As you read the article below, ask yourself this: Is your doctor your ‘legal’ drug dealer?
Frank Morris was only 23 when he ended up in rehab. But he was already a full-blown junkie, smoking crack on the streets of San Francisco, and nearly losing his left arm after accidentally pumping a full shot into his artery. He tells me the drug that led him down this path — that helped him accelerate from a teenager smoking pot in his parent’s basement to a young man shooting heroin in a filthy apartment — was OxyContin, a pain medication that has proved dramatically helpful to those in pain, and dangerously addictive too.
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.”
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
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.
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.
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
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
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.”
NEW YORK – Attorney General Eric T. Schneiderman today announced the arrest of Long Island Internist Dr. Anand Persaud, who is accused of illegally selling prescriptions for the narcotic medication oxycodone. The arrest occurred after investigators from the New York State Attorney General’s Medicaid Fraud Control Unit executed a search warrant at Persaud’s medical offices located at 1019 Atlantic Avenue in Baldwin and 173-25 Jamaica Avenue in Queens.
Persaud was arrested at his Baldwin office and is expected to be arraigned in Nassau County District Court in Hempstead. A felony complaint filed today charges Persaud, age 44, with two counts of Criminal Sale of a Prescription for a Controlled Substance, a class C felony. If convicted, he faces up to 15 years in prison.
“It’s unconscionable that a doctor, a trusted licensed professional, would violate his professional duties and abuse his license to traffic in prescriptions for narcotics,” said Attorney General Schneiderman. “My office will hold accountable those who contribute to the growth of the prescription drug abuse epidemic in New York State.”
Persaud is charged with selling a prescription for oxycodone without providing medical documentation or conducting a medical examination of his patient on both November 13, 2012 and March 19th, 2013. New York State law prohibits physicians from prescribing controlled substances, such as oxycodone, other than in good faith in the course of their professional practice. Oxycodone is one of a number of highly addictive opiates classified as Schedule II-(b) controlled substances. Under New York State Penal Law, Scheduled II-(b) controlled substances are considered narcotic drugs.
Persaud maintained a two-tiered practice. He had “medical” patients, those with regular medical issues, who were charged $110 for an office visit, and “pain management” patients, drug users and addicts, who were charged $250 or more for an office visit that included a prescription for a controlled substance. On both dates in question, Persaud charged a patient $250 or more to receive a prescription for oxycodone. Persaud did not conduct a physical examination of either patient or even question them about their need for the medication.
Both patients were Medicaid recipients eligible for no-cost medical care from Persaud who is an enrolled Medicaid provider. By enrolling in the State’s Medicaid program, a provider agrees to accept payment from Medicaid as payment in full for all care, services and supplies billed under the program, except where specifically provided in law to the contrary (18 NYCRR §504.3(c)). The patients in question presented themselves to Persaud as Medicaid recipients.
In Nassau and Suffolk Counties, admissions to drug treatment that involve opiates have increased 57 percent and 40 percent, respectively, for crisis admissions from 2007 to 2010. Non-crisis admissions have shockingly increased almost 70 percent in Nassau over the same time period. Since 2006, oxycodone has contributed to more deaths than any other prescription opioid in Nassau County, and prescriptions for the drug increased 42 percent from 2008 to 2010.
In June 2012, the New York State Legislature unanimously passed Attorney General Schneiderman’s Internet System for Tracking Over-Prescribing Act, or I-STOP; it was signed into law on August 27, 2012. On August 27th of next month, one of the key components to the plan will take effect: doctors will be required to consult a real-time database of their patients’ prescription drug history before prescribing controlled substances like oxycodone.
I-STOP will make New York the first state in the nation with such a requirement. The system will also eliminate most paper prescriptions by August 2014. It will make it harder for dirty doctors to fuel the black market in prescription drugs and will make it next to impossible for addicts and drug peddlers to go “doctor shopping” to get their pills.
“With I-STOP, we are creating a national model for smart, coordinate communication between health care providers and pharmacists to better serve patients, stop prescription drug trafficking and provide treatment to those who need help,” said Attorney General Schneiderman.
The Attorney General’s investigation of Persaud is ongoing.
Attorney General Schneiderman thanked the Rockville Centre Police Department, and in particular, Commissioner Charles Gennario, Lieutenant James Vafeades and Detective Frank Marino, for their assistance in this investigation.
The charges against the defendants are accusations and the defendants are presumed innocent unless and until proven guilty.
The investigation was conducted by Investigators Steven Broomer and Thomas Dowd and Special Auditor Investigator Joshua Berry who are supervised by Supervising Investigator Thomas Burke, Chief Investigator Thaddeus Fisher, Supervising Special Auditor Investigator Emmanuel Archer and Regional Chief Auditor Thomasina Smith.
The criminal case is being prosecuted by Special Assistant Attorney General Crystal Barrow of the Attorney General’s Medicaid Fraud Control Unit, under the supervision of Regional Director Christopher M. Shaw, and Chief of Criminal Investigations Thomas O’Hanlon, under the overall supervision of MFCU Special Deputy Attorney General Monica Hickey-Martin and Executive Deputy Attorney General for Criminal Justice Kelly Donovan.
The article below was taken from HERE.
I am Ann Blake Tracy, author of Prozac: Panacea or Pandora? – Our Serotonin Nightmare. Since early 1990 I have devoted every minute of my life to researching and writing about the SSRI antidepressant drugs. Since 1992 I have been testifying as an expert court witness on their adverse effects. I also head an international organization, the International Coalition for Drug Awareness (www.drugawareness.org), designed to educate the medical profession, patients, government authorities and others about these adverse effects and their impact upon our society. To see a full bio of who I am and what I have been doing over the past two plus decades you can go to http://www.drugawareness.org/mission/board/
In the beginning I had NO idea the overwhelming opposition I would face in my attempt to point out the obvious faults in the hypothesis behind these new antidepressants. I quickly learned that opposition was due to the massive amount of income produced by this group of drugs. But when I saw the damaging results I have seen from these drugs upon our society, I was determined to help save the lives of so many that are being needlessly lost. So concerned was I about the violence we were seeing in women and children I called the NRA and asked them to help me warn of the dangers of these drugs telling them that in the end these drugs would be the means by which enough violence would be produced that there would be a call to take America’s guns. Two decades later that is exactly where we are. Once you understand the science behind the drugs you will be able to see that such a prediction was only simple deduction.
Most important to learn is that SSRI (selective serotonin reuptake inhibitors) antidepressants are the most similar drugs to LSD and PCP– long known to produce indescribable violence, we have ever seen. Yet LSD, was patented in 1956 by Eli Lilly, the makers of Prozac which was the first of these SSRI antidepressants to be produced. They marketed LSD as a cure for mental illness and alcoholism and as an aid in psychoanalysis even though initially LSD was introduced by Sandoz Pharmaceuticals as a way to chemically induce insanity in someone so that scientists could then determine what was the root cause OF insanity.
PCP was introduced by Parke Davis Pharmaceutical and thought to be such a safe and effective prescription drug that it was on the market 7 years before pulling it. Its removal from the market was NOT due to concerns of the AMA or FDA, but at the insistence of law enforcement and judges who were tired of dealing with the violence produced by the drug. In fact over the past decade now scientists have even suggested that Ketamine (Special K), a sister drug to PCP, is the perfect antidepressant … with only one major drawback being the hallucinations/psychosis it produces. Of course since PCP and Ketamine are anesthetics they should know the drugs would stop all feeling, but do we really want a huge portion of society walking around under anesthesia? Yet since these antidepressants are so similar in action that is exactly what we have now.
In the early 2000′s law enforcement began to ask why violence for seemingly NO reason at all was appearing everywhere. And in February of 2004 Sheriff Richard Mack testified before the FDA on this same type of violence being produced as a result of these antidepressants. He ended his comments with: “”Some people don’t have the adverse reaction to these drugs, some do. I learned the same with LSD when I investigated that as an undercover narcotics officer. I can only say that the evidence is mounting over and over [as we investigate]. We cannot, as law enforcement officials, ignore such circumstantial evidence. I doubt very seriously if you could either… I am an advocate for state’s rights and I do believe that if the FDA fails to take action, the state and local authorities will have to.” (Sheriff Mack’s full testimony can be viewed here: http://youtu.be/t9wLpnu-iSc)
As you look at the following information I believe you will agree that it is time for state and local authorities to take action.
ANTIDEPRESSANTS & SCHOOL VIOLENCE: This is a very long list of school violence/shootings we have documented which have been linked to antidepressant use since 1988 – 67 cases on the list: http://www.youtube.com/watch?v=JpFoivbZH1o&feature=youtu.be
A direct link to this list where you can read more on each individual case is at http://www.drugawareness.org/ssri-nightmares/school-shootings and an entire database of almost 5000 cases like this ending in workplace violence, murder/suicides, etc. is at www.ssristories.drugawareness.org
Two other videos which you will find extremely enlightening are Corey Baadsgard’s video interview with him and his father about his own experience as the only school shooter I am aware of to talk about what happened, “Why I Took a Gun to School…”http://www.drugawareness.org/recentcasesblog/why-i-took-a-gun-to-school-1
Mark Taylor was the first boy shot at Columbine High School. He took 7 -13 bullets and survived. He became known as the Columbine Miracle Boy. This is Mark’s story about a new nightmare worse than what happened the day he was shot Mark Taylor’s Fight for Columbine.” You will learn about the cause of Columbine which includes Michael Moore stating it was NOT the guns, but the antidepressants that caused Columbine: http://www.drugawareness.org/recentcasesblog/mark-taylors-fight4columbine
Here is Mark’s testimony before the FDA: http://www.drugawareness.org/fda-testimony/mark-taylors-testimony-before-the-fda-9132004
For the science behind the violence I would point out that these drugs have suicidal and homicidal ideation listed as side effects. Ideation is not just thoughts of either suicide or homicide. Ideation is ruminating compulsive thoughts or actions resulting in suicide or homicide. Once again I ask why is it okay to have prescription medications on the market known to cause both suicide and homicide? I refer also you to my brief September 2004 FDA testimony. http://www.drugawareness.org/fda-testimony/dr-ann-blake-tracys-september-13-2004-to-the-fda and my 2006 FDA testimony to give you more in depth information on other types of cases these drugs are producing other than school shootings: http://www.drugawareness.org/fda-testimony/dr-ann-blake-tracys-december-13-2006-to-the-fda
Another very serious issue I have been tracking this entire time is the problems in the military with these drugs. Hopefully you noticed the last two mass shootings in the military, the Navy Yard shooting and the Fort Hood shooting were both committed by someone taking antidepressants. Besides that since about 2007 the number of suicides in the military have outnumbered the deaths in battle – a first in our military while young recruits are being told they must take these antidepressants to go into combat. At this point we now have 660 suicides and another 1600 suicide attempts per month! I know the very large majority are being caused by these drugs, but it needs to be documented and then it needs to stop!
It is also important to note that I just testified before the Danish Parliament on the brain damage, endocrine damage and terrible long term withdrawal associated with antidepressants. Critical to understand is that the FDA has issued warnings that ANY abrupt change in dose of an antidepressant (whether increasing or decreasing the dose) can produce suicide, hostility, and/or psychosis. The withdrawal MUST be extremely (months and even years) in order to avoid these deadly effects!
Please feel free to contact me after viewing this information if I can answer any question left unanswered or if I can be of any further assistance.
According to a study published in the Public Health Reports, driving under the influence of prescription drugs is becoming a large problem in society, causing more fatal driving accidents than ever before.
Today, driving fatalities due to driving under the influence of prescription drugs, including Xanax, Cymbalta, Zoloft, Wellbutrin, Lexapro, Sarafem and Abilify, are surpassing those caused by drunk drivers.
“While we’ve seen a decrease over the years in motor vehicle fatalities involving people under the influence [of alcohol], the nature of those crashes is changing,” said study author Fernando Wilson, Ph.D., associate professor at the University of Nebraska Medical Center.
How psychotic medicine logically increases risky driving behaviors
The study shows an alarming increase in motor vehicle accidents due to prescription drugs. The mind altering medications do not allow the person’s mind to cope naturally with life’s stressors and periods of depression. The prescription drugs quickly change the chemical levels in the brain (with the intent of a quick fix for depression or anxiety), but confuses the normal functions of the mind. The mind naturally tries to adapt to the quick changes and can become stressed in new ways, which confuses the natural state of the person’s mind, predisposing them to act out of character. In a vehicle, this change could correlate to risky driving behaviors. According to some drug labels, suicidal behavior as a side effect could translate to violent driving patterns in a vehicle.
The use of multiple drugs increases the risk dramatically
The study investigated the characteristics of U.S. drivers involved in fatal crashes between 1993 and 2010. While drug use across the board increased significantly during that time, the percentage of impaired drivers with three or more drugs in their systems nearly doubled during that time, from 11.5% to 21.5%.
Drug use by older adults
A large number of fatal crashes came from prescription drug users (39%) who were 50 years or older. This trend correlates with the increasing reliance on prescription drugs by Americans.
According to the study, 90% of individuals 65 and older have prescription drug expenses.
The authors of the study hope that medical professionals begin counseling patients about the driving impairments posed by prescription drugs.
By 2010, prescription monitoring program were in place in 42 states. These programs, designed to curb illicit drug use and prevent overdoses, also focused on the overuse and abuse of prescription drugs.
Can we K.I.S.S. this one today (K.I.S.S. = Keep It Simple Stupid)? Sometimes, simple is better. Let’s begin to answer this question with the actual definition of Iatrogenic Addiction. By definition, Iatrogenic Addiction is any addiction caused by medical treatment (e.g., liberal use of opiate analgesics in a hospital setting or by a physician that leads to opiate addiction). For a moment, let’s take this to an analogy of whether or not a criminal should be accountable for killing someone by poisoning them with arsenic. Is the victim the one who caused this poisoning or is the murderer? Is the victim in the wrong because he ate the delicious mashed potatoes that were so skillfully prepared by his culinary school trained girlfriend? Should the murderer go free because the victim should have known that his girlfriend was a psychopath and she intended to poison the him by putting arsenic in the potatoes? Is it the victim’s fault because he didn’t know the murder’s intent? Is there any shared liability between the victim and the murderer?
There are Iatrogenic Addictions that happen as a side effect of treatment; however, without exception, each and every physician, physician’s assistant and nurse practitioner, all know that the ongoing prescribing of painkillers, tranquilizers, sleeping medications and psychiatric medications will undoubtedly always cause Addiction, organ failure, stroke, heart attack and death by accidental overdose (overdose caused by the building up of toxic drugs in the body). There is absolutely no excuse. Do I personally believe prescribing medical professionals and pharmacists should be accountable in a court of law for Addicting and Killing their patients? YES!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!
More next post.