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Home Politics & Law

The DEA’s Long Game

Daily Remedy by Daily Remedy
January 25, 2022
in Politics & Law
6

The canary in the coal mine is a metaphor alluding to the initial sign of an impending calamity.

An apt metaphor for what just transpired. Recently, the Drug Enforcement Agency (DEA) issued a public safety alert informing the public about a, “sharp increase in fake prescription pills containing Fentanyl and Meth[amphetamines]”.

The alert was the canary in the coal mine, but the impending calamity is not what we are led to believe. We knew of a rise in counterfeit prescription pills for many years. It was a rise induced directly by DEA policies inflicted upon patients.

The impending calamity is not the risks counterfeit pills pose to the public, but the legal liability the DEA faces for its failed policies.

For years, federal agencies and physician advocacy groups remained in lockstep on the causes of the opioid epidemic. Lax prescription guidelines, overprescribing by willing physicians, and the addictive nature of opioids – we heard it all.

Unfortunately, these purported causes proved erroneous at best or deliberately misrepresented at worst. And implementation of policies based on these purported causes led to a rise in suicide and clinical stigmatization among chronic pain patients and patients with substance use dependencies.

This is an atrocity the DEA bears direct responsibility for.

The DEA orchestrated a culture of fear that can be described as medical McCarthyism, in which the fear of prosecution defined the quality of care for stigmatized patients. Accusations formed the basis of convictions as we saw physicians imprisoned for providing care and patients abruptly abandoned without legal recourse.

That is until now.

The American Medical Association (AMA) recently issued a report through its newly formed Substance Use and Pain Care Task Force recommending significant policy changes it believes would more effectively address the nation’s opioid epidemic. Stopping short of outright criticizing the DEA, the report proposes policy recommendations that diametrically oppose the DEA’s approach to the epidemic.

The report is simply the latest in a long line of published studies casting doubt on long held assumptions about the opioid epidemic. We know there is no correlation between opioid-related mortality and the number of opioid prescriptions. We know abruptly discontinuing opioids leads to adverse patient outcomes. And we know forcing physicians to reduce the number of opioid prescriptions leads to a rise in counterfeit prescription opioids.

All of which makes the public health alert by the DEA even more curious.

It is absurd to believe the DEA is not aware of the clinical consequences of its failed policies. And to issue a public health alert without acknowledging the basis for such an alert is deliberately deceptive – disrespecting the lives of patients lost through these policies and conveying a lack of accountability on the part of the DEA.

But lacking accountability is different from lacking awareness. The DEA is clearly aware that its aggressive approach to criminalizing the patient encounter has led to a rise in counterfeit prescription medications and adverse patient outcomes.

In Kentucky, a federal judge deemed a pain management practice liable for the suicide of a patient unable to receive adequate pain relief, who then committed suicide as a result of the untreated pain. The judge ruled that the physicians were liable for the suicide because they inappropriately reduced the patient’s opioid prescription dosage.

A ruling that implies patients have a right to be treated for pain, which when applied broadly to all chronic pain patients would hold the DEA liable for undue harms caused to patients based on its aggressive stance on opioid prescriptions.

Something the DEA is well aware of, but seems bent on assuming no accountability for, hoping the failed policies are seen as well-intentioned errors.

But in recently uncovered reports obtained through multiple FOIA (Freedom of Information Act) requests, it appears the DEA’s aggressive stance extends beyond erroneous policies and the unintended specter of clinical fear – to something far more nefarious, far more deliberate.

For years the DEA colluded with major insurance companies to obtain data on prescribing practices for physicians who treated patients in pain with prescription opioids, contracting covert, third-party data-mining companies to troll medical records without the consent of patients or the knowledge of physicians.

In 2016, these data-mining companies modified the data analysis, changing the definition of a high risk opioid prescriber to encompass a majority of physicians who prescribed opioids. The adjustment was a blatant attempt to coordinate and expedite the indictment of physicians, and to strengthen the likelihood of convictions.

It should come as no surprise that this is when we began to see a rise in physician imprisonments and a rise in counterfeit opioids. Both of which are a direct consequence of deliberately misrepresenting the trolled medical data.

Now, years later, lacking the support of physician advocacy groups, or the protection of public perception, the DEA finds itself confronting the ugly reality of its failed policies – and the ensuing liability.

But liability comes in different forms. Liability can be characterized as a harmless mistake or as a deliberate misrepresentation. The behavior of the DEA elucidated through the FOIA documents would suggest the latter.

Yet the public health alert provides a convenient rebuttal. A plausible excuse for the DEA to claim its failed policies were an honest mistake. The DEA can now say that when it realized its policies were leading to a rise in counterfeit opioid prescriptions, it issued a public health alert, suggesting the adverse clinical outcomes – the suicides and stigmatizations – were nothing more than an unintended consequence, an honest mistake.

For the DEA to issue a public health alert for a crisis that began years ago through its own policies is certainly a curious course of action – something we rarely see from federal agencies.

But a broader analysis reveals that the timing of the alert is less curious and more strategic. A canary in the coal mine – for the impending liability the DEA will soon face.

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Daily Remedy

Dr. Jay K Joshi serves as the editor-in-chief of Daily Remedy. He is a serial entrepreneur and sought after thought-leader for matters related to healthcare innovation and medical jurisprudence. He has published articles on a variety of healthcare topics in both peer-reviewed journals and trade publications. His legal writings include amicus curiae briefs prepared for prominent federal healthcare cases.

Comments 6

  1. Pingback: » When the DEA prefer OPINIONS over FACTS when filing charges violating the CONTROLLED SUBSTANCE ACT PHARMACIST STEVE
  2. Keith S. says:
    4 years ago

    This is a very poignant account of an unfortunate chapter of the crisis – misplaced aggression against a terrible problem creating more problems. Our government well meaning at times and very powerful unfortunately is not always wise in its use of that power. I am grateful for the free press and people having the courage to speak out against the injustice. Silence to injustice is a threat to justice everywhere. Thank you for accurate reporting!

    Reply
  3. David Acevedo says:
    4 years ago

    “…hoping the failed policies are seen as well-intentioned policy errors.”
    Thank you. This describes the desperation of the many anti-opiate zealots.

    Reply
  4. Brian Lynch says:
    2 years ago

    Another excellent, well written post.

    I think it’s been over a year since the Chicago DEA office made that announcement about counterfeit pills. I’ve been aware of it for years as you say..

    Reply
  5. Stuart says:
    2 years ago

    I strongly believe there never was any degree of “well intentions” on behalf of the CDC, DEA, & DOJ relative to their Gestapo-like infractions on literally millions of innocent Americans, pain physicians, and military veterans. Otherwise, at least one of the previously-mentioned governmental entities would have reacted long ago to the abundance of inarguable clinical evidence that clearly proves otherwise.

    The bottom line is that all of the government’s (unsupportable, yet highly) purported causes of the Opioid Crisis were (from the very beginning) knowingly erroneous, or more likely intentionally misrepresented (and quite often exaggerated) by the CDC, DEA, & DOJ. in collusion to make it appear as if that they were actually doing something (anything) to minimize the now ever-expanding (primarily due to their failed policies) Opioid Crisis.

    ‘Unfortunately, this is merely one of the numerous human rights violations these out-of-control governmental agencies have unjustifiably foisted upon millions of innocent Americans, their physicians, and military veterans.

    Now, they all MUST bear the burden of responsibility for doing so. And the sooner the better.

    That is until now.

    Reply
  6. Robert Curtis says:
    2 years ago

    Great article, I applaud the author.
    Having said this I don’t think we will see any changes. The number one reason for my opinion is that we still see too many members of Congress holding on to the fictitious beliefs that prescribing and chronic pain patients created the illegal opioid crisis. It was as just announced that the DEA is once again cutting opioid medication production. How many years in a row has it been now 7 or 8 ? Even with healthcare workers reporting shortages and yet they continue.
    The only way I see anything changing is maybe if we find out the CDC, DOJ or the DEA was colluding with Twitter to silence the many advocates and pain patients trying to sound the alarm. I would be willing to bet they all did.

    Reply

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Videos

Summary

In this episode of the Daily Remedy Podcast, Dr. Joshi discusses the rapidly changing landscape of healthcare laws and trends, emphasizing the importance of understanding the distinction between statutory and case law. The conversation highlights the role of case law in shaping healthcare practices and encourages physicians to engage in legal advocacy by writing legal briefs to influence case law outcomes. The episode underscores the need for physicians to actively participate in the legal processes that govern their practice.

Takeaways

Healthcare trends are rapidly changing and confusing.
Understanding statutory and case law is crucial for physicians.
Case law can overturn existing statutory laws.
Physicians can influence healthcare law through legal briefs.
Writing legal briefs doesn't require extensive legal knowledge.
Narrative formats can be effective in legal briefs.
Physicians should express their perspectives in legal matters.
Engagement in legal advocacy is essential for physicians.
The interpretation of case law affects medical practice.
Physicians need to be part of the legal conversation.
Physicians: Write thy amicus briefs!
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