Showing posts with label painkillers. Show all posts
Showing posts with label painkillers. Show all posts

Tuesday, March 19, 2013

25 disturbing facts about psych drugs, soldiers and suicides

Thursday, March 14, 2013
by Mike Adams, the Health Ranger

(NaturalNews) We are living in an age of upside-downs, where right is wrong, fiction is truth and war is peace. Those who fight the wars are subjected to their own house of mirrors via pharmaceutical "treatments." Instead of providing U.S. soldiers and veterans with actual health care, the government throws pills at them and calls it "therapy."

Stimulants, antidepressants, anti-psychotics, sedatives and pain meds are the new "fuel" for America's front-line forces. While the idea of sending medicated soldiers into battle was unthinkable just three decades ago, today it's the status quo. And the cost in human lives has never been more tragic.

Here are 25 disturbing facts about psych drugs, soldiers and suicides. They are disturbing because everybody seems to be pretending there is no link between psychiatric drugs and soldier suicides. So soldiers and veterans keep dying while the Pentagon (and the VA) keep pretending they don't know why. (Sources are listed at the bottom of this article.)

1) 33% of the U.S. Army is on prescription medications, and nearly a quarter of those are on psychotropic drugs

2) In 2010, the Pentagon spent $280 million on psychiatric drugs. That number has since risen.

3) There are now over 8,000 suicides each year by U.S. soldiers and veterans; that's over 22 a day

4) 33% of those suicides are attributed to medication side effects

5) That means medications are killing more U.S. soldiers and veterans than Al-Qaeda

6) 500% more soldiers abuse prescription drugs than illegal street drugs

7) Under the Obama administration, the number of veterans waiting for VA care has risen from 11,000 in 2009 to 245,000 today

8) More active duty soldiers die from suicide than from combat: 349 dead last year

9) The number of prescriptions for Ritalin and Adderall written for active-duty soldiers has increased 1,000% in the last five years

10) For every active-duty service member who dies in battle, 25 veterans die by suicide

11) Only 1 percent of Americans have served in the Middle East, but veterans of combat there make up 20% of all suicides in the United States

12) The suicide rate of active-duty soldiers in the Civil War was only 9 - 15 per 100,000 soldiers. The suicide rate of active-duty U.S. soldiers in the Middle East is 23 per 100,000. And casualty rates were far higher in the Civil War, meaning the Civil War was more psychologically traumatic.

13) In the Korean War, the suicide rate among active-duty military soldiers was only 11 per 100,000

14) To date, the Pentagon has spent more than a billion dollars on psychiatric drugs, making it one of the largest customers of Big Pharma

15) In 2010, over 213,000 active-duty military personnel were taking medications considered "high risk" by the Pentagon

16) In the years since the Iraq War began, twice as many soldiers of the Texas Army National Guard have died of suicide than in combat

17) Defense Secretary Leon Panetta calls military suicides an "epidemic"

18) Of all the branches of the military, the Army has the highest number of suicides each year, almost 400% more than the Marines

19) Most active-duty soldiers who take psychiatric medications consume a combination of three to five prescriptions

20) The use of prescription medications by active-duty soldiers is largely unregulated. Soldiers are given a bottle of meds and sent into combat. If they run out of meds, they are given a refill, no questions asked.

21) The mainstream media says the answer to lowing suicides of veterans is to take away their guns so that they cannot shoot themselves. This is the logical equivalent to trying to fix your car's engine by removing the "check engine" light.

22) The Pentagon is initiating new research (in 2013) to try to figure out why psychiatric medications cause soldiers to commit suicide. The research involves tracking brain activity by attaching electrodes to the skull.

23) One-third of military suicides are committed by soldiers who have never seen combat

24) In the last year, the military wrote over 54,000 prescriptions for Seroquel to soldiers, and all those prescriptions were "off label," meaning the intended use has never been approved by the FDA as safe or effective.

25) Dr. Bart Billings, a retired Army Colonel and former military psychologist, refers to psychiatric drugs as a "chemical lobotomy" for soldiers.

Thursday, September 20, 2012

How Big Pharma Hooked America on Legal Heroin

by Kelly_Bourdet on Tuesday, Sep 18, 2012 - Mother Board
  • Picture_39_large

Matthew began taking painkillers – Percocet, then OxyContin – as a teenager. His father was battling cancer, so narcotics were readily available in the house. While vacationing in Florida, he was unable to take the number of pills his body had become dependent upon. At the peak of his addiction, Matthew was taking nine 80mg pills a day, for a combined 720mg. He bought them off of a local friend who was prescribed 300 per month for her Fibromyalgia, a syndrome in which a person has long-term, body-wide pain and tenderness in the joints, muscles, tendons, and other soft tissues. He told me about his confusion at his typical withdrawal symptoms – vomiting, aches, sweating, headaches. He thought he had a bad flu.

He went to the hospital because he felt so ill, though he didn’t honestly answer doctors’ questions about his drug use. Doctors were confused by his symptoms, even giving Matthew a spinal tap to investigate. After leaving the hospital, he took some pills and his horrible “flu symptoms” miraculously disappeared.

Courtney, 28, was already a seasoned drug addict at age seventeen. When she left a treatment facility after overcoming a methamphetamine addiction, she tried OxyContin, thinking it would be easier to control. She immediately liked it. Within two months she was taking it everyday – and getting extremely dope-sick when she couldn’t find it. In a familiar sequence of events, she went from snorting to shooting Oxy, and then shooting heroin when she couldn’t find any Oxys. She bought blank prescription pads on the black market, forging OxyContin prescriptions to fuel her habit. She was eventually caught trying to fill a fake prescription at a local pharmacy. She eventually detoxed in a jail cell.

Next April, the patent on the original formulation of OxyContin expires; what happens next depends upon, to a large extent, what’s already happened. And it’s been a mess.

The active ingredient behind the drug, oxycodone, isn’t new. The compound was originally synthesized in Germany in 1916. The patent on the medication had expired well before Purdue Pharma, a Stamford, Connecticut-based pharmaceutical company and the industry leader in pain medication, released it under the brand name in 1996. The genius of Purdue’s continued foray into pain-management medication – they had already produced versions of hydromorphone, oxycodone, fentanyl, codeine, and hydrocodone – was twofold. They not only created a drug from an already readily available compound, but they were able to essentially re-patent the active ingredient by introducing a time-release element. Prior to the 1990s, strong opioid medications were not routinely given for miscellaneous or chronic, moderately painful conditions; the strongest classes of drugs were often reserved for the dying.

But Purdue parlayed their time-release system not only into the patent for OxyContin. They also went on a PR blitz, claiming their drug was unique because of the time-release element and implied that it was so difficult to abuse that the risk of addiction was “under 1%.”

To cement the brand’s reputation among doctors, Purdue conducted more than 40 national pain-management and speaker-training conferences at resorts in Florida, Arizona, and California between 1996 and 2001. They invited over 5,000 physicians, pharmacists, and nurses to these all-expenses-paid symposia. Many were recruited and trained for Purdue’s national speaker bureau. Purdue offered starter coupons offering a free 7-30 day trial of their medication, a practice that’s common among pharmaceutical companies for everything from skincare medicine to contraceptives. OxyContin became an instant hit among doctors, many of whom saw it as a wonder drug in the battle against the debilitating effects of chronic pain. As the good news spread sales of the drug mushroomed, rising from $40 million in 1996 to more than $1 billion in 2001, outstripping even Viagra. Meanwhile, Purdue’s campaign to extend the use of powerful narcotics to ordinary chronic ailments – for which the drug has been well documented to help – proved highly successful. By 2003, over half of the OxyContin prescriptions written in the United States were written by a primary care physician.



Anyone who has ever had to face the sad reality of being close to a drug addict or alcoholic quickly learns an important lesson. Namely, that when it comes to getting and using mind-altering substances, active drug addicts are among the most resourceful, ingenious, and crafty humans on the planet. I’ve known people who drank hairspray in detox units to get a buzz. So how difficult was it to circumvent the time-release element of the original OxyContin?
“The fact that I could freebase it the way that I did,” Frank says, “is really freaky.”

See, the proprietary time-release mechanism was essentially a waxy coating that could be peeled off using a razor blade or dissolved using water or saliva. Turning the “safe” version of OC into a highly-abusable form was about as difficult as peeling a tiny apple. The death rate from overdoses of opioids in 2007 was roughly three times that of 1991. In 2008, deaths from opiate overdose surpassed the combined overdose deaths of cocaine and heroin. This year the CDC says that, “opioid overdose resulted in 14,800 deaths, accounting for 73.8% of all prescription overdose deaths.”

Young Markets


Many safety trials for pharmaceuticals do not test children under the age of sixteen. To combat the rampant prescription of adult drugs to kids by pediatricians, the Food and Drug Administration offers incentives for companies who design tests specifically for children. One of these incentives is a six-month patent extension.

Sometime this year, Purdue Pharma began paying dozens of clinical sites around the country to document what happens when OxyContin is given to children. This wasn’t the first time the company had conducted pediatric trials of OxyContin: they initiated tests on children in 2004, but halted the study citing financial constraints. That year, a federal District Court in Manhattan found the company guilty of deliberately misleading federal officials in order to retain exclusive patents and prevent cheaper generic versions of OxyContin from hitting the market.

When Purdue’s new trials were reported this year by The Daily, critics and especially addiction specialists, concerned about administering a highly addictive drug to children, wondered if the tests had something to do with the expiration date of Purdue’s patent for the drug: April 2013.
“[Purdue is] doing [the pediatric trial] for patent exclusivity, there’s no doubt about it in my mind – not out of largesse,” Dr. Elliot Krane of Stanford University’s Lucile Packard Children’s Hospital told The Daily in July. “That’s important for their bottom line.” In 2004, Purdue Pharma reported $1.7 billion in gross sales of OxyContin. Last year, Purdue saw $2.8 billion in sales of the drug.

Still, Purdue said that “resources” were an issue. “We reinitiated the remaining pediatric trials once we had the necessary resources to continue them,” said James W. Heins, a company representative. “These trials are challenging to conduct and can take years to complete.”

20mg and 80mg OxyContin pills (via)

However ulterior Purdue’s motives are, and however risky testing OxyContin on kids might sound, the trials aren’t without basis. Despite the skepticism of critics, Purdue says it doesn’t plan to attempt to market its drug to pediatricians, a shift that would require rigorous FDA review. But doctors already regularly prescribe Oxy for children suffering conditions of moderate or severe pain, a practice that’s accompanied by little to no data predicting how it might affect them and what their long-term outcomes might be. This phenomenon is called “off-label use,” one defined as the practice of prescribing pharmaceuticals for an unapproved indication or in an unapproved age group, unapproved dose or unapproved form of administration."

Pharmaceutical companies can’t officially promote their drugs for the treatment of any conditions for which it has not received formal FDA approval. But that doesn’t stop off-label prescribing from happening all the time. In the United States, physicians are granted generous leeway in prescribing drugs for uses and patients other than their intended ones. Last month, GlaxoSmithKline, the British multinational pharmaceutical maker, was slapped with a $3 billion fine, the largest in the industry’s history, for promoting the off-label use of the antidepressants Wellbutrin and Paxil.

Kids are a popular audience for off-label drugs. A 2008 study published in the journal Academic Pediatrics found that 62 percent of pediatric outpatient visits resulted in the prescription of a drug for off-label use. When you look at only the prescription of pain medications, the number jumps to 86 percent. Tests on children then are a good thing: without them, we might not know what the drugs we’re already prescribing to them might actually be doing to them.

By their end, the pediatric trials will have included approximately 150 children aged 6-16, all of whom are already taking opioid medications to treat moderate to severe pain. Of course, the costs of such tests on brains that aren’t fully developed aren’t yet well understood. One study from 2005, by a professor from the University of Michigan, found that children who are prescribed opioids are more likely to abuse painkillers in later life.

The Fine Points of Misbranding


Even after a barrage of criticism over it’s marketing, Purdue Pharma, per industry norms, continues to fund a dubious advertising campaign in the form of a “public service” program called “Partners Against Pain." Aimed at consumers and physicians, the 17-year-old “resource” for doctors is one of the company’s foremost marketing tools, extolling the virtues of opioid pain medication for chronic non-malignant pain while minimizing the risk of addiction. Today it centers around public endorsements – actress Jennifer Gray is its latest spokesperson, and has appeared on local TV newscasts to promote the program – and a website that’s been a goldmine of spin. It’s impossible to fully stress how misleading some of its “facts” have been over the years. To wit:
While opioids can be abused and may be habit forming, clinical experience shows that ‘addiction to opioids legitimately used in the management of pain is very rare… In trials in almost 25,000 patients with no history of drug dependence, there were only 7 cases of iatrogenic drug addiction.
Pretty impressive, right? As a general practitioner considering prescribing opioid drugs for chronic non-malignant pain, wouldn’t an approximately 0.028 percent addiction rate strike you as an extremely low risk?

Well, if you trace this claim back to the original literature, you find that this “information” is culled from three “studies.” The first of which was not even a study. It was a letter to the editor of the New England Journal of Medicine written in 1980, reporting that in 11,882 hospitalized patients who received at least one narcotic, there were only four cases of “reasonably well documented addiction.” Note that administration of narcotic painkillers took place in a hospital setting for acute pain, and so including this statistic in resources designed to inform on long-term, non-hospital prescription of narcotics is inherently misleading. (Despite being cited in academic journals an impressive 635 times, no abstract was available for this correspondence in the online U.S. National Library of Medicine.)

Another of the sources summarized here, Drug Dependency in Patients with Chronic Headaches, was a review of 2,369 patients experiencing headaches. Only 62 patients were actually included in the drug dependency study, however, as they had been taking medications frequently for at least six-months. Of these 62, only 23 were taking narcotics. Of these 23, three were thought to be abusing their narcotic medication.

In reviewing the website for the FDA, Dr. Art Van Zee concluded in 2001 that Purdue had “over-sold the benefits of opiod therapy for chronic non-malignant pain, while providing false reassurance about what the real risks are of addiction for patients taking opiods for chronic non-malginant pain.” It’s hard to overstate the negative effects of misinformation on the prescribing habits of physicians naïve about certain classes of drugs. A resource produced by Purdue Pharma claimed to represent addiction rates in almost 25,000 patients. In reality, only 23 of the patients were taking narcotics outside of a hospital setting, and for what could be termed chronic non-malignant pain (headaches). In this extremely small sample, approximately 13 percent were believed to be abusing their narcotic medication. These studies were cited not only on their website, but also in literature given to both physicians and to patients taking OxyContin.

In 2007, Purdue Pharma and three of its top executives were ordered to pay $634 million as a penalty for misbranding OxyContin. In court, Purdue Pharma admitted that “with the intent to defraud or mislead” it promoted OxyContin as a safer, less-abusable opioid drug. Documents filed by prosecutors in the Abingdon, Virginia, District Court demonstrated that, beginning in 1996, Purdue had waged the most aggressive marketing campaign ever for a narcotic medication, promoting OxyContin to general practitioners, lauding its safety, and encouraging its use for ailments like arthritis and back pain, maladies for which treatment with opioids of this strength would have been unthinkable only a decade prior.

All the while, representatives for the company proclaimed that “delayed absorption as provided by OxyContin Tablets is believed to reduce the abuse liability of the drug.” The “believed” statement was reinforced by sales officials, who were found to have fabricated phony scientific charts and to have suppressed certain findings about the drugs addictive effects. Three top executives, who pleaded guilty to misdemeanor charges of being liable for misleading regulators, the public and doctors about the risk of addiction, were fined a combined total of $35 million. None faced prison. And while the larger $600 million fine was one of the largest ever levied against a pharmaceutical company, it represented less than half of Purdue Pharma’s annual OxyContin sales.

Frank


Like many people, Frank Morris’ parents caught him smoking weed in high school. He had developed a bit of a pot habit by around age 18, but with his parents keeping a close eye on him, he quit smoking weed and snatched a few of his mother’s Vicodin pills instead. Within a year and a half he began trying OxyContin. Frank’s life deteriorated quickly. Almost immediately he started using daily. Six months later, he freebased the drug for the first time. Six months after that he shot Oxy intravenously for the first time. After another six months he shot heroin intravenously for the first time.

Some eighteen months after his introduction to Oxy, Frank was strung out, a junkie. Soon enough he was jailed for attempting to purchase heroin on the streets of San Francisco.

Street heroin (via U.S. Drug Enforcement administration)

For much of the time he was using OxyContin, Frank, who is now 27 and living in New York City, had a legitimate prescription from a doctor. His physician prescribed him 280 80mg pills per month for his migraines. After all, this is the drug that Purdue Pharma represented as a safe alternative to fast-acting narcotics, bragging that a patient only needed two pills per day, with a 12-hour release mechanism, to achieve around-the-clock pain management. Frank was prescribed enough of one of the highest doses of the medication to take roughly nine per day. At $40 to $50 a pill, the street value in 2006 of this number of 80mg OxyContin pills was $11,200 to $14,000. Frank sold enough of the pills – roughly a quarter of them – to cover his $11-per-pill cost at a local hospital pharmacy. He pocketed the rest. By the end of his opioid addiction, he switched to shooting black tar heroin. It was cheaper.

How could a doctor have legitimately prescribed so much Oxy for migraines? Wouldn’t a young man filling this outlandish prescription month after month at a hospital pharmacy raise some red flags? The same off-label prescribing guidelines in place for the prescription of drugs to children also applies to prescription for adults. Clinical trials might only test for the safety and efficacy of, say, two pills per day, but physicians are able to interpret this information any way they see fit. Over-prescription of this kind is undoubtedly morally questionable. It’s not, however, illegal.

“It Brought Me To My Knees”


There was a salient thread connecting all the OxyContin addicts I spoke with, and that’s how fast they all said it happens, how quickly they all became addicted, and how surprised they were at their physical dependence. Each of them recited a litany of opioid substances that they had abused in various combinations: Methadone, heroin, Diuladid, Percocet, Suboxone, Vicodin, and Morphine. They swallowed, snorted, shot, and free-based the pills, sometimes even mixing them with crack. But they all told me that the first opioid that really got them, the one that was easiest to get and gave the most powerful high, was OxyContin.

Original Oxy and new formula (via)

Frank told me he was once driving through central California going into heavy withdrawal. When he pulled over at a gas station to fill up, he saw a guy with telltale scratches on his face – opiate addicts often feel phantom itches while high and will scratch their faces, arms, and legs until they bleed. Frank approached the guy, asking if he knew where he could score some Oxys. The guy pulled two huge bottles out of the trunk of his car; he could get them right there.

None of the men and women I spoke with used street heroin before taking OxyContin. All of them used it after using OxyContin. In fact, since Purdue Pharma introduced a reformulated OxyContin in 2010 containing chemical safety-nets meant to render it less easily abused — the pills no longer dissolve in water, making them more difficult to cook and shoot intravenously — the number of addicts switching to heroin has skyrocketed.

In a study of 2,500 OxyContin addicts followed from July 2009 until March 2012, researchers found a 17 percent drop in OxyContin abuse. The study found that almost one-fourth of participants were able to abuse OxyContin despite the reformulation. Sixty-six percent switched to heroin. Many have also latched onto to Opana, another painkiller. But according to the National Association of Drug Diversion Investigators, OxyContin’s falling street price is a sign that the $100 million reformulation is working at thwarting abuse of the drug. Getting high on the new Oxy requires swallowing three or four pills rather than one, but abusers are still finding unusual ways to break down their safety mechanism, through microwaving and freezing, as well as carefully filing them down to powder.

A fourth recovering addict I spoke with, Richard, a 29-year-old living in New York, seemed near tears when describing his addiction. “It brought me to my knees,” he said. When I mentioned that Purdue would be testing the safety of their drug on children, he seemed horrified. “I wouldn’t wish [OxyContin] on anyone.” Richard also watched his father’s difficult journey quitting OxyContin after being prescribed the drug. His grandfather is currently an addict after he was prescribed OxyContin for pain.

After the Backlash


Make no mistake: OxyContin is a powerful treatment for people suffering from severe and chronic pain. Users say it has changed their lives, and anyone suffering from the effects of back surgery or a violent accident can attest to the relief that opioids bring. And addiction is a complex beast, one whose roots lie far beyond a simple pill, no matter how addictive it may be.

But having heavily promoted a drug so easily abused while downplaying the danger of that abuse – and having come under heavy criticism from regulators – Purdue Pharma has in recent years changed its approach to marketing OxyContin. After being fined for their fraudulent claims, Purdue invested in several informational sites and programs to educate doctors, pharmacists, and patients on prescription drug addiction. Rxsafetymatters.org is mainly geared towards the parents of teens abusing prescription drugs. It offers links to resources for addicted persons, tips for parents on storage and disposal of commonly abused drugs, and the signs of symptoms of addiction. Purdue financially supported The Partnership at drugfree.org in their production of Time to Get Help, a resource for parents seeking addiction treatment for drug- and alcohol-abusing children.

Additionally, Purdue provides training and information to pharmacists and law enforcement on safety and proper protocol during pharmacy heists. The number of armed robberies on pharmacies in the United States rose 81 percent between 2006 and 2010, concurrent with the rise of opioid abuse and addiction. Purdue launched Rx Patrol as a resource for pharmacists.

They provide up-to-the-minute crime statistics — as of September 16, 2012, there have been 2,527 robberies and 1,541 burglaries at pharmacies since the site began compiling data in 2002 — and offer a reward of $2,500 to anyone providing a tip leading to arrests in a “significant pharmacy crime.” They also provide a “Tip of the Month” in thwarting theft. In August Purdue advised pharmacists to, “determine whether [their] building provides easy access to the roof, which is a popular entry for more seasoned criminals.”

Some pharmacies, after repeated robberies, have stopped carrying the stuff. They display signs, “No OxyContin Here,” alerting would-be robbers that holding them up wouldn’t be worth the effort.

Some pharmacies have stopped stocking Oxy to drive away robbers (via)


One wonders whether Purdue’s efforts to educate pharmacists on safety measures, though doubtless partially motivated by concern, also functions as a way to soothe pharmacists who might be coming to the conclusion that stocking the drug is more trouble than it’s worth. After all, most pharmacists didn’t anticipate a career filled with the threat of gun-wielding, ski-masked thieves and Mission Impossible -style burglars cracking the roof and shimmying down the ventilation ducts. The more prescription drug abuse creates desperate addicts, the more the pharmacy staff unwittingly fulfills the role of a drug cartel’s security, guarding a shipment of drugs prior to distribution.

The End of Oxy


Addiction to and abuse of prescription drugs will exist no matter what pharmaceutical companies do. It’s impossible to know the number of addicts directly “created” by any drug, legal or illegal, and there is likely some proportion of society that would fall prey to drug addiction or abuse regardless of the specific substances involved. The crucial question surrounding OxyContin is, how many inadvertent addicts has the drug and its marketing created? Opioids in general are highly addictive – that’s not alarming. It’s not news that Purdue admittedly defrauded the public concerning the safety of their drug. What’s disturbing is that the practice of deception and data suppression, physicians and regulators acknowledge, is common throughout the industry.

Perhaps one of the most intriguing aspects to the OxyContin story is that it asks what, exactly, we expect from pharmaceutical companies. Purdue Pharma knew, on some level, that the amount of OxyContin they were selling absolutely couldn’t all have been used for legitimate pain. The CDC famously reported that enough painkillers were sold in 2010 to medicate every adult in America, around the clock, for one month. We can’t all be in that much pain.

Purdue had to have known it was profiting off of addiction and dependence. If it didn’t, I question why the company would’ve waited for such extreme social pressure to create a less abusable form of their drug. Maybe they really did believe they had found a magic bullet, an opioid medication with the power to “cure” pain without cultivating dependence. We’ll never really know. But now that their drug is practically synonymous with addiction and crime, now that so many exposés have explored both their marketing practices and the personal stories of addicts, now maybe we can all look more clearly and critically at a culture that reveres pharmacological solutions.

Purdue’s patent for the original formulation of OxyContin is almost up, but the era of pushing Oxy as a drug safe-for-management-of-chronic-conditions isn’t quite over. The company is now fighting to protect its reformulated version of OxyContin, which has patent protection until 2025, by lobbing 16 patent-infringement lawsuits pending against 10 generic-drug manufacturers. And unless Purdue can manage to keep its original patent, cheaper generic versions of Oxy will begin to arrive in pharmacies next year. Regulators are already worried. In a June 6 letter, Ontario’s Minister of Health, Deb Matthews, asked her federal counterpart not to approve generic versions of the drug, stating that “Ontario believes that the costs to society of the reintroduction of the more-easily abused version far outweigh the financial benefits that would accrue from the reduced price.”

I didn’t even have to cook it to shoot it. I could just drop it in some water and pump it right into my arm

_
The drug industry is based around the concept of making us “well”. We get sick, and they make us better. But there are a host of medications and disorders – the use of narcotics for some types of pain and the use psychiatric drugs for some disorders – that are often dubiously thrust into this paradigm. Since all pain and psychiatric disorders exist on a spectrum, there is a danger in overmedicating those in the middle, those who might not need it and who might not take drugs if they were aware of all the possible negative outcomes related to doing so.

Drugs aren’t always necessarily making people better, though they might make things easier (in some ways, for some time). Through its aggressive marketing, Purdue Pharma pushed the concept of more liberal narcotics prescribing behavior as a human rights issue. People deserve to not be in pain. They have the right to not be in pain. This is a seductive argument and it fits neatly into the current paradigm of what we expect from drugs and the medical community. But they buried the counterargument to making people’s pain easier: It’s not always easy to put down the thing that takes away your pain.

In a society where direct-to-consumer marketing of many pharmaceuticals is legal, where pharmaceutical companies are legally allowed to entice physicians with all manner of incentives and perks, and where we elevate the power of drugs to near-mythic levels, it’s no surprise that drug companies are able to write their own narrative on sickness, cures, and risk. And we believe them, on some level, just like an entire generation believed that a powerful opioid medication wasn’t addictive or easily abused. We believe them until we reach the end of an era, until the data and stories and robberies pile up so high that we can’t ignore the fact that we were duped. As a generation of Oxy addicts suffers, as Purdue continues to make billions a year in sales of the drug, and cheaper versions are bound for pharmacies next year, what have the rest of us learned? When the next miracle pill comes along, with all its easy promises and assurances, how low will the highs go?

When I asked Frank about his thoughts on Purdue and their business practices, he was ambivalent. “I always knew I was a drug addict, so I don’t blame them for that,” he admits. Besides, it was easy: “I didn’t even have to cook it to shoot it. I could just drop it in some water and pump it right into my arm.”

But in a telling, almost poignant admission, Frank says he’s actually happy that Oxy was available to him simply because it hastened the sink to rock bottom. He even goes so far to say that Oxy has “in a weird way” granted him a life he never could’ve imagined. What disappoints him, though, is that Purdue had to know “what the deal was” with Oxy. “They just had to know what was capable with it, due to the fact that they must go through strenuous testing,” he continues. “So, its a little disheartening that this company would knowingly produce pills like that, and just say that it wasn’t so bad.”

Thursday, July 5, 2012

OxyContin For Kids: What Could Possibly Go Wrong?

by Abby Zimet

Tuesday, July 3, 2012

Government-sponsored study destroys DEA’s classification of marijuana

By Stephen C. Webster - RAW Story 

Tuesday, July 3, 2012
 
 
A government-sponsored study published this month in The Open Neurology Journal concludes that marijuana provides much-needed relief to some chronic pain sufferers and that more clinical trials are desperately needed, utterly destroying the U.S. Drug Enforcement Agency’s (DEA) classification of the drug as having no medical uses.

While numerous prior studies have shown marijuana’s usefulness for a host of medical conditions, none have ever gone directly at the DEA’s placement of marijuana atop the schedule of controlled substances. This study, sponsored by the State of California and conducted at the University of California Center for Medicinal Cannabis Research, does precisely that, driving a stake into the heart of America’s continued war on marijuana users by calling the Schedule I placement simply “not accurate” and “not tenable.”

Reacting to the study, Paul Armentano, director of the National Organization for the Reform of Marijuana Laws (NORML), told Raw Story that the study clearly proves U.S. drug policy “is neither based upon nor guided by science.”

“In fact, it is hostile to science,” he said. “And despite the Obama Administration’s well publicized 2009 memo stating, ‘Science and the scientific process must inform and guide decisions of my Administration,’ there is little to no evidence indicating that the federal government’s ‘See no evil; hear no evil’ approach to cannabis policy is not changing any time soon.”

Schedule I is supposedly reserved for the most inebriating substances that have no medical value, like LSD, ecstasy, peyote and heroin. As the DEA describes it: “Drugs listed in schedule I have no currently accepted medical use in treatment in the United States and, therefore, may not be prescribed, administered, or dispensed for medical use. In contrast, drugs listed in schedules II-V have some accepted medical use and may be prescribed, administered, or dispensed for medical use.”

And that’s the problem, the study’s authors portend.

“The classification of marijuana as a Schedule I drug as well as the continuing controversy as to whether or not cannabis is of medical value are obstacles to medical progress in this area,” they wrote. “Based on evidence currently available, the Schedule I classification is not tenable; it is not accurate that cannabis has no medical value, or that information on safety is lacking. It is true cannabis has some abuse potential, but its profile more closely resembles drugs in Schedule III (where codeine and dronabinol are listed). The continuing conflict between scientific evidence and political ideology will hopefully be reconciled in a judicious manner.”

They add that their evidence showed marijuana reliably reduced chronic neuropathic pain and muscle spasticity due to multiple sclerosis versus trials where a placebo was used. They also specifically tested marijuana’s effects when smoked, calling the delivery method “rapid and efficient” but noting that vaporization is a better choice because it produces less carbon monoxide.

The study adds that, like all medicines, there are negative side effects associated with marijuana, such as dizziness, fatigue, lightheadedness, muscle weakness and pain and heart palpitations — all of which can pose a risk in some chronic pain patients with co-occurring conditions like cardiovascular disease or substance abuse disorders. However, they call these side effects “dose-related” and “of mild to moderate severity,” adding that they “appear to decline over time, and are reported less frequently in experienced than in naïve users.”

Researchers also noted that “fatal overdose with cannabis alone has not been reported.”

Authors additionally found that marijuana does cause withdrawal symptoms within 12 hours of use, noting the symptoms are mild in experienced users and typically abate within 72 hours. They added that ingesting marijuana “can acutely impair skills required to drive motor vehicles,” but noted that the data on marijuana and traffic accidents is “inconclusive.”

Ultimately, they concluded that more clinical trials are needed to determine which individual components of the marijuana plant are causing the medicinal effects, and whether the plant can be used to treat a host of other ailments.

“Medical marijuana is mostly used for chronic pain, and has enabled countless patients to either reduce or eliminate their pharmaceutical drug regimen,” Kris Hermes, a spokesman for Americans for Safe Access (ASA), one of the nation’s leading medical marijuana advocacy groups, told Raw Story. “However, it can also be used for: arthritis, nausea or as an appetite stimulant for people living with HIV/AIDS or cancergastrointestinal disorders, and movement disorders (not just for people with multiple sclerosis). That is only a sampling of health conditions for which cannabis has been found helpful in alleviating symptoms. Other health conditions include: [post-traumatic stress disorder], [attention deficit disorder], [attention deficit hyperactivity disorder] and other mental health conditions, glaucoma, and migraines.”

In hopes of forcing recognition of marijuana’s medical value, ASA sued the federal government last year after a long-running appeal for the reclassification of marijuana was shot down nearly a decade after it was filed. That case should go before the U.S. Court of Appeals District of Columbia Circuit later this year.

“The federal government’s strategy has been delay, delay, delay,” ASA chief counsel Joe Elford said in an advisory. “It is far past time for the government to answer our rescheduling petition, but unfortunately we’ve been forced to go to court in order to get resolution.”

“Reform advocates can and should use this study to show their congressional representatives that our country’s leading medical marijuana researchers agree that it should be reclassified,” Hermes added. “…This certainly should also have a bearing on the D.C. Circuit’s deliberations in the appeal of the rescheduling petition denial.”

Medical marijuana is currently legal in just 17 states and Washington, D.C.

Sunday, February 5, 2012

Placebos and Distraction

New Study Shows How to Boost the Power of Pain Relief, Without Drugs

ScienceDaily (Feb. 3, 2012) — Placebos reduce pain by creating an expectation of relief. Distraction -- say, doing a puzzle -- relieves it by keeping the brain busy. But do they use the same brain processes? Neuromaging suggests they do. When applying a placebo, scientists see activity in the dorsolateral prefrontal cortex. That's the part of the brain that controls high-level cognitive functions like working memory and attention -- which is what you use to do that distracting puzzle.

Now a new study challenges the theory that the placebo effect is a high-level cognitive function. The authors -- Jason T. Buhle, Bradford L. Stevens, and Jonathan J. Friedman of Columbia University and Tor D. Wager of the University of Colorado Boulder -- reduced pain in two ways -- either by giving them a placebo, or a difficult memory task. lacebo. But when they put the two together, "the level of pain reduction that people experienced added up. There was no interference between them," says Buhle. "That suggests they rely on separate mechanisms." The findings, published inPsychological Science, a journal of the Association for Psychological Science, could help clinicians maximize pain relief without drugs.

In the study, 33 participants came in for three separate sessions. In the first, experimenters applied heat to the skin with a little metal plate and calibrated each individual's pain perceptions. In the second session, some of the people applied an ordinary skin cream they were told was a powerful but safe analgesic. The others put on what they were told was a regular hand cream. In the placebo-only trials, participants stared at a cross on the screen and rated the pain of numerous applications of heat -- the same level, though they were told it varied. For other trials they performed a tough memory task -- distraction and placebo simultaneously. For the third session, those who'd had the plain cream got the "analgesic" and vice versa. The procedure was the same.

The results: With either the memory task or the placebo alone, participants felt less pain than during the trials when they just stared at the cross. Together, the two effects added up; they didn't interact or interfere with each other. The data suggest that the placebo effect does not require executive attention or working memory.

So what about that neuroimaging? "Neuroimaging is great," says Buhle, "but because each brain region does many things, when you see activation in a particular area, you don't know what cognitive process is driving it." This study tested the theory about how placebos work with direct behavioral observation.

The findings are promising for pain relief. Clinicians use both placebos and distraction -- for instance, virtual reality in burn units. But they weren't sure if one might diminish the other's efficacy. "This study shows you can use them together," says Buhle, "and get the maximum bang for your buck without medications."

Journal Reference:Jason T. Buhle, Bradford L. Stevens, and Jonathan J. Friedman and Tor D. Wager. Distraction and Placebo: Two Separate Routes to Pain Control. Psychological Science, 2012

Thursday, January 12, 2012

Cannabis Treatment Threatens Deadly Painkiller Industry

Anthony Gucciardi - 01.10.12

Pharmaceutical painkillers are now responsible for more deaths in the United States than heroin and cocaine combined.

These pharmaceuticals are responsible for more than 15,000 deaths conservatively in 2008 alone. With no sign of slowing down, the painkiller industry is becoming wildly popular among Americans — as a result, so is the high rate of painkiller abuse.

Classified as dangerous by the U.S. government, cannabis (even in THC-free form, or free of psychoactive effects) has been identified as a powerful pain reliever in more than 80 peer-reviewed studies.

You may be aware of the fact that marijuana is usually quite high in THC (delta-9 tetrahydrocannabinol), which is the compound responsible for the psychoactive effect of cannabis.

In contrast, it is also low in CBD (cannabidiol) content. Both THC and CBD are known as cannabinoids, however, which interacts with your body in a very unique way.

In fact, cannabinoids are key when it comes to pain relief. While this information alone is enough to shatter the traditional beliefs on government marijuana regulation, the relationship between CBD and THC is even more revealing.

What you may not be familiar with is how CBD has been shown to block the effect of THC in the nervous system. This allows for marijuana to be used with little or no psychoactive effects. Hemp, on the other hand, is high in CBD and low in THC. This is due to the fact that it is bred to maximize its fiber, seeds, and oil. Of course these key properties are what it is most commonly used for.


Trials Indicate Cannabis as an Effective Treatment for Chronic Pain

In a 2011 study published in the British Journal of Clinical Pharmacology, researchers examined the effects of cannabinoids on chronic pain and proper sleep. What they found in their trials challenges federal government claims that cannabis has ‘no accepted medical use’. The researchers conducted 18 trials using cannabinoids in the treatment of chronic pain, and found that cannabinoids demonstrated a significant painkilling effect as well as noticeable improvements in sleep in 15 of trials. Compared, to placebo, the cannabinoids were extremely effective.

Most importantly, there were no adverse effects.

Another study, performed in 2002, reached similar conclusions. Finding cannabis to aid in pain relief as well as quality of sleep, researchers from the McGill University Health Centre stated in summary that cannabis can be used as an effective way of improving pain, mood, and sleep in some patients with chronic pain.

There are many forms of the cannabis plant, many without mind-altering properties, many of which can be utilized without adverse reactions, as detailed in the peer-reviewed research. It is also quite clear that the painkiller industry simply cannot continue to wreak havoc on the lives of many, and a natural alternative must soon emerge to prevent another 15,000 plus deaths this year.

Why is the federal government refusing to admit the medicinal properties of cannabis and the unique ability of this substance to curb pain, insomnia, and impaired mood? This is only one example of how the government decides what is and what is not good for your health.

Sunday, January 1, 2012

The 10 Most Dangerous Meds Driving America's Pill Crisis

More Americans now die from prescription pills than car accidents. The nation's response to the trend will define an era, but corporate influence threatens reform. 
By Kevin Gray, The Fix
Posted on December 26, 2011
For the first time in nearly a century, automobile accidents are no longer the nation’s leading cause of accidental deaths, according to a major report released Tuesday by the National Center for Health Statistics.

The new number one killer is drugs—not smack, crystal meth or any other stepped-on menace sold in urban alleyways or trailer parksbut bright, shiny pills prescribed by doctors, approved by the government, manufactured by pharmaceutical companies and sold to the consumer as “medicine.”

Yet of the billions of legit pills Americans pop every year for medical conditions serious and otherwise, the vast majority of lives are claimed by only a select few classes—painkillers, sedatives and stimulants—that all share a common characteristic: they promote abuse, dependence and addiction.

“This is just the tip of the iceberg of the prescription drug abuse problem,” says Dr. Margaret Warner, the federal report’s lead author. “The take-home here is, this should be a wake-up call.” Some 41,000 Americans died from what the report refers to as “poisonings” in 2008, compared with 38,000 traffic deaths. That tally marks a 90 percent increase in poisonings and a 15 percent decrease in car accidents since 1999.

Nearly nine out of ten of those poisonings were caused by prescription drug overdoses, with the chief culprit being opiate-based pain relievers such as Vicodin (hydrocodone), OxyContin and Percocet (oxycodone), codeine, morphine—and let’s not forget Actiq (fentanyl), the infamous berry-flavored lollipop that is 100 times stronger than morphine and—like most opiate analgesics—so overprescribed that only about 10% of its sales come from its original indication to treat cancer pain.

These legal opiates accounted for 40 percent, or 15,000, of the fatalities, up from 25 percent, or 4,000, in 1999. Deaths by painkiller now outpace the combined nationwide number of deaths by cocaine (5,100) and heroin (3,000); these fatal overdoses often involve mixing painkillers with other prescription drugs—for example, Klonopin, Xanax, Valium or another benzodiazepines, which are the second most lethal class.

Other report findings: Three quarters of the poisoning are unintentional—likely the result of overdoses rather than drug interactions or allergic reactions—and some 13 percent are suicides. The five states with the highest oxy-type drug death rates (per 100,000 of the population) were New Mexico (30.8), West Virginia (27.6), Alaska (24.2), Nevada (21.0), and Utah (20.8).The most likely to die: white men, American Indians and Native Alaskans, usually between the ages of 45 to 54.

Warner’s death report is but the latest in a disturbing accumulation of evidence, ranging from scientific surveys to celebrity deaths, that underscore what we already know about our painkiller nation: pill mills and doctor shoppers are not just creating a land of bathroom-cabinet addicts—their bodies are packing morgues.

With our surging “oxy addiction” showing no signs of letting up, the Centers for Disease Control and Prevention this year officially named it an “epidemic.” President Obama has repeatedly invoked prescription drug abuse as the nation’s leading drug problem responsible not only for a rising number of overdoses and deaths but also ratcheting up the incidence of break-ins and burglaries of pharmacies.

Warner and her colleagues at the agency, which is overseen by the CDC, are at pains to draw comparisons between oxy-type drug deaths and those from auto accidents, because they hope that the same comprehensive approach that helped cut traffic deaths in half during the previous decade can save just as many lives on the drug front. Auto fatalities fell following a concerted government focus on national highway safety, resulting in car safety improvements as well as a wide range of regulatory, legal, and public health measures. Seat belt laws were enforced; drunk driving laws became stricter. The fact that alcohol—yet another legal intoxicant—is responsible for close to 40% of all traffic fatalities indicates how difficult it is to apply policy to substance abuse and get significant results. Still, drunk driving is playing a smaller and smaller role in automobile fatalities, falling by close to 40% since 1982.

You need to look at policy, laws, individual behavior, community behavior and health care provider behavior,” says Dr. Chris Jones, a consulting pharmacist with the CDC. One of the most innovative interventions includes building a database on patients who abuse painkillers and identifying doctors who overprescribe (or do so without examining the patient or his medical history). So far, five states have adopted specific pill-mill laws to flush out such doctors. “We’re looking at these laws to evaluate them and for guidance on policy,” says Jones.

That includes sharing information from state medical licensing boards and pharmacy licensing boards to monitor prescribers and set thresholds for how many pills are hitting the street and why.

The Drug Enforcement Administration launched an annual National Prescription Take-Back Event; the third drug dump, in October, collected 188 tons of old pills nationwide. The agency also operates 26 Tactical Diversion Squads—agents specializing in identifying wholesale traffickers and suppliers of black-market pharmaceuticals.

Some 48 states have adopted prescription monitoring programs (PMPs), which typically encourage (rather than require) doctors to record the data of every controlled drug prescribed, but only 37 are currently operational.  In 2011, Florida implemented its PMP after its Tea Party governor reversed his controversial opposition to the surveillance tool, and the Sunshine State has already seen an exodus of pill mills to Georgia, which still has no PMP.

These federal and state campaigns come not a moment too soon, either. Painkillers have become the most common drug taken by adults between the ages of 20 to 59. The trends in sales, deaths and abuse treatment admissions for oxy and the like have all risen fourfold or more since 1999, according to a new state-by-state study. In 2009, for the first time, emergency-room visits resulting from prescription drug ODs topped 1 million, with some 343,000 due to opiate analgesics like oxy, 363,000 due to benzodiazepines and other sedatives, and 22,000 due to stimulants. (For a ranking of the top 10 drugs whose use or abuse led to overdose deaths or survival in ER visits in 2009, see the list at the end of the article.)

In 2010, enough prescription painkillers were sold nationwide to keep every American medicated around the clock for an entire month. Some 12 million Americans admitted that they were using painkillers without a prescription, and at least 14% of these nonmedical users met the criteria for abuse or dependence. In one recent survey, more than 5 million Americans reported using them to get high—in a single month period. The majority of those people say they obtained (or stole) them from friends or their family.

Jones does see one bright spot in the otherwise grim report. Methadone, which is used as a pain reliever as well as to treat opioid dependency, had been on the uptick for nearly a decade—from about 800 deaths in 1999 to about 5,500 in 2007. But for reasons not yet clear, that number dropped by remarkable 600 deaths in 2008. “For  many years it had been the most common opioid in overdose deaths,” says Jones. “We don’t know if it’s just that people have shifted to these other drugs of what. But it’s promising. We’ve have to wait and see what we find when we look at  2009.”

In terms of the big picture, however, the fact that prescription drugs have overtaken automobiles as the nation’s leading cause of accidental deaths marks a deeper societal transformation. One of the most defining developments in twentieth-century America was motorization; as more people bought more cars and drove more miles, more accidents, injuries and deaths were the inevitable result until government intervention bent the curve. 

The 21st century is shaping up to be about, among other things, the pharmaceuticalization of America, as lifelong prescription drug use starting in early childhood becomes the norm.

How will pill popping transform our lives? Certain things are predictable: The drug industry will develop and sell more and more chemicals targeted at the brain, which remains medical science’s “black box”; that will result in treatments to enhance the performance of mood, cognition, attention, memory and other mental functions that will have become, in due course, “medical conditions.” Any pill that promises to make you smarter or happier invites abuse, and some will be as addictive as Oxy or the “morphine popsicle.” But with the enforcement of effective policies—the seat belts and DUI laws of pharmaceuticalization—the drug industry’s off-label marketing and the medical profession’s overprescribing could be dramatically curtailed.

Given the current state of corporate influence over politics, these reforms are anything but predictable. What's at stake is nothing less than the nation’s expanding medicine cabinet doubling as its morgue.

The Top 10 Most Dangerous Rx Drugs in America
This list of brand name and generic drugs was compiled from the Drug Abuse Warning Network's (DAWN's) database of emergency room visits in 2009, including drug poisonings that lead to both deaths and survivals.
  1. Xanax (alprazolam) 112,552 (benzodiazepine class)
  2. OxyContin (and other oxycodone drugs) 105,214 (opiate class) 
  3. Vicodin (and other hydrocodone drugs) 86,258 (opiate class)
  4. Methadone 63,031 (opiate class)
  5. Klonopin (clonazepam) 57,633 (benzodiazepine class)
  6. Ativan (lorazepam) 36,582 (benzodiazepine class)
  7. Morphine drugs 31,731 (opiate class)
  8. Seroquel (quetiapine) 29,436 (antipsychotic class)
  9. Ambien (zolpidem) 29,127 (sedative class)
  10. Valium (diazepam) 25,150 (benzodiazepine)

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