Test Id : CSMTU
Controlled Substance Monitoring Targeted Profile, 17 Drug Classes, Mass Spectrometry, Random, Urine
    
        Useful For
            
                
                
                    
                    Suggests clinical disorders or settings where the test may be helpful
                
            
    
    Detecting drug use involving stimulants, benzodiazepines, and opioids
This test is not intended for use in employment-related testing.
    
        Profile Information
            
                
                
                    
                    A profile is a group of laboratory tests that are ordered and performed together under a single Mayo Test ID. Profile information lists the test performed, inclusive of the test fee, when a profile is ordered and includes reporting names and individual availability.
                
            
    
    | Test Id | Reporting Name | Available Separately | Always Performed | 
|---|---|---|---|
| LPCM | List Patient's Current Medications | No | Yes | 
| ADULT | Adulterants Survey, U | Yes | Yes | 
| TOPSU | Targeted Opioid Screen, U | Yes, (order TOSU) | Yes | 
| TABSU | Targeted Benzodiazepine Screen, U | Yes, (order TBSU) | Yes | 
| TSTIM | Targeted Stimulant Screen, U | Yes, (order TSPU) | Yes | 
    
        Testing Algorithm
            
                
                
                    
                    Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
                
            
    
    Testing begins with an adulterant survey. If the sample is found to be adulterated, testing will end, and the remaining tests will be canceled.
If the specimen is normal or only diluted, testing will proceed.
    
        Method Name
            
                
                
                    
                    A short description of the method used to perform the test
                
            
    
    ADULT: Spectrophotometry
TOPSU, TABSU, TSTIM: Liquid Chromatography Tandem Mass Spectrometry, High-Resolution Accurate Mass (LC-MS/MS HRAM)
    
        NY State Available
            
                
                
                    
                    Indicates the status of NY State approval and if the test is orderable for NY State clients.
                
            
    
    
    
        Reporting Name
            
                
                
                    
                    Lists a shorter or abbreviated version of the Published Name for a test
                
            
    
    
    
        Aliases
            
                
                
                    
                    Lists additional common names for a test, as an aid in searching
                
            
    
    6-monoacetylmorphine (heroin metabolite)
7-Amino Flunitrazepam (Metabolite of Flunitrazepam (Rohypnol)
7-Aminoclonazepam
Adderall (Amphetamine)
ADHD
Adipex-P (Phentermine)
Adzenys ER (Amphetamine)
Alprazolam (Xanax)
Amobarbital (Amytal)
Amphetamines
Amytal (Amobarbital)
Angel Dust (Phencyclidine)
Ativan (Lorazepam)
Benzodiazepines
Benzoylecgonine (Cocaine Metabolite)
Buprenorphine (Buprenex, Suboxone)
Chlordiazepoxide (Librium)
Clonazepam
Clorazepate (Tranxene)
Codeine
Codeine (Tylenol #3)
Codeine-6-beta-glucuronide (codeine metabolite)
Compliance monitoring
Concerta (Methylphenidate)
Dalmane (Flurazepam)
Date Rape Drug (Rohypnol [Flunitrazepam])
Desalkyl Flurazepam (Metabolite)
Desoxyn (Methamphetamine)
Dexedrine (Amphetamine)
Diazepam (Valium)
Dihydrocodeine(hydrocodone metabolite)
Drug Screen
Drugs of Abuse
Dyanavel XR (Amphetamine)
Ecstasy
EDDP (Methadone metabolite)
Fentanyl (Actiq, Duragesic, Fentora)
Flunitrazepam (Rohypnol)
Flurazepam (Dalmane)
Halcion (Triazolam)
Heroin
Hydrocodone (Lortab, Norco, Vicodin)
Hydromorphone (Dilaudid, Exalgo)
Hydromorphone-3-beta-glucuronide (hydromorphone metabolite)
Hydroxy-Ethyl Flurazepam (Metabolite of Flurazepam) (Dalmane)
Killer Weed (Phencyclidine)
Librium (Chlordiazepoxide)
Lomaira (Phentermine)
Lorazepam (Ativan)
MDA (Methylenedioxyamphetamine) Metabolite for Methylenedioxyethylamphetamine (MDEA) and Methylenedioxymethamphetamine (MDMA)
MDMA (Methylenedioxymethamphetamine)
Meperidine (Demerol)
Methadone (Dolophine)
Methadone metabolite (EDDP)
Methamphetamines (Desoxyn)
Methylenedioxyamphetamine (MDA) Metabolite for Methylenedioxyethylamphetamine (MDEA) and Methylenedioxymethamphetamine (MDMA)
Methylenedioxymethamphetamine (MDMA)
Morphine (Avinza, Kadian, MS Contin)
Morphine-6-beta-glucuronide (morphine metabolite
N-desmethyltapentadol (Tapentadol metabolite)
Naloxone (Narcan)
Naloxone-3-beta-glucuronide (Naloxone metabolite)
Norbuprenorphine (Buprenorphine metabolite)
Norbuprenorphine glucuronide (Buprenorphine metabolite)
Nordiazepam (Tranxene)
Norfentanyl (fentanyl metabolite)
Norhydrocodone (hydrocodone metabolite)
Normeperidine (Meperidine metabolite)
Noroxycodone (oxycodone metabolite)
Noroxymorphone (Oxymorphone metabolite)
Norpropoxyphene (propoxyphene metabolite)
O-desmethyltramadol (Tramadol metabolite)
Opiates
Opioid
Oxazepam (Serax)
Oxycodone (Endocet, Percocet, Oxycontin)
Oxymorphone (Numorphan, Opana)
Oxymorphone-3-beta-glucuronide (Oxymorphone metabolite)
Pain Management
PCP (Phencyclidine)
Phencyclidine (PCP)
Propoxyphene (Darvon, Darvocet)
Qsymia (Phentermine)
Restoril (Temazepam)
Ritalin (Methylphenidate)
Rocket Fuel (Phencyclidine)
Rohypnol (Flunitrazepam)
Serax (Oxazepam)
Speed (Amphetamines)
Sudafed (Pseudoephedrine)
Super Weed
Tapendtadol-beta-glucuronide (Tapentadol metabolite)
Tapentadol (Nucynta)
TCP (Phencyclidine)
Temazepam (Restoril)
Toxicology Screen, Drugs
Tramadol (Tradol, Ultram, Ultracet)
Tranxene (Clorazepate)
Triazolam (Halcion)
UDS
Valium (Diazepam)
Vicodin (Hydrocodone)
Vyvanse (Amphetamine)
Xanax (Alprazolam)
    
        Testing Algorithm
            
                
                
                    
                    Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
                
            
    
    Testing begins with an adulterant survey. If the sample is found to be adulterated, testing will end, and the remaining tests will be canceled.
If the specimen is normal or only diluted, testing will proceed.
    
        Specimen Type
            
                
                
                    
                    Describes the specimen type validated for testing
                
            
    
        Urine
    
        Ordering Guidance
    
    This test does not screen for drug classes other than those listed in Reference Values.
    
        ORDER QUESTIONS AND ANSWERS
    
    | Question ID | Description | Answers | 
|---|---|---|
| LPCM | List patient's current medications | 
    
        Specimen Required
            
                
                
                    
                    Defines the optimal specimen required to perform the test and the preferred volume to complete testing
                
            
    
    Supplies: Urine Tubes, 10 mL (T068)
Collection Container/Tube: Plastic urine container
Submission Container/Tube: Plastic, 10 mL tube
Specimen Volume: 5 mL
Collection Instructions:
1. Collect a random urine specimen.
2. Submit 5 mL in 1 plastic bottle.
3. No preservative
Additional Information:
1. No specimen substitutions.
2. Submitting less than 5 mL may compromise the ability to perform all necessary testing.
3. STAT requests are not accepted for this test.
    
        Special Instructions
            
                
                
                    
                    Library of PDFs including pertinent information and forms related to the test
                
            
    
    
            
    
        Forms
    
    If not ordering electronically, complete, print, and send a Therapeutics Test Request (T831) with the specimen.
    
        Specimen Minimum Volume
            
                
                
                    
                    Defines the amount of sample necessary to provide a clinically relevant result as determined by the testing laboratory. The minimum volume is sufficient for one attempt at testing.
                
            
    
    2 mL
    
        Reject Due To
            
                
                
                    
                    Identifies specimen types and conditions that may cause the specimen to be rejected
                
            
    
    
    
        Specimen Stability Information
            
                
                
                    
                    Provides a description of the temperatures required to transport a specimen to the performing laboratory, alternate acceptable temperatures are also included
                
            
    
    | Specimen Type | Temperature | Time | Special Container | 
|---|---|---|---|
| Urine | Refrigerated (preferred) | 14 days | |
| Frozen | 14 days | 
    
        Useful For
            
                
                
                    
                    Suggests clinical disorders or settings where the test may be helpful
                
            
    
    Detecting drug use involving stimulants, benzodiazepines, and opioids
This test is not intended for use in employment-related testing.
    
        Testing Algorithm
            
                
                
                    
                    Delineates situations when tests are added to the initial order. This includes reflex and additional tests.
                
            
    
    Testing begins with an adulterant survey. If the sample is found to be adulterated, testing will end, and the remaining tests will be canceled.
If the specimen is normal or only diluted, testing will proceed.
    
        Clinical Information
            
                
                
                    
                    Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test
                
            
    
    The targeted opioid, benzodiazepine, and stimulant screen portions are performed by liquid chromatography tandem mass spectrometry, high-resolution accurate mass (LC-MS/MS HRAM) and are completed for all opioids, benzodiazepines, and stimulants.
Opioids are a large class of medications commonly used to relieve acute and chronic pain or help manage opioid abuse and dependence. Medications that fall into this class include buprenorphine, codeine, fentanyl, hydrocodone, hydromorphone, methadone, morphine, oxycodone, oxymorphone, tapentadol, tramadol, and others. Opioids work by binding to the opioid receptors that are found in the brain, spinal cord, gastrointestinal tract, and other organs. Common side effects of opioids include drowsiness, confusion, nausea, constipation, and, in severe cases, respiratory depression. These are dose dependant and vary with tolerance. These medications can also produce physical and psychological dependence and have a high risk for abuse and diversion, which is one of the main reasons many professional practice guidelines recommend compliance testing in patients prescribed these medications.
 
Opioids are readily absorbed from the gastrointestinal tract, nasal mucosa, lungs, and after subcutaneous or intermuscular injection. Opioids are primarily excreted from the kidney in both free and conjugated forms. This assay does not hydrolyze the urine sample and looks for both parent drugs and metabolites (including glucuronide forms). The detection window for most opioids in urine is approximately 1 to 3 days with longer detection times for some compounds (eg, methadone).
 
Benzodiazepines represent a large family of medications used to treat a wide range of disorders from anxiety to seizures and are also used in pain management. With a high risk for abuse and diversion, professional practice guidelines recommend compliance monitoring for these medications using urine drug tests. However, traditional benzodiazepine immunoassays suffer from a lack of cross-reactivity with all the benzodiazepines, so many compliant patients taking either clonazepam (Klonopin) or lorazepam (Ativan) may screen negative by immunoassay but are positive when confirmatory testing is done. The new targeted benzodiazepine screening test provides a more sensitive and specific test to check for compliance to all the commonly prescribed benzodiazepines and looks for both parent drug and metabolites in the urine.
 
Stimulants are sympathomimetic amines that stimulate the central nervous system activity and, in part, suppress the appetite. Amphetamine and methamphetamine are also prescription drugs used in the treatment of narcolepsy and attention-deficit disorder/attention-deficit hyperactivity disorder (ADHD). Methylphenidate is another stimulant used to treat ADHD. Phentermine is indicated for the management of obesity. All other amphetamines (eg, methylenedioxymethamphetamine: MDMA) are Drug Enforcement Administration-scheduled Class I compounds. Due to their stimulant effects, the drugs are commonly sold illicitly and abused. Physiological symptoms associated with very high amounts of ingested amphetamine or methamphetamine include elevated blood pressure, dilated pupils, hyperthermia, convulsions, and acute amphetamine psychosis.
 
This test is intended to be used in a setting where the test results can be used to make a definitive diagnosis.
    
        Reference Values
            
                
                
                    
                    Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.
                
            
    
    ADULTERANT SURVEY:
Cutoff concentrations
Oxidants: 200 mg/L
Nitrites: 500 mg/L
 
TARGETED OPIOID SCREEN:
Not detected (Positive results are reported with qualitative "Present" results)
 
Cutoff concentrations:
Codeine: 25 ng/mL
Codeine-6-beta-glucuronide: 100 ng/mL
Morphine: 25 ng/mL
Morphine-6-beta-glucuronide: 100 ng/mL
6-Monoacetylmorphine: 25 ng/mL
Hydrocodone: 25 ng/mL
Norhydrocodone: 25 ng/mL
Dihydrocodeine: 25 ng/mL
Hydromorphone: 25 ng/mL
Hydromorphone-3-beta-glucuronide: 100 ng/mL
Oxycodone: 25 ng/mL
Noroxycodone: 25 ng/mL
Oxymorphone: 25 ng/mL
Oxymorphone-3-beta-glucuronide: 100 ng/mL
Noroxymorphone: 25 ng/mL
Fentanyl: 2 ng/mL
Norfentanyl: 2 ng/mL
Meperidine: 25 ng/mL
Normeperidine: 25 ng/mL
Naloxone: 25 ng/mL
Naloxone-3-beta-glucuronide: 100 ng/mL
Methadone: 25 ng/mL
2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP): 25 ng/mL
Propoxyphene: 25 ng/mL
Norpropoxyphene: 25 ng/mL
Tramadol: 25 ng/mL
O-desmethyltramadol: 25 ng/mL
Tapentadol: 25 ng/mL
N-desmethyltapentadol: 50 ng/mL
Tapentadol-beta-glucuronide: 100 ng/mL
Buprenorphine: 5 ng/mL
Norbuprenorphine: 5 ng/mL
Norbuprenorphine glucuronide: 20 ng/mL
 
TARGETED BENZODIAZEPINE SCREEN:
Not detected (Positive results are reported with qualitative "Present" results)
 
Cutoff concentrations:
Alprazolam: 10 ng/mL
Alpha-hydroxyalprazolam: 10 ng/mL
Alpha-hydroxyalprazolam glucuronide: 50 ng/mL
Chlordiazepoxide: 10 ng/mL
Clobazam: 10 ng/mL
N-desmethylclobazam: 200 ng/mL
Clonazepam: 10 ng/mL
7-Aminoclonazepam: 10 ng/mL
Diazepam: 10 ng/mL
Nordiazepam: 10 ng/mL
Flunitrazepam: 10 ng/mL
7-Aminoflunitrazepam: 10 ng/mL
Flurazepam: 10 ng/mL
2-Hydroxy ethyl flurazepam: 10 ng/mL
Lorazepam: 10 ng/mL
Lorazepam glucuronide: 50 ng/mL
Midazolam: 10 ng/mL
Alpha-hydroxymidazolam: 10 ng/mL
Oxazepam: 10 ng/mL
Oxazepam glucuronide: 50 ng/mL
Prazepam: 10 ng/mL
Temazepam: 10 ng/mL
Temazepam glucuronide: 50 ng/mL
Triazolam: 10 ng/mL
Alpha-hydroxytriazolam: 10 ng/mL
Zolpidem: 10 ng/mL
Zolpidem phenyl-4-carboxylic acid: 10 ng/mL
 
TARGETED STIMULANT SCREEN:
Not detected (Positive results are reported with qualitative "Present" results)
 
Cutoff concentrations:
Methamphetamine: 100 ng/mL
Amphetamine: 100 ng/mL
3,4-Methylenedioxymethamphetamine (MDMA): 100 ng/mL
3,4-Methylenedioxy-N-ethylamphetamine (MDEA): 100 ng/mL
3,4-Methylenedioxyamphetamine (MDA): 100 ng/mL
Ephedrine: 100 ng/mL
Pseudoephedrine: 100 ng/mL
Phentermine: 100 ng/mL
Phencyclidine (PCP): 20 ng/mL
Methylphenidate: 20 ng/mL
Ritalinic acid: 100 ng/mL
    
        Interpretation
            
                
                
                    
                    Provides information to assist in interpretation of the test results
                
            
    
    A positive result derived by this testing indicates that the patient has used one of the drugs detected by these techniques in the recent past.
For information about drug testing, including estimated detection times and Result Interpretations, see Controlled Substance Monitoring on MayoClinicLabs.com.
    
        Cautions
            
                
                
                    
                    Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances
                
            
    
    No significant cautionary statements
    
        Clinical Reference
            
                
                
                    
                    Recommendations for in-depth reading of a clinical nature
                
            
    
    1. Physicians' Desk Reference: 60th ed. Medical Economics Company; 2006
2. Bruntman LL Lazo JS, Parker KL, eds. Goodman and Gilman's: The Pharmacological Basis of Therapeutics. 11th ed. McGraw-Hill Book Company; 2006
3. Langman LJ, Bechtel LK, Holstege CP. Clinical toxicology. In: Rifai N, Chiu RWK, Young I, Burnham CAD, Wittwer CT, eds. Tietz Textbook of Laboratory Medicine. 7th ed. Elsevier; 2023:chap 43
4. Gutstein HB, Akil H: Opioid analgesics. In: Brunton LL, Lazo JS, Parker KL, eds. Goodman and Gilman's: The Pharmacological Basis of Therapeutics. 11th ed. McGraw-Hill Companies; 2006:chap 21
5. Rovine T, Ferrero CL, American Pain Society: Chronic Pain in America: Roadblocks to Relief. Roper Starch Worldwide, Inc; 1999. Updated 2001. Accessed December 12, 2024. Available at http://accurateclinic.com/wp-content/uploads/2016/04/Chronic-Pain-In-America-Roadblocks-To-Relief-1999.pdf
6. Magnani B, Kwong T. Urine drug testing for pain management. Clin Lab Med. 2012;32(3):379-390
7. Jannetto PJ, Bratanow NC, Clark WA, et al. Executive summary: American Association of Clinical Chemistry Laboratory Medicine Practice Guideline-using clinical laboratory tests to monitor drug therapy in pain management patients. J Appl Lab Med. 2018;2(4):489-526
8. McMillin GA, Marin SJ, Johnson-Davis KL, Lawlor BG, Strathmann FG. A hybrid approach to urine drug testing using high-resolution mass spectrometry and select immunoassays. Am J Clin Pathol. 2015;143(2):234-240
9. Cone EJ, Caplan YH, Black DL, Robert T, Moser F. Urine drug testing of chronic pain patients: licit and illicit drug patterns. J Anal Toxicol. 2008;32(8):530-543
    
        Method Description
            
                
                
                    
                    Describes how the test is performed and provides a method-specific reference
                
            
    
    Adulterant:
All results are measured using spectrophotometry at wavelengths specified by the reagent manufacturer. The use of a refractometer may also be used in the specific gravity measurement.(Package inserts: Specimen Validity Test Creatinine. Roche Diagnostics; V3.0, 08/2015; Specimen Validity Test Nitrite. Roche Diagnostics; V3.0, 08/2018, Specimen Validity Test Oxidant. Roche Diagnostics; V 3.0, 08/2018; Specimen Validity Test pH Roche Diagnostics; V3.0, 02/2019, Specimen Validity Test Specific Gravity. Roche Diagnostics; V4.0, 08/2022)
 
Targeted Screening Panels for opioids, benzodiazepines, and stimulants:
The urine sample is diluted with internal standard and clinical laboratory reagent water and then analyzed by liquid chromatography tandem mass spectrometry using a high-resolution accurate mass orbitrap detector.(Unpublished Mayo method)
    
        PDF Report
            
                
                
                    
                    Indicates whether the report includes an additional document with charts, images or other enriched information
                
            
    
    
    
        Day(s) Performed
            
                
                
                    
                    Outlines the days the test is performed. This field reflects the day that the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time before the test is performed. Some tests are listed as continuously performed, which means that assays are performed multiple times during the day.
                
            
    
    Monday through Saturday
    
        Report Available
            
                
                
                    
                    The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.
                
            
    
    
    
        Performing Laboratory Location
            
                
                
                    
                    Indicates the location of the laboratory that performs the test
                
            
    
    
    
        Fees :
            
                
                
                    
                    Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
                
            
    
    - Authorized users can sign in to Test Prices for detailed fee information.
- Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their account representative. For assistance, contact Customer Service.
    
        Test Classification
            
                
                
                    
                    Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.
                
            
    
    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.
    
        CPT Code Information
            
                
                
                    
                    Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CPT codes are provided by the performing laboratory.
                
            
    
    CPT codes are provided by the performing laboratory.
G0482
80347 (if appropriate for select payers)
80364 (if appropriate for select payers)
80326 (if appropriate for select payers)
    
        LOINC® Information
            
                
                
                    
                    Provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.
                
            
    
    | Test Id | Test Order Name | Order LOINC Value | 
|---|---|---|
| CSMTU | CSM Targeted Drug Profile,17,HRMS,U | 69739-1 | 
| Result Id | Test Result Name | Result LOINC Value 
                                        
                                        Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
                                     | 
|---|---|---|
| 20606 | Creatinine, U | 2161-8 | 
| 22312 | Specific Gravity | In Process | 
| 23509 | pH | 2756-5 | 
| 23511 | Oxidants | 58714-7 | 
| 23510 | Nitrites | 32710-6 | 
| 30914 | Comment | 48767-8 | 
| 42323 | Codeine | 19411-8 | 
| 42324 | Codeine-6-beta-glucuronide | 89310-7 | 
| 42325 | Morphine | 19597-4 | 
| 42326 | Morphine-6-beta-glucuronide | 89308-1 | 
| 42327 | 6-monoacetylmorphine | 19321-9 | 
| 42328 | Hydrocodone | 19482-9 | 
| 42329 | Norhydrocodone | 89304-0 | 
| 42330 | Dihydrocodeine | 19446-4 | 
| 42331 | Hydromorphone | 19486-0 | 
| 42332 | Hydromorphone-3-beta-glucuronide | 89309-9 | 
| 42333 | Oxycodone | 19642-8 | 
| 42334 | Noroxycodone | 89303-2 | 
| 42335 | Oxymorphone | 19646-9 | 
| 42336 | Oxymorphone-3-beta-glucuronide | 89301-6 | 
| 42337 | Noroxymorphone | 89302-4 | 
| 42338 | Fentanyl | 59673-4 | 
| 42339 | Norfentanyl | 43199-9 | 
| 42340 | Meperidine | 19532-1 | 
| 42341 | Normeperidine | 27920-8 | 
| 42342 | Naloxone | 42618-9 | 
| 42343 | Naloxone-3-beta-glucuronide | 89307-3 | 
| 42344 | Methadone | 19550-3 | 
| 42345 | EDDP | 93495-0 | 
| 42346 | Propoxyphene | 19429-0 | 
| 42347 | Norpropoxyphene | 19632-9 | 
| 42348 | Tramadol | 19710-3 | 
| 42349 | O-desmethyltramadol | 86453-8 | 
| 42350 | Tapentadol | 72485-6 | 
| 42351 | N-desmethyltapentadol | 89306-5 | 
| 42352 | Tapentadol-beta-glucuronide | 89300-8 | 
| 42353 | Buprenorphine | 93494-3 | 
| 42354 | Norbuprenorphine | 82371-6 | 
| 42355 | Norbuprenorphine glucuronide | 89305-7 | 
| 65059 | Opioid Interpretation | 69050-3 | 
| 604871 | Alprazolam | 94116-1 | 
| 604867 | Alpha-Hydroxyalprazolam | 19325-0 | 
| 604891 | Alpha-Hydroxyalprazolam Glucuronide | 94115-3 | 
| 604872 | Chlordiazepoxide | 19385-4 | 
| 604889 | Clobazam | 94114-6 | 
| 604890 | N-Desmethylclobazam | 94113-8 | 
| 604873 | Clonazepam | 19399-5 | 
| 604267 | 7-aminoclonazepam | 94112-0 | 
| 604874 | Diazepam | 19443-1 | 
| 604880 | Nordiazepam | 19624-6 | 
| 604875 | Flunitrazepam | 19466-2 | 
| 604866 | 7-aminoflunitrazepam | 94111-2 | 
| 604876 | Flurazepam | 19474-6 | 
| 604868 | 2-Hydroxy Ethyl Flurazepam | 94110-4 | 
| 604877 | Lorazepam | 19520-6 | 
| 604878 | Lorazepam Glucuronide | 94109-6 | 
| 604879 | Midazolam | 19585-9 | 
| 604869 | Alpha-Hydroxy Midazolam | 94108-8 | 
| 604881 | Oxazepam | 19638-6 | 
| 604882 | Oxazepam Glucuronide | 94107-0 | 
| 604883 | Prazepam | 19678-2 | 
| 604884 | Temazepam | 19698-0 | 
| 604885 | Temazepam Glucuronide | 94106-2 | 
| 604886 | Triazolam | 19714-5 | 
| 604870 | Alpha-Hydroxy Triazolam | 94105-4 | 
| 604887 | Zolpidem | 94104-7 | 
| 604888 | Zolpidem Phenyl-4-Carboxylic acid | 94103-9 | 
| 604949 | Benzodiazepine Interpretation | 69050-3 | 
| LPCM | List Patient's Current Medications | 66423-5 | 
| 610273 | Methamphetamine | 19554-5 | 
| 610274 | Amphetamine | 19343-3 | 
| 610275 | 3,4-methylenedioxymethamphetamine (MDMA) | 19568-5 | 
| 610276 | 3,4-methylenedioxy-N-ethylamphetamine (MDEA) | 59844-1 | 
| 610277 | 3,4-methylenedioxyamphetamine (MDA) | 19565-1 | 
| 610278 | Ephedrine | 99108-3 | 
| 610279 | Pseudoephedrine | 99109-1 | 
| 610280 | Phentermine | 19674-1 | 
| 610281 | Phencyclidine (PCP) | 19659-2 | 
| 610282 | Methylphenidate | 19577-6 | 
| 610283 | Ritalinic acid | 99110-9 | 
| 610284 | Stimulant Interpretation | 54247-2 |