Paroxetine Quantitative, Serum or Plasma
0090786
 
Ordering Recommendation
Mnemonic
PAROXE SP
Methodology
Quantitative Liquid Chromatography-Tandem Mass Spectrometry
Performed
Varies
Reported
3-10 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
 
Collect
Plain red, lavender (EDTA), or pink (K2EDTA).  
Specimen Preparation
Separate serum or plasma from cells within 1 hours. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.4 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Separator tubes.  
Remarks
 
Stability
Ambient: 2 week; Refrigerated: 1 month; Frozen: 1 month  
Reference Interval
By report
Interpretive Data
Note
CPT Code(s)
80299
Components
Component Test Code*Component Chart Name
0090773Paroxetine Quantitative, Serum or Plasma
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, contact interface support at interface.support@aruplab.com.
Cross References
  • Paxil
Performed at National Medical Services (NMS)