Taking audio/video recordings to protect your rights

Over the last couple of weeks, we have seen several videos … concerning how the flying public is being mis-treated on various airlines…  American, United, Delta have made the news…

We have seen a person dragged off a plane… experiencing a concussion, broken nose and losing two teeth

A female with a baby in her arms was confronted by a flight attendant over a baby stroller

A male was tossed from a flight because after telling the flight attendant that he had to use the restroom and told him he would have to wait… after a 30+ minute wait .. he got up and quickly used the bathroom… 

The above video sort of reminds you of civil forfeitures… telling a father that he must relinquish a seat that he had PAID FOR.. and just one of the FOUR SEATS that he had paid for… one that a infant was sitting in – in a legal car seat..

He was lied to that it was a FAA rule that infants < 2 y/o could not fly in a car seat… Was threatened with him and his wife being thrown in jail and kids put in foster care unless he forfeited the four seats he had paid for.

When are we going to start see such audio/video of healthcare providers denying care, lying to pts, technically abusing pts ?

I have had pts tell me that they have been threatened by Pharmacists – normally chain store employees – have threatened to have pts ARRESTED because they asked for reason why their legal/on time/medically necessary prescriptions were being denied.

What are they wanting… pts getting down on their knees and BEGGING them to DO THEIR JOB ?

YouTube is a powerful platform for engagement, and uploading videos about protecting your rights can help to engage viewers and start a conversation about the topic. This can lead to increased awareness, advocacy, and action around protecting one’s rights. Visit this site to start your campaign from here and gain more youtube likes.

Corporations do not want BAD PRESS… and employees that cause them to get BAD PRESS .. may get suspended, fired or at least given a final warning…

Corporations typically don’t really care what their employees do.. as long as they don’t steal from the company, allow others to steal from the company and as long as HQ doesn’t get any complaints. The only time they will care and come looking for a problem is when revenues fall because pt/customers have taken their business elsewhere … where they are treated better.

IMO, many employees in healthcare neither respect nor fear pts nor care about their rights, and until they are taken to task to change how pts are treated… it will not improve and will probably get worse.

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Beware of worthless procedures and epidural steroids for your back pain

Beware of worthless procedures and epidural steroids for your back pain

www.kevinmd.com/blog/2017/04/beware-worthless-procedures-epidural-steroids-back-pain.html

CLICK ON GRAPHIC TO GO TO AMAZON TO PURCHASE

 

 

Is this document enough to start filing grievance with www.cms.gov if pt is on Medicare/Medicaid … or with your insurance company … or if your insurance is from an employer and self insured (ERISA) then file a grievance with the person/dept that is making decisions about what is to be paid for by the company.  The employer may go after the insurer for refunds of all the monies that was paid out for unnecessary and discouraged procedures.

If this was not so absurd … it would be funny… CDC and the like says that there is no proof (clinical studies) that opiates work long term.. because there has been no double blind studies on such, all there is … is anecdotal evidence from pts that it works… yet.. there is no clinical evidence that ESI using cortisone has been proven to be beneficial, and in fact more evidence that they have the potential to be harmful to the pt.  Technically, for a healthcare professional to provide a product/service that is not medically necessary… and insurance is billed for such… is considered INSURANCE FRAUD.

Many healthcare providers seem to have neither respect for nor fear of pts.  If you wish to file the claim anonymously, then hire an attorney to file the complaint and the pt can “hide” behind the attorney/client privilege.  This could also be a potential area of class action against a healthcare provider… Providing unnecessary/unapproved procedures to hundreds of pts.

Near my office, there’s a breakfast-and-lunch joint where strangers sit down at shared tables. When Joseph, an attorney in his early seventies, heard that I was writing a book about the back pain industry, he started asking questions.

That afternoon, he was scheduled to have the first of three epidural spinal injections meant to relieve the symptoms of spinal stenosis, a condition in which the spinal cord narrows to the point where it squeezes the nerves. The weakness and cramping in his legs were so bad that he couldn’t walk a long city block without stopping to recover.

The injections were his best hope, he said, making it even harder for me to break the news. A few months earlier, in a 2015 review of the medical literature, the Agency for Healthcare Research and Quality had found no evidence that epidural steroid injections were effective in treating symptoms of spinal stenosis or typical lower-back pain. Even in the presence of a recent disc herniation and ensuing sciatica, the benefits of injections were small and not sustained over time. That news followed on the heels of an FDA statement warning that injection of the active medication in these shots, glucocorticoids — a class of corticosteroids — into the epidural space of the spine could result in rare but serious neurological problems, including loss of vision, stroke, paralysis and death. Based on those and other findings, the Journal of the American Medical Association ( JAMA) advised physicians to refrain from recommending injection therapy to patients with any kind of chronic back pain.

That news did not go over well with the doctors known as “interventional pain physicians,” who make a living performing such procedures. In the United States, more than ten million epidural steroid injections are delivered each year, a number that makes them the bread and butter of interventional pain management practices.

I was not surprised that my lunch partner didn’t have the facts. Primary care physicians who ordered the shots were rarely informed about the lack of evidence and the risks of treatment. Even young, healthy people, explained anesthesiologist James Rathmell, the chair of the Department of Anesthesiology, Perioperative and Pain Medicine at Boston’s Brigham and Women’s Hospital, could go in with manageable low-back-pain symptoms and come out with catastrophic neurological injuries. “The bottom line,” said Rathmell, “is that if you come into my clinic with chronic axial back pain, you’re not going to get epidural steroid injections — because they don’t work.

“People should get the best evidence-based treatment they can,” he added. “As a rule of thumb, if you pay practitioners to do stuff, they will do more stuff. Frankly, what’s happened in interventional pain management is just a microcosm of what’s happened in all of medicine.”

As I explained these things to Joseph, he paled. Why would his doctor advise him to undergo a worthless and risky procedure?

Three decades ago, anesthesiologists had no trouble getting jobs in hospital ORs. On a busy morning, they could run five cases at once, and get paid for them all, while depending on registered nurses to keep an eye on individual patients. Starting in the early 1990s, cost-conscious health management organizations (HMOs) realized that the nurses could manage without supervision, and they stopped paying fees to doctors who at best were marginally present. Many anesthesiologists found themselves underemployed. They knew little about treating musculoskeletal disorders or how to address the feelings of depression, anger, and isolation that often afflict back pain patients, but when they retooled, they set up pain management practices.

Torpedoed into entrepreneurship, the most successful interventional pain physicians offered an ever-expanding menu of injections, including facet and sacroiliac joint blocks, selective nerve blocks, discography, needle electromyography, radio-frequency and thermal facet ablations, botulinum toxin, and trigger point injections. They implanted intrathecal drug delivery pumps and spinal cord stimulators and cemented together vertebral compression fractures. They used medical lasers to heat, shave and slice soft tissue. By the turn of the new millennium, interventional pain management, which a decade before had barely existed, had become one of the most profitable aspects of spine care.

There are, indeed, people who undergo one perfectly targeted epidural steroid injection and hit the golf course the next morning, completely cured. In the more typical scenario, however, the first injection — if in fact, it provides any relief at all — is only briefly effective. Then the numbing medicine and the anti-inflammatory effect of the glucocorticoid wear off, and the pain returns.

Generally, the shots are ordered in a series of three, although no expert I asked could say why, and the American Society of Anesthesiologists’ guidelines do not advise the administration of a specific number. “You always do three, even if the first two do no good at all,” wisecracked neurosurgeon Charles Burton, who publicly questioned the safety and effectiveness of the procedure, long before JAMA and the FDA got on board. Some doctors construed the “rule of three” to mean that, in a single visit, they could give three shots at each affected vertebral level, thereby exposing a patient to a colossal dose of glucocorticoid. In fact, when Colorado researchers mined an insurance company’s database, they found that one doctor had billed a single patient for fifty-one such injections in one year. The same database showed that a New Jersey patient had received thirteen shots in a five-month period and had subsequently developed kidney failure.

The FDA had been issuing cautionary statements about epidural steroid injections since 1981. But in 2014, the agency took a further step compelling pharmaceutical manufacturers that produced the injectable glucocorticoids to clearly state the risks on every vial’s label, advising that “serious neurologic events, some resulting in death, have been reported with epidural injection,” and that the “safety and effectiveness of epidural administration of corticosteroids have not been established.” The FDA stopped short of requiring manufacturers to notify physicians or their purchasing departments that things had changed, and most did not notice. One pain physician, Cleveland Clinic’s Richard Rosenquist, told Bloomberg reporter David Armstrong that because he’d used such drugs for his entire career, unless he was alerted to do so, he was “unlikely to go back and spend time reading the package insert.”

The implications were significant: Properly “consented,” a patient who was about to receive an epidural steroid injection would hear about specific risks, including damage to the dura mater (the sturdy sleeve surrounding the spinal cord), nerve root injury, elevated cholesterol levels, vertebral fractures, the death of muscle and bone tissue, staph infection, epidural abscess, immune system deficits, stroke and death. But in reality, if this information was conveyed at all, it was in boilerplate format, which the patient signed after only a cursory glance.

There are two dominant techniques for administering epidural steroid injections. In the first, known as “interlaminar,” the needle is directed into the epidural space, around the spinal nerves. In the second approach, referred to as “transforaminal,” the needle is inserted at an angle, which places it closer to the targeted nerve but also in the vicinity of vessels and arteries. Incorrectly placed, the needle can sever an artery or deliver medication into the blood vessels, clogging them and preventing adequate blood flow to the brain. The result, in either case, may be stroke or paralysis.

Whether the approach is transforaminal or interlaminar, research shows that a quarter of epidural steroid injections miss their targets. In “blind” injections, performed without fluoroscopic guidance, the needle is incorrectly placed in up to half of epidural steroid procedures.

In roughly six percent of epidural steroid injections (a number that sounds small but is not, because thousands of injections are delivered every day), the needle nicks the dura mater, the sturdy sleeve surrounding the spinal cord, allowing cerebrospinal fluid to leak out. Typically, this is not terribly serious. It results in a severe headache, which goes away after the patient lies flat for a couple of days. Sometimes, another procedure, known as a “blood patch,” is used to stop the leak of cerebrospinal fluid.

But when the needle actually punctures the dura mater, it’s a different story. Then the payload of glucocorticoid and anesthetic may be delivered into a region of fragile nerve tissue called the subarachnoid space. From there, the cerebrospinal fluid, bearing its toxic load, circulates to the brain, where the cortisone solution efficiently strips the insulating (and essential) myelin layer of neurons. One result is “adhesive arachnoiditis,” a condition so grossly debilitating that neurologist Dewey Nelson described it as akin to “having a blowtorch up your rectum. It binds the nerves, like gunky cooked spaghetti, and the result is unrelenting pain that may last for a lifetime.”

Cathryn Jakobson Ramin is an investigative journalist and author of Crooked: Outwitting the Back Pain Industry and Getting on the Road to Recovery.  Reprinted with permission of Harper, an imprint of HarperCollins Publishers

 

 

FL Implementation Bill Dies

    Implementation Bill Dies

The House and Senate have adjourned the 2017 session. The medical marijuana bills are among scores of bills that didn’t make it through both the House and Senate.

Lawmakers had created massive new regulation driven by special interests.

The House and Senate both gave lip service to working in the interests of the patients while taking tens of thousands of dollars from the “Have’s” (those who have a license) and the “Have Not’s” (those who want a license).

Drug-Free America was a leading voice in the drafting of House bill 1397. The bill was amended and re-written dozens of times. The final hours of the debate had nothing to do with patients and everything to do with the people who want to profit off the patients.

100 stores per license – was the final sticking point for the dart thrown between infinity and 3.

The Senate, in an earlier committee, attempted to block the seven license holders from growing so fast they would hold a market monopoly. They put a cap on the number of storefronts per license. The House rejected the cap on storefronts. (Could the thousands of dollars Leader Rodrigues got from the current license holders be part of the reason they held out?)

This session, those of us up here in Tallahassee working for you without compensation came to think of ourselves as the “Have Compassion” and “Have a Conscience”. Well, we lost this session. WE would like to thank our allies, Gary Stein, the team from the Minorities for Medical Marijuana, supporters of NORML and all those who came up to speak. We worked long and hard, but we couldn’t overcome the influence of money on the process.

Because the House and Senate failed to provide a framework for the implementation of Amendment 2 the Department of Health Office of Compassionate Use will finish the rule making process. You will remember they have already held public hearings.

Already attorneys are considering their options for lawsuits. This is an expensive and uncertain process.

For now, if you know someone who uses cannabis then be sure to encourage them to use caution.

Leading from the Front,
FLCAN Team
Florida Cannabis Action Network | Leading The Grassroots Since 1998
Anonymous Donations to P.O. Box 360653, Melbourne, FL 32936 | Tel: 321-253-3673

Lawsuit: State threatened to take children after false positive drug test

Lawsuit: State threatened to take children after false positive drug test

http://www.cincinnati.com/story/news/2017/05/05/lawsuit-state-threatened-take-children-after-false-positive-drug-test/101328170/

according to : Research shows that morphine and codeine can sometimes be detected in the urine up to 48 hours after ingestion of poppy seeds from some pastries, such as bagels, muffins, and cakes (see reference one for a free article on this topic).  http://www.usada.org/can-poppyseeds-cause-a-positive-drug-test/  

So these “investigators” knew or should have know this fact… when Holly asked if eating poppy seeds on Bagel Chips could have caused the positive urine test…   Also this information states that the poppy seeds MAY CONTAIN Morphine and Codeine… and Heroin is metabolized in the body into Morphine so these “investigators” jumped to the conclusion that Holly was using Heroin… Just another illegal process by “people in authority” … to gain  “extra money” for their agency. Kind of reminds you of civil asset forfeitures ?

Holly Schulkers said they knew she wasn’t on heroin before she left the St. Elizabeth hospital in Edgewood, but that didn’t stop state social workers and hospital staff from threatening to take her children and putting her through a two-month “nightmare.”

Now, she’s suing the Kentucky Cabinet for Health and Family Services and St. Elizabeth Healthcare in federal court in Covington.

Schulkers walked into the hospital Feb. 8 to deliver her child through induced labor. She and her husband, David Schulkers, each have two children from previous marriages. This would be their first child together, and Schulkers said likely their last.

The labor went smoothly and she gave birth to a seven-pound baby girl on Feb. 9, a Thursday. She breastfed her new daughter within the first hour, and began discussing discharge with her doctors.

On Friday morning, according to the lawsuit, the Schulkers received an unexpected visit to their room from a hospital social worker who told her she had tested positive for opioids.

 The suit, filed Thursday in U.S. District Court, states Schulkers was told she couldn’t leave the hospital with her child, who would have to be monitored for 72 hours for withdrawal symptoms.

Schulkers agreed to a second urine test and was told her baby’s umbilical cord would also be tested. But, she said, before the results of those tests came back, the Kentucky Cabinet for Health and Family Services was contacted and social workers came to her room.

“They started asking me how the heroin, is what they said, got in my system,” Schulkers said. “I said, ‘There’s a mistake. Somebody mixed up the urine. I’m not a heroin addict.'”

She said she asked if the poppy seeds on the “Stacy’s Everything Bagel Chips” she had eaten before she gave birth could have thrown off the test, and was told the result could not be affected by that.

The state workers asked where she lived, how many children they had, where the kids were and where they went to school, according to the suit.

“She said she was going to run a background check on me, and asked what drug charges they would find,” Schulkers said. “I told them they weren’t going to find anything. I work with children. I volunteer at the kids’ school. They run background checks on me to make sure I’m not a criminal coming into the kids’ school.”

Schulkers said the cabinet even called her mother-in-law to ask if there was any history of drug abuse.

The suit states a supervisor with the cabinet told Schulkers, still in the hospital with her newborn, to “let me get the help you need so you can be a better mother to your children.”

When Schulkers insisted she did not do drugs, the suit states, she was told “until this gets figured out you are no longer allowed to be around any children without supervision of (an) approved individual.”

The suit states Schulkers’ second urine test and the umbilical cord test came back negative over the weekend, but that Schulkers and her husband weren’t off the hook.

According to the suit, they signed a prevention plan, which barred Holly Schulkers from being alone with any of her children. Stamped at the bottom of the plan, in capital letters: “Absent effective preventative services, placement in foster care is the planned arrangement for the child.”

The couple signed “under duress” and “coercive conditions,” the suit states, because they were worried that their children would be removed from their care.

Schulkers was allowed to take her daughter home Sunday. She said her the baby never showed any signs of withdrawal.

On Monday, Schulkers’ husband stayed home to “supervise” his wife and newborn. Their older children went to school where they were met by cabinet investigators, according to the suit. Schulkers said she was not told this was happening, and didn’t learn about it until afterward.

“They pulled my kids out [of class], my husband’s kids out and questioned them about if I took any prescription medicine, if they ever saw me smoking anything,” Schulkers said. “They asked if my husband and I fought, if we fought did we hit each other?

“My oldest daughter said she was really nervous and scared. My son thought they were getting information to kidnap him and break into our house. No child at that age should have their innocence taken away.”

She took yet another drug test, a hair test that would show any long term abuse. The suit states that test came back negative, too, and the results were sent to the cabinet.

It wasn’t until April 7 that the Schulkers received a letter stating the prevention plan was over and that “the claim of abuse was unsubstantiated.” Schulkers said it was a two-month “nightmare” in which she lived in fear of losing her children, sometimes worried to even answer the door to her Fort Thomas home.

“The birth of my last child has been ruined by these people,” Schulkers said. “I was basically guilty in their eyes. It wasn’t ‘innocent until proven guilty.’ It was, ‘This lady is on drugs and we’re going to do what we need to do to prove that.'”

Her legal team argues the cabinet may have had financial incentives for keeping the case open as long as it did. The suit claims  the prevention plan’s language matches the language required for the cabinet to receive federal funding for investigations.

“If the investigation is terminated, they quit receiving the funding. In our mind, that explains why the cabinet may have kept this open for two months,” said Schulkers’ attorney, Paul Hill. “If that was done to this family for money from the federal government, it’s pure evil.”

The Kentucky Cabinet for Health and Family Services did not respond to requests for comment on the lawsuit.

“We cannot comment on any prospective or active litigation matters,” a spokesperson at St. Elizabeth said in a statement Friday. “St. Elizabeth follows all necessary protocols and procedures to ensure the safety and health of all patients.”

For Schulkers, the lawsuit extends beyond her family.

“I’m sure this has happened to other people,” she said. “I want to make sure it never happens to anyone else again.”

it’s not valid to call for use of a compound because the treatment is cheaper

Attorney Advises Caution in Use of Compounded Meds

https://www.bloodhorse.com/horse-racing/articles/221412/attorney-advises-caution-in-use-of-compounded-meds

Many pain clinics use compounding pharmacy to prepare injectables for ESI’s or to fill implanted pumps.  While this article talks about using these compounds with animals/horses… but if you want to see how bad it can get  with compounders.. suggest that you read this  https://en.wikipedia.org/wiki/New_England_Compounding_Center_meningitis_outbreak

Where compounding pharmacy produced Methylprednisolone was contaminated with a FUNGUS… abt 70 pts DIED and around 700 got seriously ill… and the medications to treat this fungal meningitis is a pretty NASTY MEDICATION.

It has been reported that pain doc can purchase these compounded medications for 10%-25% of the cost of commercial products

An attorney who handled a prominent negligence case against a Kentucky compounder advises veterinarians and horse owners to make sure they are acting legally when administering a compounded drug to a horse, because without such care they could lose out on legal protections should anything go wrong with the treatment.

During the National Conference on Equine Law May 4 at Keeneland, Tom Nicholl, an attorney and veterinarian in Orlando, Fla., advised vets and horsemen who treat a horse with a compounded drug to acquire in writing from the compounder that the administration of the substance is legal.

Nicholl outlined some of the gray areas that compounders operate under, specifically in the horse industry. He noted that while there has been some added oversight of compounded drugs, most of that focus has been on compounds for human use, and to a lesser extent compounded drugs in animals to be sold for meat. He said the lowest of regulatory concern is the use of compounded drugs in animals not sold for human consumption, like horses.

He said this environment has allowed compounding pharmacies, which are supposed to be used to mix two or more FDA-approved drugs to suit a specific patient, wide latitude in operations and has led to misconceptions.

Nicholl said while compounders are supposed to address specific patients, some have been found to make large batches of product, which blurs the line between a compounder and drug manufacturer. A drug manufacturer, whether a brand name or generic, is subject to FDA oversight. Compounders are largely regulated at the state level, although some federal restrictions have been added in recent years.

A patient who needs a specific dose—say a large or small animal—that may not be available in that dosage size would likely be a candidate for a compounded version of the medication. Or a patient who cannot receive an injection of a drug may have to have an oral version of the drug compounded.

If an FDA-approved drug is no longer manufactured, a compounded alternative is allowed to be made and substituted. Nicholl noted that this situation comes up frequently in animals.

Also, a valid client-patient relationship is required that documents why the patient, in this case a horse, needs a compounded medication as opposed to the FDA-approved drug.

Nicholl cautioned that some sellers try to equate compounded drugs with generic drugs. He said that sales pitch is not accurate, as generic drugs do receive FDA oversight but compounded drugs do not.

“Compounded drugs are not FDA approved,” Nicholl advised. “There’s no quality standards, no stability standards, no consistency standards.”

In using compounded drugs in racing, this can put a horse in danger of a positive drug test, as withdrawal standards are based on FDA-approved drugs, but compounded medications can see fluctuation in the concentration of the drug from batch to batch. Such a post-race positive, of course, would impact a vet, trainer, and owner.

Furthermore, compounded drugs can be a danger to the health of horses as well. Nicholl is familiar with that situation, as he represented horse owners who sued Wickliffe Pharmaceutical Inc. (also known as Wickliffe Veterinary Pharmacy) and some of its board members, after alleging that six horses became sick and two others died at an Ocala training center after receiving a compounded drug to treat equine protozoal myeloencephalitis from the Lexington, Ky., pharmacy. 

The 2014 lawsuit alleged a Wickliffe compound of toltrazuril and pyrimethamine had more than 13 times the amount of pyrimethamine that was supposed to be in the product, as listed on the label. The FDA reported a similar finding in the Wickliffe product in question, noting that adverse events associated with high doses of pyrimethamine include seizure, fever, and death.

The case was settled out of court in early 2015. Nicholl believes by filing the case in federal court, his clients were in a better settlement negotiating position, because in that court Wickliffe also was subject to punitive damages should the case go forward. Nicholl said the dosage levels and documentation of the mixture did not match what testing revealed to actually be in the compounded medication.

Nicholl noted that, had the horses involved received a compounded drug that didn’t meet legal standards of administration, it’s doubtful any court would have recognized their case. He said the compounded drug administered in this case met legal standards, because there was a valid vet-patient relationship, the medication was properly prescribed, the compound was a mix of FDA-approved drugs, the vet involved noted that an FDA-approved drug had not been effective as some patients had relapsed, and it was properly labeled.

He said it’s not valid to call for use of a compound because the treatment is cheaper. He also said saying its use is “common practice” will not meet legal standards.

 

Walgreen & opiate crisis.. no mention of “I’m not comfortable” .. “Good Faith Policy

Walgreens Fights the Opioid Crisis

What a large national chain is doing to combat opioid abuse.

http://drugtopics.modernmedicine.com/drug-topics/news/walgreens-fights-opioid-crisis

As the opioid epidemic spirals out of control, all pharmacies from independent to major chain to health-systems are starting to take steps in fighting it. A recent APhA study looked at one of those chains, Walgreens, to analyze just how effective their strategy for fighting the opioid crisis really is, and the results provide insights for pharmacists in every corner of the industry.

One goal of the APhA 2017 annual meeting was to increase awareness about pharmacists’ roles in combatting the opioid crisis. As a part of this, the APhA journal, JAPhA, put out a special issue on the topic. One article, “A nationwide pharmacy chain responds to the opioid epidemic,” quantifies the success of Walgreens’ efforts to combat opioid abuse and makes suggestions for how other chains and independent pharmacies can use these same strategies.

The study looked at three strategies: providing kiosks for the disposal of unused medications, expanding access to naloxone, and providing counseling on the risks of opioids and how to avoid overdose. These strategies include increased training for pharmacists on how to dispense naloxone, which can be dispensed without a prescription in 33 states, as well as training on specific-state policies, how to recognize an overdose and the risk factors for an overdose, how to handle an overdose, as well as an overview of the impact of overdoses in the United States.

The pharmacist counsels each patient who receives naloxone on its use. This counseling covers topics including risk factors for opioid overdose, strategies to prevent overdosing, how to recognize an overdose, how to respond to an overdose, and how to administer naloxone.

The study analyzed naloxone distribution in states between 2012 and August of 2016. In 2012, Walgreens dispensed only 18 naloxone prescriptions in 11 states and Puerto Rico. In comparison, in the first eight months of 2016, Walgreens had dispensed 10,478 naloxone prescriptions in 49 states.

By October of 2016, Walgreens had installed more than 500 medication-disposal kiosks, and the program had disposed of more than 10 tons of medication.

A major challenge that Walgreens, or any other chain in more than a few states, faced was how naloxone dispensing laws were changing in each state. Because of this lack of coherence, a large-scale roll-out of the naloxone strategy was difficult. The study recommends creation of national policies that would streamline the roll-out process and make uniform training possible.

The study also found challenges for individual pharmacists. In community pharmacies especially, the plan could be prohibitively time-consuming, the authors noted. In addition, there is no reimbursement plan in place for this extra time spent documenting and counseling. Developing strategies thus requires the cooperation of many organizations. The authors recommend “broad efforts” to adopt new CDC guidelines for opioid prescribing and that more organizations adopt similar opioid addiction programs.

The study concludes by saying that access to naloxone, patient education, and disposal kiosks are “key initiatives to address the opioid epidemic and reduce the increasing national burden of opioid overdose.”

Here is a article from 2013 about Walgreens “Good Faith Policy”

Walgreens’ “secret checklist” reveals controversial new policy on pain pills

After Walgreen’s implemented this policy… all too many of Walgreen’s Pharmacist became “uncomfortable” in filling  prescriptions for controlled substances…. even for those pts that Walgreens had filled these same medications for years… all of sudden they were persona non grata… Surprisingly, these same Pharmacists seem to have little problem filling non-controlled prescriptions for these same pts… written by the same prescribers…

DEA: what they say in front of a TV camera and what they tell prescribers/Pharmacists ?

I would like to know if the FDA has recently passed a new law stating if you are on opiates for pain, that you can no longer take benzodiazipines? I have been on both for 23 years (alprazolam) due to MS, defective sleep structures in my brain, etc… I do not sleep without alprazolam. My pain doctor told me in April he would not write my script for oxycodone if I took alprazolam. I slept a total of 9 1/2 hours  the whole month of April. My visit with the pain doc on May 3rd, I was told this was a new FDA ruling that just went into effect. I had to make a choice of taking alprazolam or oxycodone. I choose the alprazolam because it also helps tamper the pain I have from 2 failed back surgeries in the 70’s, severe osteoporosis & osteoarthritis with many breaks, spinal hemangiomas,, several surgeries to correct some of these problems to no avail just more pain problems. I will now be weaned off of the oxycodone by the pain management doctor. I took my alprazalom last night, got 8 1/2 hours hour of restful restorative sleep, & did not have to take a oxycodone this morning. Lack of sleep & increase of pain go hand in hand. I don’t believe the alprazalom will relieve all the pain so wonder if this law is true or not, or if this pain doc just wants me to get off of everything that lets me function as a normal human being. I have much to do as my husband is totally bedridden, plus life in general! Am I to just sign up for a nursing home myself? If this is a new rule, we must fight it!

There is something called BEERS CRITERIA

http://chpw.org/resources/Providers/Beers_Criteria.pdf

INTENDED USE
The goal of this clinical tool is to improve care of older adults by reducing their exposure to Potentially Inappropriate Medications (PIMs).
This should be viewed as a guide for identifying medications for which the risks of use in older adults outweigh the benefits.
These criteria are not meant to be applied in a punitive manner.
This list is not meant to supersede clinical judgment or an individual patient’s values and needs. Prescribing and managing disease conditions should be individualized and involve shared decision-making.
These criteria also underscore the importance of using a team approach to prescribing and the use of non-pharmacological approaches and of having economic and organizational incentives for this type of model.
Implicit criteria such as the STOPP/START criteria and Medication Appropriateness Index should be used in a complementary manner with the 2012 AGS
Beers Criteria
to guide clinicians in making decisions about safe medication use in older adults.
The criteria are not applicable in all circumstances (eg, patient’s receiving palliative and hospice care). If a clinician is not able to find an alternative and chooses to continue to use a drug on this list in an individual patient, designation of the medication as potentially inappropriate can serve as a reminder for close monitoring so that the potential for an adverse drug effect can be incorporated into the medical record and prevented or detect early
This is just CRITERIA… doesn’t get up to the level of GUIDELINES…  first question is what is an OLDER ADULT ? Some of us believe that Beers is a bunch of academic BS.  They made recommendations and then they put statements such as these in the guideline:
This list is not meant to supersede clinical judgment or an individual patient’s values and needs.
What this pt is running into is that the DEA claims that they don’t tell prescribers what medication to give which pts.. then because some people take excessive doses of opiates, benzos, and muscle relaxants like Soma… maybe mix with alcohol and end up DEAD… the DEA comes out and said that there is no valid medical use of those three medications being used in the same pt.  Doesn’t make any difference that millions of people have taken those medications together and in appropriate doses and get improved quality of life… and NONE HAVE OD’d…

Jeff Walsh, DEA Asst. Special Agent, sits down with WESH 2’s Matt Grant to discuss issues patients are having getting legitimate prescriptions filled.
JEFF WALSH is one of those DEA agents that spends the majority of his time – sitting behind a desk… I have spoke with Pharmacists who relay what they are being told by DEA agents in the field… and what Agent Walsh states in this video interview does not match up with what community pharmacists and prescribers  are being told.
Report Matt Grant at www.wesh.com in Orlando did a couple of dozen of pieces – including two-30 minute specials – on the denial of care in FL… you can find most of them on www.youtube.com
My suggestion to pts when they are told by a prescriber that “it is the law”.. simply as for a copy of the law and or the state statue number… so you can look it up on the web… if they can’t/won’t provide the information… most likely it is because there is no such LAW … so they can’t enforce  a LAW that doesn’t exist.
When the prescriber states that “THEY” are putting pressure on the prescriber… politely ask who in the hell “THEY” are ?
Healthcare professionals are suppose to function on FACTS… they don’t start you on hypertension, diabetes, cholesterol or other chronic disease medications without some sort of labs/testing to document that they have FACTS that you do in fact need medication to treat a verified disease.

Reports: White House plans 95 percent budget cut to the anti-drugs office

Reports: White House plans 95 percent budget cut to the anti-drugs office

Health 28 minutes ago
A budget proposal would cut the Office of National Drug Control Policy’s budget by 95 percent, from $388 million in 2017 to $24 million in 2018, Politico, CBS and Mother Jones are reporting.

SCOOP: White House plans to effectively kill Office of National Drug Control Policy, currently the lead agency fighting the opioids crisis.

‘Narcan parties,’ ‘narc-me parties,’ ‘Lazarus parties

http://www.ksl.com/?sid=44109931&nid=148

SALT LAKE CITY — There is new concern that naloxone, the drug that counteracts an opiate overdose, could be used in what Utah’s Drug Enforcement Administration is calling “Narcan parties.”

“Anytime you have something good, a criminal will capitalize on that and use it to their own advantage,” said DEA special agent Brian Besser.

Besser said the demand for prescription pills in our state is unprecedented and because of that, when users can no longer get their prescriptions filled, they turn to drugs like heroin. He said 80 percent of Utah’s heroin users started out with prescription drugs.

Naloxone, also known by its brand name Narcan, is a fast-acting drug that reverses the effects of heroin and prescription painkiller overdoses and restores breathing. As a result, naloxone has become prevalent, but lately not for the reasons intended.

“We are hearing them called ‘Narcan parties,’ ‘narc-me parties,’ ‘Lazarus parties.’ You know, like raising someone from the dead,” he said.

Dr. Jennifer Plumb with Naloxone Utah said pairing things like heroin and naloxone is not as good as it sounds.

“When you receive naloxone as an opioid-dependent person, it feels awful,” she said. “It sends you immediately into withdrawal.”

Plumb said in some cases, it takes more than one dose to counteract the overdose, which is why she finds it hard to believe someone would voluntarily participate in a “Narcan party.”

“One, you feel terrible, and two, to lose their last resources or potentially their last fix, it just defies all common sense to me,” she said.

DEA officials said although there is no evidence of it happening in Utah, they are doing everything they can to stay informed.

“Just because it appears to be below the radar here, I don’t want to be naïve and think that it does not exist,” Besser said.

What is more important medication PRICE or QUALITY ? FDA – ASLEEP AT THE SWITCH

FDAFDA slams Indian API firm for faking certificates of analysis

http://www.fiercepharma.com/manufacturing/fda-slams-indian-api-firm-for-faking-certificates-analysis

The FDA put India’s Sal Pharma on its import alert list and then issued it a warning letter for putting fake COAs on products that were manufactured by companies that are not approved by the agency and selling them in the U.S.