MyPharmaGenes® PGx

DNA test to guide individual drug therapy
Comprehensive DNA test for the definition of personalized medication strategies.

PHARMACOGENETICS: VARIABILITY IN DRUG RESPONSE

Genetics contributes to individual differences, not only in characteristics such as height or skin colour but also at the pharmacological level. Pharmacogenetics studies the relationship between genetic variability and how we respond to drugs. This information assists doctors in therapeutic management, which includes selecting active compounds and adjusting doses. The ultimate goal of this approach is to maximize therapeutic effects and minimize the risk of side effects.

MyPharmaGenes® PGx is a comprehensive pharmacogenetic test designed to create a personalized pharmacological plan. This test evaluates 121 drugs commonly used in various medical specialities, including:

Psychiatry

Neurology

Pain management

Cardiology

Oncology

Gastroenterology

Immunosuppression

Rheumatology

Urology

Infectiology

An interactive WebApp

MyPharmaGenes® PGx is supported by an interactive WebApp where patients can:

  • Manage their own drug portfolio;
  • Register drugs that have triggered side effects;
  • Have rapid access to which drugs may or may not be recommended for them;
  • Find more specific information regarding the genes evaluated.

MyPharmaGenes® PGx is indicated for:

  • Patients who are starting new therapies;
  • Patients who are not achieving therapeutic goals and/or experience moderate to severe adverse effects with the current therapy;

What is analysed?

The MyPharmaGenes® PGx test analyses genetic variants associated with the metabolism and response to specific drugs, scientifically validated and with proven clinical utility.

MyPharmaGenes® PGx highlights:

  • Coverage of 121 drugs;
  • Evaluation of 28 genes and 85 genetic variants;

With the evaluation of the patients’ genotypic profile is it possible to:

  • Prescribe more adequate drug dosages;
  • Evaluate the patient’s response to the treatment;
  • Avoid/minimise adverse drug reactions;
  • Select alternative agents, if necessary.

And, consequently, offer better treatment to more patients.

Drugs evaluated by therapeutic areA


Turnaround time

15 working days

Scientific Studies

[1] Bouvy, J.C., De Bruin, M.L. & Koopmanschap, M.A. “Epidemiology of Adverse Drug Reactions in Europe: A Review of Recent Observational Studies”. Drug Saf 38 (2015): 437–453.
[2] Steve Connor (2003) “Glaxo chief: Our drugs do not work on most patients”, Independent/UK, 8/12/2003.
[3] Spear, B.B., Heath-Chiozzi, M. & Huff, J., “Clinical Application of Pharmacogenetics”. Trends Mol Med 7.5 (2001):201-204.
[4] Böhm, R. & Cascorbi, I., “Pharmacogenetics and Predictive Testing of Drug Hypersensitivity Reactions”. Front Pharmacol 7 (2016): 396.
[5] Lauschke, V.M., Milani, L. & Ingelman-Sundberg, M. “Pharmacogenomic Biomarkers for Improved Drug Therapy—Recent Progress and Future Developments”. AAPS J 20.1 (2018): 4.
[6] Gaedigk, Andrea, et al. “Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles: A GeT-RM Collaborative Project”. J Mol Diagn 21.6 (2019): 1034-1052.