Search form

Transportation Department Expands Drug Testing Panel to Include Certain ‘Semi-Synthetic’ Opioids

By Kathryn J. Russo
  • November 16, 2017

Employers regulated by the U.S. Department of Transportation (DOT) should revise their drug and alcohol testing policies to conform to new DOT regulations that added four “semi-synthetic” opioid drugs to the DOT drug testing panel. The new regulations go into effect on January 1, 2018.

DOT announced in a rule published in the Federal Register on November 13, 2017, that it will expand its drug testing panel to include the following four “semi-synthetic” opioid drugs:

  • Hydrocodone;
  • Hydromorphone;
  • Oxycodone; and
  • Oxymorphone.

DOT-regulated employers include those regulated by the Federal Motor Carrier Safety Administration (FMCSA), Federal Aviation Administration (FAA), Federal Railroad Administration (FRA), Federal Transit Administration (FTA), Pipeline and Hazardous Materials Safety Administration (PHMSA), and the United States Coast Guard (USCG).

The changes were made to harmonize DOT’s drug testing regulations with recent revisions to U.S. Department of Health and Human Services (HHS) Mandatory Guidelines for Federal Workplace Drug Testing Programs that took effect on October 1, 2017. The new DOT rule also includes other revisions to DOT drug and alcohol testing regulations.

Prescription Painkiller Epidemic

The addition of the four semi-synthetic opioid drugs is intended to address the nationwide epidemic of prescription painkiller abuse.

Hydrocodone, hydromorphone, oxycodone, and oxymorphone are Schedule II controlled substances. They are more commonly known as Vicodin, OxyContin, Lortab, Norco, Percocet, and Dilaudid, among other names. DOT still refers to its drug testing panel as a “5-panel,” but “opiates” is being changed to “opioids” and will include the four synthetic substances in addition to heroin, morphine, and codeine.

HHS had explained that the four prescription pain medications were added to the standard testing panel because data indicates that, although they are prescribed, they are the prescription pain medications that are most frequently used without medical authorization.

DOT regulations still permit an employee to produce a legitimate medical explanation for the presence of drugs in his or her system, but the Medical Review Officer (MRO) is not permitted to question whether the prescribing physician should have prescribed the substance.

In addition, DOT will add methylenedioxyamphetamine (MDA) as an initial test analyte, and remove methylenedioxyethylamphetamine (MDEA) as a confirmatory test analyte.

Drug Panel and Cut-Off Concentrations

As of January 1, 2018, all DOT-regulated employers must utilize the following drug test panel and cut-off concentrations:

Drug Initial Confirmatory
Marijuana 50 ng/ml 15 ng/ml
Cocaine 150 ng/ml 100 ng/ml
Phencyclidine (PCP) 25 ng/ml 25 ng/ml
Amphetamines (includes Methamphetamines, MDMA, MDA) 500 ng/ml 250 ng/ml
Opioids    
    Codeine/Morphine 2000 ng/ml 2000 ng/ml
    6-AM (Heroin) 10 ng/ml 10 ng/ml
Hydrocodone/Hydromorphone 300 ng/ml 300 ng/ml
Oxycodone/Oxymorphone 100 ng/ml 100 ng/ml

 

Other Revisions

DOT’s new rules also make certain technical amendments, clarify certain definitions, and remove the requirement for employers and Consortium/Third Party Administrators to submit blind specimens. Among other things, the definition of “drugs” has been revised to include “opioids” instead of “opiates,” and the definitions of “evidential breath testing device” and “alcohol screening device” have been revised.

The regulation addressing direct observation collections is revised to require service agents who learn that a direct observation collection should have been collected, but was not, to inform the employer to direct the employee to have an immediate recollection under direct observation. (Previously, this requirement applied only to collectors.)

The regulation addressing MRO verification of valid prescription medication use also is being revised as follows:

You [the MRO] must also advise the employee that, before informing any third party about any medication the employee is using pursuant to a legally valid prescription consistent with the Controlled Substances Act, you will allow 5 business days from the date you report the verified negative result for the employee to have the prescribing physician contact you to determine if the medication can be changed to one that does not make the employee medically unqualified or does not pose a significant safety risk. If, in your reasonable medical judgment, a medical qualification issue or a significant safety risk remains after you communicate with the employee’s prescribing physician or after 5 business days, whichever is shorter, you must follow §40.327. If, as the MRO, you receive information that eliminates the medical qualification issue or significant safety risk, you must transmit this information to any third party to whom you previously provided information under §40.327.

DOT will require Medical Review Officers, Substance Abuse Professionals, Breath Alcohol Technicians, and Screening Test Technicians to subscribe to the Office of Drug & Alcohol Policy & Compliance’s list-serve to receive ODAPC email updates.

DOT’s new regulations also confirm that no specimens, other than urine, may be tested for drugs. Only urine specimens screened and confirmed at HHS-certified laboratories are permitted; point-of-collection testing, or instant tests, are not authorized.

***

Jackson Lewis attorneys are available to assist employers in revising their drug and alcohol testing policies and practices to conform to the regulations.

©2017 Jackson Lewis P.C. This Update is provided for informational purposes only. It is not intended as legal advice nor does it create an attorney/client relationship between Jackson Lewis and any readers or recipients. Readers should consult counsel of their own choosing to discuss how these matters relate to their individual circumstances. Reproduction in whole or in part is prohibited without the express written consent of Jackson Lewis.

This Update may be considered attorney advertising in some states. Furthermore, prior results do not guarantee a similar outcome.

Jackson Lewis P.C. represents management exclusively in workplace law and related litigation. Our attorneys are available to assist employers in their compliance efforts and to represent employers in matters before state and federal courts and administrative agencies. For more information, please contact the attorney(s) listed or the Jackson Lewis attorney with whom you regularly work.

See AllRelated Articles You May Like

October 27, 2017

What Employers Need to Know about OSHA’s Respirable Crystalline Silica Rule for Construction

October 27, 2017

Full enforcement with the Occupational Safety and Health Administration’s new respirable crystalline silica rule in the construction industry began on October 23, 2017, according to the agency. The silica rule is one of the most comprehensive health standards ever issued for the construction industry and significantly reduces the... Read More

August 23, 2017

Mine Safety Agency Implements Medical Standards Action Plan for Inspectors, Technical Personnel

August 23, 2017

The Mine Safety and Health Administration will implement an action plan for employees who do not meet the agency’s medical standards.   As a condition of employment, MSHA inspectors and technical personnel must undergo periodic medical examinations, including vision and hearing tests, and meet medical standards set by the Office... Read More

August 23, 2017

OSHA Schedules Second Public Meeting on Voluntary Protection Programs

August 23, 2017

The Occupational Safety and Health Administration has scheduled the second of two meetings to “reshape” the Voluntary Protection Programs (VPP) for August 28, 2017. The first meeting was held on July 17, 2017. OSHA established the VPP on July 2, 1982, to promote cooperation between government, industry, and labor to improve worker... Read More

Related Practices