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Back to Test Catalogue
Test ID: LEFLUN

Leflunomide Metabolite (Teriflunomide) LC-MS/MS, Serum

Test Overview

Clinical Utility

Leflunomide is rapidly and extensively metabolized to teriflunomide,which is the active form of the medication. Therapeutic monitoring of teriflunomide is important to ensure adequate dosage. It is recommended that women of childbearing potential who discontinue leflunomide therapy undergo the cholestyramine drug elimination procedure.This procedure includes verification that plasma levels of teriflunomide are less than 20 ng/mL by two separate tests at least 14 days apart.

Method

Liquid chromatography-tandem mass spectrometry (LC-MS/MS)

Result Included

Teriflunomide

Specimen

Specimen Type

Avoid gel separator tubes
Serum
Plasma (Na Heparin)
Plasma (Li Heparin)

Volume

Sample Volume

1.0 mL

Minimum Volume

0.5 mL

Specimen Comment

Avoid gel separator tubes.

Collection & Handling

Handling Information

Store and send cold or frozen.

Stability

Ambient Refrigerated Frozen
5 days 14 days 30 days

Rejection Criteria

Criteria Specification
Specimen Gel-separator tubes

Performance & Interpretation

Turnaround Time

10 days

Results

Name
Units
Reference Range
Conversion
  1. Leflunomide Metabolite
    ng/mL
    Therapeutic: See note
    Elimination: <20

    Comment

    Mean steady state plasma concentrations of teriflunomide from patients on daily dosages of 5, 10, or 25 mg of leflunomide were 8,800, 18,000 and 63,000 ng/mL, respectively.

Referral Location

Out-of-Country

Interface & Setup

HL7 Interface Codes

Order Code Result Name Result Codes Units
LEFLUN TERIFLUNOMIDE 38058 ng/mL

Test Version

Last Updated

2023-05-26