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Pharmacogenomic (PGx) Decision Support

Pharmacogenomic (PGx) Decision Support

Ability to select treatment plans based on interactions between a patient's genome and a prescribed drug or drugs.

Pharmacogenomic (PGx) Decision Support: Products


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24 products
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# of Clients- low to high
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Alphabetical
Highest rated

Filter products


EMR compatibility

Star rating

Product attributes
  • Covid-19
  • Pediatric
  • In Epic App Orchard
  • In Cerner App Gallery

Keywords

Solutions

Filter products by clients


Used by

EMR used

Organization size

Type
  • AMC
  • Pediatric Facilities
  • ACO
  • Rural Presence
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EpicCare Ambulatory, one of the top ten ambulatory EHRs in the country, specializes in outpatient primary care. The module is used for documenting visits, placing orders, sending prescriptions, and viewing and communicating test results.
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Our unique approach uses complex assays and treatment algorithms to help your doctor prescribe the right high blood pressure drugs that will work for you. With Geneticure, you’ll discover the personalized physiology and genetics associated with your hypertension that show the function of your heart, kidneys and blood vessels. Our method goes beyond most DNA tests that only look at drug metabolizing enzymes — how much of a drug gets into your bloodstream. Drug metabolizing enzymes are primarily used to help guide the correct dosage, independent of whether or not it’s the right medication in the first place. With Geneticure, you’ll find out which medications might be most likely to work best for you, based not only on drug metabolism, but also enzymes, hormonal pathways, and drug receptors in your DNA. Geneticure has 3 clinical trials on nearly 700 subjects demonstrating clinical and health economic utility, with 5 peer reviewed publications.
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Phosphorus provides comprehensive genetic testing across most specialties, including: cardiology, lipidology, oncology, neurology, obstetrics and gynecology, fertility, reproductive endocrinology, pharmacology, and more. In addition to operating as a reference lab and conducting genetic testing for your patients, we also provide genetic counseling services. Providers that are interested in moving testing in house, can reach out to our company for lab management and in-house opportunities for partnership.
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By InsightRX

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Achieve therapeutic targets and improve sample efficiency. InsightRX Nova standardizes precision dosing across your institution, improving efficacy, minimizing variability, and reducing adverse events—all while lowering blood sampling by up to 50%. Improve model accuracy and stay up to date. InsightRX Nova gives you access to the most up to date, clinically validated models developed by our partners and curated from the literature. In addition, dosing guidance improves over time as we update models using our proprietary human-assisted AI framework and data from the InsightRX network. Capture results and outcomes. InsightRX Nova includes reports on your institution’s target performance compared to national benchmarks or your institutional data. For more powerful analytics, InsightRX Apollo provides dashboards enabling you to understand how targets are being met across drugs, providers, and subpopulations.
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By Invitae

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Our clinical decision support tool synthesizes the evidence impacting drug response, including pharmacogenomic testing, to support doctors and pharmacists in making faster, more proactive decisions at the point of care. YouScript is the only clinical decision support system validated in multiple clinical and real world studied system. In a recent study, utilization of YouScript and pharmacogenomic testing revealed 52% reduction in readmissions and 42% reduction in ED visits. And we’re successfully integrated into the clinical workflow of Epic, Cerner, Allscripts, and Telus Health. Equally important is that our team includes pioneers in genetics, medicine, technology, and genetic counseling, and is trusted by experts to provide the most comprehensive, reliable genetic screening, technology, and support available. In pursuit of our mission, we aim to be a trusted partner to value-based healthcare organizations, providers, and payers who want to lower the barriers of precision medicine through transforming clinical decisions through genomics.
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