The Manufacturer of PROZAC (ELI LILLY) … must be so PROUD !

Carrie Fisher’s Urn Is Her “Prized Possession” Antique Prozac Pill

http://www.hollywoodreporter.com/news/carrie-fishers-urn-is-a-huge-prozac-pill-961625

I wonder where she got that “Prozac pill” in the 50’s… since Prozac was not brought to market until 1987 ?

The family will plan a public memorial for Fisher and mother Debbie Reynolds in the future.

Carrie Fisher was always making people crack a smile in life, and she made sure she got just one more out of them in death.

It was revealed on Friday that Fisher’s ashes were placed in a gigantic Prozac-pill urn.

“It was a porcelain antique Prozac pill from the ’50s that was one of Carrie’s prized possessions,” Todd, Fisher’s brother, told The Hollywood Reporter.

Fisher died after suffering a heart attack late last month. She was 60. Her mother, the iconic starlet Reynolds, died a day later. She was 84.

Fisher was honest and open about her battles with drugs and mental illness throughout her career. She also had a kooky sense of humor, so it makes sense the Princess Leia actress would want her urn to resemble an antidepressant pill.

A private gathering for friends and family was held in Beverly Hills on Thursday. Meryl Streep was among those in attendance.

Todd Fisher has said the family will plan a public memorial for the two actresses in the future.

More “PAIN DOCS” that have decided to practice “cookie-cutter – by the numbers” medicine.

Below  (IN BLACK)  is the second email that I have received in the last couple of days from chronic pain pts where their “pain clinic” has decided to CAVE to the CDC guidelines… SCREW … practicing medicine… just care for pts “BY THE NUMBERS”..  That is NOT PRACTICING MEDICINE… that is just filling in the blanks on a bill and collecting money for doing so.. A grade schooler could do that … Apparently we have another epidemic going on… pain specialists and prescribers that are becoming SPINELESS and BALL-LESS. 

Below is my response to this pt (IN BLUE) ..might save me having to answer a number of similar emails that I presume it is just a matter of time before they start flooding my email inbox.  Feel free to share this to the far corners of our country.

Medicare/Medicaid/Medicare Advantage have a new Star Rating System and the less STARS a healthcare provider ends up for the year ( hospitals, prescribers, pharmacies , Part D, Medicare Advantage provider, etc ) the less they get reimbursed the following year… and if they don’t have ONE YEAR out of three getting at least a THREE STAR RATING… they could be toss out of being a Medicare/Medicaid provider.  They lose STARS by pts filing GRIEVANCES with www.cms.gov (800-MEDICARE) for “PISS-POOR CARE”.  Here is a recent post   769 Hospitals Penalized For Patient Safety In 2017: Data Table  where 769 hospitals are getting REDUCED REIMBURSEMENTS in 2017  because pts FILED GRIEVANCES with www.cms.gov… if pts don’t SPEAK UP when they are provided poor/bad care.. they will continue to receive poor/bad care.  Most healthcare providers don’t want their reimbursements lowered….nor.. do they wish to get booted from the Medicare/Medicaid provider network. Over 200,000 people die every year from medical errors….but … the general public hears very little about this…  IT IS A BIG SECRET !!  That is like 800 commercial airliners FALLING OUT OF THE SKY EVERY YEAR and everyone on board DYING…  If that happened… how many people would continue to fly …but we keep going to hospitals and healthcare providers !!!!

Get you a copy of the CDC guidelines and point out to them that pts who are terminal, cancer, Hospice or require palliative care are EXEMPT from the dosing limits… Here is the World Health Organization’s definition of palliative care  https://palliative.stanford.edu/overview-of-palliative-care/overview-of-palliative-care/world-health-organization-definition-of-palliative-care/

 

The idiots who wrote the CDC guidelines.. apparently believed that palliative is part of Hospice but in reality palliative care can be its own singular stand alone modality and is not totally inclusive of Hospice.  There are two ICD10 codes (diagnostic codes) that are to be used for a pt needing palliative care…  IMO.. most/all chronic pain pts can easily have the ICD10 palliative care code added to their lists of diagnoses.

 

Have they performed the CYP450 enzyme testing on you to determine if you are a fast/ultra fast metabolizer ?  https://www.practicalpainmanagement.com/treatments/pharmacological/opioids/cytochrome-p450-testing-high-dose-opioid-patients    Looking at the two particular enzymes 2D6 & 2C9 for abnormalities.  This should also help justify your higher than CDC  dosing limits.

 

If this does not budge them.. and you have a spouse or significant other there is always suing them for your significant other suing them for loss of consortium and companionship. https://www.pharmaciststeve.com/?p=12615  These type of lawsuits normally have a 300,000 – 400,000 limit on damages and should be large enough for an attorney take a case on …on a contingency basis… they take a per-cent of award.  Since this appears to be more than a single prescriber practice… and this is a decision of all the prescribers and the practice itself… might find an attorney to go after class action… surely a pain clinic has a fair number of pts that fit in the same mold that you do.  I just looked up DNA Advanced Pain Treatment Center and they have TEN PRESCRIBERS listed on their website… that is a lot of deep pockets for a law firm to go after…

 

If they still insist on pulling your dose back … especially if they fail to do the CYP 450 testing and/or they do and you are a fast/ultra fast metabolizer… presuming that you are on Medicare/Medicaid/Medicare Advantage you should file a GRIEVANCE with www.cms.gov ( 800-MEDICARE) for failing to follow standard of care and pt/senior abuse.. because cutting back your dose will make you house/chair/bed confined and unable to do personal care items… take a bath, brush your teeth, prepare meals etc…  I would also file a grievance with the state medical licensing board for the same.  Once the new AG/head of DOJ gets into place.. I would file similar grievances with Americans with Disability act.

 

 

 

Hi Steve, well I received the infamous letter from the pain clinic I have been going to for 7 years.  It states”DNA Advanced Pain Treatment Center will be following the CDC recommendations & policies on the dispensing of controlled substances including opiate medications.  Because of these policies, there will be adjustments made to your medications that will result in a result in a reduction in your dosage.  If this is not satisfactory to you we can provide you with a list of providers that may be willing to continue your medication. If you would like to discuss the changes with your practitioner, we would be happy to schedule an appointment to give you an opportunity to do so….Steve I would appreciate anything you could suggest to fight this uphill battle as u hav in the past made suggestions.   I hav had 4 hip surgeries & am in chronic pain & unable to walk very well or live life to it’s fullest extent.  I am om opana er 40mg tid & oxymorphone 10 IR QID prn  opana 15mg ER prn bid. These meds hav made life so much easier to get the activities of daily living done along wth being more apt to socialize.  Can you suggest what to do to reclaim my existence again?  I would so appreciate your help Steve.

Judge Rules Insurance Company Must Pay for Injured Worker’s Medical Marijuana

Judge Rules Insurance Company Must Pay for Injured Worker’s Medical Marijuana

hightimes.com/news/judge-rules-insurance-company-must-pay-for-injured-workers-medical-marijuana/

In what could become a precedent-setting decision, New Jersey Judge Ingrid French ordered an insurance company to pay for medical marijuana for an injured worker who suffers from lingering neuropathic pain after an accident involving a power saw at an 84 Lumber outlet in 2008.

The worker, 39-year-old Andrew Watson, was seeking reimbursement for MMJ he’d bought in 2014 after enrolling in the New Jersey’s medical marijuana program. He also sought to be covered for the treatment in the future.

French found that Watson’s intractable neuropathic pain fell under New Jersey’s list of qualifying conditions.

The judge took into account testimony from a psychiatrist/neurologist who said medical marijuana was an appropriate treatment for Watson to reduce prescription opiates to treat his complex regional pain syndrome (CRPS), an uncommon form of chronic pain.

“Evidence presented in these proceedings show that the petitioner’s ‘trial’ use of medicinal marijuana has been successful,” French said. “While the court is sensitive to the controversy surrounding the medicinal use of marijuana, whether or not it should be prescribed for a patient in a state where it is legal to prescribe it is a medical decision that is within the boundaries of the laws in the state.”

In her eight-page decision, French wrote that Watson’s testimony was credible: “Ultimately, the petitioner was able to reduce his use of oral narcotic medication… The court found the petitioner’s approach to his pain management needs has been cautious, mature, and overall, he is exceptionally conscientious in managing his pain.”

Another expert witness, psychiatrist Dr. Edward H. Tobe, described the benefits of medical marijuana and the risks of opiates.

“Opiates can shut down breathing (whereas) marijuana cannabinoids won’t,” he said,according to an excerpt of his testimony, reported The Inquirer. “Marijuana does not affect the mid-brain. The mid-brain is critical in controlling respiration, heart rate, many of the life-preserving elements.”

John Gearney, a labor attorney who writes a weekly blog on workers’ compensation cases, said the ruling was the first in New Jersey to address whether an insurer should pay for medical marijuana.

“There are about 50 workers’ compensation judges in the state, and they will read it and see what the judge thought when a case like it comes before them,” Gearney said.

Philip Faccenda, the lawyer who represented Watson, said the decision might also benefit insurance companies.

“We believe this will offer very powerful cost savings with respect to the entire workers’ compensation industry in New Jersey,” Faccenda said. “More costly pharmaceuticals can be reduced and medical marijuana would be a less expensive treatment modality.”

Thankfully, lawyers representing 84 Lumber said in an email on Thursday that they don’t intend to appeal the decision.

“With respect to the recent decision, we respect the court’s decision,” the email read. “At this juncture there is no plan to appeal.”

Philadelphia residents up in arms over soda tax hit


Philadelphia residents up in arms over soda tax hit

http://www.foxnews.com/politics/2017/01/06/philadelphia-residents-up-in-arms-over-soda-tax-hit.html

just wait until Senator Manchin gets his opiate prescription tax to help fund treating addicts

Clinton backs Manchin plan to tax opioids

Philadelphia residents are getting hit by the first big-city soda tax in the country, and they’re not happy. Pictures are going viral of hefty receipts that show the 1.5 cent-per-ounce tax adding up to several dollars extra on a single purchase.

“The magnitude of this tax is historic and Philadelphian consumers can’t afford it,” said David McCorkle, CEO of the Pennsylvania Food Merchants Association. 

When the levy was approved last year, Philadelphia became the largest city in the nation to create a specific tax for soda and sugary beverages. The tax took effect on Jan. 1, with a per-ounce rate 24 times more expensive than the state’s tax on beer.

The 1.5 cent-per-ounce rate sounds small. But it can add up on purchases of packs and large bottles.

In one photo that went viral after being posted to Facebook, a receipt shows more than $3 in tax added to the cost of a $5.99 12-pack of Propel, an energy drink. Because of the broad language, the tax captures not only sodas but energy drinks, zero-calorie diet beverages, juice and even milk substitutes for lactose-intolerant people.  

 

Other shoppers also sounded off.

 

Philadelphia Mayor Jim Kenney first proposed the tax in March 2016; it passed the City Council 13-4. The revenue will be used to fund initiatives for areas in need of improvement like community schools, parks, rec centers, and libraries – and for expanding the city’s pre-K programs.

But the city has been in a legal battle with the American Beverage Association, which opposes the measure. And the Kenney administration has gone to the state Supreme Court seeking a final legal decision. A spokesperson for Kenney told FoxNews.com that without the tax, the city cannot fund additional pre-K seats come September – and stressed it’s not technically a sales tax.

“The Philadelphia Beverage Tax is a tax on the distribution of sweetened beverages intended for retail; it is not a sales tax to be paid by the consumer and collected by the retailer,” spokesman Mike Dunn said. “There are thousands of Philadelphians who are thrilled with the infrastructure this tax will pay for, so it depends on who you’re speaking to.”

The mayor’s office said there was no “mandate” on consumers, but rather on dealers and distributors who could choose whether to increase prices.  

“Since it is not a sales tax, distributors … do not have to pass it down to their customers, the dealers,” Dunn said. “They could choose to slightly lessen their seven-figure bonuses, for example.”

But McCorkle, a plaintiff in the case against the tax, said despite what the mayor’s office says, the tax will be passed onto consumers.

“I would ask anyone in the mayor’s office to walk through a supermarket or convenience store—the consumers are seeing a dramatic increase in the price of products in these Philadelphia stores and Philadelphians will vote with their feet by finding a neighboring community where they can buy the products they want at prices they did prior to January 1st,” McCorkle said. “If Philadelphians shop outside the city, sales decline, not only in the beverage category, but in all categories.”

McCorkle said the Philadelphia economy in general could be affected.

“I think the city needs to take a hard look at the potential impact, and we suspect that if store revenue declines, cuts have to be made somewhere,” McCorkle said.

According to the mayor’s office, Philadelphia has established a Healthy Beverages Tax Credit to help those small stores and bodegas McCorkle is concerned about. The credit is offered to “qualifying merchants who increase their inventory of healthy beverages.”

Philadelphia’s experience could shape how the soda tax debate plays out across the country. Illinois is considering a statewide soda tax, and cities including Santa Fe, N.M., are considering new local levies. 

Could this be why the DEA wants to RESCHEDULE CBD ?

GW Pharmaceuticals Announces Positive Results from Phase 3 Cannabidiol Trial

http://www.epilepsy.com/article/2016/3/gw-pharmaceuticals-announces-positive-results-phase-3-cannabidiol-trial

Monday, March 14, 2016

GW Pharmaceuticals has announced positive results from the first of two Phase 3 studies of Epidiolex® (cannabidiol or CBD) in the treatment of Dravet syndrome. Median seizure reduction was 39% with Epidiolex versus only 13% with placebo, a scientifically significant finding. In addition, the side-effect profile was acceptable for an anti-epileptic drug and secondary endpoints were supportive of a robust treatment effect.

“This is a very important day for the epilepsy community and families struggling with Dravet and other devastating epilepsies,” said Dr. Jacqueline French, chief scientific officer for the Epilepsy Foundation. “Although anecdotal evidence supported an effect of CBD in serious childhood epilepsies, this is the first scientific evidence that confirms this effect.”

Since 2014, the Epilepsy Foundation has called for an end to Drug Enforcement Administration (DEA) restrictions that limit clinical trials and research into medical marijuana for epilepsy. Learn more.

In referring to the recent study results, Dr. French added, “This data should support eliminating barriers to CBD research. GW Pharmaceuticals is leading the development of an FDA pipeline for CBD and this represents a significant step forward.”

“The Epilepsy Foundation is thrilled to see positive results in this first controlled clinical study of GW Pharmaceuticals’ Epidiolex in children living with Dravet syndrome,”  said Warren Lammert, a founder of the Epilepsy Therapy Project of the Epilepsy Foundation. “We are proud to have contributed a small grant to support the early trials of Epidiolex, and we continue to advocate on behalf of those individuals and families with uncontrolled seizures and their doctors for the ability to participate in clinical trials and to access cannabis therapies.”

Epidiolex has both Orphan Drug Designation and Fast Track Designation from the U.S. Food and Drug Administration (FDA) in the treatment of Dravet syndrome, a rare and debilitating type of epilepsy for which there are currently no treatments approved in the U.S. GW Pharmaceuticals is also pursuing two Phase 3 trials in Lennox-Gastaut syndrome and the second pivotal trial in Dravet syndrome.”

“One third of those living with epilepsy suffer uncontrolled seizures and many live with unacceptable side effects from existing therapies,” said Mr. Lammert. “This success underscores the importance of our mission and focus on advancing new therapies to eliminate seizures and mortality from epilepsy.“

Learn more about the Epidiolex study here.

24 dead as flu slams Washington; hospitals and state coordinate to fight epidemic

24 dead as flu slams Washington; hospitals and state coordinate to fight epidemic

http://www.thenewstribune.com/news/local/article125032549.html

Getting a flu shot is a CDC GUIDELINE… just like the opiate dosing guideline… so should healthcare professionals be held liable/responsible for deaths from catching the flu because the healthcare professional did not mandate that their pts get a flu shot ?… Healthcare professionals are held liable for deaths of pts that take too many controlled substances and/or put under the spot light if they prescribe opiates mgs/day more than the CDC guidelines ?  Is it that certain CDC guidelines bear more weight – have more importance … than other CDC guidelines… Or is it just that some pt deaths are acceptable than others ?

Washington is under attack from the flu virus and hospitals all over the state are struggling to find beds for the sick. The state’s death toll now stands at 24, including four from Pierce County.

Caught in the midst of a flu epidemic some hospitals are canceling elective surgeries and sending patients to other facilities. The state, meanwhile, is urging only the sickest or at-risk flu patients to use emergency rooms.

Based on Centers for Disease Control statistics Washington might be part of one of the hardest hit regions in the U.S. The region, which also includes Oregon, Alaska and Idaho, had the highest rate of positive flu tests in the nation (27.4 percent) in the week ending Dec. 31. That’s a sharp increase from the previous week’s rate of 18.5 percent.

The next closest region was the inner mountain West at 15.2 percent.

Those numbers translate into more patients seeking help at health care facilities.

“They are seeing a high volume of patients,” said Nigel Turner, a communicable disease control expert with the Tacoma-Pierce County Health Department. “This is something that is partly due to the flu but also just a lot of other bugs around this time of year.”

Turner, who participated in a conference call late Thursday between hospitals and health departments, said the coordination between those agencies is an annual occurrence.

“But this may be a more severe year than we’ve seen in some recent times,” Turner said of the epidemic. “I haven’t seen it at this level in a number of years.”

The conference call was organized by the Washington State Hospital Association in conjunction with the Washington State Department of Health.

“From that call it does sound like many of those hospitals are working at capacity,” said Dr. Kathy Lofy, the state’s health officer at DOH.

“(Sick) people are taking their beds,” said Mary Kay Clunies-Ross, a spokeswoman with the Hospital Association.

Hospitals are activating “surge plans,” Clunies-Ross said. The plans are used for a mass casualty event but also for general overcrowding in emergency departments.

“A surge plan includes canceling elective surgeries, for example,” she said. Surgical beds could then be used for admitting patients coming in through the emergency department.

Providence Regional Medical Center in Everett has opened a satellite emergency room to handle more patients, KOMO TV reported.

“We are actively looking at things to do if things should get worse from where they are now,” Lofy said. That might include opening a flu hotline to direct callers to the best medical option.

Also impacting the system are flu outbreaks at long term health care facilities. Those patients, who are mostly elderly, are often sent to hospitals when they become ill. The facilities themselves have reported 41 new outbreaks of influenza-like illnesses in the week ending Dec. 31.

The epidemic likely hasn’t peaked yet.

“I don’t think anyone thinks this is the high point,” Clunies-Ross said.

Health care providers say the best prevention against the flu is to get vaccinated. With the state in epidemic status many are rushing to get vaccinated.

Two of those on Friday were Gov. Jay Inslee and First Lady Trudi Inslee. They were getting their flu shots Friday morning at a CVS pharmacy in Olympia.

Inslee spokeswoman Jaime Smith said that the couple’s schedules had prevented any earlier vaccinations.

“As with so many people, (they have) busy lives,” Smith said. “They’re going to (get vaccinated) today,”

OGT with Ken McKim: S1E4 – Christmas Angel

Don’t Rush to Ban or Use Kratom, Expert Says

Don’t Rush to Ban or Use Kratom, Expert Says

http://www.medscape.com/viewarticle/872535?

A new review contends that the herbal remedy kratom has some beneficial properties and suggests that a Drug Enforcement Administration (DEA) proposal to make it illegal could bring legitimate research to a standstill.

The leaves from the kratom tree (Mitragyna speciosa), which is found in Southeast Asia, have been used for hundreds of years to treat pain and reduce fatigue, but until recently, it was more or less “a well-kept secret in that part of the world,” review author Walter Prozialeck, PhD, chairman of the Department of Pharmacology at the Chicago College of Osteopathic Medicine, Midwestern University, in Illinois, told Medscape Medical News.

Use of the product has been increasing in the United States and Europe during the past decade, in part because of increased restrictions on opioid prescribing and dissemination of information via the Internet, said Dr Prozialeck.

“It’s real important that physicians know about this stuff,” especially given that patients may be using kratom, he said. Dr Prozialeck added that he believes the substance is not as harmful as opioids, but that many questions about safety and efficacy need to be resolved.

In August 2016, the DEA proposed making kratom a Schedule I drug. It would then join the list of restricted substances that includes heroin and LSD. However, the DEA has delayed that decision.

A public comment period on the drug closes on December 1, but Dr Prozialeck said that given the many questions about the substance, he believes the agency may further put off making a final scheduling decision.

In reviews conducted in 2012 and again this year, Dr Prozialeck and colleagues found that kratom likely has some legitimate and important uses.

“There’s no question kratom compounds have complex and potentially useful pharmacologic activities, and they produce chemically different actions from opioids,” Dr Prozialeck said in a statement

In the latest review, published in the December issue of the Journal of the American Osteopathic Association, Dr Prozialeck notes that kratom differs from opioids in that it does not produce intense euphoria and does not depress respiration.

Not the Same as Opioids

He cites several studies that offer proof that the mitragynines — the active substances in kratom — have different molecular actions than opioids.

 

Andras Váradi, PhD, PharmD, and colleagues at Memorial Sloan Kettering Cancer Center, New York City, showed in a cell culture study that although mitragynines bind to mu opioid receptors, they only partially activate the signaling pathway, and therefore it is likely they do not have the same characteristics, such as the development of dependence or euphoria, as opioids, said Dr Prozialeck.

They also correlated results in mice, and the results showed that mitragynine compounds were as good at relieving pain as opioids but were less likely to produce dependence, and withdrawal symptoms were milder, Dr Prozialeck said.

“These animal studies were really compelling,” he told Medscape Medical News.

Another study by Dr Váradi and colleagues at Columbia University in New York City similarly found that the kratom components might represent “a novel framework for the development of functionally biased opioid modulators, which may exhibit improved therapeutic profiles.”

 

Dr Prozialeck said his review of various websites found thousands of user reports that kratom’s effects were subjectively quite different from those of opioids.

“As a pharmacologist, I would certainly not classify kratom or the mitragynines as opioids,” he said.

Cautionary Note

Despite his optimism that kratom may hold potential, Dr Prozialeck is urging against use of the plant, in large part because the herbal product is unregulated. This makes it hard to evaluate safety and efficacy, as well as determine dosing and purity, he said.

 

Recent reports have shown that some commercially available products may contain substances other than kratom or may have high doses of some of the constituent elements.

In October 2016, researchers in the Boston area who bought kratom off the shelf reported that the products contained artificially elevated concentrations of 7-hydroxymitragynine, “the alkaloid responsible for M speciosa’s concerning mechanistic and side effect profile.”

In this case, it appears that “unscrupulous vendors” were “adulterating products to enhance their activity and make them more drugs of abuse,” said Dr Prozialeck.

 

In another study, researchers bought and tested 15 kratom products. They found that all contained mitragynine, a stimulant, but none had any 7-hydroxymitragynine, the compound responsible for kratom’s narcotic properties.

Dr Prozialeck said he understands that the DEA’s proposed ban was due to concern about increasing reports of toxicity. But given the lack of regulation of kratom products in the United States, “it’s not clear that kratom is the culprit,” said Dr Prozialeck.

“In a perfect world, there should be some way short of a total ban to regulate, or at least provide some quality control measures over the production and sale of kratom,” he said.

Dr Prozialeck reports no relevant financial relationships.

J Am Osteopath Assoc. 2016;116:802-809. Full text

Misguided Repeal to Cure Opioid Crisis Ignores Patients’ Pain

Misguided Repeal to Cure Opioid Crisis Ignores Patients' Pain by Lynn R. Webster @LynnRWebsterMDMisguided Repeal to Cure Opioid Crisis Ignores Patients’ Pain

thepainfultruthbook.com/2016/12/misguided-repeal-to-cure-opioid-crisis-ignores-patients-pain/

Once again, I read the Intractable Pain Act (along with the section of it known as the “Pain Patient’s Bill of Rights”) which was passed by the Tennessee House and Senate in 2001 and repealed in 2015.

I did not see anything in the legislation that supports the statement made by Knox News columnist Frank Cagle that “when a patient was discharged from the hospital, they had to sign a form saying they have been issued all the pain medicine they wanted. If they didn’t get all the pain pills they wanted, the doctor could be sanctioned.”

What the Intractable Pain Act States

Instead, the now-defunct Intractable Pain Act states the following:

  • A patient suffering from severe chronic intractable pain should have access to proper treatment of his or her pain.
  • Opiates can be an accepted treatment for patients in severe chronic intractable pain who have not obtained relief from any other means of treatment.
  • A physician treating a patient who suffers from severe chronic intractable pain may prescribe a dosage deemed medically necessary to relieve severe chronic intractable pain as long as the prescribing conforms with the provisions of this section.
  • The patient’s physician may refuse to prescribe opiate medication for a patient who requests the treatment for severe chronic intractable pain. However, that physician shall inform the patient that there are physicians whose primary practices are the treatment of severe chronic intractable pain with methods that include the use of opiates.

Did Drug Industry Lobbyists Play a Role?

The author of the article claims the drug industry pushed the 2001 legislation through the legislature. I don’t know what role, if any, the “drug industry lobbyists” played in passing this law, but I don’t see anything in this bill that isn’t reasonable in providing relief to people in pain. There is no mandate in the Act to prescribe opioids. The Act, however, enables doctors to treat pain patients with opioids when that is the best available treatment.

The ubiquitous view that treating pain is the reason for the opioid crisis mischaracterizes the problem. Worse, it conflates the needs of people in pain with the efforts to curb illegal drug use, and it leaves chronic pain patients with few treatment options.

Tennessee repealed the Intractable Pain Treatment Act in 2015 in response to a record high of opioid overdoses. But the repeal didn’t address the cause of the problem. According to a recent article in the Tennessean, the increase in overdose deaths is largely due to illegally produced and distributed synthetic fentanyl, not prescription painkillers.

The legislators in Tennessee meant well. They were right in thinking that the opioid crisis is a serious problem that causes far too much carnage.

No Reduction in Overdoses in the Aftermath of the Repeal

However, their effort to curb the opioid crisis has not reduced the availability of illicit drugs nor the number of overdoses, while it has made it more difficult for people in pain to find relief. The lesson to be learned is that most of the harm from opioids in Tennessee comes from illicit or diverted opioids and that repealing the Intractable Pain Act, thus far, has not curbed the opioid crisis or reduced the number of opioid-related overdoses.

 

 

Maybe we should go back to being a English colony ?

UK Reclassifies CBD Oil as Medicine Just as America Puts It in Class With Heroin

http://www.alternet.org/drugs/uk-reclassifies-cbd-oil-medicine-america-puts-class-heroin

After the DEA moved to further constrain Americans’ access to medically miraculous CBD oil by classifying it alongside heroin and cocaine, Britain chose compassion and common sense — and just classified cannabidiol (CBD) as a medicine.

On Monday, Britain’s Medicines & Healthcare products Regulatory Agency (MHRA) decided CBD — which can treat illnesses and conditions from severe childhood epilepsy to autism to cancer — warranted the classification as a medicine based on credible evidence of its efficacy.

Thus, unlike in the U.S. — where the substance is now considered devoid of medical benefit by the DEA — CBD meeting quality and regulatory standards may be legally obtained by any British citizens who need it, reports High Times.

“We have come to the opinion that products containing cannabidiol (CBD) used for medical purposes are a medicine,” an MHRA spokesperson said in a statement on the agency’s website.

“Our primary concern is patient safety and we wish to reiterate that individuals using cannabidiol (CBD) products to treat or manage the symptoms of medical conditions should discuss their treatment with their doctor.

“MHRA will now work with individual companies and trade bodies in relation to making sure products containing CBD, used for a medical purpose, which can be classified as medicines, satisfy the legal requirements of the Human Medicines Regulations 2012.”

This rational approach stands in sharp and tragic contrast to draconian drug laws in the U.S., where, as of January 13, CBD oil — which does not contain the psychoactive chemical THC, which gives people a high — and all cannabinoids will be considered dangerous substances.

Healthcare and cannabis rights advocates have excoriated the DEA’s brash and baseless move, noting lives will now be in jeopardy.

“The whole policy around this plant is just so illogical,” Robert J. Capecchi, director of federal policies at the Marijuana Policy Project, told Vice. “Even when you look at the criteria you’re supposed to be looking at under the law, they’re just not following it. It’s just a stupid policy for lack of a better term.”

THC-containing cannabis — also medically beneficial for the treatment of post-traumatic stress disorder, among many other conditions — still remains as a Schedule I substance in the U.S., and is not considered medicine in Britain.

But the latter has taken steps in the right direction with the new classification for CBD — a complete reversal of cease and desist orders sent by MHRA to vendors only months ago, as High Times notes, ordering it to be “removed from sale in the UK.”

“The change really came about with us offering an opinion that CBD is in fact a medicine,” Gerald Heddel, director of inspection and enforcement at the agency, explained to Sky News, “and that opinion was based on the fact that we noted that people were making some quite stark claims about serious diseases that could be treated with CBD.”

Decades of government propaganda about the putative dangers of ‘marijuana’ — amplified exponentially by President Nixon’s administration’s agenda to, in essence, criminalize black people and the anti-war left — still linger in the stigmatization of all the cannabis plant’s myriad derivatives.

Despite the DEA’s war on cannabis and its users, onerous prohibition has been voted out in an increasing number of states — forcing those who need it to uproot their lives and move, in order not to face arrest over their medicine. Medical research into cannabis and cannabinoids continues to evince the miraculous assets the plant offers. In just one example, as High Times explains,

“In early December, researchers from the University of Alabama found that CBD oil reduces both the frequency and severity of seizures in children and adults with with severe, intractable epilepsy. In two-thirds of the 81 participants, the severity was reduced by at least 50 percent.”

In classifying CBD as medicine, MHRA recognizes such benefits — and the improved health of British citizens — eclipse the value in blindly continuing dangerous and inaccurate propaganda.

Sadly, the highly profitable war on drugs and influence of pharmaceutical corporations have the DEA feigning ignorance about cannabis and CBD — at the expense of people’s lives.