Quetiapine, Serum or Plasma
2003118
 
Ordering Recommendation
Mnemonic
QUETIAP
Methodology
Quantitative Liquid Chromatography-Tandem Mass Spectrometry
Performed
Tue, Fri
Reported
1-5 days
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
 
Collect
Plain red. Also acceptable: Lavender (K2 or K3EDTA) or pink (K2 EDTA).  
Specimen Preparation
Separate serum or plasma from cells within 2 hours of collection. Transfer 1 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.5 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
Whole blood. Gel separator tubes, light blue (citrate), or yellow (SPS or ACD solution).  
Remarks
 
Stability
Ambient: 1 week; Refrigerated: 1 month; Frozen: 1 month  
Reference Interval
Interpretive Data
The following therapeutic ranges and toxic values have been suggested but have not been validated.
Adverse effects may include somnolence, dizziness, fatigue, constipation, weight gain.

See Compliance Statement B: www.aruplab.com/CS
Predose Draw (Trough) -​ Preferred
Therapeutic range 70-​170 ng/mL
Toxic: Greater than 1000 ng/mL

Peak Draw (1.5 hour post dose) -​ Not recommended
Therapeutic range 100-​1000 ng/mL
Toxic: Greater than 1500 ng/mL
Note
CPT Code(s)
80299
Components
Component Test Code*Component Chart Name
2003119Quetiapine, Serum/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
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