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Duloxetine Quantitative, Serum or Plasma
2006473
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.
Submit With Order
ARUP Consult®
Disease Topics
Specimen Required
Patient Preparation
 
Collect
Plain red or lavender (EDTA) or pink (K2EDTA). 
Specimen Preparation
Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.4 mL) Requires light protection when submitted at Room Temperature. 
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


Note
CPT Code(s)
Components
Component Test Code*Component Chart NameLOINC
2006474Duloxetine Quantitative, Serum or Plasma46227-5
* 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)

Performed at National Medical Services (NMS)