Pharmacogenomic (PGx) testing will help uncover your biological response to different medications.

CQuentia provides a comprehensive, industry-leading PGx testing covering 43 genes and its 183 variants (mutation) addressing the response to over 24,000 medications and multiple conditions such as the patients risk to Malignant Hyperthermia, Pseudocholinesterase Deficiency, and the patients Thrombosis Profile.

CQuentia’s Pharmacogenomic testing program explore the patients unique individual genetic profile identifying how they will respond to the various medications used during and after surgery. CQuentia also defines when a patient has a genetic risk for malignant hyperthermia, a pseudocholinesterase deficiency or has a thrombosis risk. The combined view of medication efficacy and risk factors provides a greater level of patient detail that directly impacts the success of the surgical event.

We ensure that the results of our comprehensive pharmacogenomic tests are made accessible at point-of-care. PGx guided medication management has shown to reduce narcotic use during surgery, decrease instances of post-operative side effects (such as nausea/vomiting) and improve post-operative pain scores.

Genes Being Tested and Interpreted at CQuentia
ABCB1CFTRDRD1HTR2CSLC6A2
ABCG2COMTDRD2IFNL3SLCO1B1
ADRA2ACYP2D6DRD3KCNIP1VKORC1
ADRB1 CYP1A2EDN1KORC1
AGTCYP2B6 F2LDLR
APOECYP2C19F5MTHFR
BCHECYP2C9GNB3NR1H3
CACNA1CCYP3A4GRIK4OPRM1
CACNA1S CYP3A5HTR1ATMPT
CES1DPYDHT2ARYR1

If you would like to order a PGx Test