Table 1. Potential safety implications for incorrect medication list.
| Discrepancy classification | Potential consequence for PGx | Potential implication for patient safety |
|---|---|---|
| Missing/wrong dose | Some PGx guidelines/package labeling contain specific dosing recommendations | Dosing outside of prescribed dosage could result in either under or overdosing, each of which could affect safety/efficacy |
| Wrong frequency | – | Altered frequency dosage could result in either under or overdosing, each of which could affect safety/efficacy |
| Wrong medication | PGx recommendations may be missed, or incorrect recommendations may be made, implications if wrong medication is a strong inhibitor | Taking alternative medications unbeknownst to the treatment team could result in significant drug-drug interactions or could trigger an adverse event thought to be a new symptom thus triggering the prescribing cascade |
| Discontinued medication | Incorrect recommendations may be made; implications if discontinued medication is a strong inhibitor | Not taking medications that the healthcare team believes are being taken can result in less effective alternative medications being used |
| Duplicate medications | – | Can result in prescriber and healthcare team confusion with cluttered medication lists |
| Omissions | PGx recommendations may be missed, implications if added medication is a strong inhibitor | Taking alternative medications unbeknownst to the treatment team could result in significant drug-drug interactions or could trigger an adverse event thought to be a new symptom thus triggering the prescribing cascade |
| Added PRN indication | – | Joint Commission requirement; clarifies patient taking medication for correct reason |
PGx, pharmacogenomic; PRN, pro re nata.