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DNA testing for medicines

DNA testing for medicines, also called pharmacogenetics, examines variants that can influence how certain medicines are processed or work. For some well-studied combinations, the result can help guide the choice of medicine or dose, but does not predict with certainty whether a medicine will work or cause side effects.

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  • Pharmacogenetics examines inherited DNA variants that can affect the action, breakdown or safety of specific medicines.
  • A result does not apply to ‘all medicines’. Each gene–medicine combination has its own evidence and recommendations.
  • A genotype can be translated into an expected phenotype, such as slow, normal or ultrarapid metabolism, but these categories are not the same for every enzyme.
  • Other medicines and illnesses can change the behaviour predicted from genetics. This is sometimes called phenoconversion.
  • The result supports shared decision-making and does not replace a medical diagnosis, medicine safety checks or follow-up.

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