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PAIN PATIENTS Washington State!
Is this what the chronic pain community needs?
Presidential candidate VP Kamala Harris brings to DC the experience of a PROSECUTOR for THREE DECADES. The above video is her first campaign stop where she states that she is going to get women to be allowed to make their own decisions about their bodies and medical decisions and keep the government out of medical decisions- but apparently when it only involves abortion!
Does this mean that no pts- especially those who are dealing with medical disabilities – do not have the right to be involved in their medical care – especially subjective diseases – like pain, depression, and anxiety?
Just ask chronic pain pts in Florida, where they elected a state Attorney General who is married to a DEA AGENT!
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CVS LIES UNDER OATH over their PBM’ jacking up Rx prices
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House criticizes PBMs for pushing patients to higher-priced drugs
House criticizes PBMs for pushing patients to higher-priced drugs
An investigation by federal lawmakers found that pharmacy-benefit managers promised to control costs but have instead steered patients toward higher-priced medicines and affiliated pharmacies that reduce patient choice, The Wall Street Journal reported July 23.
A House Committee on Oversight and Accountability investigation found PBMs devised formulas for preferred medications that encouraged use of higher-priced drugs. It also found that Express Scripts sent messages to patients saying they would pay more to fill at their local pharmacy, but less for a three-month supply by using the affiliated mail-order pharmacy.
“While this is made to appear to benefit the patient, what it is instead doing in practice is limiting a patient’s ability to choose their own pharmacy,” the committee wrote.
The report followed a 32-month investigation. Leaders from three large PBMs are set to testify before the House committee this week.
A Pharmaceutical Care Management Association spokesperson told the Journal the firms help reduce costs to patients and health plans. He declined to comment on the report because the organization had not seen it.
“The critically important role of PBMs in our healthcare system in driving affordable access to prescription drugs is undeniable, saving patients and health plans $1,040 per person per year on drug costs,” the spokesperson said.
The three largest PBMs — CVS Caremark, Cigna’s Express Scripts and UnitedHealth’s OptumRx — handle 79% of U.S. medical prescriptions for approximately 270 million people. Integrating further with health insurers allows even more control over medication prices and access, according to a Federal Trade Commission report issued in July. On top of that, PBMs contributed to a 10% closure rate of independent pharmacies in rural locations between 2013 and 2022.
An investigation by the FTC into pharmacy benefit managers revealed PBM favoritism toward their own pharmacies and vast market control, which affects both medication access and affordability, according to the agency’s report.
The House committee also criticized the largest PBMs for lack of transparency and said they sent House investigators only a handful of pages about the groups they established to buy drugs, the Journal reported.
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15 health systems dropping Medicare Advantage plans | 2024
15 health systems dropping Medicare Advantage plans | 2024
Medicare Advantage provides health coverage to more than half of the nation’s seniors, but some hospitals and health systems are opting to end their contracts with MA plans over administrative challenges.
Among the most commonly cited reasons are excessive prior authorization denial rates and slow payments from insurers.
In 2023, Becker’s began reporting on hospitals and health systems nationwide that dropped some or all of their Medicare Advantage contracts.
In January, the Healthcare Financial Management Association released a survey of 135 health system CFOs, which found that 16% of systems are planning to stop accepting one or more MA plans in the next two years. Another 45% said they are considering the same but have not made a final decision. The report also found that 62% of CFOs believe collecting from MA is “significantly more difficult” than it was two years ago.
Fifteen health systems dropping Medicare Advantage plans in 2024:
Editor’s note: This is not an exhaustive list. It will continue to be updated this year
1. Canton, Ohio-based Aultman Health System‘s hospitals will no longer be in network with Humana Medicare Advantage after July 1, and its physicians will no longer be in network after Aug. 1.
2. Albany (N.Y.) Med Health System stopped accepting Humana Medicare Advantage on July 1.
3. Munster, Ind.-based Powers Health (formerly Community Healthcare System) went out of network with Humana and Aetna’s Medicare Advantage plans on June 1.
4. Lawton, Okla.-based Comanche County Memorial Hospital stopped accepting UnitedHealthcare Medicare Advantage plans on May 1.
5. Houston-based Memorial Hermann Health System stopped contracting with Humana Medicare Advantage on Jan. 1.
6. York, Pa.-based WellSpan Health stopped accepting Humana Medicare Advantage and UnitedHealthcare Medicare Advantage plans on Jan. 1. UnitedHealthcare D-SNP plans in some locations are still accepted.
7. Newark, Del.-based ChristianaCare is out of network with Humana’s Medicare Advantage plans as of Jan. 1, with the exception of home health services.
8. Greenville, N.C.-based ECU Health stopped accepting Humana’s Medicare Advantage plans in January.
9. Zanesville, Ohio-based Genesis Healthcare System dropped Anthem BCBS and Humana Medicare Advantage plans in January.
10. Corvallis, Ore.-based Samaritan Health Services’ hospitals went out of network with UnitedHealthcare’s Medicare Advantage plans on Jan. 9. Samaritan’s physicians and provider services will be out of network on Nov. 1.
11. Cameron (Mo.) Regional Medical Center stopped accepting Aetna and Humana Medicare Advantage in 2024.
12. Bend, Ore.-based St. Charles Health System stopped accepting Humana Medicare Advantage on Jan. 1 and Centene MA on Feb. 1.
13. Brookings (S.D.) Health System stopped accepting all Medicare Advantage plans in 2024.
14. Louisville, Ky.-based Baptist Health went out of network with UnitedHealthcare Medicare Advantage and Centene’s WellCare on Jan. 1.
15. San Diego-based Scripps Health ended all Medicare Advantage contracts for its integrated medical groups, effective Jan. 1.
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Healthcare: nothing more.. nothing less than a FOR PROFIT BUSINESS
WHO Warns of Counterfeit Ozempic in the Global Supply Chain—Here’s What to Know
WHO Warns of Counterfeit Ozempic in the Global Supply Chain—Here’s What to Know
https://jamanetwork.com/journals/jama/fullarticle/2821502
The World Health Organization (WHO) is warning of counterfeit Ozempic discovered in 2023 in regulated supply chains in Brazil, the UK, and the US, amid an uptick in similar reports worldwide. Besides potentially being ineffective, fake versions of the drug pose a serious, perhaps life-threatening risk because they are injected under the skin, according to the alert.
Ozempic, a branded version of the drug semaglutide, is a once-weekly injection to treat type 2 diabetes and cardiovascular disease; it’s also prescribed for weight management off-label or at a different dose under the brand name Wegovy. Demand for these hugely popular glucagon-like peptide 1 (GLP-1) receptor agonists has often exceeded supply—at least 25 000 patients are starting Wegovy every week in the US, according to drug maker Novo Nordisk—and earlier this year, the WHO linked shortages of drugs like Ozempic to a rise in counterfeit versions sold though unregulated outlets including social media platforms.
The recent WHO warning is the first public alert to verify falsified Ozempic’s infiltration into legitimate drug supply chains in 3 different countries. It asks health care professionals, regulatory authorities, and the public worldwide to be on the lookout for suspicious medicines and to report any irregularities.
“WHO has received reports of falsified Ozempic detected in at least 14 countries across 4 different WHO regions,” Rutendo Kuwana wrote in an email to JAMA Medical News. Kuwana is the team lead for substandard and falsified medical products at WHO, which has been actively monitoring and responding to reports of counterfeit Ozempic since September 2022. WHO does not know how many people were affected or how many units were counterfeit in Brazil, the UK, or the US, he said.
According to Kuwana, no serious or uncommon adverse reactions were noted in the incidents reported to WHO. “WHO is however aware of media reports of adverse effects, especially when the incorrect active substance is used,” he added.
“Counterfeit drugs are illegal, and they could contain the wrong ingredients, other harmful ingredients, or contain too little, too much or no active ingredient at all,” Sangeeta Chatterjee, PharmD, deputy director of the US Food and Drug Administration (FDA) Office of Drug Security, Integrity, and Response, wrote in an email.
What Are Signs of Fake Ozempic?
The WHO’s medical alert is a roundup and verification of previously reported fakes, which Ozempic manufacturer Novo Nordisk confirmed were falsified.
In December, the FDA reported:
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Thousands of units of counterfeit Ozempic (1 mg) with serial number 430834149057, lot NAR0074—a combination that does not correspond to genuine manufacturing records
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Needles from the lot were also counterfeit and of unknown sterility and read “NovoFine” rather than the authentic “NovoFine Plus.”
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Packaging and prescribing information were also falsified.
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Some of these counterfeit products may still have been available for purchase in December 2023.
In October, the UK Medicines and Healthcare products Regulatory Agency (MHRA) reported:
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Counterfeit prefilled Ozempic pens (1 mg) identified at 2 UK wholesalers that were bought from legitimate suppliers in Austria and Germany.
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Batch number MP5E511 of the pens is genuine but the product is counterfeit.
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Dose selectors protrude beyond the counterfeit pens when setting doses, unlike authentic Ozempic pens.
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None of the falsified pens were dispensed to patients, and there were no reports of harm.
Also, in October, Novo Nordisk informed Brazil’s national health surveillance agency about counterfeit Ozempic batch number LP6F832.
How Did Fake Ozempic Get Into Regulated Drug Supply Chains?
In the US, the regulated supply chain for drugs starts with a manufacturer like Novo Nordisk, and includes repackagers, wholesale distributors, third-party logistic providers, and pharmacies.
“The US has a very safe drug market, but it’s not unheard of that [counterfeits] happen,” said Kristina Acri, PhD, an economist at Colorado College who studies counterfeit medications.
A buyer at a midsize pharmaceutical distributor warehouse in New York purportedly found the fake batch, according to a Vanity Fair article, and the New York Times quoted a Novo Nordisk representative who said the falsified products were found in warehouses outside the company’s authorized supply chain. The FDA recommends that pharmacies only buy Ozempic through distributors authorized by Novo Nordisk.
As of March 2024, the FDA is aware of 9 adverse event reports for products with the lot number of the counterfeit Ozempic, Chatterjee wrote.
“The agency continues to monitor adverse event reports through MedWatch. However, we are not able to provide additional details about an ongoing investigation,” Chatterjee wrote in response to a request for information about the counterfeit products’ quality and safety and how they came into the legitimate supply chain.
The UK has a similarly regulated drug market to the US, Acri said, adding that some developing countries with less sophisticated markets can present more opportunities for counterfeit drugs to slip in.
“Producing counterfeit drugs and inserting them into the legitimate supply chain is an illegal activity and puts patients at considerable risk,” a spokesperson for Novo Nordisk said in an email.
What Other Counterfeits Are Out There?
In June 2023, Novo Nordisk reported that a counterfeit Ozempic pen, reportedly bought at a retail pharmacy in the US, actually contained insulin and led to an adverse reaction.
Novo Nordisk has filed 21 lawsuits as of May 2024 against businesses such as medical spas, weight loss clinics, and pharmacies selling compounded versions of semaglutide that could be harmful and deceptively marketed. A compounded version of a drug may be allowed when a commercially available drug appears on the FDA’s drug shortage list. Compounded drugs are not approved by the FDA, and the agency cannot verify their safety or effectiveness. Novo Nordisk said it does not directly or indirectly sell bulk semaglutide to compounding pharmacies.
A search of the FDA’s site showed that between last October and early July of this year, the agency sent warning letters to 6 online retailers selling unapproved or misbranded semaglutide or tirzepatide. The latter is a GLP-1 and glucose-dependent insulinotropic polypeptide agonist drug that works similarly to semaglutide to suppress appetite and delay gastric emptying. It’s sold by Lilly under the name Mounjaro for diabetes and as Zepbound for weight management.
Lilly has filed lawsuits against business purporting to sell products containing tirzepatide and in an open letter said it “is deeply concerned about the proliferation of online sales and posts on social media involving counterfeit, fake, compounded, and any other unsafe or untested versions of what they say is tirzepatide.”
Why Are Counterfeits Happening?
John Buse, MD, PhD, a professor of medicine at University of North Carolina School of Medicine, said his patients with diabetes and obesity continue to intermittently struggle to fill prescriptions for semaglutide and tirzaptide, often calling dozens of pharmacies to find inventory. “It is driving doctors and patients crazy.”
Wegovy, Mounjaro, and Zepbound continue to be in short supply, according to the FDA. These shortages coupled with increasing demand has fueled the market for counterfeit Ozempic, Acri noted.
“It comes down to economics,” she said. “There is a tremendous amount of money that can be made in making and passing along counterfeit drugs, and that’s a great incentive for some really evil people.”
In addition to fighting counterfeits, drug manufacturers are trying to relieve shortages fueling the market for fakes. In late June, Novo Nordisk announced it plans to invest $4.1 billion in a North Carolina manufacturing facility to expand production of its obesity drugs and other medications, but the construction is not expected to be complete until between 2027 and 2029.
To avoid purchasing falsified medications, the FDA recommends that consumers only buy Ozempic from state-licensed pharmacies that require a valid prescription and that they check the packaging for signs of counterfeiting. Clinicians and consumers should report adverse effects to FDA’s MedWatch program by submitting an online report or downloading a report that they can fax to 1-800-FDA-0178.
Acri and Buse said consumers may never know if they used a counterfeit version of a drug unless they have an adverse reaction.
Buse said, “If someone is good at creating counterfeit material, unfortunately, I think it’s going to be very difficult for patients and pharmacists to know when they might have these bootleg products.”
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Could the Chevron Doctrine overturning muzzle the DEA?
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United Health: apparently does not like protesters outside of HQ
Protesters say 11 arrested outside UnitedHealthcare HQ in Minnetonka
https://www.startribune.com/unitedhealth-protest-minnetonka-arrests/600380907/
Warren Blasts United Health CEO for Monopolistic Practices that Harm Patients
Critics have held a series of events highlighting what they describe as a pattern of improper coverage denials by the nation’s largest health insurer.
Protest organizers say 11 people were arrested Monday outside UnitedHealthcare’s headquarters in Minnetonka during an event spotlighting what critics say is a pattern of improper coverage denials by the nation’s largest health insurer.
Protestors blocking a road were arrested by the Minnetonka Police Department, according to a news release from People’s Action Institute, a consumer group that protested at UnitedHealth Group’s Optum headquarters in Eden Prairie in April.
Minnetonka police said the protestors were cited with misdemeanors and released from the scene. Three of those arrested were from Minnesota, according to police, while others came from Illinois, Maine, New York, Texas and West Virginia.
“UnitedHealthcare policyholders and medical professionals have petitioned, protested and spoken directly to the chief medical officer of UnitedHealth Group about our concerns, but their leadership has refused to acknowledge that prior authorizations and claim denials are a widespread problem,” Aija Nemer-Aanerud, a director with Chicago-based People’s Action Institute, said in a news release Monday.
In a statement, UnitedHealthcare said: “The safety and security of our employees is a top priority. We have resolved the member-specific concerns raised by this group and remain open to a constructive dialogue about ensuring access to high-quality, affordable care.”
UnitedHealthcare is the health insurance business at Minnetonka-based UnitedHealth Group, the largest company in Minnesota by revenue. Its Optum division runs clinics, manages pharmacy benefits and consults with health care providers on data and information technology needs.
Health policy experts say there’s been a lack of comprehensive data on the frequency of and causes for insurance coverage denials.
Critics in recent years have focused on prior authorization rules that patients and health care providers say have wrongly led to coverage denials, blocking needed care in the process. Insurers contend the rules help control costs and can improve quality.
UnitedHealthcare announced in March 2023 that it was dialing back some requirements for prior authorizations. The subject, however, has been a source of controversy for decades, including a pledge by UnitedHealthcare in 1999 to move away from “restrictive ‘mother-may-I-medicine,'” the Wall Street Journal reported at the time.
People’s Action Institute says it launched a campaign in 2022 to fight back against coverage denials by health insurers. After the protest at Optum headquarters in April, critics met with UnitedHealthcare executives, pushing to help individual patients and for broader reforms at the company.
“Health insurance coverage has expanded in America,” Nemer-Aanerud said, “but we are finding it is private health insurance corporations themselves that are often the largest barrier for people to receive the care they and their doctor agree they need.”
In Monday’s incident, Minnetonka police said, public nuisance citations were issued for interfering/obstructing/rendering dangerous for passage any public highway or right-of-way.
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Today: Make America SAFE ONCE AGAIN
In this interview on Fox Cable Fox & Friends today, they were actually talking about illicit street fentanyl analog that is killing our citizens. Not just stating that the person OD’d from Fentanyl.
There are some 100-200 known different Fentanyl analogs and only two are approved by the FDA to be used in humans. Fentanyl citrate is the one most – and longest being used in humans.
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