Gene2Rx - Pain Pharmacogenetics Report
Pain Pharmacogenetics Report
Report Information
Name: Leslie Knope
Date of Report: June 22, 2025
Data Source: 23andMe
Report Version: v2.0
About This Report

This report contains pharmacogenetic alleles and implications for drug response for the genetic data submitted. Both the genotypes presented and implicated medications are predictions based on the submitted data and published pharmacogenetics literature. This is not a clinical report and the data contained here in no way should be used as clinical guidance.

The information presented in this report is based on allele mappings and therapeutic implications developed by the Clinical Pharmacogenomics Implementation Consortium (CPIC®) and the US Food and Drug administration (FDA). Gene2Rx is not affiliated with CPIC or the FDA in any way. The contents of this page have not been endorsed by CPIC or the FDA and are the sole responsibility of Gene2Rx.

This report includes information about how your pharmacogenetics may influence your response to drugs used for pain relief. This report does not contain information about all drugs used for pain relief, only those that have known pharmacogenetic interactions. If you do not see your medication listed here, there is currently no prescription guidance based on pharmacogenetics published by either the FDA or CPIC.

The implications of taking medication for which you may have an atypical response are based on probabilities. You may or may not experience any side effects or altered efficaciousness. Consult your healthcare provider before making any changes to your healthcare.

The quality of uploaded data is not verified and may contain errors that result in alterations to your pharmacogenetic report. Genotyping panels (such as those used by direct to consumer genetics services) offer an incomplete representation of an individual's genetics. You may harbor additional genetic variation that can affect drug response.

⚠️ Disclaimer: Do not alter your medication dose or stop your medication without first consulting your healthcare provider.
Table of Contents
Pharmacogenetics Summary

This table contains the specific variants identified in each of the genes assessed for your Gene2Rx report. These genes are important for modulating response to medications and have been determined to be clinically actionable for some medications.

The "Genotype" column indicates the specific alleles identified in your DNA. These correspond to patterns of genetic variants within each gene. There are two alleles for each gene, one for each copy.

The "Phenotype" column indicates the predicted effect that your genotype will have on the function of the proteins encoded by each gene. These phenotypes will determine how you will respond to different medications. See the legend below for descriptions of the symbols associated with each phenotype.

Gene Genotype Phenotype
CYP2C19 *1/*2 Intermediate Metabolizer
CYP2C9 *1/*2 Intermediate Metabolizer
CYP2D6 *4/*4 Poor Metabolizer
Legend

Symbols in the Gene Summary table represent the predicted function of the gene. A non-normal allele does not necessarily lead to a change in drug response.

Normal function
Decreased function
Increased function
Severely decreased or no function
Unknown function
Drugs with Potential Atypical Response

Based on your genetics, you may have an atypical response to medications listed in this section. Listed below are drug classes followed by tables containing drugs within those classes and how your pharmacogenetics may influence how you respond to the drug.

Each table contains generic names for the drug, brand names, the associated gene, your gene phenotype, and a description of how your genotype may affect your drug response. Each row also contains a link to the CPIC guideline or FDA drug label from which the information was derived, which also contains therapeutic recommendations for your healthcare provider.

Some drugs have guidance based on multiple genes. Results are assessed for each gene individually and grouped together in the report.

Drugs are often used for multiple indications and can belong to multiple drug classes. We have grouped the drugs in this report based on their most common use, but you may find that some drugs are used for purposes other than indicated by the drug classes in this report.

Therapeutic Guidance Legend
Normal therapeutic guidance
Alternate dosing recommended
Alternate drug recommended

Note: Phenotypes with an unknown effect on drug response will have normal therapeutic guidance, despite the effect being unknown.

Pain Management

Generic Name Brand Names Gene Your Gene Phenotype Implication Source
CodeineTylenol 3CYP2D6 Poor MetabolizerCPIC: Implication: Greatly reduced morphine formation leading to diminished analgesia.Therapeutic recommendation: Avoid codeine use because of possibility of diminished analgesia. If opioid use is warranted, consider a non-tramadol opioid.
FDA: Results in lower systemic active metabolite concentrations and may result in reduced efficacy.
CPIC, FDA
MeloxicamMobicCYP2C9 Intermediate MetabolizerCPIC: Implication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the meloxicam prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.
FDA: No FDA guidance for this phenotype
CPIC, FDA
OliceridineOlinvykCYP2D6 Poor MetabolizerResults in higher systemic concentrations and higher adverse reaction risk (respiratory depression and sedation). May require less frequent dosing.FDA
PiroxicamFeldeneCYP2C9 Intermediate MetabolizerCPIC: Implication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.
FDA: Results in higher systemic concentrations.
CPIC, FDA
PitolisantWakixCYP2D6 Poor MetabolizerResults in higher systemic concentrations. Use lowest recommended starting dosage. Refer to FDA labeling for specific dosing recommendations.FDA
TramadolUltram, ConZipCYP2D6 Poor MetabolizerImplication: Greatly reduced O-desmethyltramadol (active metabolite) formation leading to diminished analgesia.Therapeutic recommendation: Avoid tramadol use because of possibility of diminished analgesia. If opioid use is warranted, consider a non-codeine opioid.CPIC
Drugs with Typical Response

Based on your genetics, you are likely to respond normally to medications listed in this section.

Pain Management

Generic Name Brand Names Gene Your Gene Phenotype Implication Source
CarisoprodolSomaCYP2C19 Intermediate MetabolizerNo FDA guidance for this phenotypeFDA
CelecoxibCelebrexCYP2C9 Intermediate MetabolizerCPIC: Implication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.
FDA: No FDA guidance for your genotype
CPIC, FDA
FlurbiprofenAnsaid, Ocufen, StrepfenCYP2C9 Intermediate MetabolizerCPIC: Implication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.
FDA: No FDA guidance for your genotype
CPIC, FDA
IbuprofenAdvilCYP2C9 Intermediate MetabolizerImplication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.CPIC
LornoxicamXefoCYP2C9 Intermediate MetabolizerImplication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.CPIC
TenoxicamMobiflexCYP2C9 Intermediate MetabolizerImplication: Mildly reduced metabolismTherapeutic recommendation: Initiate therapy with recommended starting dose. In accordance with the prescribing information, use the lowest effective dosage for the shortest duration consistent with individual patient treatment goals.CPIC
Frequently Asked Questions
What do I do now?

If you find that you may have an atypical response to a medication you take or are considering taking, it is important that you first consult with your healthcare provider or a genetic counselor before making any changes. The guidelines linked next to each finding (either CPIC or FDA) provide therapeutic guidance that include treatment recommendations.

Should I change medications or dosage based on my report?

No! Do not alter your medication dosage or stop taking your medication without first consulting your healthcare provider. Direct-to-consumer data is not clinical grade, so anything included in the report should be used as a conversation starter with your healthcare provider to seek the appropriate clinical laboratory test. Again, do not alter your medication dosage or stop taking your medication without first consulting your healthcare provider.

Why shouldn't I change my medication based on this report?

Our service relies on the genetic information provided to you by the direct-to-consumer service you paid for. Unfortunately, direct-to-consumer data is not clinical grade, so anything included in the report should be used as a conversation starter with your healthcare provider to seek the appropriate clinical laboratory test. DO NOT alter your medication dosage or stop taking your medication without first consulting your healthcare provider. Read more here and read primary research here.

Are these expert annotations?

Yes, The Clinical Pharmacogenetics Implementation Consortium (CPIC®) is a group of PGx experts that volunteer their time to curate genetic guidance for drug response, based on the most recent research. They have high standards for the evidence required to include a drug-gene guideline. The US Food and Drug Administration (FDA) has evaluated all pharmacogenetic associations presented in this report and believes there is sufficient scientific evidence to provide clinical guidance for prescribing practices. Read more here.

Why would my PGx annotations change?

While your genetics don't change over the course of your life, research is an ongoing process and what we know about how an individual's genetics influences their drug response changes over time. As new research is conducted and published, the CPIC guidelines and FDA drug labels are updated accordingly. These updates only happen once new research meets strict validation requirements and experts agree it's time for a guideline change. Gene2Rx provides the most recent CPIC and FDA guidance at the time of the report.

I don't see my medication in the report. Why not?

Not all drugs are influenced by pharmacogenetics, and some need more research to verify an association. If you don't see your medication listed, it means that there is not yet a CPIC guideline for providing clinical guidance for pharmacogenetic dosing.

Does Gene2Rx determine structural variants for CYP2D6?

Structural variations for CYP2D6 are not called and may affect your response to drugs metabolized by CYP2D6.

More questions?

Contact us at contact@gene2rx.com.

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