Fentanyl Screen w/Reflex, Qualitative, Urine
Test Mnemonic
UFENTSRF
CPT Codes
- 80307 - QTY (1)
LOINC ®
59673-4
Performing Laboratory
Cleveland Clinic Laboratories
FDA Category
In Vitro Diagnostic
Specimen Requirements
| Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
|---|---|---|---|---|---|
| 3 mL | Urine Yellow No additive | Refrigerated |
Alternate Specimen Requirements
| Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
|---|---|---|---|---|---|
| 3 mL | Urine Yellow No additive |
Minimum Specimen Requirements
| Volume | Type | Container | Collect Temperature | Transport Temperature | Special Instructions |
|---|---|---|---|---|---|
| 3 mL |
Stability
| Environmental Condition | Description |
|---|---|
| Ambient | 4 weeks |
| Refrigerated | 4 weeks |
| Frozen | 6 months |
Days Performed
7 days a week
Turnaround Time
8 hours
Methodology
| Name | Description |
|---|---|
| Enzyme Immunoassay (EIA) |
Reference Range
Special Info
All non-negative results are sent for confirmation and billed. Please see the Urine Fentanyl and Metabolite results
Clinical Info
Evaluation of suspected acute overdose. This test should not be used for therapeutic drug or compliance monitoring; the quantitative pain panel, urine (UQNTPP) should be ordered instead.