Phenotype | Characteristics | Clinical Consequence |
---|---|---|
PM | Major variants: CYP2D6*3, -*4, -*5, -*6 | High plasma drug level |
Enzyme inactive | Risk of drug-related side effects | |
5–10% White; 1–2% Chinese and Japanese | Use of reduced drug dose | |
IM | Major variants: CYP2D6*9, -*10, -*41 | Lower dose for some patients |
Low residual enzyme activity | ||
EM | Not a uniform group | Standard dose for most patients |
Normal rate of metabolism | ||
UM | Multiple copies of CYP2D6 | Very low plasma drug level |
Very high enzyme activity | Loss of drug efficacy | |
1–2% Whites; 30% Ethiopians | Higher drug dose required |
IM, intermediate metabolizer.