logo
These discounted versions of popular weight-loss drugs are going away: What to know

These discounted versions of popular weight-loss drugs are going away: What to know

USA Today02-03-2025

These discounted versions of popular weight-loss drugs are going away: What to know
Show Caption
Hide Caption
Will Ozempic, Wegovy be affordable in the near future?
Could the high cost of hugely popular weight loss drugs Ozempic and Wegovy be coming down in the near future?
Cheddar
Many Americans have turned to compounding pharmacies to get popular weight-loss drugs due to lack of availability or expensive retail price tags. But this option will soon close for consumers.
The federal government allows compounding pharmacies to sell copies of drugs when the medications are in short supply. Yet federal regulators recently declared the blockbuster weight-loss drugs Wegovy and Zepbound are no longer in shortage. That means consumers who use telehealth companies or medical spas to get less expensive, compounded versions will need to get their medications elsewhere.
That has panicked consumers such as Amanda Bonello, a Marion, Iowa, mother of three, who worries the supply cutoff will force her to buy the brand-name version of a drug she can't afford. She takes a compounded version of tirzepatide, Eli Lilly's drug sold under the name Mounjaro to treat diabetes and Zepbound for weight loss. The average retail price for Zepbound is nearly $1,300, according to GoodRx, a prescription drug discount provider.
"It leaves me up a creek without a paddle," Bonello said. "It feels like we're all on an island and Big Pharma has the only food source, and they're letting everyone who can't afford it starve."
Industry groups that represent compounding pharmacies and suppliers have sued to continue selling these drugs. And patients have started an online petition to extend the time in which they can use compounded GLP-1, or glucagon-like peptide-1, medications. Alternatively, the petition requests the Food and Drug Administration authorize generic versions or encourage drugmakers to lower retail prices. The petition also seeks to compel health insurers to cover these drugs.
What's status of compounded Wegovy and Zepbound?
Compounding suppliers and pharmacies will soon no longer be allowed to make and sell weight-loss drugs for the mass market. The federal government has authorized a transition period that's already partly closed for compounded versions of Zepbound and Mounjaro. Consumers will have a bit longer to get compounded semaglutide, which is sold under the brands Wegovy for weight loss and Ozempic for diabetes.
In December, the FDA declared Eli Lilly's tirzepatide was no longer in short supply. The FDA said pharmacies had until Feb. 18 to discontinue compounding, distributing or dispensing tirzepatide. Suppliers that produce batches of the drug and sell to others have until March 19 to cease distribution. The industry trade group Outsourcing Facilities Association sued the FDA in U.S. District Court in Texas and filed a motion seeking to delay such enforcement.
In a legal response to the industry trade group's motion, the FDA urged the court to reject the group's request. The agency argues rejecting the request would "maximize patient safety" and adhere to Congress' intent to incentivize drug development while allowing compounding during temporary drug shortages.
Last month, the FDA said the shortage of shortage of Novo Nordisk's semaglutide is over. Pharmacies must cease selling compounded semaglutide by April 22. Facilities that supply compounded semaglutide injections must cease distributing the drug by May 22.
I take compounded weight-loss drugs. What will my doctor or pharmacist tell me?
Pharmacists who supply compounded weight-loss and diabetes drugs already are discussing the situation with customers. Some aren't refilling prescriptions. Others don't want to start new customers on the compounded medications because they'll soon need to switch to brand-name medications.
Within a year of discontinuing semaglutide, a group of 327 patients in the U.S., Europe and Japan regained two-thirds of weight lost while on the medication, one study found. The study said also said the patients were less healthy than they were while on the medication.
Jennifer Burch, who runs an independent compounding pharmacy in North Carolina, said she informs all her patients about how compounded drugs are available only when a brand name is on the FDA's shortage list.
She fields questions from people who are interested in starting on compounded tirzepatide. With the drug shortage ending, she advises patients to not start taking compounded drugs if they won't be able to access or afford the brand-name drugs.
"We try to make sure they know that up front," said Burch, who is president of the Pharmacy Compounding Foundation. "We don't want to pull the rug out from under them."
Burch added some patients want doctors to write longer-term prescriptions so they can stockpile the compounded medication for up to one year. But doctors are reluctant to do that because they must monitor patients weight loss and overall health while on the medication, she said.
"I had a provider yesterday who said, 'I'm really scared to write 12 months for a patient. They'll come back to me and they'll weigh 100 pounds. That's not really what I want,'" Burch said.
The industry group Alliance for Pharmacy Compounding urged the FDA to approve the transition period for people taking compounded weight-loss medications to give them time to prepare for such as change, said CEO Scott Brunner.
Brunner said patients often must go back to their doctor or telehealth provider and get a new prescription for their weight-loss medications. This transition period gives pharmacies enough time to prepare for the change without abruptly changing patients prescriptions.
"This is all about continuation of care, assuring patients don't experience some interruption of therapy," Brunner said. "Abruptly ending these GLP-1 drugs can have potential health consequences."
What's being done to make brand name versions of weight-loss drugs more affordable?
Most large companies that provide health insurance benefits for workers and private insurance companies cover diabetes drugs such as Ozempic and Mounjaro.
But a survey last year by the benefits consultant Mercer said fewer half of large employers covered GLP-1 drugs for obesity. That means consumers often face large bills for drugs that retail for about $1,300 per month, before rebates or discounts.
While Congress has scrutinized pharmaceutical companies over the retail price of these medications, drugmakers have rolled out some discounted, direct-to-consumer options.
Last week, Eli Lilly slashed the monthly price for lower-dosage vials of Zepbound by $50 for consumers who pay cash via the drugmaker's LillyDirect website. Consumers who buy a month's supply of 2.5-mg vials will now pay $349 and 5-mg vials will cost $499. Lilly also announced higher dosages of 7.5 and 10 mg at monthly prices $599 and $699 respectively. Those higher dosage prices will be discounted to $499 per month for the first fill, as well as refills within 45 days.
Meanwhile, drug compounders are still pressing legal challenges to the FDA's decision to declare the weight-loss drug shortages over. The Outsourcing Facilities Association sued the FDA on Monday over its decision to declare Novo Nordisk's Wegovy and Ozempic are no longer in shortage. The industry group earlier sued the agency over declaration that Lilly's tirzepatide was no longer in short supply.
In the tirzepatide lawsuit, the OFA filed a motion arguing the FDA's shortage decision was effectively a new rule that requires a more comprehensive regulatory process. A federal judge has not yet ruled on the motion. The FDA said it won't enforce its Feb. 18 deadline for compounding pharmacies to discontinue the drug until the court rules on the motion.
After the FDA declared the tirzepatide shortage over, Bonello said she planned to ask her doctor to switch her to compounded semaglutide. Now, she realizes that's not a lasting solution, either.
Her workplace insurance plan covers GLP-1 diabetes medications but it doesn't cover weight-loss medications. Although she has elevated blood sugar, she doesn't have diabetes, even though other family members have been diagnosed.
Even with Lilly's discounted price of $499 for the higher dosages announced this week, Bonello said she can't afford that amount and still pay daily living expenses.
"That's more than my phone bill and car insurance combined," she said.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Long-lasting HIV prevention shot heads toward approval
Long-lasting HIV prevention shot heads toward approval

Yahoo

time34 minutes ago

  • Yahoo

Long-lasting HIV prevention shot heads toward approval

June 6 (UPI) -- A new vaccine to prevent HIV is expected to be approved by the U.S. Food and Drug Administration later this month. If approved, the shot -- lenacapavir -- would be given twice a year and could be a big step forward in the fight against HIV. Drugmaker Gilead Sciences tested the shot in a study of women and girls. None of the participants who received the injections got HIV. That early success helped boost Gilead's stock by 73% over the past year, The Wall Street Journal reported. "We know it's challenging to take a daily pill for prevention, and we see an incredible opportunity here," said Johanna Mercier, Gilead's chief commercial officer Right now, more than 400,000 people in the United States use pills to prevent HIV, The Wall Street Journal added. These medications are referred to as PrEP, short for pre-exposure prophylaxis. Gilead expects the number of users to top 1 million by the next decade. Many people already say they'd prefer a shot over daily pills. In one survey of more than 500 PrEP users, 95% said they would switch to a long-acting injection. Sales of other long-acting options, like the shot Apretude from GSK, have risen sharply - up 63% in the past year. Even with strong results, Gilead faces several hurdles. One is reaching the people who need PrEP the most. Black Americans represent 39% of new HIV cases but only 14% of current PrEP users. Many people still face stigma or lack insurance coverage, which can limit access. Gilead says reaching underserved groups is a top goal. Most current PrEP users have commercial insurance, but Medicaid will be key for expanding access to lower-income communities. Another concern: Some experts worry the new shot may simply replace current Gilead products, like the daily pill Descovy, which now holds about 40% to 45% of the market. But Gilead says the shot should help expand the overall number of people using PrEP in both the U.S. and abroad. "We're thinking globally about the public health impact we can have," Mercier said. The company is working with governments and health groups in the United Kingdom and low-income countries to raise awareness and make these products more available. More information The National Institutes of Health has more on Pre-Exposure Prophylaxis (PrEP). Copyright © 2025 HealthDay. All rights reserved.

RFK Jr. will ‘end the war' against alternative medicine at the FDA, from stem cell therapy to chelation. Here's what to know
RFK Jr. will ‘end the war' against alternative medicine at the FDA, from stem cell therapy to chelation. Here's what to know

Yahoo

timean hour ago

  • Yahoo

RFK Jr. will ‘end the war' against alternative medicine at the FDA, from stem cell therapy to chelation. Here's what to know

Health and Human Services Secretary Robert F. Kennedy, Jr. doubled down on his support for non-pharmaceutical health treatments during a recent podcast appearance, saying, 'We're going to end the war at the FDA against alternative medicine.' Speaking on the Ultimate Human podcast with host Gary Brecka, a 'renowned Human Biologist, biohacker, and longevity expert,' according to the website, Kennedy said he would fix the U.S. Food and Drug Administration's bias against the following: stem cell treatments, chelating drugs, vitamins and minerals, amino acids, peptides, and hyperbaric chambers. 'Our position is that the FDA has a job: Just do the science on these kinds of issues and then tell the public what they've learned from the science … but don't tell physicians what they can and cannot prescribe,' he said. And as far as the patients go, he said, 'If you want to take an experimental drug … you ought to be able to do that.' RFK Jr. added, 'We don't want to have the Wild West. We want to make sure that information is out there. But we also want to respect the intelligence of the American people' to decide what treatments will benefit them the most. He acknowledged that, with this approach, there will be 'charlatans' as well as 'people who have bad results' from various alternative treatments. 'But ultimately,' he said, 'you can't prevent that either way, and leaving the whole thing in the hands of pharma is not working for us.' Brecka called Kennedy's pronouncements 'music to my ears.' Below, what you need to know about the alternative therapies RFK Jr. is advocating for. What is it: It's a way to repair diseased or injured tissue in the body using stem cells—cells that can self-renew or become other types of tissues—typically grown in a lab, manipulated, and then be implanted into the patient. What it does: Though it's considered to be largely experimental, the FDA does permit stem cell therapies for blood and immune disorders. Leukemia, lymphoma, neuroblastoma, and multiple myeloma, for example, are also often treated this way, with bone marrow treatments, which are backed by decades of science. Other types of the treatment are still in clinical trials, while more and more wellness centers are offering the treatment for unapproved reasons, using cells drawn from the patient's body and injected back in without manipulation for everything from autism and ALS to Parkinson's and better skin, according to the New York Times. Kennedy told Brecka that he received the treatment for his voice disorder, spasmodic dysphonia, and that it helped him 'enormously,' but that he had to go to Antigua to access it. Risks: For starters, wellness clinic treatments cannot guarantee they are using actual stem cell, reported the Times. And improper injections can lead to a host of terrible consequences—clots, infections, blindness, and even the formation of tumors, which the FDA warned of in 2021. What it is: Chelation involves the use of certain chemicals to remove toxic heavy metals, such as mercury and lead, from the body; all FDA-approved chelation therapy products require a prescription and can only be used safely under the supervision of a healthcare practitioner. What it does: Some alternative medicine practitioners offer chelation therapy, through pill or injection, as a way to treat Alzheimer's, autism, diabetes, high blood pressure, or Parkinson's disease, all of which are unapproved and risky. Children's Health Defense, founded by Kennedy, has written about chelation as a way to treat autism, which compares 'autism with mercury poisoning' due to childhood vaccines that contained the preservative thimerosal (largely mercury) before it was removed in 2001. Some flu shots still contain the preservative, but, says the Centers for Disease Control and Prevention, 'There is no evidence of harm caused by the low doses of thimerosal in vaccines.' Risks: The FDA warns specifically about using chelation therapy for autism, and notes, 'Chelating important minerals needed by the body can lead to serious and life-threatening outcomes.' While minor risks may include fever, headache, muscle pain, and nausea or vomiting, severe reactions range from heart failure and kidney damage to respiratory failure and seizures, according to the Cleveland Clinic. What they are: Dietary supplements in almost every letter of the alphabet, from A to zinc, are over-the-counter pills or liquids that contain nutritional boosts of vitamins and minerals. What they aim to help: Vitamin and mineral supplements aim to fill in with necessary nutrients that a person is not getting through food—though nutritionists believe that healthy food is the best source of such vitamins and minerals. Studies have found supplements may help with practically any issue under the sun—energy, heart issues, cognitive function, gut health, sleep, and more. Risks: The U.S. Food and Drug Administration regulates supplements, but doesn't approve them for safety or effectiveness before they are sold to the public. Some may cause liver damage and toxicity, while others may just be a waste of money. What it is: Amino acids are often referred to as the 'building blocks of proteins,' needed for building proteins, hormones, and neurotransmitters. are compounds that play many critical roles in your body. You need them for vital processes such as building proteins, hormones, and neurotransmitters. Amino acids are concentrated in protein-rich foods such as meat, fish, and soybeans, and foods that contain all nine essential amino acids are called complete proteins. Peptides are short proteins, and come in the form of hormones such as follicle-stimulating hormone (FSH), and creatine and collagen. What they aim to help: Amino acid supplements may help with various issues—such as L-arginine for blood flow and inflammation; tryptophan for mood and sleep; and valine, leucine, and isoleucine to help with energy and athletic performance. Taking collagen supplements may help strengthen nails and bones, while people take creatine for boosting workouts and building muscle growth. Risks: Side effects of taking either can range from toxicity and gastrointestinal issues to effects on brain function muscle protein balance. Creatine may cause muscle cramps and digestive problems (and may not have many benefits), while tryptophan may cause dizziness, headache, or nausea. And again, as with all supplements, the U.S. Food and Drug Administration regulates them, but doesn't approve them for safety or effectiveness before they are sold to the public. What it is: Hyperbaric oxygen therapy in a medical-grade, FDA-approved chamber lets you breathe pure oxygen—as opposed to everyday air, which is just 21% oxygen mixed with nitrogen. Hyperbaric oxygen is also highly pressurized, thereby allowing the lungs to take more in. Home chambers (used by folks including Lebron James, LeAnn Rimes, and Mayim Bialik), as well as those offered in many wellness clinics, do not deliver 100% oxygen. Instead, they use regular air that is 30% more pressurized than normal for what's known as 'mild hyperbarics.' What it aims to help: The FDA has been regulating HBOT chambers since 1976, and has officially cleared 13 medical conditions—such as decompression sickness, burns, radiation injury, and certain wounds—for such treatment. But it's used off-label for many other reasons, including concussions, traumatic brain injury, long COVID, age reversal, stroke recovery, fibromyalgia, and improved brain function, many of which are being looked at in ongoing clinical trials. Risks: For medical-grade chambers, risks include ear and sinus pain, middle ear injuries, temporary vision changes, and lung collapse, which is rare, according to the FDA. For mild hyperbarics, risks include potential exposure to toxic oils from some compressors, carbon dioxide buildup that brings a risk of hypoxia inside the chamber—or, according to some experts and a body of inconclusive evidence, that the treatment may simply be ineffective. This story was originally featured on

Nearly 100 House Democrats urge RFK Jr. to restore millions in family planning grants
Nearly 100 House Democrats urge RFK Jr. to restore millions in family planning grants

Yahoo

timean hour ago

  • Yahoo

Nearly 100 House Democrats urge RFK Jr. to restore millions in family planning grants

Nearly 100 House Democrats are calling on Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. to restore tens of millions of dollars in federal family planning grants to more than a dozen organizations that have been frozen for more than two months. In a letter to Kennedy sent Friday and seen first by The Hill, 95 lawmakers said the organizations that had their Title X funding frozen on March 31 — including nine Planned Parenthood clinics — are still in the dark about the status of their grants. At the time, the clinics said they received letters from the administration saying the grants were being 'temporarily withheld' due to possible civil right violations and President Trump's executive orders prohibiting the promotion of diversity, equity and inclusion (DEI) and 'taxpayer subsidization of open borders.' More than two months later, the lawmakers said the grantees 'remain without funding and have received no communication from the administration regarding the status of the investigations, the expected timeline, or the future of their funding.' HHS declined to comment, citing ongoing litigation. The agency is being sued over the freeze by the National Family Planning and Reproductive Health Association (NFPRHA) and the American Civil Liberties Union (ACLU). 'Congress has already appropriated these funds, and the administration has a responsibility to distribute them without undue delay or obstruction, ensuring that critical care is not disrupted for millions of people who rely on Title X services,' the group of lawmakers wrote. The letter was led by Reps. Josh Gottheimer (D-N.J.), Judy Chu (D-Calif.), Lizzie Fletcher (D-Texas) and Sharice Davids (D-Kan.) and signed by 91 other Democrats. Title X is the country's only federal program dedicated to providing affordable birth control and other sexual and reproductive health care to low-income Americans and has done so since the 1970s. The lawmakers timed the letter to coincide with the 60th anniversary of the U.S. Supreme Court's ruling in Griswold v. Connecticut, which established a constitutional right to privacy regarding contraception and reproductive decisions. 'However, due to the actions of this administration, reproductive freedom is under threat,' the lawmakers wrote. The first Trump administration prohibited providers from receiving Title X funding if they mentioned abortion or referred patients for abortions. It also required clinics to construct separate facilities for the procedure and other services. More than a dozen grantees, including all Planned Parenthood affiliates nationwide, left the program in protest because of the rule. The Biden administration reversed Trump's Title X rule in 2021. Updated at 3:26 p.m. Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store