GeneMedRx is the first software tool available to prescribers that predicts potential drug-drug and drug-gene interaction risk based on both cytochrome P450 metabolism and genetic testing. This information helps physicians gain enhanced understanding of metabolism-based adverse drug interactions and/or lack of efficacy.
GeneMedRx is the upgraded, pharmacogenetics-ready version of Mental Health Connections P450 Interactions program, the most extensive coverage of cytochrome P450s available and in use by physicians since 1997.
Constantly updated to keep pace with the dozens of relevant reports appearing each month. The database currently contains:
- 2500 Drugs and Metabolites (Over 7500 names)
- 5000 PubMed Links
- 80000 Unique Notes
- 1500 Substrates
- 1000 Inhibitors and Inducers
Unlike other DDI programs GeneMedRx uses an algorithm to predict and weight DDIs for drug combinations not reported in the literature.
Designed For Accessibility
- API available for integration into your current EHR or EMR for seamless use. Request an API demo.
- Available from any computer with Internet access.
- Colors and icons highlight interactions of concern.
- Optional entry of patient’s genetic profile provides information based on drug-gene interactions
- Program allows for what-if scenarios.
- A clinical confidence rating is given for those predictions that are supported by clinical data.
- Not unduly alarmist.
- Results are presented in a simple form with detailed notes and references readily available.
How GeneMedRx Works
1. Input patient prescription, Over the counter, herbal medicine regimens, food intakes, patient factors (pregnancy, cigarette smoking, etc.), and chemical exposures. If available, input patient’s pharmacogenetic test results (For information on obtaining this testing, Visit http://www.genemedrx.com
2. Scan the results for potential drug-drug interactions based on the metabolism of the drugs in question. Please note that results do not include the minority of drug-drug interactions for which metabolism is not understood.
3. Determine the effect removing or adding a particular drug has on the predicted change.
4. If needed, pick an alternate drug or dosage based on the predicted change profile
Choice Browser: In Windows the Firefox browser loads the drug list quicker and displays the windows more attractively than does Internet Explorer. On the Mac a Firefox browser works properly. We are working to make the program work with other Mac browsers as well.
Jane’s physician added paroxetine to her other meds after consulting GeneMedRx to determine there were no significant interactions noted. When Jane experienced nausea and sleeplessness, pharmacogenetic testing was ordered. Jane is a CYP2D6 poor metabolizer with a genotype of *4/*4. She was normal for other CYP genotypes. Her physician again consulted GeneMedRx and found that paroxetine was a high-risk medication for Jane’s genotype. By querying the program he found that citalopram, a CYP2C19 substrate, might be safer for Jane.
Jessica R. Oesterheld, M.D., a practicing psychiatrist and educator, is a frequent author and lecturer on metabolism-based pharmacology in adults and children. Her interest arose from clinical experiences with adverse drug reactions caused by CYP based drug interactions.
Neil B. Sandson, M.D., is Director of the Division of Education and Residency Training at Sheppard Pratt Health System.
David N. Osser, M.D., is a clinical psychopharmacology consultant and a member of the International Psychopharmacology Algorithm Project.
The software is available as an internet subscription. Further details or order online.