Heroin Boom: Afghanistan Producing 25 Times More Opium Since U.S. Invasion

Heroin Boom: Afghanistan Producing 25 Times More Opium Since U.S. Invasion

http://www.breitbart.com/national-security/2016/10/24/heroin-boom-afghanistan-producing-25-times-opium-since-u-s-invasion/

The estimated opium poppy plant production and its cultivation area in Afghanistan have increased more than 25-fold over the course of the ongoing war in the country to 4,800 metric tons and 201,000 hectares (ha), respectively, according to the United Nations.

Meanwhile, eradication efforts appear to have collapsed this year despite the estimated $8.5 billion in American taxpayer funds that the United States has already spent on anti-narcotics measures in Afghanistan since the war started in October 2001.

Each year, the UN Office on Drugs and Crime (UNODC) issues the Afghanistan Opium Survey to show production and cultivation trends of the deadly drug in the country, considered the world’s top producer of opium and its heroin derivative.

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“The potential opium production in 2016 might be an underestimation,” acknowledges the UNODC, noting that it had to rely on satellite images to calculate estimates due to the worsening security conditions in top opium-producing regions.

According to the latest UN survey, since the U.S. invaded Afghanistan on October 7, 2001, the area under opium cultivation has increased nearly 25 times from 8,000 ha in 2001, when the ruling Taliban regime had imposed an opium ban across the country, to 201,000 ha this year, which is equivalent to an area more than 11 times the size of Washington, D.C.

 

Both the increase in cultivation area and the decrease in eradication efforts were attributed to deteriorating security conditions across the country. Taliban jihadists, who use proceeds from the sale of opium and heroin to fund their terrorist activities, are primarily responsible for the crumbling security conditions in Afghanistan.

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Meanwhile, estimated opium production shot up to 4,800 metric tons in 2016, from 185 tons when the U.S. invaded. The dramatic increase in opium production is reportedly not only the result of a larger area under cultivation but also due to the higher opium yield per hectare.

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Opium production and cultivation have increased dramatically since 2015 alone, notes the latest survey. The UN reports that estimated production jumped 43 percent and cultivation rose 10 percent this year compared with 2015 levels.

Areas under cultivation this year marked the third-largest in two decades, following historic highs in 2013 and 2014.

UNODC Executive Director Yury Fedotov indicated that the most recent survey shows “a worrying reversal in efforts to combat the persistent problem of illicit drugs and their impact on development, health and security.”

Eradication efforts appear to have disappeared this year with an area of 355 ha uprooted, marking a 91 percent drop when compared to 3,760 ha in 2015.

Most (54 percent) of the opium in Afghanistan is cultivated and produced in southern provinces that border Pakistan and have historically been Taliban strongholds, namely Helmand and Kandahar, the deadliest provinces for U.S.-led coalition forces of the ongoing war.

Opium is cultivated and/or produced in nearly two-thirds (21) of the 34 provinces that make up Afghanistan, the UN reveals.

U.S. government officials maintain Afghan heroin is not fueling the growing heroin overdose epidemic taking American lives on a daily basis in the United States.

In June, the DEA reported, “In 2014, 10,574 Americans died from heroin-related overdoses, more than triple the number in 2010.”

In its latest National Drug Threat Assessment, the DEA notes that only a small portion of Afghan heroin makes it into the U.S., smuggled primarily by Nigerian traffickers on commercial airlines.

In 2012, the latest year for which data is provided, Afghan heroin reportedly accounted for about four percent of estimated total weight of heroin seized in the United States.

The DEA acknowledges that most of the heroin flowing into Canada primarily originates in Afghanistan, but it maintains that Mexico and “to a lesser extent Colombia” are the top providers of the fatal drug in the United States.

Nevertheless, the White House and other government agencies have sounded the alarm on the Afghanistan heroin going into Canada, suggesting it may be flowing into the U.S.

Some American soldiers in Afghanistan have been investigated “on suspicion of using or distributing heroin, morphine or other opiates during 2010 and 2011,” the Associated Press (AP) pointed out in 2012.

Pentagon data analyzed by Breitbart News shows the number of U.S. service members testing positive for heroin has increased over the course of the war in Afghanistan.

In December 2014, the U.S. Special Inspector General for Afghanistan Reconstruction (SIGAR), reported that some U.S. taxpayer-funded reconstruction efforts, “such as improved irrigation, roads, and agricultural assistance,” may have contributed to the booming opium trade in Afghanistan.

In 2014, the DEA drug threat assessment shows, Mexico produced an estimated 42 metric tons of heroin. Afghanistan produced 6,400 metric tons of opium that same year.

Only ONE PERCENT of trauma pts are still taking opiates ONE YEAR LATER

If You’re Prescribed Opioids after Injury or Surgery, Will You Become Dependent?

nationalpainreport.com/if-youre-prescribed-opioids-after-injury-or-surgery-will-you-become-dependent-8831759.html

We’ve all seen the massive media attention on the opioid epidemic and as the dust settles and changes are made to how opioids are viewed, we are left with a few takeaways.  One of them is that if someone is injured or has had surgery, prescribing opioids is a bad thing because many will become dependent.

A new study presented at the American College of Surgeons refutes this notion, reporting that up to one year after discharge from the hospital, only about 1 percent of trauma patients were reportedly still taking prescription opiates, or opioids, such as hydrocodone, oxycodone, morphine, and fentanyl.

“Our findings in patients who sustain traumatic injury contradict the popular narrative about the role that appropriate use of opioids may play in the rate of opioid abuse in this country,” said senior investigator Andrew Schoenfeld, MD, an orthopaedic surgeon at Brigham and Women’s Hospital and assistant professor at Harvard Medical School, Boston.

 

This new study is one of the largest investigations of prescription opiate use among patients who sustained trauma and may have the longest continued follow-up one year after hospital discharge.

Their research was conducted using the 2007 to 2013 database of TRICARE, the Department of Defense health care system that insures active-duty military, reserve members, retired veterans, and their dependents. Because most TRICARE plan members are currently civilians, Dr. Schoenfeld said the study findings are generalizable to the U.S. population.

Included in the study were patients aged 18 to 64 years whose injuries were severe, as indicated by an Injury Severity Score of 9 or higher.  Patients with major trauma could be expected to receive opiate prescriptions after their hospitalization.  In all, 15,369 patients were included and none of the patients had filled an opiate prescription within six months before their injuries.

Although more than half of the patients in the study, or 8,282, filled at least one opiate prescription soon after discharge, only 8.9 percent (1,371 patients) continued to fill opiate prescriptions three months later, the investigators reported.  Continued prescription opiate use reportedly dropped to 3.9 percent (597 patients) at six months and 1.1 percent (175 patients) at one year.

“We were really surprised by how low the numbers were for long-term opiate use,” Dr. Schoenfeld said.  “It appears that traumatic injury is not a main driver for continued opioid use in patients who were not taking opioids prior to their injuries.”

To identify predictors of continuing use of prescription opiates after hospital discharge, the researchers evaluated patients’ demographic and medical factors and found increased risk of continued opioid use among the following:

  • Patients ages 45 to 64 compared to those 18 to 24.
  • Lower socioeconomic status
  • Those who are married (although these finding probably cannot be generalized to the U.S. population, according to Dr. Schoenfeld, because military families tend to marry earlier than civilians do.)

“We wish to emphasize that health care providers should not withhold opiate painkillers because a patient has any of the identified risk factors from this study,” Dr. Schoenfeld said.  “At-risk patients can benefit from closer follow-up with their health care providers and, for those at high risk, a referral to the hospital’s pain management service.”

The study results were presented at the 2016 Clinical Congress of the American College of Surgeons.

Healthcare is just a business and “bodies” are just a revenue stream

The time a 28-year-old MBA told a physician where to round first

www.kevinmd.com/blog/2016/05/the-time-a-28-year-old-mba-told-a-physician-where-to-round-first.html

The last couple of decades have seen a dramatic shift of power and clout away from individual physicians and towards administrators and the business side of health care. In many ways, physicians have nobody but themselves to blame collectively; because for any large and respected group of people to surrender so much autonomy so quickly, a lack of strong leadership must always be a factor.

So many different reasons for this sea change can be discussed, but the consequences are very palpable. To name but a few, we’ve seen the relentless push towards consolidation and mass employment of physicians, a rise in mandates and bureaucratic requirements, and a general explosion in the number of administrative folks while the number of physicians appears to be shrinking! Then there’s the more subtle changes that the medical profession has also allowed to happen right under their noses, such as the refusal of many in the hierarchy to even call doctors by their true job title anymore — instead labeling them only as “providers” (a subject I’ve written about including an open letter to the AMA and all State Medical Boards).

Speaking as someone who maintains a large network of physician friends and colleagues across the country, some of the stories I’ve heard about what happens nowadays are astonishing. Fortunately, after a few bad experiences, I’m now part of an organization where the relationship between physicians and administrators is probably as good as it can be. But from what I see, this is a rarity.

I relate one recent story in particular. I have a very close friend in the Midwest who is quite a brilliant doctor. He went to a top US medical school and got stellar USMLE scores.  I’ve known him for years and am proud to have trained with him. He is sub-specialty board certified, but decided to practice hospital medicine.

He told me that his group, which is essentially run by non-clinicians, is completely (and unsurprisingly) focused on the bottom line only. Administrators aggressively monitor their physicians’ whereabouts and try to review all of their patient interactions (mostly how it pertains to billing). To cut a long story short, he told me that the administration for some reason or another wanted him to round first on a particular floor. He didn’t think it was the right thing to do for patient care (apparently another floor frequently had patients who required closer and more immediate attention), and it culminated in him basically being scolded by a 28-year-old MBA who informed him that he had to round on that particular floor first, like it or not. Needless to say, he didn’t take too kindly to this interaction and that particular experience persuaded him that the time was right to move on.

This story bothered me on multiple different levels, as I’m sure it would any self-respecting physician. First and foremost, how did the medical profession surrender so much to the business of medicine that a situation like this could happen? I wonder what our more esteemed colleagues in perhaps their 50s and 60s would have done twenty years ago if a 28-year-old MBA had dared tell them where to round first? Secondly, how did that young man feel so empowered to scold a highly qualified physician and feel so convinced that “he was the boss”? And thirdly, perhaps most worryingly, is this the future of medicine in the United States? If so, is there any way that physicians can wrestle back a bit of control over their own profession to avoid situations like this becoming the norm? Because if we can’t, and the practice of medicine is no longer led by doctors, it’s not only the doctors who lose.

Patients will too.

DEA’s Latest Ban Plan: Kratom

DEA’s Latest Ban Plan: Kratom

www.addictionnow.com/2016/09/29/deas-latest-ban-plan-kratom/

Kratom is an unusual, natural substance consumed in Asian countries including Thailand and Malaysia, since the early 1800s, to help treat anxiety and depression, alleviate fatigue, promote strength, relieve chronic pain, PTSD symptoms, diarrhea and combat lack of energy.

Kratom – thom, biak, ketum, kakuam or thang –  is mostly consumed orally in gel capsule form, but its leaves (from kratom trees) can also be crushed and chewed, smoked or brewed with tea. At low doses, it has a similar, stimulating effect one would get from drinking a strong cup of coffee. At higher doses it is a powerful sedative and painkiller, and arguably an addictive one.

DEA Ban

Because of claims the substance can be addictive and abused, the US Drug Enforcement Administration (DEA) announced they intend to make Kratom a Schedule I drug – grouped with LSD, heroin, marijuana, and ecstasy.

Around the same time last month, the US Food and Drug Administration (FDA) alerted the public that it will be detaining supplements that contain Kratom without any physical examination.

The federal agencies are yet to evaluate the substance but claim there’s no legitimate medical use for Kratom in the United States, and that it has caused psychosis, hallucinations and other dangerous side effects in its users.

The DEA also linked 15 deaths to the use of Kratom in the last two years, but 14 of those 15 people who died also had other drugs in their systems. That’s a very small number when you take in consideration millions of doses are being consumed regularly around the US. The number of people who allegedly died after consuming Kratom doesn’t even come close to the number of kids who die every year from being trapped inside hot vehicles.

Pros vs. Cons

One of the best assessments available so far regarding the drug’s effects can be found in a study published last year in the Journal of Psychoactive Drugs. After stating that there hasn’t been any rigorous scientific research regarding Kratom and humans, the study analyzed hundreds of profiles from a popular website for drug users and drug researchers. Researchers then… 

gathered a list of negative side effects including stomach pain, headaches, itching, and nausea, alongside a list of positive effects like relaxation, increased energy, and enhanced sociability.

The study showed that Kratom alone has an extremely low overdose risk, which catches the attention of health care providers working to combat the  rising numbers of overdose deaths.

The most revealing information about Kratom in the study was its great ability to relieve pain, which gives a natural alternative to those who seek highly addictive and potentially deadly painkillers.

Proponents point to Kratom’s success as a method of treatment

The American Kratom Association was founded last year to protect the rights of Americans using the substance, to inform the general public about Kratom’s benefits and to raise awareness while representing a community of responsible consumers who share successful stories about using Kratom.

The increasing number of enthusiasts includes doctors, lawyers and law enforcement officers, and other professionals who found hope through the use of Kratom. Some use the new association as a platform to talk about how they’ve been cured from their lifelong addictions while others talk about how they’ve gained the ability to deal with depression, OCD, ADD/ADHD, migraines, debilitating cases of Lupus, Fibromyalgia, and Lyme Disease – among other serious illnesses – since they started using the natural analgesic. There’s still a lot to learn about Kratom, but it does seem to be a much better alternative than other popular maintenance medications for opiate addiction, such as methadone and buprenorphine, both known for causing death.

Many agree that banning Kratom would clearly affect many Americans who have  found it to be a good alternative to cure their addiction to heroin, among other opiates and legal narcotics.

Chronic pain advocate, consultant and licensed pharmacist for about 50 years Steven R. Ariens said he knows of a patient who has been on Kratom for six years and will be back on a wheelchair unable to move from pain after the federal ban. 

Best Interest (or not)

Kratom is legal in 44 states, but the ban could take place on the last day of September, although it is evident there isn’t a great deal of information or research regarding the medical benefits of the tree leaf product.

People using Kratom will not only be criminally charged if they continue to use it after the ban, but they would also have a hard time getting informed about the substance. Once the DEA lists a substance as Schedule I, medical research and scientific studies hardly ever take place since it becomes much more difficult for researchers to gain access to such substances – and that rarely changes.

“There’ll be no lift from the DEA because they profit from the ban,” Ariens said.

With the data gathered so far, and all the positive anecdotal evidence, one would wonder if banning the natural substance is potentially more harmful than beneficial. Is it in our best interest to have a regulating agency crippling its own need for scientific research? If we aim to protect people or aid recoveries, shouldn’t we be making room for more flexibility in the way that controlled drugs are studied?

Trending News Today: Researcher Allegedly Withheld Deaths Caused by Cancer Therapy

Trending News Today: Researcher Allegedly Withheld Deaths Caused by Cancer Therapy

http://www.specialtypharmacytimes.com/news/trending-news-today-researcher-allegedly-withheld-deaths-caused-by-cancer-therapy

A National Cancer Institute researcher waited several months before notifying authorities that 2 patients in a lymphoma trial died of fungal infections that may have been caused by the treatment. According to The Washington Post, the early-stage trial was examining the efficacy of a treatment that combines the drug ibrutinib with a cocktail of chemotherapy drugs. Steroids were also used to help reduce swelling in the brain. In 2015 and 2016, there were 4 patients who developed an aggressive form of aspergillus, a common fungal infection. Additionally, another 3 patients may have possibly had the infection. In May and December of 2015, two of the patients died of infections. Although concerns began to increase and enrollment was stopped in April, principal investigator Kieron Dunleavy did not file an official unanticipated problem report until May that recorded the suspected association between the treatment and the infections. Dunleavy has been suspended from clinical research until he undergoes additional training.
 
There are currently many medical myths that remain in existence, therefore a new report by Live Science, address some of these myths in order to demystify them, according to The Washington Post. Although the flu shot contains dead flu viruses, these flu vaccinations do not actually cause the flu. It’s commonly believed that the weather turning cold causes people to get sick; however, the report stated that individuals are not more likely to get sick from colder temperatures. One of the most commonly believed myths is that eating turkey at thanksgiving makes you tired, pointing fingers at the tryptophan found in the meat. However, the drowsiness is most likely due to people overeating and ingesting lots of carbohydrates or alcoholic beverages. Lastly, sitting too close to a TV or computer or reading in the dark does not damage your eyes. According to the study authors, there is no evidence that this causes any long-term damage.
 
In an attempt to combat the steady rise of the opioid epidemic, the DEA launched an aggressive campaign nearly a decade ago that targets wholesale companies distributing these addictive pills to corrupt pharmacies and pill mills. According to The Washington Post, investigators from the agency’s Office of Diversion Control began filing civil cases against distributors and issuing orders that immediately suspended the drugs, producing hefty fines. Unfortunately, the industry fought back and hired former DEA and Justice Department officials to begin pushing for a softer approach. Soon after a meeting between the deputy attorney general and the DEA’s diversion chief, who was chastised for going after the industry, officials at the DEA headquarters began delaying and blocking enforcement actions, which caused the number of cases to nose dive, according to the Post. In fiscal 2011, civil case filings against distributors, pharmacies, manufacturers, and physicians reached 131, before plummeting to 40 in fiscal 2014. Meanwhile, the amount of immediate suspension orders dropped from 65 to 9 during the same period. This major slowdown started in 2013 after DEA lawyers began requiring a standard of proof before cases could move forward. In a statement issued by the department, they said that the drop in diversion cases was a reflection of the shift from crackdowns on ubiquitous pill mills to a small group of physicians, companies, and pharmacists who continue to violate the law, reported the Post.

Maybe the chronic pain community needs to listen to the two Presidential candidates ?

Maybe the chronic pain community needs to listen to the two Presidential candidates ?

stronger-togetheramerican-great-again

 

 

 

 

There is an estimated 116 million chronic pain pts and in the last president election.. there was 5 million votes between the winner and loser and an estimate 106 million eligible voters – DIDN’T VOTE !

Our country cannot be GREAT.. if we keep denying millions of chronic pain pts their necessary medication and intentionally throwing them out of a productive life and their quality of live for them and their families – INTO THE CRAPPER !

People march for "yoga pants parade" in Barrington, R.I., Sunday, Oct. 23, 2016. Hundreds of women, girls and other supporters proudly donned their yoga pants Sunday afternoon as they peacefully paraded around the Rhode Island neighborhood of a man who derided the attire as tacky and ridiculous. (Kris Craig/Providence Journal via AP) Photo: Kris Craig, AP / Providence Journal

http://www.thehour.com/news/us/article/Yoga-pants-parade-a-protest-against-misogyny-10135273.php

More people showed for a protest in a small RI town (pop 16,000) over a man who wrote a letter to a editor about women wearing yoga pants in public… than showed up for a recent national rally supporting appropriate pain care for chronic pain pts.

Just in the last few days to Governors (Vermont & Arizona) have come out to set daily opiate limits that pts can have.  Another state governor assumes the authority to practice medicine without a license ?  The question has to be asked… do these Governors and other politicians/bureaucrats that are attempting to practice medicine without a license… have any LEGAL AUTHORITY to do what they are doing ?

Unless they are challenged in our courts… they are going to continue TO DO AS THEY PLEASE … There is more and more information being published that chronic pain pts are not abusing their medications and >90% of those ODing on opiates do not have a legal prescription for the opiate that shows up in toxicology.

STRONGER TOGETHER…. if someone puts together a organization to create a legal defense fund to challenge all these possible ILLEGAL ACTIONS… and if just TEN PERCENT of the chronic pain community contributed the cost of a fast food lunch $5- $7.50… ONE TIME … SEVENTY MILLION (70,000,000.00) could be raised…  for a “war chest”.

The BEST LAW FIRMS in the country would be beating a path to the chronic pain community’s door… wanting to defend your rights that have been taken away.

There is no WHITE KNIGHT or a person name “george” coming over the horizon to save your ass… the anti-opiate groups are being well funded by groups that have FOR PROFIT companies that attempt to treat people suffering from addictive substance disorder and the various State/Federal agencies and opiophobic bureaucrats.

You can’t sue the government… but… the legality of their actions can be challenged in a court of law.  A few of their edicts/mandates are declared illegal/unconstitutional… it will stop them in their tracks on implementing any more of these basic violations of human rights.

Another state governor assumes the authority to practice medicine without a license ?

Gov. Ducey order limits opioids for Arizona employees

http://www.12news.com/mb/news/local/arizona/governor-ducey-order-limits-opioids-for-arizona-employees/340796576

 

congressstupidVermont Governor Proposes Limits on Painkiller Prescriptions

I guess that the Gov of Arizona has never hear of The Americans with Disability Act that provides certain accommodations in the work place.

Arizona Gov. Doug Ducey on Monday issued an executive order limiting opioid prescriptions for employees insured through the State of Arizona and individuals insured through the state’s Medicaid program, Arizona Health Care Cost Containment System (AHCCCS).

The order limits the first fill of prescription opioids to seven days and limits all fills for children, except those suffering from cancer, chronic disease or traumatic injury, according to a news release from the governor’s office.

“This action is essential to help prevent future drug addictions,” Ducey said in a prepared statement.

“The numbers are staggering. In 2015, 401 people in Arizona – more than 1 a day – died from prescription opioid overdoses. And in 2013 there were enough prescription pain medications dispensed to medicate every adult in Arizona around the clock for two weeks.”

 

Ducey signed the order Monday on the Capitol lawn. The signing is part of national Red Ribbon Week, focusing on drug prevention.

 

CDC “waiting till hell freezes over” to realize that legal opiates and OD’s: NO RELATIONSHIP

liarliarFewer Pain Meds but More Overdoses in Massachusetts

http://www.painnewsnetwork.org/stories/2016/10/20/fewer-pain-meds-but-more-overdoses-in-massachusetts

Apparently CDC is putting “common sense” ON HOLD.. when it comes to finally admitting that legal opiates and OD… have little in common..  Only 8.3 percent of those who died had a prescription for an opioid drug
Where is a recent article from the BOSTON GLOBE that stated that ONLY 8.3% of the people ODing on opiates … had a legal prescription for the opiate that toxicology showed in their system.

By Pat Anson, Editor

Opioid prescribing fell by 15 percent for members of Blue Cross Blue Shield of Massachusetts after the insurer adopted policies that discourage the dispensing of opioid pain medication, according to a new analysis by the Centers for Disease Control and Prevention.

The CDC’s Morbidity and Mortality Weekly Report found that 21 million fewer opioid doses were dispensed to Blue Cross Blue Shield members from 2012 to 2015. But the new policies failed to slow the growing number of opioid overdose deaths in Massachusetts, which more than doubled during the same period.

The CDC said it will “take time” before overdoses start to decline.

“Reducing the level of opioid prescribing is a long term strategy to limit exposure to these drugs. Mortality outcomes would not be expected to change for several years after implementation, and impact would be complicated by the increasing supply of illicit opioids,” Courtney Lenard, a CDC spokesperson, said in an email to Pain News Network.  

“Long-term strategies like the one outlined in the report take time to make an impact and therefore no immediate impact can be expected during the first several years of program implementation. Assessing what happened before and after the policy at the mortality level is inappropriate.”

Blue Cross Blue Shield (BCBS) of Massachusetts is the state’s largest insurer, with about 2.8 million members.

In 2012, the insurer adopted policies that discourage opioid prescribing by requiring doctors to develop treatment plans that consider non-opioid therapies; requiring pre-authorization for all opioid prescriptions after an initial 30 day supply; and limiting some pain patients to use of a single pharmacy.

The effect was immediate, with an average monthly decline of 14,000 prescriptions for both short and long-acting opioids.

Although cancer patients were exempt from the policies, there was a 9% decline in opioid prescriptions to BCBS members with a cancer diagnosis. The CDC attributed that to a “sentinel effect” in which doctors implement the same policies for all of their patients regardless of diagnosis.

“I think oncologists were becoming more thoughtful and maybe more vigilant about how much narcotics they were prescribing and I think that’s why we saw that decrease in cancer patients,” said Tony Dodek, MD, associate chief medical director for BCBS of Massachusetts. “We’ve only received one complaint about the program in terms of people having access to necessary pain medications.”

Like the CDC, Dodek said it may take years before the stricter prescribing policies start to have an impact on overdoses. So far the signs are not encouraging.

Opioid overdoses in Massachusetts rose from 698 deaths in 2012 to 1,659 deaths in 2015. The trend has continued in the first six months in 2016, with nearly a thousand opioid overdoses reported. Two-thirds of this year’s deaths were related to fentanyl, a synthetic opioid that is increasingly appearing on the black market. Illicit fentanyl is often combined with heroin and cocaine, or used in the manufacture of counterfeit pain medication.

MASSACHUSETTS DEPARTMENT OF HEALTH

MASSACHUSETTS DEPARTMENT OF HEALTH

“It’s not surprising to me that overdoses have not gone down because there is still a lot of drugs in circulation,” said Dodek. “What we did was slow the supply of new medication that’s in circulation. The fact is there is already way too much medication sitting in people’s medicine cabinets at home and that is what was available to start this epidemic.”

The Drug Enforcement Administration has said the U.S. is being “inundated” with counterfeit painkillers and there are anecdotal reports of some patients turning to street drugs for pain relief as opioid medication has become harder to get. But Dodek says it is recreational users – not pain patients – who are resorting to the black market.

“Any pain patient isn’t having access problems to getting opioids,” he said. “Those who may be using it for recreational purposes or for diversion probably are having a more difficult time (getting prescriptions). We still need to figure out what to do about illicit drugs, but I think decreasing the amount of prescriptions drugs will only be a good thing in the end.”

And what about the effect on pain patients as these policies are adopted? The CDC report ends with this telling statement:

“Finally, it is not known from these data how patient pain and function were affected by limiting access to opioid prescriptions.”

Enough INCOMPETENCE and GUILT to go around ?.. and CPP end up suffering ?

How drugs intended for patients ended up in the hands of illegal users: ‘No one was doing their job’

https://www.washingtonpost.com/investigations/how-drugs-intended-for-patients-ended-up-in-the-hands-of-illegal-users-no-one-was-doing-their-job/2016/10/22/10e79396-30a7-11e6-8ff7-7b6c1998b7a0_story.html

As the worst of a nationwide opioid epidemic raged in Appalachia, DEA investigators went after companies distributing millions of highly addictive pills. Then, their cases ground to a halt. (Lee Powell/The Washington Post)

UNNATURAL CAUSES SICK AND DYING IN SMALL-TOWN AMERICA: Since the turn of this century, death rates have risen for whites in midlife, particularly women. In this series, The Washington Post is exploring this trend and the forces driving it. Related: The DEA slowed enforcement while the opioid epidemic grew out of control

For 10 years, the government waged a behind-the-scenes war against pharmaceutical companies that hardly anyone knows: wholesale distributors of prescription narcotics that ship drugs from manufacturers to consumers.

The Drug Enforcement Administration targeted these middlemen for a simple reason. If the agency could force the companies to police their own drug shipments, it could keep millions of pills out of the hands of abusers and dealers. That would be much more effective than fighting “diversion” of legal painkillers at each drugstore and pain clinic.

Many companies held back drugs and alerted the DEA to signs of illegal activity, as required by law. But others did not.

Collectively, 13 companies identified by The Washington Post knew or should have known that hundreds of millions of pills were ending up on the black market, according to court records, DEA documents and legal settlements in administrative ­cases, many of which are being reported here for the first time. Even when they were alerted to suspicious pain clinics or pharmacies by the DEA and their own employees, some distributors ignored the warnings and continued to send drugs.

“Through the whole supply chain, I would venture to say no one was doing their job,” said Joseph T. Rannazzisi, former head of the DEA’s Office of Diversion Control, who led the effort against distributors from 2005 until shortly before his retirement in 2015. “And because no one was doing their job, it just perpetuated the problem. Corporate America let their profits get in the way of public health.”

A review of the DEA’s campaign against distributors reveals the extent of the companies’ role in the diversion of opioids. It shows how drugs intended for millions of legitimate pain patients ended up feeding illegal users’ appetites for prescription narcotics. And it helps explain why there has been little progress in the U.S. opioid epidemic, despite the efforts of public-health and enforcement agencies to stop it.

At the peak of the crisis, the DEA retreated from the battle. A Post investigation published Saturday revealed that beginning in 2013, some officials at DEA headquarters began to block and delay enforcement actions against wholesale drug distributors and others, frustrating investigators in the field.

Several former DEA officials told The Post that the shift in approach undercut the cases­­­ against some of these distributors, who were ignoring signs that their customers were ordering suspicious quantities of narcotics.

“We could not get these cases­ through headquarters,” said Frank Younker, a DEA supervisor in the Cincinnati field office who retired in 2014 after a 30-year career. “We were trying to shut off the flow, and we just couldn’t do it.”

The 13 companies include Fortune 25 giants McKesson, Cardinal Health and Amerisource­Bergen, which together control about 85 percent of all pharmaceutical distribution in the United States. They also include regional wholesalers such as Miami-Luken and KeySource Medical, both based in Ohio, as well as Walgreens, the nation’s largest retail drugstore chain. Many of the distributors are tiny operations with just a few employees.

It is not clear how many other cases exist. Because the DEA handles its enforcement actions administratively, few details surface unless the agency or the company discloses them, or if one side appeals in civil court.

The DEA declined to disclose how many enforcement actions it has brought against distributors, requiring a Freedom of Information Act request that The Post filed in April. The request is pending. The DEA also would not make any officials available to discuss this article, but provided a statement from acting administrator Chuck Rosenberg defending the agency’s enforcement actions.

“We now have good folks in place and are moving in the right direction,” he said.

Some of the 13 companies have fought the DEA’s enforcement efforts in court and in hearings before the agency’s administrative law judges. All have lost or settled, except in two cases that are pending. Using its civil authority, the DEA stopped the flow of narcotics from some company warehouses, and U.S. attorneys levied fines totaling more than $286 million.

Most of the 13 wholesalers involved in these cases declined to be interviewed. In court filings and congressional testimony, they said they have developed large and sophisticated systems to help prevent drug diversion. They have complained that it is difficult to police the activities of far-flung drug dispensers and have noted that drugs could not be sold to illegal users without prescriptions written by corrupt doctors. They also criticized the DEA’s past approach to the problem as punitive and its rules as vague and confusing.

But the problem is clearly ongoing. Prescription narcotics cause more overdose deaths every year than any street drug, including heroin. The painkiller epidemic has taken 165,000 lives since the turn of the century, with the number of deaths soaring from 3,785 in 2000 to 14,838 in 2014.

Opioid overdoses, mainly from prescription drugs, are also the leading cause of the recent unexpected rise in the mortality rate of middle-aged white Americans, particularly women in rural areas, after decades of steady decline.

But it is impossible to estimate how much of the opioid supply is siphoned away to illicit use.

“No one knows, because it’s impossible to track what happens to an individual prescription once it leaves the pharmacist,” said Susan Awad, director of advocacy and government relations for the American Society of Addiction Medicine.

***

One of the first wholesalers targeted by the DEA under its “Distributor Initiative” was Southwood Pharmaceuticals, a small company based in Lake Forest, Calif., that sent controlled substances to Internet pharmacies. Because these online businesses typically allowed people to obtain drugs without being seen by a doctor, they were ripe for abuse.

In 2005, for example, Southwood supplied one Florida online drugstore, Medipharm-Rx, with 8.6 million doses of hydrocodone — the opioid found in Vicodin and Lortab, according to the DEA.

But Southwood failed to file a single suspicious order report, even after the DEA warned the company in July 2006 about the growth in the volume of its shipments. The DEA had seen the trend in its own monitoring of drug-sales data.

“Even after being advised by agency officials that its internet pharmacy customers were likely engaged in illegal activity, [Southwood] failed miserably to conduct adequate due diligence,” Michele Leonhart, then the DEA’s deputy administrator, wrote in a 2007 decision to revoke the company’s license to distribute narcotics.

“The direct and foreseeable consequence of the manner in which [Southwood] conducted its due diligence program was the likely diversion of millions of dosage units of hydrocodone,” Leonhart wrote, adding that the company had reason to know that the 44 million doses of hydrocodone it distributed were probably being diverted.

That amount would provide a 30-day supply of narcotics for everyone in the city of Dallas, according to Express Scripts, a pharmacy benefit management company.

Southwood got out of the business of selling controlled substances and six years later lost its pharmacy license in California.

The company’s president, John Sempre, recently told The Post that the company did not understand at first that it was supplying Internet pharmacies. He said it is very difficult for companies to monitor the sales of faraway retailers.

“If companies like McKesson can’t control it, what does that tell you?” Sempre asked.

In 2008, McKesson, the nation’s largest drug distributor, settled a case that accused three of its U.S. warehouses of failing to report hundreds of suspicious orders from Internet pharmacies. “As a result, millions of doses of controlled substances were diverted from legitimate channels of distribution,” the Justice Department said in a news release. The company paid a $13 million fine to U.S. attorney’s offices in Florida, Maryland, Colorado, Texas, Utah and California.

“By failing to report suspicious orders for controlled substances that it received from rogue Internet pharmacies, the McKesson Corporation fueled the explosive prescription drug abuse problem we have in this country,” Leonhart, then the acting DEA administrator, said in a statement at the time.

Seven years later, after being caught up in a second diversion case, McKesson agreed to pay a $150 million fine and accepted license suspensions at four warehouses, according to a company filing with the Securities and Exchange Commission. No other details of that case have become public, and both the company and the DEA declined to discuss it.

A McKesson spokeswoman said in a statement to The Post, “We welcome the ongoing dialogue with the DEA aimed at developing effective controlled substances monitoring programs and successfully mitigating prescription drug abuse and diversion.”

AmerisourceBergen, another member of the so-called Big Three distributors, lost its license to send controlled substances from an Orlando warehouse on April 24, 2007, amid allegations that it was not controlling shipments of hydrocodone to Internet pharmacies. The facility was back in business by August of that year and did not pay a fine, according to a company spokeswoman.

Few details of the case have surfaced.

Cardinal, the third member of the Big Three, paid a $34 million fine in 2008 after seven of its warehouses across the country filled thousands of suspicious orders from Internet pharmacies without reporting them, despite an earlier warning from the DEA, according to a Justice Department news release.

On Oct. 5, 2010, when Cardinal investigator Vincent Moellering visited Gulf Coast Medical Pharmacy, a drugstore in Fort Myers, Fla., he found evidence of diversion everywhere, records show, including suspicious customers who came in groups to fill their prescriptions.

The pharmacy owner told Moellering that he could sell even more narcotics if Cardinal would supply them, according to Moellering’s report, which the DEA introduced in a court proceeding.

Moellering labeled the store “high risk” and wrote: “I am not convinced that the owner is being forthright pertaining to his customers’ origin or residence. I have requested permission to contact DEA to resolve this issue.”

But Cardinal didn’t notify the agency or cut off Gulf Coast’s drug supply, the DEA contends. Instead, the shipments kept going out. In 2011 alone, Cardinal sent more than 2 million doses of oxycodone to Gulf Coast. Cardinal typically shipped 65,000 doses of the opioid annually to comparable pharmacies, the DEA said.

Even as Cardinal was increasing its shipments to Gulf Coast, another wholesale drug distributor, H.D. Smith, was cutting off its supply of painkillers to the pharmacy. Smith took action after one of its compliance officers visited Gulf Coast and found “impaired and lethargic” customers “with glassy eyes” in November 2010, a few weeks after Moellering’s visit, court records show.

The Smith inspector learned that the pharmacy filled 300 prescriptions a day, nearly half for controlled substances. Smith considered anything over 20 percent to be a red flag.

Gulf Coast owner Jeffrey R. Green and manager Karen S. Hebble sometimes waited after hours to sell narcotics, even without a pharmacist present, court records show.

Drug dealers said they brought groups of fake patients — known in the trade as “spuds” or “skidoodies” — to Gulf Coast to fill bogus prescriptions obtained from cooperating prescribers, court records state. They always paid cash.

One drug dealer would call ahead to make sure Gulf Coast had enough pills for his fake customers; sales were so brisk that Gulf Coast sometimes ran out of painkillers. Cardinal only stopped shipments to Gulf Coast in October 2011, shortly before the DEA demanded information from the distributor. The next month, Gulf Coast surrendered its license.

Green and Hebble were ultimately convicted in federal court on conspiracy and money-laundering charges.

Cardinal contended that volume of drug sales alone is not an accurate measure of lack of compliance. The company noted that Gulf Coast served a hospital complex and hundreds of physicians.

In 2012, Cardinal settled the administrative case, but no fine has been levied. Negotiations are ongoing, according to a federal prosecutor and the company.

In a statement to The Post, Brett Ludwig, Cardinal’s vice president of public relations, said the company deploys “advanced analytics, technology, and teams of anti-diversion specialists and investigators who are embedded in our supply chain. This ensures that we are as effective and efficient as possible in constantly monitoring, identifying, and eliminating any outside criminal activity.”

At Walgreens, an employee at one of the 13 warehouses the drugstore chain operated in the United States, grew suspicious of the large orders being sent to some of its pharmacies, court records show.

Kristine Atwell, who managed distribution of controlled substances for the company’s warehouse in Jupiter, Fla., sent an email on Jan. 10, 2011, to corporate headquarters urging that some of the stores be required to justify their large quantity of orders.

“I ran a query to see how many bottles we have sent to store #3836 and we have shipped them 3271 bottles between 12/1/10 and 1/10/11,” Atwell wrote. [A bottle sent by a wholesaler generally contains 100 doses.] “I don’t know how they can even house this many bottle[s] to be honest. How do we go about checking the validity of these orders?”

Walgreens never checked, the DEA said. Between April 2010 and February 2012, the Jupiter distribution center sent 13.7 million oxycodone doses to six Florida stores, records show — many times the norm, according to the DEA.

In March 2011, the situation became so alarming at two Walgreens drugstores in the small town of Oviedo, Fla., that Police Chief Jeffrey Chudnow wrote to the company’s top executives: Alan G. McNally, who was chairman at the time; and Gregory D. Wasson, then its president and chief executive.

Chudnow asked that they prohibit Walgreens pharmacists from filling orders where the quantities of narcotics were split over two prescriptions.

“These types of prescriptions overtly denote misuse and possible street sales of these drugs,” Chudnow wrote. He said he never heard back from the executives.

In 2012, the DEA launched a six-month investigation of Walgreens’s Jupiter facility. The probe found that Walgreens failed to maintain an effective system for detecting suspicious orders or reporting them to the DEA.

Even when suspicious orders were identified, the warehouse often shipped the drugs anyway, without making inquiries, the DEA said in court papers. A company spokesman said Walgreens would have no comment on the case.

Walgreens settled with the DEA in 2013, agreeing to pay an $80 million fine — a record for a diversion case at the time. The company acknowledged that its “suspicious order reporting for distribution to certain pharmacies did not meet the standards identified by DEA.”

In 2013, DEA officials at the agency’s headquarters began requiring a higher burden of proof before investigators in the field could take enforcement action. One case that was underway became entangled in that shift, according to interviews and records.

Beginning in 2011, the DEA had repeatedly warned Miami-Luken, an Ohio-based distributor, about suspicious sales of opioids, according to Jim Geldhof, then the agency’s program manager in Detroit.

“We went to management of the company and told them they have to look at their sales. They are pretty extraordinary,” said Geldhof, who retired in January after more than four decades with the agency. “We spoke to them on multiple occasions, and we were pretty much ignored.”

Yet investigators couldn’t convince lawyers at DEA headquarters to allow them to take action.

Geldhof said that he requested orders to show cause in 2013 and that they were not issued until November 2015.

“It sat there for two years. I don’t know why there was a delay,” Geldhof said. “We went between back and forth. The ball was always moving. We had all of this going on, overdose deaths, what part of this are we not getting them to understand. We said, ‘You tell us what you want and we’ll give it to you.’ ”

Inside Miami-Luken headquarters, employees had also seen troubling signs. Two of them sent word up the chain. A pharmaceutical buyer and a customer-service representative were concerned about large oxycodone orders by a southern Ohio pain clinic.

The warnings reached senior company officials, including then-chief executive Anthony Rattini. But little changed.

Cindy Willet, the senior pharmaceutical buyer, told investigators in 2015 that she eventually “stopped talking to [Rattini] about her concerns because he wasn’t doing anything about it. It was as if it was falling on deaf ears. Tony never stopped an order.”

The pain clinic, Unique Pain Management, was based in Wheelersburg, Ohio, a town of 6,500 at the epicenter the opioid epidemic. The clinic was run by a father-daughter team of physicians, John and Margy Temponeras. Between December 2009 and June 2010, the clinic’s monthly orders of oxycodone rose from 67,800 doses to 104,400. Miami-Luken did not investigate the surge, according to the DEA.

Despite signs that something was amiss, “Miami-Luken not only continued to ship Dr. [Margy] Temponeras oxycodone, but also shipped increased amounts,” the DEA alleged.

But Margy Temponeras ordered so much OxyContin from Miami-Luken that in August 2010 she drew the attention of Purdue Pharma, the drug’s manufacturer. Purdue cut Miami-Luken’s OxyContin supply by 20 percent, prompting Miami-Luken to halt drug shipments to Temponeras, records show.

Last year, a federal grand jury indicted the Temponerases and a pharmacist on charges that they conspired to illegally sell medication, alleging that at least eight people had died of overdoses connected to the drugs.

Three of those people died while the clinic was receiving drugs from Miami-Luken between November 2008 and August 2010, according to the indictment and DEA records. It is unclear whether Margy Temponeras also purchased drugs from other distributors, or whether any of those who died consumed drugs distributed by Miami-Luken.

The Temponerases are scheduled to stand trial early next year. Their attorneys declined to comment. An attorney for the pharmacist, Raymond Fankell, who is also scheduled to stand trial next year, said Fankell’s involvement was limited to helping Margy Temponeras set up the dispensary in her office and to filling her prescriptions at his drugstore.

During one of their interviews with Rattini, DEA investigators asked how the company documented suspicious orders. Rattini pointed to his compliance officer, who put a finger to his head. “It’s all just up here,” he said.

The agency is now attempting to revoke Miami-Luken’s license. The company has asked for a hearing before a DEA administrative law judge and is battling the DEA in federal court over a subpoena for agency records.

Not All Drug Abuse Is From Health Providers and Oxycodone

Not All Drug Abuse Is From Health Providers and Oxycodone

http://www.anesthesiologynews.com/Commentary/Article/10-16/Not-All-Drug-Abuse-Is-From-Health-Providers-and-Oxycodone/38050/ses=ogst?

Over the last few months, there has been an explosion of interest in the legislature to rein in oxycodone and to limit its use for pain management. Health care providers are painted as the major culprits who are causing an explosion of drug abuse, as reported by the media. Many excellent physicians in the field of pain medicine have been put under the microscope regarding their management of narcotics prescribed for certain patients, including those with terminal disease pain. This is not to say that health care providers should not be policed with medically based data on how to balance pain management with narcotics and nonnarcotic modalities.

The media is also filled with reports of raids on methamphetamine laboratories in our communities. This ongoing battle with illicit drugs has become a major political issue at both the local and federal level. Political debate has focused on how oxycodone and fentanyl are overprescribed, diverted and at the heart of our drug problem.

Public health care providers and politicians may not be aware of a more overwhelming supply chain of illicit addictive drugs. These drugs that are flooding our streets are being manufactured not in a debilitated trailer in rural America, but in a factory at an industrial level. Want to get your hands on the latest designer street drug or slightly tweaked version of fentanyl? It’s as easy as typing “Research Chemicals” into Google. You can scroll through an endless list of websites such as Alibaba.com and Guidechem.com, to name a few. Some of these offer free samples, bargain prices and home delivery by Express Mail. All you have to do is wire a few thousand dollars or use your credit card with an English-speaking customer service representative, and you get drugs delivered to your door. No need to doctor-shop or use criminal drug dealers.

 

This globalized marketplace, in which Chinese chemical companies pump out large volumes of ever-changing isomers that are too new to be banned in the United States or internationally, leaves our local and federal law enforcement officials virtually powerless to slow the influx of synthetic drugs. Those companies also manufacture some of the precursors of illicit drugs, which are used by many of the major drug cartels. In a country that has perfected the art of internet censorship and electronic spying, the open online drug market is a blatant example of what law enforcement has said is China’s reluctance to take action, as it has today become the major supplier of deadly synthetic drugs.

Since 2008, the number of new psychoactive substances added to the United Nations Office on Drugs and Crime has soared more than eightfold to 541, far more than the 244 drugs listed as controlled substances that are sold on these websites as “legal highs,” “research chemicals,” “not for human use” and fertilizers.

Our local governments have to deal with these temporarily legal substances until legislation can be passed. A great example is “spice” or “synthetic marijuana,” which flooded smoke shops and gas stations and was sold alongside tobacco products. Some of the most popular names included K2, Yucatan Fire, Skunk and Moon Rocks. Spice was often promoted as being “natural,” but in reality it was plant material treated with manufactured psychoactive chemicals and synthetic cannabinoid compounds. Spice users and poison control centers across the country have reported rapid heart rates, agitation, confusion, hallucinations, self-destructive behavior and psychosis. These agents have triggered heart attacks, strokes and permanent neurologic damage.

Bath salts are another drug that has triggered a major drug problem and has filled our ERs and ICUs. Websites market these compounds as keyboard cleaners, plant food and jewelry cleaners. The main component of most bath salts is methylenedioxypyrovalerone or new derivatives to skirt the law. Popular types of bath salts include “Ivory Wave,” “Purple Wave,” “Vanilla Sky” and “Bliss.” These drugs trigger agitation, paranoia, hallucinations, hypertension, tachycardia and suicidal thinking. A major danger is depression or suicidal behavior that can last even after the stimulatory effects of the drugs have worn off. There have been cases of suicides reported a few days after use.

Flakka (or alpha-PVP), which is manufactured in China, is sold by over 150 companies. It is a highly addictive synthetic drug that has overwhelmed hospital systems, some of which report 20 Flakka-related emergencies a day. Many deaths also have been attributed to this cheaply priced drug. Some of the dealers even guarantee that if your shipment is seized, they will send you another package. To elude U.S. Customs and Border Protection agents, the shipment may be labeled as industrial solvent or cleaner. A kilogram can be purchased for $1,500 online and sold for many-fold more on our streets.

These chemical companies may be responsible for the explosion in narcotic overdose deaths that have affected all social classes across the country. The media is filled with reports of fentanyl deaths and ever-increasing drug-related deaths. This has triggered the wide availability of Narcan (naloxone, Adapt Pharma) to first responders and the public. However, much of the problem may be triggered by the widespread availability of industrially produced fentanyl analogs.

The Drug Enforcement Administration is working to classify these specific analogs. An example of the frustration that law enforcement must deal with is a compound called furanylfentanyl. Once it is listed as illegal, the laboratories in China will be automatically changing the formula to come up with the next analog acetyl fentanyl drug configuration.

What can we do as health care providers who must deal with these problems on a daily basis in our ERs, operating rooms and ICUs? I believe that education is a key factor. We need to educate our political leaders about any and all industrially produced, addictive drugs and their terrible effects on our society. Our national government should address this problem with authorities in China. At the grassroots level, health care providers must educate the public on these dangerous, synthetic drugs with widely varying potencies.