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Duloxetine Quantitative, Serum or Plasma
2006473
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Ordering Recommendation
Mnemonic
DULOX SP
Methodology
Quantitative High Performance Liquid Chromatography-Tandem Mass Spectrometry
Performed
Varies
Reported
7-10 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
Collect
Plain Red, Lavender (K2EDTA), or Pink (K2EDTA).
Specimen Preparation
Separate from cells ASAP or within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.4 mL) Requires light protection when submitted at Room Temperature.
Test is not performed at ARUP; separate specimens must be submitted when multiple tests are ordered.
Storage/Transport Temperature
Refrigerated or frozen. Also acceptable: Room temperature (must be light protected).
Unacceptable Conditions
Separator tubes.
Remarks
Stability
Ambient: 1 month; Refrigerated: 1 month; Frozen: 1 year
Reference Interval
By Report
Interpretive Data
Compliance Category
Performed by non-ARUP Laboratory
Note
Hotline History
N/A
CPT Codes
80332 (Alt code: G0480)
Components
| Component Test Code* | Component Chart Name | LOINC |
|---|---|---|
| 2006474 | Duloxetine Quantitative, Serum or Plasma | 46227-5 |
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
- Cymbalta(R)
Duloxetine Quantitative, Serum or Plasma
National Medical Services (NMS)
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