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Back to Test Catalogue
Test ID: FMIRT

Mirtazapine (Remeron), Serum/Plasma

Test Overview

Method

High performance liquid chromatography-fluorescence detection (HPLC-FID)

Result Included

Mirtazapine

Aliases/Synonyms

Remeron

Specimen

Specimen Type

Avoid gel separator tubes Serum (Preferred)
Plasma (Acceptable)

Containers

Preferred Containers

Red top (no additive)

Acceptable Containers

Green top (Sodium heparin)

Volume

Sample Volume

2 mL

Minimum Volume

0.3 mL

Specimen Comment

Avoid gel separator tubes.

Collection & Handling

Handling Information

Store and send cold or frozen.

Stability

Ambient Refrigerated Frozen
72 hours 14 days 180 days

Rejection Criteria

Criteria Specification
Specimen Gel-separator tubes

Performance & Interpretation

Turnaround Time

11 days

Results

Name
Units
Reference Range
Conversion
  1. Mirtazapine
    ng/mL
    4.0 - 40.0

    Comment

    Expected steady state trough mirtazapine concentrations in patients receiving recommended daily dosages: 4.0-40.0 ng/mL
    Toxic range not established
    Test performed at: Medtox Laboratories Inc., 402 W. County Road D, St. Paul, MN 55112

Referral Location

Out-of-Country

Interface & Setup

HL7 Interface Codes

Order Code Result Name Result Codes Units
FMIRT Mirtazapine 64814 ng/mL

Test Version

Last Updated

2023-03-23