PGx Analysis (Pharmacogenomics) A DNA based test to determine how a patient will respond to a particular medicine or a combination of medicines and identifies their unique sensitivities to possible drug effects. The rate of drug metabolism varies by individual. PGx testing can assist healthcare providers with minimizing or completely avoiding trial-and-error dosing, as well as substantially reducing the risk of serious prescription related side effects. In-Home Test. FDA Approved
Check AvailabilityOur tests analyze specific genes and markers associated with immunodeficiency, providing accurate and actionable results. The screening can help diagnose primary immunodeficiency disorders, autoimmune diseases, and other conditions that may impact the immune system. A DNA based multi-gene panel that accurately identifies the presence of an inherited gene mutation or alteration which may create a predisposition for cancer. Patients who receive a positive test result will benefit from the opportunity to better understand and make informed decisions about managing future risks and their medical care. In Home Self-Test. FDA Approved.
Check AvailabilityA DNA based test used to analyze particular gene(s) to determine if there are genetic changes present that significantly increase your risk for developing Diabetes-Obesity. Genetic testing provides a more precise estimate of a person’s risk for Diabetes-Obesity than using your personal and family history alone. In some cases, the results of this test may also provide information about risks for medical conditions that are not related to Diabetes-Obesity. In Home Self-Test. FDA Approved.
Check AvailabilityA DNA based multi-gene panel used to ascertain a patient’s risk factors for inherited cardiovascular diseases. The panel includes all known genes currently associated with the development of inherited cardiovascular diseases that can present as sudden death or other major adverse events. Cardiac Genetic Testing can be ordered in disease-specific panels or in one comprehensive panel. In Home Self-Test. FDA Approved.
Check AvailabilityA neurological exam consists of a physical examination to identify signs of disorders affecting your brain, spinal cord and nerves (nervous system). Neurological examination is the best way for healthcare providers to check the function of your brain and nervous system. It helps them determine which tests to run. Every neurological exam is different depending on your symptoms. Sometimes, it can take time to complete the physical examination and the interview, as your nervous system is very complex. In Home Self-Test. FDA Approved.
Check AvailabilityAbout Safe Medical Screening
Safe Medical Screening and our partners, provide advanced hereditary risk assessments. Connecting patients and their Primary Care Physicians with CLIA certified testing laboratories, to help understand the results that impact you and your family.
Hereditary Risk Assessments – A Multi-Generational Approach to Medicine
Genetic testing can provide important medical insights about how your body metabolizes and reacts to different medications, as well as identifying predispositions to certain hereditary diseases (including cardiac related illnesses and cancer).
And since genetics are hereditary, these tests can also provide risk information for your family as well.
• We only contact your Primary Care Physician and ask them if the genetic test is medically necessary.
• Laboratories we are contracted with are Licensed and CLIA Certified
• Representatives are HIPAA Certified and Compliant
Welcome Message
Safe Medical Screening and our partners, provide advanced hereditary risk assessments and health solutions to both patients and providers across the United States. From connecting patients to a network of trusted physicians and certified testing laboratories, to understanding the results that impact you and your family, Safe Medical Screening is committed to providing affordable and accessible healthcare solutions.