MN: bureaucrats pass law that pharmas have to provide – FREE OF CHARGE – insulin or fined upto $600k/month

Why so many people at the Capitol are so pissed off about the drug industry’s lawsuit against Minnesota’s new emergency insulin program

https://www.newsbreak.com/news/0PV2NyWt/why-so-many-people-at-the-capitol-are-so-pissed-off-about-the-drug-industrys-lawsuit-against-minnesotas-new-emergency-insulin-program

From the day they introduced it to the day it passed the Minnesota Legislature, backers of a bill to provide insulin to diabetics who can’t afford the hormone said it wouldn’t draw a lawsuit from drug makers.

Citing assurances from unnamed industry executives, those proponents of the bill, which relies on the companies’ existing patient assistance program charities instead of substantial fees on drug companies, was less of a lawsuit magnet. In April, the DFL-controlled Minnesota House approved the bill by 111-22. The Senate responded with a vote of 67-0.

They were wrong.

On Tuesday night, just hours before the Alex Smith Insulin Affordability Act was to take effect, the Pharmaceutical Research and Manufacturers of America — the industry trade group better known as PhRMA — filed suit to get the new law declared unconstitutional.  “A state cannot simply commandeer private property to achieve its public policy goals,” states the suit, which names the Minnesota Board of Pharmacy and MNsure as defendants. “Because the Act takes private property for public use without paying just compensation, it is unconstitutional and should be enjoined.” 

Walz’s reaction: ‘What the hell?’

Minnesota’s plan, brokered by Republicans in the state Senate, relies on existing patient assistance programs run by pharmaceutical companies like Eli Lilly, Sanofi and Novo-Nordisk. Only if the companies refused to participate in the program do they face fees or fines: $200,000 per month for six months, and increasing to $400,000 per month for the next six. After a year of non-participation, fines go to $600,000 a month.

The suit does not ask for a temporary injunction against the act taking effect, and Gov. Tim Walz and Lt. Gov. Peggy Flanagan stressed at a press conference on Wednesday that the program was still available for those who need it.  A 90-day supply can be received either through a pharmacy or directly from the manufacturer’s patient assistance program. No more than a $50 copay can be charged for that three month supply. Those same diabetics can then apply for longer-term supplies by verifying income eligibility through MNsure.

Walz called Wednesday “one of the most enjoyable days” as governor because the new law resulted from the advocacy of diabetics and their families. The law is named for Alec Smith, who died three years ago after rationing his insulin after aging off his parent’s health insurance. Walz declared Wednesday “Alec Smith Day” in Minnesota. His parents, Nicole Smith-Holt and James Holt, Jr., accepted the proclamation from Walz.

But the lawsuit put something of a damper on the celebration. The plan had been sold as a compromise with the industry, and advocates had to swallow hard to accept it, making the news of the suit galling to some. Flanagan found out about the suit Tuesday night via social media and told Walz about it the same night. His reaction: “What the hell?”

On Wednesday, Flanagan said of the drug industry: “They may continue fighting, but so will we. And we have the advantage of being right.”

Gov. Tim Walz
MinnPost photo by Peter Callaghan
Gov. Tim Walz called Wednesday “one of the most enjoyable days” as governor because the new law resulted from the advocacy of diabetics and their families.

James Holt said his family is outraged by the lawsuit, but said he thinks it was filed because other states were looking at Minnesota as a potential model for similar programs. “They’re scared,” Holt said. 

State Sen. Matt Little
State Sen. Matt Little

Sen. Matt Little, DFL-Lakeville, said the industry has only itself to blame for the law since they are the ones who continued to impose large increases in the price of insulin, which created the unaffordability problem. He also had a message for the industry in their fight against advocates like Alec Smith’s parents and Concordia University student Alexis Stanley, all of whom were instrumental in getting the legislation passed. “I do not like your odds.”And Attorney General Keith Ellison said he will fight the lawsuit. “Today — the very day that our state finally put Minnesotans’ lives ahead of drug companies’ profits — Big Pharma is telling Minnesotans that their obscene profits come before your lives,” he said. “My office and I will defend it with every resource we have.”

Industry: insulin price increases aren’t our fault

The lawsuit challenges the law under both the takings clause and the commerce clauses of the U.S. Constitution. “If Minnesota believes that, despite the insulin manufacturers’ affordability programs, there is a need for further action to help some Minnesota residents obtain insulin, it could have created a state‐run program in which it purchases insulin from PhRMA’s members and distributes it to residents in need,” the suit states. “But instead of using public funds to address a matter of public concern, Minnesota chose to enact a law that effects per se takings of the manufacturers’ property without compensation, so that the state can achieve its policy objectives at no expense to its taxpayers.

“In addition to being forced to give away their insulin for free according to the state’s terms, manufacturers will also incur significant expenses in developing and administering the Continuing Safety Net Program and Urgent Need Program.”

The suit also blames health plans and pharmacy benefit managers for cost increases of insulin and other drugs and seeks to have the industry’s legal costs covered by the state.

Both Democrats and Republicans criticized the industry’s decision to file suit. “PhRMA is missing the mark by wasting time and money on this lawsuit. Minnesotans would be far better off if the pharmaceutical industry would focus on fairness in pricing,” said Sen. Michelle Benson, R-Ham Lake, the chair of the Senate’s Health and Human Services Finance and Policy Committee. “You shouldn’t have to be a powerful government or a special interest group to have access to fair prices. All Minnesotans want to be treated fairly.”

Senate Majority Leader Paul Gazelka also said he was disappointed with the suit. “Senate Republicans remain committed to providing emergency insulin for those in crisis no matter what happens with this poorly timed lawsuit,” the East Gull Lake Republican said.

And Little took issue with one of suit’s key arguments:  “The cost of producing insulin is so low that to say this is taking is gonna be really tough for them,” he said.

Did PhRMA mislead lawmakers?

DFL Rep. Mike Howard of Richfield dubbed the industry “soulless” for filing suit and said he thinks PhRMA misled the Senate GOP backers of the compromise that eventually became the law. “Everything about this process has shown that there is ill intent by the pharmaceutical industry,” he said. “They have not been honest; they have not been clear; they have not been straightforward; they have not been willing to come before a committee to show their face. The reason that things are confusing is by design.”

Yet the industry did raise constitutional issues with the program when it testified on the program in March. “The majority of our concerns would be around clarifying any constitutional issues we have,” Sharon Lamberton, deputy vice president for PhRMA, said at the time. “We are concerned with how manufacturers would be compensated for the insulin product, which would be a takings clause of the 5th amendment concern.”

Before that meeting, Sen. Scott Jensen, R-Chaska, said he was comfortable that the industry would let the proposal become law without challenge, largely because it didn’t impose huge licensing fees — around $38 million per year — to fund it, as the version of the program proposed by House DFLers did. “The pharmaceutical manufacturers don’t like the bill, they may even today be opposing the bill,” Jensen said before the first hearing on the compromise bill. “But they will come along and they are saying yes to this. This is not something where we’ll have to say, ‘Oh my stars it’ll end up in court.’”

State Sen. Scott Jensen
State Sen. Scott Jensen

On Wednesday, Jensen said: “I think we knew there was a risk. But we’d done so much stakeholder work that I thought everyone was comfortable. As they saw movement toward the Senate bill, they made it very clear this was their preference,” Jensen said. “The intensity of their concern was very mild and was popping up less and less often. I felt that at the table we’d reached a high comfort level.”Jensen now thinks the Legislature should look at changing the program to limit its takings clause implications. One idea would be to use other funds for the 30-day emergency program, which now requires the industry to compensate or provide insulin to pharmacies to replace what was distributed to diabetics. Jensen proposed using the health care access fund, which is paid for via a tax on health care providers.

But such a proposal is unlikely to win support in the DFL-controlled House and Walz, given their belief that any costs should be borne by the industry that made insulin unaffordable.

Lija Greenseid, an advocate who is the mother of a diabetic daughter, said she favors imposing a fee on the industry for that portion of the program.

Greenseid said she believed Jensen and Sen. Eric Pratt, R-Prior Lake, who first proposed using the patient assistance programs as the basis for the state’s plan, when they told her they were convinced the Senate’s version would not be challenged in court. “I think Sen. Jensen needs to be held accountable, either for some miscommunication from PhRMA or that it was all about politics; they needed to sweep this away in an election year,” she said. “If that was the plan, it backfired because this looks very bad.”

Little was even more critical of the Senate GOP’s management of the issue. “I believe there’s a possibility here that we have to face that (PhRMA) told GOP members they wouldn’t sue on this because their argument — that it was unconstitutional — was actually stronger against the Senate version” of the proposal. 

The license fee that House DFL members had proposed to fund the program is legal and constitutional, Little said. “They wanted to avoid a license fee because they knew they couldn’t beat that in court,” he said of insulin makers. “I think we have to face the reality that they did this on purpose.”

Coronavirus: Rand Paul, Dr. Fauci debate when to reopen schools amid COVID-19 pandemic

Sen. Rand Paul delivered an emotional statement during Tuesday’s Senate hearing on safely returning to work and school amid the COVID-19 pandemic, stating data has shown that “young children rarely spread the virus,” and that some countries who have reopened schools amid the pandemic have not had surges in virus cases. Dr. Anthony Fauci, the top infectious disease expert in the U.S. said that he “strongly” agrees with Paul that the country needs to “do whatever we can to get the children back to school.” For more info, please go to http://www.globalnews.ca Subscribe to Global News Channel HERE: http://bit.ly/20fcXDc Like Global News on Facebook HERE: http://bit.ly/255GMJQ Follow Global News on Twitter HERE: http://bit.ly/1Toz8mt Follow Global News on Instagram HERE: https://bit.ly/2QZaZIB #GlobalNews #coronavirus #COVID19

84 yo Native American Veteran cut off his pain pills. Tragic and disgusting

CVS: Anything for a buck ?

I just thought I’d share this info with you. You may post anonymously if appropriate.
My store is a covid testing store! Initially, there was a cap on # of tests we did per day. Things got somewhat difficult, since a tech spent 10 mins approximately to get test done. So 20 X10 = 200 tech minutes lost. We survived that, so CVS decided to lift the cap. We now have a tech administering tests all day, therefore we loose 9 tech hours ( testing occurs from 9am -6pm). No extra help provided! We are now behind in our daily script filling! Staff is stressed including pharmacist & techs! Front store is tired of ringing for us. Customers are calling from drive through yelling because it’s taking so long to pick up Rx.
This plan was supposed to help minute clinic testing volume. It’s a nightmare. Pharmacist must add ice packs to testing sample box to maintain temperature,this means leaving the building, walking in front of cars at DT to place ice in collection box!
Testing info is recorded on the Epic hospital system which was added to our already antiquated cvs system.
The final straw for me was yesterday. I heard a tech telling patient you must sign up on cvs.com & you must indicate you have at least one symptom. So I say they should not lie about symptoms. Her response DL told us to tell them that!!! One guy is getting tested weekly! WTH! Anything for a buck CVS!

celebrating 50 years as a Pharmacist

50 years ago this month, after 5 yrs and 168 academic hours and 2000 hrs of working in a pharmacy… I headed off to Frankfort Kentucky to take my first “boards”.  1970 was the first year of “national pharmacy boards”, before this year the Pharmacy boards in the various states designed their own tests that had to be passed in order to be licensed in the state.  Kentucky was one of the first… if not the first to use this national board testing.    I had graduated from Butler University Pharmacy school just abt 5 weeks earlier.

There was no tutorial books to prepare for this test, there was no one who had taken the board the year before to ask about what was on it..  I was one of the “guinea pig” recent pharmacy graduates that was the first to take this national test.  NO PRESSURE HERE !

The first day – a Monday – started very early and I remember having to compound some meds and the day ended late that night with the “orals” portion of the test… the pharmacy board members individually questioned us about our knowledge of pharmacy.  The next day started early and we were given either 4 different written tests or 6 different written tests… totally 6 hrs… no restroom break, no meal break… and you got done around 2 PM… and drove back to our home in Southern Indiana.

It did not take them long to grade the tests… by the end of the same week,  you were suppose to get a letter from the KY Board of Pharmacy…  One thing that everyone knew was that when you got that letter out of your mailbox.. and if your name on the envelope did not have R.Ph. (Registered Pharmacy) behind your name… you didn’t have to even have to open the envelope…. because you knew that you didn’t pass.  Luckily mine had those initials on the envelope and I had achieved a passing grade of 87 !!!  I could exhale !!

I had just went from $2.00/hr working as a pharmacy student to $235.00/wk…. working as a Pharmacist. My income had just about TRIPLED !!!  I had a job lined up at a small regional chain that I had been working summers since after my second year in pharmacy school.

Is Walgreens monetizing personal data from their pt$/cu$tomer$ ?

Walgreens steps up Microsoft partnership, adds Adobe deal to roll out new digital tools

https://www.fiercehealthcare.com/tech/walgreens-steps-up-microsoft-partnership-to-roll-out-new-digital-tools

Walgreens Boots Alliance is expanding its 18-month partnership with Microsoft to roll out new technology tools to personalize the healthcare and retail experiences for its 100 million customers.

Working with the tech giant and Adobe, the drugstore company plans to implement new customer analytics and outreach tools to help it better serve customers.

The digital experience and customer insights platform will advance Walgreens into the second phase of its digital transformation, the company said.

“At WBA, our mission is to deliver extraordinary experiences that enrich our customers’ lives. Capabilities to combine previously disparate customer data sets, including information from more than 100 million members of our loyalty programs, into a more singular, unified view of the customer—powered by these modern technology platforms—will enable us to truly personalize our omnichannel healthcare and retail offering,” said Vineet Mehra, global chief marketing officer at Walgreens Boots Alliance.

Walgreens announced its partnership with Microsoft last year to develop new healthcare delivery models, including technology and retail innovations to disrupt the healthcare delivery space.

The strategic partnership with Microsoft and the new deal with Adobe allows Walgreens to harness insights to deliver more engaging and personalized experiences while respecting and protecting the privacy choices of patients and customers, the company said.

Walgreens and other drugstore giants have been feeling the pressure from pharmacy competitors Walmart and Amazon, which bought PillPack in 2018.

Walgreens’ new digital capabilities also help give the company a leg up against emerging pharmacy startups such as Capsule.

“There’s no denying that the retail industry has been in a constant state of change over the past several years and consumers expect personalized interactions, connected online and in-store experiences, and high-quality customer service when they shop,” said Shelley Bransten, Microsoft’s corporate vice president for retail and consumer goods industries, in a statement.

In a recent interview, Rick Gates, Walgreens’ senior vice president of pharmacy and healthcare, said industry collaborations will be valuable as Walgreens continues to innovate during the COVID-19 health crisis and after the crisis subsidies. SEO personal injury can help law firms stand out in competitive search engine results.

“The need to accelerate the pace of innovation is going to be very important. There is going to be a lot more collaboration to solve things quickly and it’s going to be less about building things yourself,” Gates told Fierce Healthcare.

Walgreens plans to leverage Microsoft’s Dynamics 365 and Power Platform along with the Adobe Experience Cloud to collect data and develop customer profiles to engage customers and create personalized experiences.

Microsoft Dynamics 365 will serve as Walgreens’ customer data platform to provide a unified, 360-degree view of the customer while Adobe’s customer experience management solutions will enable the company to deliver those experiences through the industry’s only end-to-end solution for analytics, content management, personalization and campaign orchestration, Walgreens said.

The company plans to launch an individually tailored prescription experience for patients at Walgreens. It will also roll out a bespoke beauty experience for customers by enabling Boots Beauty Consultants to provide custom product recommendations.

The new platform also will power the company’s strategic initiative around mass personalization—delivering the right offers and content to the right customer whether they shop in the store, online or through the mobile app.

“COVID-19 has created a world that is more digital while redefining the value of physical stores,” said Anil Chakravarthy, Adobe’s executive vice president and general manager for its digital experience business, in a statement.

The deal with Adobe will help the retail and pharmacy giant better blend online and offline customer experiences, Chakravarthy said.

hydroxychloroquine and chloroquine can prevent COVID-19

https://www.medscape.com/viewarticle/933227

HCQ Trial to Resume

A global randomized controlled trial testing whether the antimalarial drugs hydroxychloroquine and chloroquine can prevent COVID-19 in healthcare workers or other high-risk workers will resume, Reuters reports. The UK Medicines and Healthcare Products Regulatory Agency had paused the COPCOV trial after another British trial found hydroxychloroquine to have no benefit for already-infected COVID-19 patients.

“Hydroxychloroquine could still prevent infections, and this needs to be determined in a randomized controlled trial,” said the trial’s co-leader. “The question whether (it) can prevent COVID-19 or not remains as pertinent as ever.”

NACDS urges mandatory electronic prescriptions for controlled substances

NACDS urges mandatory electronic prescriptions for controlled substances

https://drugstorenews.com/nacds-urges-mandatory-electronic-prescriptions-controlled-substances

The National Association of Chain Drug Stores is urging the Drug Enforcement Administration to make electronic prescriptions for controlled substances, or EPCS mandatory.

In comments on the reopening of the Interim Final Rule for EPCS, the organization described the significant benefits associated with EPCS and recommendations on how best to achieve them.

“For more than 20 years NACDS has collaborated with DEA on the development and implementation of policies and standards for EPCS. We remain committed to the use of electronic prescriptions for all medications, especially controlled substances,” NACDS wrote.

NACDS noted that further DEA action would build on an NACDS-backed federal law that requires electronic prescribing of controlled substances in Medicare Part D, beginning in 2021. It also would build on NACDS-backed action by more than half of the states to require electronic prescribing of opioids, all controlled substances, or all prescriptions.

In addition, the organization also strongly supports the use of electronic prescribing as an important tool to improve safety and security in the prescribing process and to combat the abuse, misuse and diversion of controlled substances.

Significant benefits of electronic prescribing include: safeguards against unauthorized changes, reproduction and diversion of controlled substance prescriptions; further reductions in medication errors; improved patient care and outcomes — including clinical decision-making at the point of care; enhanced workflow in healthcare settings; and cost savings due to improved patient outcomes.

NACDS’ recommendations for enhancing the rule flow from the fact that pharmacies have been engaged in the effective use of electronic prescribing for quite some time and modifications in the rule are necessary to reflect the advancements that pharmacies have made. NACDS recommends changes to the audit requirements for software applications to make them consistent with pharmacies’ current practices in ensuring the use of the latest technologies, and to prevent duplicative and unproductive audits.

“Pharmacies remain absolutely committed to serving as a part of the solution to opioid abuse and addiction,” NACDS president and CEO, Steve Anderson said. “Considering the significant and substantial benefits of EPCS, further action by the DEA to make electronic prescriptions mandatory is the logical next step in helping to address this ongoing issue, and in improving patient health outcomes in every community.”

While the DEA allows a pharmacy to legally do a electronical transfer a C-II prescription to another pharmacy, if the first pharmacy receiving the electronic Rx from the prescriber doesn’t have stock or the Pharmacist is “not comfortable” filling the Rx.  They cannot print out a valid C-II Rx because to be legal it has to have a signature from the prescriber.   The potential catch here  if the pharmacy can’t/won’t fill the C-II, is that their computer software has not been updated to allow the electronic transfer to another pharmacy and/or a particular state has laws that prohibit such transfers and/or not updated their state laws to conform with national DEA laws.

There is also the possibility that some pharmacists that don’t like to fill controlled meds could tell the pt that there is no way that they can transfer the Rx or give the pt a copy and they are out of stock.

Other electronically sent controlled substance Rxs (C-III thru C-V) and other Rxs for all other Rx only meds can be verbally transferred to another pharmacy, if the first pharmacy can’t/won’t fill the Rx.

COVID-19 drug remdesivir to cost $3,120 for typical patient on private insurance

COVID-19 drug remdesivir to cost $3,120 for typical patient on private insurance

https://www.foxbusiness.com/healthcare/covid-drug-remdesivir-private-insurance

Gilead Sciences Inc. detailed its pricing plans for Covid-19 drug remdesivir, saying it will charge U.S. hospitals $3,120 for a typical patient with commercial insurance.

The drugmaker on Monday disclosed its pricing plans as it prepares to begin charging for the drug in July. The U.S. has been distributing remdesivir donated by Gilead since the drug was authorized for emergency use in May.

Ticker Security Last Change Change %
GILD GILEAD SCIENCES INC. 74.56 -0.01 -0.01%

Under the company’s plans, Gilead will charge a higher price for patients with private insurance in the U.S., and a lower price for U.S. government health programs like Medicare and all other developed countries that insure their patients directly.

The government price will be $390 per dose or $2,340 per patient for the shortest treatment course and $4,290 for a longer treatment course.

Gilead said in the U.S. it will charge nongovernment buyers such as hospitals about $520 per dose, or a third more than the government price, for patients who are commercially insured. That works out to $3,120 for a patient getting the shorter, more common course of treatment, and $5,720 for the longer treatment duration.

The U.S. is the only developed country where Gilead will charge two prices, Gilead Chief Executive Daniel O’Day said in an interview. In other nations, governments negotiate drug prices directly with drugmakers. “The logic is that we wanted a single government price around the developed world,” Mr. O’Day said.

In this March 2020 photo provided by Gilead Sciences, a vial of the investigational drug remdesivir is visually inspected at a Gilead manufacturing site in the U.S. (Gilead Sciences via AP)

The higher price for U.S. commercially insured patients is because government health programs such as Medicaid typically receive statutorily-defined discounts off the prices companies receive in the private market.

“This medicine is priced far below the value it brings to health-care systems and that’s true for private payers and government payers,” Mr. O’Day said.

On average, the drug should help reduce hospital costs by $12,000 per patient, he said. Gilead estimated the savings based on data showing that each day of hospitalization costs $3,000 and that patients taking remdesivir are discharged four days sooner than those receiving standard treatment, Mr. O’Day said.

Covid-19 patients get two doses of remdesivir by infusion on the first day, and one dose daily afterward. The shortest treatment course is five days, while a longer treatment course takes 10 days.

Currently, 90% to 95% of patients receive five-day treatment courses, Mr. O’Day said.

Remdesivir is the first antiviral drug shown to be effective at treating Covid-19 in a major clinical trial, reducing patients’ recovery times by four days compared with the placebo group in a large study funded by the National Institute of Allergy and Infectious Diseases.

So far, few other drugs have proven in human testing to help coronavirus patients. One drug that recently produced positive results in a clinical trial was the steroid dexamethasone.

The drug, which treats Covid-19 by a different mechanism than remdesivir, has been on the U.S. market for decades to treat other diseases. It hasn’t been authorized in the U.S. to treat Covid-19, but doctors are allowed to prescribe it “off-label” under U.S. regulations.

Given its unique status, remdesivir’s pricing has been widely anticipated–and hotly debated–among doctors, health insurers and investors. It could serve as the starting point for other drugs that eventually prove to safely treat coronavirus patients.

The Institute for Clinical and Economic Review, a nonprofit group that analyzes pharmaceutical prices, said last week that a cost-effective price for remdesivir would be $2,520 to $2,800 per patient if dexamethasone becomes a standard medication for Covid-19.

Without dexamethasone, a cheap generic medication, remdesivir would be cost-effective at a range of $4,580 to $5,080 a patient, ICER said.

The U.S. Food and Drug Administration on May 1 authorized emergency use of remdesivir through the course of the pandemic. Gilead plans to seek a full, permanent approval.

In July, Gilead will start charging for the drug, but federal and state officials will continue deciding which hospitals receive it. In September, Gilead expects to have enough supply to meet demand and will distribute the drug in the same way it distributes other medicines.

One issue that has already factored into debate over what remdesivir should cost is the U.S. government’s role in funding its development.

The NIAID funded the study that showed it sped the recovery of hospitalized Covid-19 patients, and expects to spend at least $30 million on the study through the end of the fiscal year, an NIAID spokesman said in February.

Gilead has also invested in researching remdesivir. The company previously developed the drug to treat Ebola patients, but it didn’t work as well as other drugs. Gilead and other researchers explored remdesivir’s Covid-19 use after the virus emerged.

Gilead has said it spent about $50 million on research and development related to the drug in the first quarter, or about 4.5% of its total R&D spend. Through the end of 2020, Gilead expects to spend more than $1 billion on developing and manufacturing remdesivir, Mr. O’Day said.

Some generic drugmakers have said they plan to charge less than $1,000 per treatment course in India and Bangladesh, where Gilead has licensed rights to sell the drug. ICER estimates that the raw materials needed to make remdesivir cost about $10 per patient for a 10-day treatment course, citing a recent academic paper

Write to Joseph Walker at joseph.walker@wsj.com

Here is another EPIDEMIC… chain pharmacists… JUST SAYING NO to filling controlled Rxs

Sir I’ve been trying To get my prescription  filled,, but the pharmacy keeps turning it down  C V S, Walgreens,  and Walmart.. I’m a amputee with Fandom  pain and constant burning, plus on  Dialysis 3 times a week.. I’ve been on my pain killers for over 5 years and now they don’t want to give them to me. What options do I have.  please  Help me

Are we drifting back to the “Reagan years” ? Maybe the spirit of Nancy Reagan is haunting many that have a pharmacy/pharmacist license.  This woman is from Texas and I wonder why people keep going back to chain stores ? Do they like to be abused and intimidated ?

Once again here is website that will help “abused chain pts” to find a independent pharmacy  https://ncpa.org/pharmacy-locator