Some people are apparently on some sort of “trip”

I went to Walgreens today to fill my prescription and they refused to fill even though said I could fill today. The lady Pharmacist told me she didnt care what the prescription said it was a couple days to soon. I told her I was a pain patient and am on full disability due to botched bone tumor surgery where both the main nerves in leg were severely damaged. I told her to give me my prescription back and I will go elsewhere and she went into this spill how she don’t understand pharmacy jumpers and that I shouldn’t do that. I explained to her tha I have used Walmart pharmacy for 20 plus years and the only reason I came to Walgreens is because my meds would be 20 dollars cheaper there. She continued to treat me like a criminal and she has know what I go through every day just to get by with my pain issue. I was wondering if you have any advice for me sir that could help me . Thanks in advance 

 

Desperately seeking SOLITUDE

Few seem to see the similarities between those in the chronic pain community and those in the mental health community dealing with addictive personality disorders. It really doesn’t matter if those with addictive disorders has a preference for Alcohol, Nicotine, Caffeine, Methamphetamine, Cocaine, Opiates, Gambling, Food, sex, etc..etc…

Those in the chronic pain community is “seeking” place of solitude from their unrelenting pain… just like those with addictions are “seeking” a solitude from the monkeys on their back and/or demons in their heads, what they personally consider more “normal” for them.

Addicts will generally state that they take/abuse the substance does so because they “like the way that it makes them feel”

Could it be said of chronic pain pts when they get adequate pain management that they “like the way that it makes them feel” – which they usually refer to as “normal”.

We have no idea how many of the deaths of addicts is actually a suicide.. they are “sick & tired” of trying to find their next “fix” they are sick and tired of dealing with “dope sick”.. which is what they call withdrawals.

There has been other countries that have decided that prohibition will not work and helping addicts to be mostly “functional” and reduce the number of OD’s because addicts get a “known strength” of their drug of choice. This could reduce several things… cartels would have fewer customers, we would have fewer OD’s, and fewer hostile family of those addicts who have OD’d because they got a opiate that was not what they were expecting.  Hopefully, a lot fewer families of the “former addict” who are hostile about chronic painers being  adequately treated for their chronic health issues.

Of course, to get to this point, Congress is going to have to force the DEA/judicial system into viewing addiction as the disease that it is and not the crime that they have been declaring for over 100 yrs. After all, the DEA/judicial system is the common denominator that is impacting untold number of pts and healthcare providers. Of course, with abt 40% of Congress  being attorneys… part of the judicial system … may make that a “mission impossible”. Being that the war on drugs employs some 500,000 to ONE MILLION people.

Mental health is a serious health issue, otherwise we would not have 50,000 suicides each year and ONE MILLION attempts.

Deadly fentanyl overdoses in Maryland were up more than 70 percent in 2017 when compared to 2016

Hogan: Greater federal support needed to fight opioids

http://www.wbaltv.com/article/hogan-greater-federal-support-needed-to-fight-opioids/19180214

Maryland Gov. Larry Hogan took the fight against opioids to Capitol Hill Thursday.

Hogan testified in front of the U.S. Senate Committee on Health, Education, Labor and Pensions to speak about what needs to be done on the federal level to fight the epidemic.

He cited the synthetic opioid fentanyl as the leading cause of deadly overdoses, and he called on lawmakers to address the problem. First, he wants more federal funding aimed at fighting addiction.

Hogan said he also wants increased availability to naloxone, education programs focused on the dangers of fentanyl and legislation to address the flow of drugs into the country.

“The majority of this fentanyl is being shipped in from China or it’s crossing the border and being smuggled in from Mexico, and we simply can’t stop it without the federal government stepping up,” Hogan said.

Deadly fentanyl overdoses in Maryland were up more than 70 percent in 2017 when compared to 2016.

The following is a transcript of the governor’s remarks as prepared for testimony, courtesy the governor’s office.

“During my campaign for governor in 2014, I traveled across Maryland with my running mate, Boyd Rutherford, asking voters one question: Which issue facing your community are you most concerned about? The answer we heard again and again, in every corner of our state, was heroin and opioid addiction.

“Immediately after taking office, we set up a Heroin and Opioid Emergency Task Force, chaired by Lt. Gov. Rutherford, which developed 33 specific recommendations focused on a four-pronged approach: education, prevention, enforcement and treatment. We have acted to address or move forward on nearly all of these recommendations.

“In March 2017, Maryland became the first state in the nation to declare a full-scale state of emergency in response to the heroin, opioid, and fentanyl crisis. In order to truly treat this crisis as we would a natural disaster or public safety emergency, we activated an Opioid Operational Command Center to more rapidly coordinate between state and local agencies, and dedicated an additional $50 million in funding over the next five years. In total, we have spent nearly half a billion in state and federal funding to combat opioid and substance use disorders.

“Through legislation we have taken positive strides, we’ve expanded our state’s Good Samaritan Law and Prescription Drug Monitoring Program, imposed strict penalties on individuals distributing fentanyl, and passed legislation limiting the amount of opioids a health care provider can prescribe. This past June, our Department of Health issued a standing order allowing all Marylanders to be able to receive the life-saving drug Naloxone from pharmacies, and in January, I authorized our attorney general to file suit against opioid manufacturers and distributors that have helped create the addiction crisis gripping our state and nation.

“Yet, in spite of all of our efforts, in spite of us fighting with every tool we have at our disposal, this crisis continues to evolve, particularly with the threat of fentanyl and other synthetic additives, which can be 50 times to 100 times stronger than heroin.

“Combatting a crisis of this scale requires all levels of government working together. No state or community can go it alone. The majority of the deadly fentanyl is being shipped in from China or smuggled in from Mexico and we need the federal government to step in and stop this poison from ravaging our state and our nation.

“Maryland is working tirelessly to fight this epidemic, alongside our counties and municipalities, in neighborhoods and schools, with public health, human services and public safety. We need greater federal support, especially more targeted and aggressive federal enforcement efforts for fentanyl and other synthetic opioids.

“Ultimately, this is about saving lives. It will take all of us to do that.”

Should Kratom Be Legal? New Research Provides Clearer Picture of the Plant’s Risks and Benefits

https://merryjane.com/health/kratom-controversy-new-research-on-plant-provides-clearer-picture-of-risks-benefits

The most comprehensive review on kratom to date challenges claims of the opioid-like substance being “deadly,” and provides a blueprint for future research into its clinical benefits and side effects.

by Laura Dorwart

While the U.S. is in the thick of an opioid epidemic, an increasing number of Americans have turned to kratom, which users say can provide much-needed relief of opioid withdrawal symptoms. The plant-based supplement, derived from leaves of the kratom tree (Mitragyna speciosa), is also commonly used to relieve chronic pain, depression, and anxiety. Used in Thailand and Malaysia for centuries, kratom has sparked significant controversy in the U.S. and was nearly classified by the DEA as a Schedule I drug in 2016 before those plans were scrapped due to major public outcry.

As public debates about the best ways to combat opioid addiction rates in the U.S. continue, many Americans have sought out alternative remedies for self-treatment of withdrawal and dependency. Kratom is a (currently) legal, widely-available substance with a lower risk of adverse side effects and acute dependency than other treatments, and many users claim it helps them manage their pain while simultaneously easing their reliance on opioids. Others have begun to use it as a milder alternative to prescription antidepressants and other psychiatric medications. As it’s grown in popularity, so have concerns about its potential risks.

Still, the FDA and DEA have persisted in painting kratom as potentially risky and even lethal, and media coverage has followed suit, calling the supplement potentially “deadly” and dangerous. A recent systematic review — the most comprehensive review to date on kratom’s potential risks — calls those claims into question, however, and provides a blueprint for future research into kratom’s clinical benefits and side effects.

Dr. Marc T. Swogger, a clinical psychologist and Associate Professor in the Department of Psychiatry at the University of Rochester Medical Center, and Dr. Zach Walsh, an Associate Professor at the University of British Columbia’s Department of Psychology, published their findings in Drug and Alcohol Dependence in February 2018. “We reviewed the literature to date on kratom and mental health, looking at all the studies that had reported on a variety of mental health outcomes,” Dr. Walsh told MERRY JANE by phone of his and Dr. Swogger’s work. “The main findings were that people are using kratom for a variety of purposes, mostly to help with opioid withdrawal. We also didn’t find evidence of kratom increasing negative mental health outcomes.”

More specifically, Dr. Walsh clarifies, “It doesn’t appear to cause depression, anxiety, or suicidal ideation” — despite some claims that it’s driven frequent users to suicide. In fact, their review of over 57 years of available research on kratom suggests that the plant can improve mood and relieve symptoms of mild to moderate anxiety. In other words, the review has profound implications for the future of kratom, which has risked veering quickly into a pattern of public stigmatization and a frenzy of media demonization, not unlike what we’ve seen with cannabis. Instead, Dr. Swogger told the University of Rochester Medical Center Newsroom, “The bulk of the available research supports kratom’s benefits as a milder, less addictive, and less-dangerous substance than opioids, and one that appears far less likely to cause fatal overdose.”

The review also indicated that, while kratom does carry some risk of dependence syndrome, its potential for dependency is mild — potentially resulting in symptoms like nausea, irritability, and headaches — compared to that of opioids. This makes sense, says Dr. Walsh, because kratom is from the coffee family, not the opioid family. The mild stimulating, mood-boosting effects many report with kratom may be akin to the kinds of effects we see with coffee. The problem, the study’s authors claim, is not kratom itself, but the fact that there’s not yet enough empirical work on kratom at all — so the public isn’t totally certain about its risks or benefits.

These findings contradict recent claims by the FDA that kratom carries an equal risk of addiction and overdose to opioids. In February 2018, the agency released a new report that left kratom users and experts alike scratching their heads. In it, FDA Commissioner Scott Gottlieb, M.D., emphasized kratom’s opioid-like properties, which were determined using predictions made by a computational model. Dr. Gottlieb claimed, “The data from the PHASE model shows us that kratom compounds are predicted to affect the body just like opioids,” and thus potentially carry a similar risk of dependence.

Along with the report, the FDA released information on the 36 deaths they’d referenced in a November 2017 press release, along with a public health advisory about the risks of kratom and its potential for addiction and overdose. But the accompanying death reports raised further suspicions about kratom’s real risks, rather than alleviating them. In all but one of the 36 deaths cited, Nick Wing writes in the Huffington Post, there are multiple substances listed in the toxicology reports — from Xanax and alcohol to high concentrations of prescription medications. There’s only one listed case where mitragynine — the main active ingredient in kratom — is the only substance involved, save for one death that’s since been redacted and is listed elsewhere as death by gunshot wound.

According to Dr. Walsh, some of the growing hysteria about kratom might be derived from cultural biases and prejudices. “It’s a plant medicine from Southeast Asia, from outside of the North American and Western European pharmaceutical families. So immediately, that arouses suspicion.”

Moreover, the treatment of kratom is in line with the historical pattern about how marijuana was painted in the media before being stigmatized and demonized by governmental agencies, politicians, and pharmaceutical companies. “It’s hard to speculate on why the War on Drugs would have a component that’s harmful to public health,” Dr. Walsh says, “but that’s been a main theme. It’s in keeping with the general dysfunctional madness of the last 75 years of drug policy.”

The dubiousness of recent claims by the FDA add to Dr. Walsh’s concerns that the risks of kratom are being preemptively overblown. And though the theoretical model described in the recent FDA press release has been one of the agency’s “guiding lights” in developing theories about the kratom, Dr. Walsh clarifies that “this model hasn’t been empirically validated” and is thus an unreliable source of hard data.

Still, he says, the study shouldn’t be taken as proof that kratom isn’t harmful. “Lack of evidence doesn’t mean an evidence of lack,” he warns. Before we can come to any final conclusions about kratom, we’ll need to study it further. And since all painkillers have their own negative side effects, it’s likely that kratom has some side effects for long-term users. “It’s not yet meeting a standard of evidence where it’s something that you’d recommend,” says Dr. Walsh.

A current salmonella outbreak across several states among kratom users underscores the need for regulation and scientific study of kratom rather than steps towards criminalization or FDA scheduling. Without clearly delineated consumer standards, it’s easy for kratom to go underground and risk contamination. But to get to that point, Dr. Walsh and Dr. Swogger argue, it will require large cohort studies that follow kratom users over a period of time, measuring both its harms and medicinal benefits, as well as clinical trials.

FDA commissioner to health insurers: You’re doing it wrong

https://www.cnbc.com/2018/03/07/fda-commissioner-to-health-insurers-youre-doing-it-wrong.html

  • “Sick people aren’t supposed to be subsidizing the healthy,” Scott Gottlieb said Wednesday.
  • The FDA commissioner was speaking at the National Health Policy Conference of AHIP, the health insurer industry group.
  • In his critique, Gottlieb homed in on an increasingly popular target in the drug pricing debate: rebates.

Insurance is designed, theoretically, to protect against the catastrophic: tornadoes, floods, hurricanes — or, where our health is concerned, cancer or another devastating disease.

To make that financial protection affordable, many pay into the system: the healthy are supposed to subsidize the sick.

But at a conference Wednesday organized by the health insurance industry, FDA Commissioner Scott Gottlieb delivered a startling message: You’re doing it wrong.

“Sick people aren’t supposed to be subsidizing the healthy,” Gottlieb told an audience at the National Health Policy Conference of AHIP, the health insurer industry group. “That’s exactly the opposite of what most people thought they were buying when they bought into the notion of having insurance.”

Gottlieb’s remarks were focused on the health of the market for biosimilars — copycats of complex, biologic medicines — and his concerns that industry consolidation and what he called rigged payment schemes may be stifling their development.

But they rang out as a critique of the U.S. system for pricing and paying for drugs more broadly, a system in which Gottlieb said each faction of the health-care industry is complicit in thrusting prices upward — at the expense of the sickest patients.

In his critique of health insurance constructs, he homed in on an increasingly popular target in the drug pricing debate: rebates. Those are discounts on medicines negotiated by pharmacy benefit managers on behalf of insurers.

But because the rebating system is opaque, and because of consolidation among PBMs and insurers, that system can result in ever-higher drug prices and everyone from drugmakers to the middlemen to insurers taking a slice of the pie, Gottlieb said.

Moreover, he posited, there’s a “perverse incentive” to spread the benefit of those rebates across plan members, rather than applying them directly to lower the costs of drugs for the sickest patients — thus, a system where the sick subsidize the healthy.

“Patients shouldn’t face exorbitant out-of-pocket costs, and pay money where the primary purpose is to help subsidize rebates paid to a long list of supply chain intermediaries, or is used to buy down the premium costs for everyone else,” Gottlieb said.

What reason is there, he asked, for a cancer patient to shoulder a large co-pay on their costly medicine?

“Is a patient really in a position to make an economically based decision?” he continued. “Is the co-pay going to discourage overutilization? Is someone in this situation voluntarily seeking chemo?”

The answer, of course, is no. “Yet the big co-pay or rebate on the costly drug can help offset insurers’ payments to the pharmacy, and reduce average insurance premiums,” Gottlieb said.

His comments were applauded by industry observers.

“Too many benefit plans operate like reverse insurance,” Adam Fein, CEO of Drug Channel Institute, wrote in an email to CNBC. “The sickest people taking medicines for chronic illnesses generate the majority of manufacturer rebate payments. These funds are then used to subsidize the premiums for healthier plan members.”

Others heralded Gottlieb’s citation of rebates as a key deterrent to uptake for biosimilars.

“This is impressive, from the head of the FDA,” tweeted Walid Gellad, director of the Center for Pharmaceutical Policy & Prescribing at the University of Pittsburgh.

Health insurers and pharmacy benefits managers, unsurprisingly, disagreed.

“It’s unfair to blame payers — who pay 2/3 the cost of drug benefits — for seeking the lowest costs in a marketplace where they have no control over the prices drugmakers set,” the Pharmaceutical Care Management Association, the PBM industry group, said in a statement. “Likewise payers — not the pharmacy benefit managers they hire to negotiate discounts — determine how rebates and other savings are allocated to reduce premiums, out-of-pocket costs and other expenses.”

AHIP took issue with the idea that insurers play a role in rising drug prices.

“Health plans welcome the introduction of generic biologics, or biosimilars, as a way to give patients quicker access to more affordable medicines,” the group said in a statement. And it pointed fingers back at drugmakers. “The trend among pharmaceutical companies to hike the prices of brand name biotech drugs before generic competition arrives is forcing makers of biosimilars to set their prices higher.”

Some pointed out Gottlieb’s position is an unusual one for an FDA commissioner to take; the agency officially doesn’t take a role in drug pricing.

Gottlieb told CNBC Wednesday afternoon that ensuring biosimilars have a pathway to market is a public health concern.

“Part of my job is to worry about the effectiveness and viability of the biosimilars pathway and achieving the access and competition it was intended to create,” Gottlieb said. “If ill-conceived payment arrangements serve to discourage investment in a way that forestalls that pathway from ever really taking root, that’s a public health concern. And when I look at the biosimilars pipeline, I’m worried that may be happening.”

The focus on rebates is spurring change: this week, UnitedHealth said it would apply drug rebates directly to lower costs for patients on their prescriptions starting next year. The company said it’s part of a move to “simplify pharmacy benefits, deliver savings directly to its customers and improve their healthcare experience.”

Alex Azar, newly minted secretary of the Department of Health and Human Services, praised the move, calling it a “prime example of the type of movement toward transparency and lower drug prices for millions of patients that the Trump Administration is championing.”

But, as many analysts pointed out, it may mean premiums across the board go up.

“Most plan sponsors use manufacturer rebates in aggregate to subsidize the cost of beneficiary premiums, keeping the premiums artificially low,” RBC Capital Markets’ George Hill wrote in a Tuesday research note. “This strategy has historically been effective, but has in recent years created a disconnect where the sickest and most expensive patients have been generating the rebates used to subsidize much healthier patients.”

So by reversing that trend, as Gottlieb and Azar encourage, the health insurance model may become less backwards. But it won’t necessarily result in lower costs, just a redistribution of them.

One pharmacy tried to charge me 10 TIMES the normal price!

Hello Steve, I am a 100% Disabled Vietnam Era Veteran. I am a retired USPS letter carrier. My wife passed away and I had lost our family plan health insurance. Though I am covered by the VA it is an hour drive from my home. Once  there I may wait for hours to see a different doctor every month. I am a chronic pain patient. I have been seeing the same doctor every month in Florida for the past 15 years. He is a Board Certified physician and the Chairman of the board of the largest hospital in my County. My question is: Is it legal for CVS to deny filling my prescription because I do not have private health insurance anymore? Driving several hours, and waiting around to get a 30 day supply of medication, at my age, is more than inconvenient. It is humiliating and very hurtful. I have an old minivan and I can wind up stranded somewhere. It costs $672 a month for private health insurance at my age! I can go into shock if I can not get my medication. What can I do? Furthermore, I wanted to add that I was denied medication because I didn’t have 6 or more medications . Uncontrolled medications can be mailed to me for free from the VA. One pharmacy tried to charge me 10 TIMES the normal price! Price gouging is definitely not ethical. Other excuses we’re we don’t have it because  ” We exceeded our quota” or we only get this for our “regular customers”. I am too sick to fight or go galavanting from pharmacy to pharmacy trying to get my medication. I won’t be able to care for myself or my two dogs anymore. I’ll lose my home, my independence, and wind up in a nursing home. What will it cost us taxpayers then?  Sorry for being too wordy, I am very scared now. Thanks for your concern and advocacy,

Pre-disease Conditions and their Symptoms

The our health care system.. when I first started as a pharmacist… it was pretty much you had a DISEASE or you DIDN’T..

Today we have all sorts of PRE-disease CONDITIONS…  think of pre-diabetes,  pre-hypertension… sometimes when I get frustrated with someone wanting to discuss all of these PRE-ISSUES on someone’s health… I try to bring things back to reality  EVERYTHING AFTER BIRTH IS PRE-DEATH !

I try to look at how the media, the various bureaucracies , and healthcare itself in a “big picture” context.  I try to to look at what is said, what is not said.. and how often the “truth” is twisted.

They routinely state that opiates are ADDICTIVE or HIGHLY ADDICTIVE

They routinely state that Fentanyl is involved with a OD… when it is one of many ILLEGAL FENTANYL ANALOGS

They tend to ignore the decrease in legal opiate prescription while OD are going dramatically in the opposite direction.

They have even changed the nomenclature:

No more accidental overdoses..  just anyone dying with a opiate in toxicology has their death certificate designate their cause of death to be “opiate related death”

No more addiction/dependence .. just anyone using opiates (legally/illegally) for >90 days… is suffering from a “opiate use disorder”

CDC published opiate dosing guidelines and the then head of the CDC made the statement that they DID NOT BEAR THE WEIGHT OF LAW. One has to ask why a Fed agency in charge of dealing with contagious disease,  elected to publish these opiate guidelines while at the same time ignore publishing any guidelines in treating addiction

Then we have various insurance companies, PBM’s and large healthcare corporation are now setting up some additional opiate guidelines. Daily MME limits, Prior Authorization, Quantity limits and the like.. while at the same time eliminating any limitations on the treatment of addiction.

Could it be that “the powers to be” have decided – for whatever reason – chronic pain is a pre-addiction symptom and thus those who are addicted are treated to change their behavior – which would suggest that they are treating addiction as the mental health issue that it really is… but treating chronic pain as symptom of an impending addition.

Anyone know a good pain doc in the Fort Worth Area

Comment
So glad I found you. I am a 62 year male who has been suffering from chronic back and neck pain for the last 15 years. I have been under the care of pain management specialist here in Fort Worth Texas for the last 13 years.
I was able to put a 10 hour day at work, fight the traffic and get home and have a couple of hours of “family life” before I had to get flat on my back because of the pain.
On weekends I could do an hour Walmart ritual, buy my groceries, come home and then cook for 2-3 hours.
Physically, that was all I was capable of doing, any more and the pain became so intense that nothing could break through.
My Doctor, per CDC guidelines has been reducing my pain meds. This means that I could no longer follow the same routine. I have to save my meds for what I think are priorities, and for me that is work.
I have been with the same company for 33 years. I am Senior Manager of Supply Chain at a multi billion dollar company.
In today’s business environment, one cannot hope to keep a job without producing and being better than average.
If I lose my job because I leave early too frequently due to pain, no one is going to touch me with a 10 foot pole once they realize that I am a cancer survivor (leukemia) who has gone through two chemo cycles, 5 years apart, each costing close to half a million dollars.
Job loss for me means a slow death sentence since I am not going to even attempt paying for the next chemo out of the retirement savings.
I am in poor health, COPD, Diabetes, high blood pressure and cholesterol and a few others. I doubt I live much longer and I am in peace with that.
My wife of 40 years has never worked a day in her life. I always thought that the life insurance from work and the 401 and social security will be enough to give her and the grand daughter we adopted a comfortable life after I am gone.
She will have to have all 3, two out of three is not sufficient.
Because of CDC Guidelines which has resulted in significant reduction in the my pain meds,I can no longer maintain a 10 hour day at work consistently. If I lose my job, I lose the insurance and her future becomes very questionable.
I have no idea what I am going to do, if I don’t die while still employed.
We all have our stories and this is mine. The stupid CDC guidelines is going to effect how my grand daughter is going to live and what her standard of living will be. Will my wife be forced to lower her standard of living in her 60’s?
Oh well, it is what it is. Best of luck.

I got this in the mail, I am not going to publish this person’s email.. but.. I have it…  if someone knows a good pain doc in Forth Worth Texas area… reach out to me and I will share this pt’s email

Opioid-related deaths in Ontario jump 52 per cent in 2017 compared to year before

Opioid-related deaths in Ontario jump 52 per cent in 2017 compared to year before

Opioid-related deaths in Ontario increased by 52 per cent from January to October 2017 compared to the same period the year before, according to newly released data from the provincial government.

The province said there were 1,053 opioid-related deaths during the 10-month period compared to 694 in 2016.

The government also said emergency department visits related to opioid overdoses jumped 72 per cent between January to December 2017 to 7,658 from 4,453 in 2016.

The province has been criticized for its lack of transparency and laggard data collection methods in response to the growing opioid crisis.

Despite changes enacted last May in the way the Ontario coroner’s office collects data on opioid-related deaths, critics say the province is still behind places like British Columbia which have month-to-month data sets readily available.

Ontario has promised to commit $280 million over three years to fight the opioid crisis, including distributing naloxone through emergency departments, pharmacies and correctional facilities, expanding access to addictions programs and improving data collection and monitoring.

The province announced it is making available “easy-to-use” nasal spray naloxone kits for free at pharmacies.

As part of the province’s strategy on opioid prevention and addiction, the Ontario government moved last year to offer naloxone kits to police and firefighters across the province.

Naloxone, the overdose-reversing medication, will be given to all 61 police services across the province and all 447 municipal fire departments.

The province said it is adding additional supports to health and addiction providers to enhance treatment services for clinics and youth groups, as well as hiring new front-line health and social service workers.

The government said it has also approved four new safe injection sites in the province, the latest being in London which opened last month. Sites are already open in Toronto and Ottawa.

 

Pharmacist: she doesn’t need to be on it, she’s the only one in town who takes it. She should just get off it.

 I read your article in Drug Topics titled ‘when valid prescriptions are refused’. I would like to explain a situation that happened today with a pharmacist and get your professional advice. The pharmacist called my mother this afternoon and said he refused to fill her prescription because he requires a code, which is for the reason she is taking the medication. He expressed that he believes she is misusing the medication. The medication he refused to fill is her pain medication. She has been on this medication for over 10 years and will have to be on this medication for the rest of her life. She suffers from chronic pain due to Reflex Sympathetic Dystrophy. She has had several surgeries in the last 20+ years, she has both hips replaced and a knee replacement that required several follow up surgeries due to complications from the RSD. She has been on a pain medication since this all began. She sees a pain management doctor once a month and has for 20+ years. That is the doctor that has prescribed the pain medication. She is also required by Comp to see a psychiatrist biweekly. Who is aware of the medication she takes. The pharmacy, that the said pharmacist is employed, has been my mother’s pharmacy since they opened their doors for business. The pharmacist has only been there since April of last year. He has prescribed this same prescription monthly without the said code he is now requiring. I believe this is his retaliation because my mother filed a complaint against him with the manager of the store in which the pharmacy is located. She made a legitimate complaint that the pharmacist has made several remarks about the medication she is on. He said she doesn’t need to be on it, she’s the only one in town who takes it. She should just get off it. Well then it progressed to him not having the prescription when it was to be filled. He would say he has to order it and she he to wait. It’s a controlled substance, she doesn’t have time to wait. She gets enough for a one month supply. Then she goes to her pain management doctor and he sends in a new prescription. It is usually within a few short days of when her previous months prescription is ending. He then said it was her responsibility to call the pharmacy ahead of time to ensure they have the medication on time. Which she did, even though I thought that was absurd. It took him shorting her pills one month before I finally pushed my mother to complain to someone. So now the bottom line is he will not fill her prescription and odds of another pharmacy carrying this particular medication is slim to none. Her prescription is to be filled in 5 days but we are in NY and if you’ve seen the weather we are in the middle of a blizzard. The pharmacist said he tried to call the doctors office and they said they don’t provide those “codes” anymore because that’s violating the patients privacy. It gets me that he specifically waited to today to call my mother and tell her this. Since I know he talked to the doctors office before toady. Since the doctors office is closed today because of the severe weather conditions. Is this right? After all these years he can just refuse? Or does he have a personal vendetta against my mother? Would should she do? Besides change pharmacies, as I’ve recommended several times. She is old school and prefers to stay where she knows. 

One of the big things that Pharmacists are suppose to do is to keep a doctor from prescribing for disease issues that are “outside of their scope of practice”.  Certain healthcare providers are suppose to limit the type of pts they treat and/or prescriptions they write for.  A pharmacist is not going to fill a prescription, written by a Dentist, for birth control pills.

But some pharmacists seem to have little/no concern about them staying within their scope of practice and/or they don’t understand what their scope of practice is.

One of the basics of the practice of medicine is the starting, changing, stopping a pt’s medication/therapy. So in this particular case with a Pharmacist telling pt that she DOESN’T NEED TO BE ON THE PARTICULAR MEDICATION AND SHOULD JUST GET OFF IT.

Since pharmacists don’t have prescriptive authority… is this pharmacist exceeding his scope of practice ?