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Tempus (Pharacogenetic Testing)

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Tempus (Pharacogenetic Testing) explained

Tempus (Pharacogenetic Testing) evaluates genetic variants that may influence how you metabolize or respond to certain psychiatric medications.

Some panels have FDA‑cleared components; overall offering typically LDT under CLIA

Tempus (Pharacogenetic Testing) helps treat

• Pharmacogenetic guidance for medication selection
• Metabolism (CYP450) and transport variants
• Side‑effect risk discussions

additional medications

• Related clinical evaluation and history
• Repeat testing to confirm abnormal results
• Additional targeted labs as recommended

medication risks

• Genetic privacy and potential insurance/employment implications
• Limited clinical actionability for some markers

side effects

• Emotional impact of unexpected findings

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FAQs

Q: Does it replace clinical judgment?
A: No—results supplement, not replace, clinician decision‑making.

Q: Guaranteed to improve outcomes?
A: No—evidence varies by drug/gene; utility depends on case.

Q: Privacy/insurance?
A: Genetic data has implications; review policies and GINA protections.

Q: Sample?
A: Usually cheek swab/saliva.

Q: Turnaround?
A: Typically 1–3 weeks.

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