Drug metabolism rates vary among patients. Some patients metabolize a drug so rapidly that therapeutically effective blood and tissue concentrations are not reached; in others, metabolism may be so slow that usual doses have toxic effects.
Drug response differences are associated with differences present in individuals’ genetic makeup. Typically, people have two copies of each gene. Those with extra gene copies produce too much of the CYP2D6 enzyme and process the drug very fast. As a result, their bodies convert the painkiller drugs like codeine to its active form morphine so quickly that a standard dose codeine leads to morphine toxicity. In contrast, some variants of CYP2D6 that vary by a single difference in their DNA sequence create an enzyme that doesn’t work. People with these variants process codeine slowly, if at all, leading to little, if any, pain relief.