Cub pharmacy admits to giving woman wrong prescription dosage for months

http://www.fox9.com/news/cub-pharmacy-admits-to-giving-woman-wrong-prescription-dosage-for-months

BLOOMINGTON, Minn. (KMSP) – A woman in Bloomington has a warning for others after she was given the wrong prescription dosage for months.

“I feel like I’m a 75, 80-year-old woman and I’m a 24-year-old single mom just trying to live,” said Megan Morales.

After years of trying to get a handle on her epilepsy, Morales says the majority of her daily pain stems from an overdose of Briviak. 

 

Last June, her doctor added the anti-epileptic prescription to her daily routine, specifically 10 milligrams twice a day. Instead, a Cub pharmacist filled the scrip for 100 milligrams. Morales refilled the prescription three times before catching the mistake.

“My trust is completely gone from them,” said Morales.

Because of the large dosage, Morales had to be weaned off the drug and suffer through withdrawal. Her conversations with those representing Cub have been going on for months while she continues to battle through pain. 

“I get people make mistakes, we all make do,” said Tammy Morales, Megan’s mom.

In a statement from Supervalu, which owns Cub, a spokesperson admits this was a human error, saying, “Since this matter was brought to our attention last fall, our team has reviewed our processes and coached our pharmacists in our commitment to reduce the potential for a future pharmacy error.”

Executive Director of the Minnesota Board of Pharmacy Cody Wiberg points out human error everywhere, including pharmacies, does happen. Wiberg believes these mistakes happen fewer times in Minnesota because of two-step process pharmacists are legally required to take. He says he would like see a rule in place mandating records of mistakes and what is done about them. 

“The board would then have the authority to go in and review those records and more importantly, make sure they are taking action to prevent future errors,” said Wiberg.

The future and not knowing how long her current pain will last is what Morales worries about most.  

“If [my son] asks questions like ‘Momma why are you twitching?’” said Morales. “I can’t explain that to my three-year-old. How can you explain to your three-year-old that? I’m scared.”

Morales hasn’t filed a lawsuit yet because her main goal is to prevent this from happening to others. 

Failure to treat pts’ pain when dying of cancer can have consequences

In the early 90’s there was two different docs in California that were sued because they refused to properly treat the pain of two different pts – so pts wouldn’t become addicted .  They were sued by the relatives of these pts and BOTH doctors were found guilty – NOT OF MALPRACTICE – but of SENIOR ABUSE. Each family was awarded ONE MILLION +.

ACLU is ready to protect illegal aliens… but how many chronic painers have contacted them and got NOWHERE ?

 

 

Hi Steve –

Since the day President Trump came into office, California has been at the forefront of the fight against his racist, anti-immigrant policies. Now Jeff Sessions’ Justice Department is suing California for daring to stand against ICE brutality. Californians know that the strength of their state owes much to its large immigrant population – and they won’t let a bigoted administration tear apart the fabric of their communities.

It’s time to put ICE back on its leash. Add your name to the petition to tell Homeland Security to rein in ICE’s lawlessness. The agency’s invasive, hateful objectives are the antithesis of the constitutional principles of this country.

California’s laws limit the ability of local law enforcement to cooperate with ICE, increase oversight of ICE detention facilities located in California, and prohibit workplace raids without a warrant. In other words, these are measures to protect immigrants from ICE’s invasive, fear-mongering objectives.

Sessions and Trump are also threatening to withhold federal funding from states and cities with laws that limit local cooperation with Trump’s deportation force, and they’re even hinting at criminal charges for politicians who support laws that push back against ICE.

This is yet another outrageous move by the Trump administration. They’ve given ICE free rein to wreak havoc on immigrant communities throughout the country, and we’ve got to stop them. Sign this petition telling the Homeland Security Department that it’s time to put ICE in check.

The good news is that we have so many people on our side as we fight against Trump’s policies of unprecedented bigotry. We need you to make your voice loud and clear: Put ICE back on its leash. Protect immigrants now.

With ICE, Trump and Sessions want to ramp up hate and division – but we won’t let them.

Thanks for your support,

Lorella Praeli
ACLU Director of Immigration Policy and Campaigns

How many chronic painers have approached the ACLU about the brutality of the DEA and violation/discrimination of the Americans and Disability Act and Civil Rights Act… and got a “not interested” from them ?

From this email… it would appear that the ACLU has a ENTIRE SECTION just to deal with illegal immigration…

Some people are apparently on some sort of “trip”

I went to Walgreens today to fill my prescription and they refused to fill even though said I could fill today. The lady Pharmacist told me she didnt care what the prescription said it was a couple days to soon. I told her I was a pain patient and am on full disability due to botched bone tumor surgery where both the main nerves in leg were severely damaged. I told her to give me my prescription back and I will go elsewhere and she went into this spill how she don’t understand pharmacy jumpers and that I shouldn’t do that. I explained to her tha I have used Walmart pharmacy for 20 plus years and the only reason I came to Walgreens is because my meds would be 20 dollars cheaper there. She continued to treat me like a criminal and she has know what I go through every day just to get by with my pain issue. I was wondering if you have any advice for me sir that could help me . Thanks in advance 

 

Desperately seeking SOLITUDE

Few seem to see the similarities between those in the chronic pain community and those in the mental health community dealing with addictive personality disorders. It really doesn’t matter if those with addictive disorders has a preference for Alcohol, Nicotine, Caffeine, Methamphetamine, Cocaine, Opiates, Gambling, Food, sex, etc..etc…

Those in the chronic pain community is “seeking” place of solitude from their unrelenting pain… just like those with addictions are “seeking” a solitude from the monkeys on their back and/or demons in their heads, what they personally consider more “normal” for them.

Addicts will generally state that they take/abuse the substance does so because they “like the way that it makes them feel”

Could it be said of chronic pain pts when they get adequate pain management that they “like the way that it makes them feel” – which they usually refer to as “normal”.

We have no idea how many of the deaths of addicts is actually a suicide.. they are “sick & tired” of trying to find their next “fix” they are sick and tired of dealing with “dope sick”.. which is what they call withdrawals.

There has been other countries that have decided that prohibition will not work and helping addicts to be mostly “functional” and reduce the number of OD’s because addicts get a “known strength” of their drug of choice. This could reduce several things… cartels would have fewer customers, we would have fewer OD’s, and fewer hostile family of those addicts who have OD’d because they got a opiate that was not what they were expecting.  Hopefully, a lot fewer families of the “former addict” who are hostile about chronic painers being  adequately treated for their chronic health issues.

Of course, to get to this point, Congress is going to have to force the DEA/judicial system into viewing addiction as the disease that it is and not the crime that they have been declaring for over 100 yrs. After all, the DEA/judicial system is the common denominator that is impacting untold number of pts and healthcare providers. Of course, with abt 40% of Congress  being attorneys… part of the judicial system … may make that a “mission impossible”. Being that the war on drugs employs some 500,000 to ONE MILLION people.

Mental health is a serious health issue, otherwise we would not have 50,000 suicides each year and ONE MILLION attempts.

Deadly fentanyl overdoses in Maryland were up more than 70 percent in 2017 when compared to 2016

Hogan: Greater federal support needed to fight opioids

http://www.wbaltv.com/article/hogan-greater-federal-support-needed-to-fight-opioids/19180214

Maryland Gov. Larry Hogan took the fight against opioids to Capitol Hill Thursday.

Hogan testified in front of the U.S. Senate Committee on Health, Education, Labor and Pensions to speak about what needs to be done on the federal level to fight the epidemic.

He cited the synthetic opioid fentanyl as the leading cause of deadly overdoses, and he called on lawmakers to address the problem. First, he wants more federal funding aimed at fighting addiction.

Hogan said he also wants increased availability to naloxone, education programs focused on the dangers of fentanyl and legislation to address the flow of drugs into the country.

“The majority of this fentanyl is being shipped in from China or it’s crossing the border and being smuggled in from Mexico, and we simply can’t stop it without the federal government stepping up,” Hogan said.

Deadly fentanyl overdoses in Maryland were up more than 70 percent in 2017 when compared to 2016.

The following is a transcript of the governor’s remarks as prepared for testimony, courtesy the governor’s office.

“During my campaign for governor in 2014, I traveled across Maryland with my running mate, Boyd Rutherford, asking voters one question: Which issue facing your community are you most concerned about? The answer we heard again and again, in every corner of our state, was heroin and opioid addiction.

“Immediately after taking office, we set up a Heroin and Opioid Emergency Task Force, chaired by Lt. Gov. Rutherford, which developed 33 specific recommendations focused on a four-pronged approach: education, prevention, enforcement and treatment. We have acted to address or move forward on nearly all of these recommendations.

“In March 2017, Maryland became the first state in the nation to declare a full-scale state of emergency in response to the heroin, opioid, and fentanyl crisis. In order to truly treat this crisis as we would a natural disaster or public safety emergency, we activated an Opioid Operational Command Center to more rapidly coordinate between state and local agencies, and dedicated an additional $50 million in funding over the next five years. In total, we have spent nearly half a billion in state and federal funding to combat opioid and substance use disorders.

“Through legislation we have taken positive strides, we’ve expanded our state’s Good Samaritan Law and Prescription Drug Monitoring Program, imposed strict penalties on individuals distributing fentanyl, and passed legislation limiting the amount of opioids a health care provider can prescribe. This past June, our Department of Health issued a standing order allowing all Marylanders to be able to receive the life-saving drug Naloxone from pharmacies, and in January, I authorized our attorney general to file suit against opioid manufacturers and distributors that have helped create the addiction crisis gripping our state and nation.

“Yet, in spite of all of our efforts, in spite of us fighting with every tool we have at our disposal, this crisis continues to evolve, particularly with the threat of fentanyl and other synthetic additives, which can be 50 times to 100 times stronger than heroin.

“Combatting a crisis of this scale requires all levels of government working together. No state or community can go it alone. The majority of the deadly fentanyl is being shipped in from China or smuggled in from Mexico and we need the federal government to step in and stop this poison from ravaging our state and our nation.

“Maryland is working tirelessly to fight this epidemic, alongside our counties and municipalities, in neighborhoods and schools, with public health, human services and public safety. We need greater federal support, especially more targeted and aggressive federal enforcement efforts for fentanyl and other synthetic opioids.

“Ultimately, this is about saving lives. It will take all of us to do that.”

Should Kratom Be Legal? New Research Provides Clearer Picture of the Plant’s Risks and Benefits

https://merryjane.com/health/kratom-controversy-new-research-on-plant-provides-clearer-picture-of-risks-benefits

The most comprehensive review on kratom to date challenges claims of the opioid-like substance being “deadly,” and provides a blueprint for future research into its clinical benefits and side effects.

by Laura Dorwart

While the U.S. is in the thick of an opioid epidemic, an increasing number of Americans have turned to kratom, which users say can provide much-needed relief of opioid withdrawal symptoms. The plant-based supplement, derived from leaves of the kratom tree (Mitragyna speciosa), is also commonly used to relieve chronic pain, depression, and anxiety. Used in Thailand and Malaysia for centuries, kratom has sparked significant controversy in the U.S. and was nearly classified by the DEA as a Schedule I drug in 2016 before those plans were scrapped due to major public outcry.

As public debates about the best ways to combat opioid addiction rates in the U.S. continue, many Americans have sought out alternative remedies for self-treatment of withdrawal and dependency. Kratom is a (currently) legal, widely-available substance with a lower risk of adverse side effects and acute dependency than other treatments, and many users claim it helps them manage their pain while simultaneously easing their reliance on opioids. Others have begun to use it as a milder alternative to prescription antidepressants and other psychiatric medications. As it’s grown in popularity, so have concerns about its potential risks.

Still, the FDA and DEA have persisted in painting kratom as potentially risky and even lethal, and media coverage has followed suit, calling the supplement potentially “deadly” and dangerous. A recent systematic review — the most comprehensive review to date on kratom’s potential risks — calls those claims into question, however, and provides a blueprint for future research into kratom’s clinical benefits and side effects.

Dr. Marc T. Swogger, a clinical psychologist and Associate Professor in the Department of Psychiatry at the University of Rochester Medical Center, and Dr. Zach Walsh, an Associate Professor at the University of British Columbia’s Department of Psychology, published their findings in Drug and Alcohol Dependence in February 2018. “We reviewed the literature to date on kratom and mental health, looking at all the studies that had reported on a variety of mental health outcomes,” Dr. Walsh told MERRY JANE by phone of his and Dr. Swogger’s work. “The main findings were that people are using kratom for a variety of purposes, mostly to help with opioid withdrawal. We also didn’t find evidence of kratom increasing negative mental health outcomes.”

More specifically, Dr. Walsh clarifies, “It doesn’t appear to cause depression, anxiety, or suicidal ideation” — despite some claims that it’s driven frequent users to suicide. In fact, their review of over 57 years of available research on kratom suggests that the plant can improve mood and relieve symptoms of mild to moderate anxiety. In other words, the review has profound implications for the future of kratom, which has risked veering quickly into a pattern of public stigmatization and a frenzy of media demonization, not unlike what we’ve seen with cannabis. Instead, Dr. Swogger told the University of Rochester Medical Center Newsroom, “The bulk of the available research supports kratom’s benefits as a milder, less addictive, and less-dangerous substance than opioids, and one that appears far less likely to cause fatal overdose.”

The review also indicated that, while kratom does carry some risk of dependence syndrome, its potential for dependency is mild — potentially resulting in symptoms like nausea, irritability, and headaches — compared to that of opioids. This makes sense, says Dr. Walsh, because kratom is from the coffee family, not the opioid family. The mild stimulating, mood-boosting effects many report with kratom may be akin to the kinds of effects we see with coffee. The problem, the study’s authors claim, is not kratom itself, but the fact that there’s not yet enough empirical work on kratom at all — so the public isn’t totally certain about its risks or benefits.

These findings contradict recent claims by the FDA that kratom carries an equal risk of addiction and overdose to opioids. In February 2018, the agency released a new report that left kratom users and experts alike scratching their heads. In it, FDA Commissioner Scott Gottlieb, M.D., emphasized kratom’s opioid-like properties, which were determined using predictions made by a computational model. Dr. Gottlieb claimed, “The data from the PHASE model shows us that kratom compounds are predicted to affect the body just like opioids,” and thus potentially carry a similar risk of dependence.

Along with the report, the FDA released information on the 36 deaths they’d referenced in a November 2017 press release, along with a public health advisory about the risks of kratom and its potential for addiction and overdose. But the accompanying death reports raised further suspicions about kratom’s real risks, rather than alleviating them. In all but one of the 36 deaths cited, Nick Wing writes in the Huffington Post, there are multiple substances listed in the toxicology reports — from Xanax and alcohol to high concentrations of prescription medications. There’s only one listed case where mitragynine — the main active ingredient in kratom — is the only substance involved, save for one death that’s since been redacted and is listed elsewhere as death by gunshot wound.

According to Dr. Walsh, some of the growing hysteria about kratom might be derived from cultural biases and prejudices. “It’s a plant medicine from Southeast Asia, from outside of the North American and Western European pharmaceutical families. So immediately, that arouses suspicion.”

Moreover, the treatment of kratom is in line with the historical pattern about how marijuana was painted in the media before being stigmatized and demonized by governmental agencies, politicians, and pharmaceutical companies. “It’s hard to speculate on why the War on Drugs would have a component that’s harmful to public health,” Dr. Walsh says, “but that’s been a main theme. It’s in keeping with the general dysfunctional madness of the last 75 years of drug policy.”

The dubiousness of recent claims by the FDA add to Dr. Walsh’s concerns that the risks of kratom are being preemptively overblown. And though the theoretical model described in the recent FDA press release has been one of the agency’s “guiding lights” in developing theories about the kratom, Dr. Walsh clarifies that “this model hasn’t been empirically validated” and is thus an unreliable source of hard data.

Still, he says, the study shouldn’t be taken as proof that kratom isn’t harmful. “Lack of evidence doesn’t mean an evidence of lack,” he warns. Before we can come to any final conclusions about kratom, we’ll need to study it further. And since all painkillers have their own negative side effects, it’s likely that kratom has some side effects for long-term users. “It’s not yet meeting a standard of evidence where it’s something that you’d recommend,” says Dr. Walsh.

A current salmonella outbreak across several states among kratom users underscores the need for regulation and scientific study of kratom rather than steps towards criminalization or FDA scheduling. Without clearly delineated consumer standards, it’s easy for kratom to go underground and risk contamination. But to get to that point, Dr. Walsh and Dr. Swogger argue, it will require large cohort studies that follow kratom users over a period of time, measuring both its harms and medicinal benefits, as well as clinical trials.

FDA commissioner to health insurers: You’re doing it wrong

https://www.cnbc.com/2018/03/07/fda-commissioner-to-health-insurers-youre-doing-it-wrong.html

  • “Sick people aren’t supposed to be subsidizing the healthy,” Scott Gottlieb said Wednesday.
  • The FDA commissioner was speaking at the National Health Policy Conference of AHIP, the health insurer industry group.
  • In his critique, Gottlieb homed in on an increasingly popular target in the drug pricing debate: rebates.

Insurance is designed, theoretically, to protect against the catastrophic: tornadoes, floods, hurricanes — or, where our health is concerned, cancer or another devastating disease.

To make that financial protection affordable, many pay into the system: the healthy are supposed to subsidize the sick.

But at a conference Wednesday organized by the health insurance industry, FDA Commissioner Scott Gottlieb delivered a startling message: You’re doing it wrong.

“Sick people aren’t supposed to be subsidizing the healthy,” Gottlieb told an audience at the National Health Policy Conference of AHIP, the health insurer industry group. “That’s exactly the opposite of what most people thought they were buying when they bought into the notion of having insurance.”

Gottlieb’s remarks were focused on the health of the market for biosimilars — copycats of complex, biologic medicines — and his concerns that industry consolidation and what he called rigged payment schemes may be stifling their development.

But they rang out as a critique of the U.S. system for pricing and paying for drugs more broadly, a system in which Gottlieb said each faction of the health-care industry is complicit in thrusting prices upward — at the expense of the sickest patients.

In his critique of health insurance constructs, he homed in on an increasingly popular target in the drug pricing debate: rebates. Those are discounts on medicines negotiated by pharmacy benefit managers on behalf of insurers.

But because the rebating system is opaque, and because of consolidation among PBMs and insurers, that system can result in ever-higher drug prices and everyone from drugmakers to the middlemen to insurers taking a slice of the pie, Gottlieb said.

Moreover, he posited, there’s a “perverse incentive” to spread the benefit of those rebates across plan members, rather than applying them directly to lower the costs of drugs for the sickest patients — thus, a system where the sick subsidize the healthy.

“Patients shouldn’t face exorbitant out-of-pocket costs, and pay money where the primary purpose is to help subsidize rebates paid to a long list of supply chain intermediaries, or is used to buy down the premium costs for everyone else,” Gottlieb said.

What reason is there, he asked, for a cancer patient to shoulder a large co-pay on their costly medicine?

“Is a patient really in a position to make an economically based decision?” he continued. “Is the co-pay going to discourage overutilization? Is someone in this situation voluntarily seeking chemo?”

The answer, of course, is no. “Yet the big co-pay or rebate on the costly drug can help offset insurers’ payments to the pharmacy, and reduce average insurance premiums,” Gottlieb said.

His comments were applauded by industry observers.

“Too many benefit plans operate like reverse insurance,” Adam Fein, CEO of Drug Channel Institute, wrote in an email to CNBC. “The sickest people taking medicines for chronic illnesses generate the majority of manufacturer rebate payments. These funds are then used to subsidize the premiums for healthier plan members.”

Others heralded Gottlieb’s citation of rebates as a key deterrent to uptake for biosimilars.

“This is impressive, from the head of the FDA,” tweeted Walid Gellad, director of the Center for Pharmaceutical Policy & Prescribing at the University of Pittsburgh.

Health insurers and pharmacy benefits managers, unsurprisingly, disagreed.

“It’s unfair to blame payers — who pay 2/3 the cost of drug benefits — for seeking the lowest costs in a marketplace where they have no control over the prices drugmakers set,” the Pharmaceutical Care Management Association, the PBM industry group, said in a statement. “Likewise payers — not the pharmacy benefit managers they hire to negotiate discounts — determine how rebates and other savings are allocated to reduce premiums, out-of-pocket costs and other expenses.”

AHIP took issue with the idea that insurers play a role in rising drug prices.

“Health plans welcome the introduction of generic biologics, or biosimilars, as a way to give patients quicker access to more affordable medicines,” the group said in a statement. And it pointed fingers back at drugmakers. “The trend among pharmaceutical companies to hike the prices of brand name biotech drugs before generic competition arrives is forcing makers of biosimilars to set their prices higher.”

Some pointed out Gottlieb’s position is an unusual one for an FDA commissioner to take; the agency officially doesn’t take a role in drug pricing.

Gottlieb told CNBC Wednesday afternoon that ensuring biosimilars have a pathway to market is a public health concern.

“Part of my job is to worry about the effectiveness and viability of the biosimilars pathway and achieving the access and competition it was intended to create,” Gottlieb said. “If ill-conceived payment arrangements serve to discourage investment in a way that forestalls that pathway from ever really taking root, that’s a public health concern. And when I look at the biosimilars pipeline, I’m worried that may be happening.”

The focus on rebates is spurring change: this week, UnitedHealth said it would apply drug rebates directly to lower costs for patients on their prescriptions starting next year. The company said it’s part of a move to “simplify pharmacy benefits, deliver savings directly to its customers and improve their healthcare experience.”

Alex Azar, newly minted secretary of the Department of Health and Human Services, praised the move, calling it a “prime example of the type of movement toward transparency and lower drug prices for millions of patients that the Trump Administration is championing.”

But, as many analysts pointed out, it may mean premiums across the board go up.

“Most plan sponsors use manufacturer rebates in aggregate to subsidize the cost of beneficiary premiums, keeping the premiums artificially low,” RBC Capital Markets’ George Hill wrote in a Tuesday research note. “This strategy has historically been effective, but has in recent years created a disconnect where the sickest and most expensive patients have been generating the rebates used to subsidize much healthier patients.”

So by reversing that trend, as Gottlieb and Azar encourage, the health insurance model may become less backwards. But it won’t necessarily result in lower costs, just a redistribution of them.

One pharmacy tried to charge me 10 TIMES the normal price!

Hello Steve, I am a 100% Disabled Vietnam Era Veteran. I am a retired USPS letter carrier. My wife passed away and I had lost our family plan health insurance. Though I am covered by the VA it is an hour drive from my home. Once  there I may wait for hours to see a different doctor every month. I am a chronic pain patient. I have been seeing the same doctor every month in Florida for the past 15 years. He is a Board Certified physician and the Chairman of the board of the largest hospital in my County. My question is: Is it legal for CVS to deny filling my prescription because I do not have private health insurance anymore? Driving several hours, and waiting around to get a 30 day supply of medication, at my age, is more than inconvenient. It is humiliating and very hurtful. I have an old minivan and I can wind up stranded somewhere. It costs $672 a month for private health insurance at my age! I can go into shock if I can not get my medication. What can I do? Furthermore, I wanted to add that I was denied medication because I didn’t have 6 or more medications . Uncontrolled medications can be mailed to me for free from the VA. One pharmacy tried to charge me 10 TIMES the normal price! Price gouging is definitely not ethical. Other excuses we’re we don’t have it because  ” We exceeded our quota” or we only get this for our “regular customers”. I am too sick to fight or go galavanting from pharmacy to pharmacy trying to get my medication. I won’t be able to care for myself or my two dogs anymore. I’ll lose my home, my independence, and wind up in a nursing home. What will it cost us taxpayers then?  Sorry for being too wordy, I am very scared now. Thanks for your concern and advocacy,

Pre-disease Conditions and their Symptoms

The our health care system.. when I first started as a pharmacist… it was pretty much you had a DISEASE or you DIDN’T..

Today we have all sorts of PRE-disease CONDITIONS…  think of pre-diabetes,  pre-hypertension… sometimes when I get frustrated with someone wanting to discuss all of these PRE-ISSUES on someone’s health… I try to bring things back to reality  EVERYTHING AFTER BIRTH IS PRE-DEATH !

I try to look at how the media, the various bureaucracies , and healthcare itself in a “big picture” context.  I try to to look at what is said, what is not said.. and how often the “truth” is twisted.

They routinely state that opiates are ADDICTIVE or HIGHLY ADDICTIVE

They routinely state that Fentanyl is involved with a OD… when it is one of many ILLEGAL FENTANYL ANALOGS

They tend to ignore the decrease in legal opiate prescription while OD are going dramatically in the opposite direction.

They have even changed the nomenclature:

No more accidental overdoses..  just anyone dying with a opiate in toxicology has their death certificate designate their cause of death to be “opiate related death”

No more addiction/dependence .. just anyone using opiates (legally/illegally) for >90 days… is suffering from a “opiate use disorder”

CDC published opiate dosing guidelines and the then head of the CDC made the statement that they DID NOT BEAR THE WEIGHT OF LAW. One has to ask why a Fed agency in charge of dealing with contagious disease,  elected to publish these opiate guidelines while at the same time ignore publishing any guidelines in treating addiction

Then we have various insurance companies, PBM’s and large healthcare corporation are now setting up some additional opiate guidelines. Daily MME limits, Prior Authorization, Quantity limits and the like.. while at the same time eliminating any limitations on the treatment of addiction.

Could it be that “the powers to be” have decided – for whatever reason – chronic pain is a pre-addiction symptom and thus those who are addicted are treated to change their behavior – which would suggest that they are treating addiction as the mental health issue that it really is… but treating chronic pain as symptom of an impending addition.