Pharmacogenomics (PGx)
Pharmacogenomics is a process that uses a non-invasive genetic test involving a cheek swab or sample of saliva to determine how an individual responds to medications. The genetic results will show how that person metabolizes certain medications. This information can be used to show if they are likely to tolerate the medication, need a different dosage, or require a different medication.
Implications for Current/Past Therapy
Pharmacogenetic results help to explain your current response to medications. We may be able to show why your dose has changed or recommend your dose be changed. We can also often explain why you are experiencing some of the medication side-effects.
Implications for Future Therapy
Your pharmacogenomic results can be applied to future therapy. Future medication considerations may be influenced by your pharmacogenomic information. Having your results available can help clinicians tailor your medication therapy towards you as an individual.
Common Challenges with Starting a New Medication Solved with PGx
Starting a new medication can be an overwhelming experience. Many people are faced with fears and anxieties with starting a new medication and considering potential side-effects can leave people feeling helpless and lacking confidence in the healthcare process. Selecting medications for many health conditions can be expensive and often take months of trial and error with repeat office visits to find the correct medication at the right dose. The aim of PGx is to provide a tool that helps patients and providers gain confidence that the right medication is being selected for the right person. The hope is to save time and preserve comfort by avoiding options that are likely to produce inadequate results or side-effects.