Controlled Substance Risks in Medical Practice

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Understanding DEA Perils

[By Dr. Charles F. Fenton III; Esq]

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The Drug Enforcement Agency (DEA) controls the issuance of DEA numbers that permit the physician to prescribe controlled substances to their patients.

The use of controlled substances is important to almost all medical specialties. 

Family practitioners use codeine to treat coughs and surgeons use narcotics to manage pain. The spectrum-of-use is wide. 

The Dilemma 

Unfortunately, there will always be a rogue physician willing to sell narcotic prescriptions. These physicians cause the DEA to cast a jaundiced eye towards all physicians.  

However, the dilemma may be that there are simply too many stories of physicians who “over-use” controlled substances in a practice designed to ease the suffering of their patients; or not?

And, how do we differentiate among them all? 

Assessment 

The physician never knows when a patient coming into the office complaining of pain and asking for pain medication – whether that patient is truly in pain or not – is an undercover agent for the DEA.

Has it come to prescriber beware? 

Conclusion 

This peril and paranoia (combined with the risk of a malpractice claim of “hooking” the patient) causes some physicians to actually under prescribe pain medication. So, your thoughts on this ME-P are appreciated.

Speaker: If you need a moderator or speaker for an upcoming event, Dr. David E. Marcinko; MBA – Publisher-in-Chief of the Medical Executive-Post – is available for seminar or speaking engagements. Contact: MarcinkoAdvisors@msn.com

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One Response

  1. Real Time Drug Surveillance

    Did you know that health insurance companies are finally beginning to mine their patient data to look for drug safety red flags?

    It’s true! WellPoint Inc., in collaboration with the Food and Drug Administration [FDA], plans to launch one of the first real-time drug-surveillance systems. Starting early next year, the insurer will systematically scan the medical information of more than half of its 35 million members to look for hidden patterns or spikes in medical problems that might be linked to certain medication or combination of drugs; as reported in the Wall Street Journal [WSJ].

    Until now, the drug-safety monitoring system used by the FDA has been spotty, slow and passive, relying largely on harried doctors and drug companies to report problems they see crop up with patients, and capturing less than 10 percent of bad reactions.

    But, are there any other covert reasons for this economic altruism?
    Like, MIB [Medical Information Bureau] reportage, for example.

    Are there any comments on this life-saving, yet potentially inflammatory issue? Is there a potential for Protected Health Information [PHI] disclosure; despite HIPAA restrictions? Please opine?

    -James

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