Test Code FLUOX Fluoxetine, Serum
Reporting Name
Fluoxetine, SUseful For
Monitoring serum concentration of fluoxetine during therapy
Evaluating potential toxicity
Evaluating patient compliance
Method Name
Liquid Chromatography Tandem Mass Spectrometry (LC-MS/MS)
Performing Laboratory
Mayo Clinic Laboratories in RochesterSpecimen Type
Serum RedSpecimen Required
Collection Container/Tube: Red top (serum gel/SST are not acceptable)
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions:
1. Draw blood immediately before the next scheduled dose (trough).
2. Centrifuge and aliquot serum into plastic vial within 2 hours of collection.
Specimen Minimum Volume
0.5 mL
Specimen Stability Information
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Serum Red | Refrigerated (preferred) | 28 days | |
Frozen | 28 days | ||
Ambient | 72 hours |
Reject Due To
Gross hemolysis | OK |
Gross lipemia | OK |
Gross icterus | OK |
Reference Values
Fluoxetine + Norfluoxetine: 120-500 ng/mL
Day(s) Performed
Wednesday
CPT Code Information
80299
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
FLUOX | Fluoxetine, S | 78437-1 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
80228 | Fluoxetine, S | 74982-0 |
251 | Norfluoxetine, S | 3868-7 |
252 | Fluoxetine+Norfluoxetine | 74948-1 |
Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.Report Available
1 to 8 daysForms
If not ordering electronically, complete, print, and send a Therapeutics Test Request (T831) with the specimen.