Test Catalog

Test Id : FDA1S

Drugs of Abuse (10 panel) and Alcohol Screen, Serum

Reflex Tests
Lists tests that may or may not be performed, at an additional charge, depending on the result and interpretation of the initial tests.

Test Id Reporting Name Available Separately Always Performed
FAMCS Amphetamines Confirmation, S No No
FBBCS Barbiturates Confirmation, S No No
FBCS Benzodiazepines Confirmation, S No No
FCANS Cannabinoids Confirmation, S No No
FCMC Cocaine and Metabolites Confirm, S No No
FETCS Ethanol Confirmation, S No No
FMMCS Methadone and Metabolite Confirm, S No No
FOFU Opiates-Free Unconjugated Conf, S No No
FPCCS Phencyclidine Confirmation, S No No

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

If appropriate, confirmation testing will be performed at an additional charge.

Method Name
A short description of the method used to perform the test

Enzyme-Linked Immunosorbent Assay (ELISA)

Headspace Gas Chromatography (GC)

NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.

Yes

Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test

Drug of Abuse 10 and Alcohol Scrn,S

Aliases
Lists additional common names for a test, as an aid in searching

Ethanol

Opiates

Cocaine/Metabolites

Benzodiazepines

Cannabinoids

Amphetamines

Barbiturates

Methadone/Metabolite

Phencyclidine

Methamphetamine/MDMA

Oxycodone/Oxymorphone

Acid

Adderall

Amfetamine

Cannabis

Coke

Crack

Desoxyn

Dextroamphetamine

Ecstasy

Heroin

Levoamphetamine

Lysergide

Marijuana

Meth

Molly

THC

Tranquilizer

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

If appropriate, confirmation testing will be performed at an additional charge.

Specimen Type
Describes the specimen type validated for testing

Serum Red

Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing

Specimen Type: Serum

Container/Tube: Red top

Specimen Volume: 5 mL

Collection Instructions:  

Collect sample using alcohol free skin preparation. Draw blood in a plain, red-top tube(s), serum gel tube is not acceptable. Spin down and send 5 mL of serum refrigerated in a plastic, preservative-free vial.

Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory

2.25 mL

Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected

Hemolysis NA
Lipemia NA
Icterus NA
Other Polymer gel separation tube (SST or PST).

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
Serum Red Refrigerated (preferred) 7 days
Frozen 14 days

Testing Algorithm
Delineates situations when tests are added to the initial order. This includes reflex and additional tests.

If appropriate, confirmation testing will be performed at an additional charge.

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.

Reporting limit determined each analysis.

 

Test

Result

Units

Ethanol

None Detected

mg/dL

Opiates

None Detected

ng/mL

Cocaine/Metabolites

None Detected

ng/mL

Benzodiazepines

None Detected

ng/mL

Cannabinoids

None Detected

ng/mL

Amphetamines

None Detected

ng/mL

Barbiturates

None Detected

mcg/mL

Methadone/Metabolite

None Detected

ng/mL

Phencyclidine

None Detected

ng/mL

Methamphetamine/MDMA

None Detected

ng/mL

Oxycodone/Oxymorphone

None Detected

ng/mL

PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information

No

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 Sunday

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.

6 to 13 days

Performing Laboratory Location
Indicates the location of the laboratory that performs the test

NMS Labs

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 Regional Manager. 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 NMS Labs. It has not been cleared or approved by the U.S. 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.

80307x2

 

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
FDA1S Drug of Abuse 10 and Alcohol Scrn,S Not Provided
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.
Z5535 Ethanol 20470-1
Z5536 Opiates 8219-8
Z5537 Cocaine/Metabolites 73823-7
Z5538 Benzodiazepines 46976-7
Z5539 Cannabinoids 8172-9
Z5540 Amphetamines 8149-7
Z5541 Barbiturates 20421-4
Z5542 Methadone/Metabolite 59705-4
Z5543 Phencyclidine 8236-2
Z5544 Methamphetamine/MDMA 91034-9
Z5545 Oxycodone/Oxymorphone 77732-6

Test Setup Resources

Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel | Pdf

Sample Reports
Normal and Abnormal sample reports are provided as references for report appearance.

Normal Reports | Abnormal Reports

SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI Normal Reports | SI Abnormal Reports