Step 1: Read the curve. A semilog or simple decay curve in which a constant fraction of the drug is removed per unit time, and the half-life (t½) stays the same at high and low concentrations, is the hallmark of first-order kinetics.
Step 2: Apply the concept. In first-order elimination the rate of elimination is proportional to the plasma concentration: as concentration falls, the absolute amount eliminated per unit time also falls, but the proportion (and hence t½) is fixed. Mathematically, \(C = C_0 e^{-kt}\) and \(t_{1/2} = 0.693/k\), independent of \(C_0\).
Step 3: Choose the answer. A constant t½ with concentration-proportional elimination = first-order kinetics, which applies to most drugs at therapeutic doses.
Step 4: Why the others are wrong - zero-order kinetics removes a constant amount per unit time (straight-line linear decline, saturated enzymes, e.g. ethanol, phenytoin, aspirin at high dose) and has no fixed t½; Michaelis-Menten at saturating dose behaves as zero-order; mixed-order shifts from zero- to first-order only as concentration falls below saturation.
Key fact: Constant t½ + concentration-proportional elimination = first-order kinetics (exponential decay).