plasma concentration of a drug after administration t max The time it takes to reach C max C min The lowest (trough) concentration that a drug reaches before the next dose is administered Volume of Distribution The volume in which a drug is distributed (varies) denoted by symbol V d calculated by the Dose divided by the initial concentration Concentration The amount of drug in a given volume (generally plasma in the case of humans) denoted by symbol C calculated by the Dose divided by the volume of distribution 0 ,C ss Elimination Rate Constant The rate at which a drug is removed from the body given as k e Elimination half-life The time required for the concentration of a drug to reach half its original value calculated by the natural log (2) divided by the elimination rate constant Clearance The volume of plasma clear of a drug per unit time, given by symbol CL Bioavailability The systematically available fraction of a drug given by symbol f Each drug will have its own C max and a different elimination rate constant, thus a different elimination half-life

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Visceral fat is metabolically active in the worst way, secreting pro-inflammatory cytokines that drive insulin resistance

Recently it was suggested that serial plasma measurements (i.e

This category is defined as: "Any pharmacological substance which is not addressed by any of the subsequent sections of the List and with no current approval by any governmental regulatory health authority for human therapeutic use (e.g