This program collects genetic and health information to help doctors choose the right medications for patients.
This study wants to understand how genes can affect how the body responds to medicines. This information will help us determine whether changing your medicine can make you healthier and improve your life. We will study your medical history for the last year and the next five years after you join the study. study goals include: * Enrolling patients who take multiple medications or have harmful side effects from their medications. * Keeping all medical information and genetic samples from patients in one place. * Helping doctors make better decisions about which medicines to prescribe. * Influencing insurance companies and the government to help pay for this kind of medical care for people who need to change their medicine to stay healthy.
Study Type
OBSERVATIONAL
Enrollment
3,000
Texas A&M Family Care
Bryan, Texas, United States
RECRUITINGFrequency and nature of ADRs on the Naranjo Scale
Patients will be referred to the Texas A\&M Interprofessional Pharmacogenomics Clinic (IPGx) by their primary care physicians. A physician or ambulatory pharmacist in the IPGx clinic or Family Care Clinic will obtain a complete medical history, physical examination, and validate the patient's current concomitant medication list at the IPGx during the office visit. Patient medical information would be input into the CSN, which functions as a computable EHR medical record analysis, evaluation of polypharmacy status, and monitoring of Adverse Drug Reactions using the Naranjo Scale questionnaire will be conducted for the duration of the study.
Time frame: 5 years
Serum/plasma drug concentrations
Patients will be referred to the Texas A\&M Interprofessional Pharmacogenomics Clinic (IPGx) by their primary care physicians for an evaluation of pharmacokinetic and pharmacodynamic (PK/PD) assessments. For drug level measurement, urine samples will be collected using provided kits and shipped to the contracted laboratory via FedEx in biosafety shipping containers.
Time frame: 5 years
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