Podcast: Is Ozempic (Semaglutide) Safe? Does It Increase Cancer Risk?

Brief Summary

This podcast episode examines the potential side effects of GLP-1 weight-loss drugs like Ozempic and Zepbound, focusing on suicide risk, thyroid and pancreatic cancer, pancreatitis, and bowel obstruction. It balances the alarming warnings with the statistical rarity of some side effects and the potential overall health benefits of weight loss, including reduced cancer risk. The episode also touches on concerns about data suppression by drug companies and the challenges of accurately assessing long-term risks.

  • GLP-1 drugs carry warnings for potential side effects like thyroid tumors, pancreatitis, kidney injury, and suicidal thoughts.
  • Studies suggest GLP-1 drugs may lower the risk of suicidal ideation.
  • GLP-1 drugs are associated with an increased risk of thyroid cancer, but the overall risk remains low.
  • GLP-1 drugs may significantly increase the risk of pancreatitis and bowel obstruction, although these events are rare.
  • Weight loss achieved through these drugs could potentially lower overall cancer risk and provide cardiovascular benefits.

Introduction to GLP-1 Weight-Loss Drugs and Their Potential Side Effects

The podcast introduces a series on Ozempic and other GLP-1 weight-loss drugs, addressing concerns about potential side effects such as suicide, pancreatitis, bowel obstruction, thyroid cancer, and pancreatic cancer. Regulatory authorities have expressed concerns about the potential risks of acute pancreatitis, thyroid cancer, and kidney failure, which are included as warnings in the drug packaging. The package inserts for Ozempic (semaglutide) and Zepbound (tirzepatide) list warnings and precautions, including thyroid tumors, acute pancreatitis, gallbladder disease, low blood sugar risk, kidney injury, allergic reactions, worsening eye disease, increased heart rate, and suicidal thoughts and behaviors.

Suicide Risk and GLP-1 Drugs

The possibility of adverse psychiatric events with GLP-1 drugs is biologically plausible due to the presence of GLP-1 receptors in the central nervous system. However, a meta-analysis of randomized controlled trials did not find any detrimental effect on mental health, including suicide risk. Newer studies with real-world subjects also showed no clear increased risk. One study found that semaglutide (Ozempic) was associated with a lower risk of suicidal ideation, potentially cutting suicidal thoughts by more than half compared to older weight-loss drugs. Weight reduction treatments can improve mood by reducing the burden of obesity.

Thyroid Cancer Risk and GLP-1 Drugs

Wegovy and Zepbound carry black box warnings for thyroid cancer risk due to dose-dependent thyroid tumors observed in rodents at clinically relevant exposures. It is currently unknown whether these drugs cause medullary thyroid carcinoma in humans. As a precaution, these drugs should not be prescribed to individuals with a personal or family history of thyroid cancer. Doctors should advise patients to watch for symptoms of thyroid tumors, such as lumps or swelling in the neck, trouble swallowing, shortness of breath, or persistent hoarseness. Research on GLP-1 drugs like Ozempic has shown an increased risk of all thyroid cancers, particularly medullary thyroid cancer, after a few years of use. A meta-analysis found a significant increase in the risk of overall thyroid cancer, with about 52 percent greater odds. However, the overall incidence of thyroid cancer in the population is low, with only about three people out of 1,000 expected to get the cancer over a decade. Even with a 50 percent increase in risk, only about four in 1,000 would get it over a decade. The five-year relative survival rate for thyroid cancer is 98.4 percent, indicating it is a relatively mild cancer.

Pancreatitis and Bowel Obstruction Risk with GLP-1 Drugs

The most common side effects of Ozempic-type weight-loss drugs are gastrointestinal issues like nausea, vomiting, diarrhea, and constipation. Ozempic may also increase the risk of pancreatitis, kidney failure, and thyroid cancer. Kidney issues may arise from dehydration due to vomiting or diarrhea caused by the drugs. GLP-1 drugs were associated with nine times more pancreatitis and a four times higher risk of bowel obstruction compared to older weight-loss drugs. GLP-1 slows down the digestive tract, which can lead to nausea but also promotes fullness and weight loss. In rare cases, it can cause the gut to become so sluggish that it stops working, leading to a blockage requiring surgery. The number needed to harm for bowel obstruction after one year of use is 1,223, meaning over 1,000 people would need to take the drug for a year to cause one extra case. The cumulative risk after 10 years of treatment is less than one percent. GLP-1 receptors are abundant in the pancreas, and GLP-1 therapy can cause the cells of the pancreas to proliferate, potentially leading to inflammation. Studies suggest GLP-1 drugs may increase the odds of pancreatitis as much as six-fold.

Pancreatic Cancer Risk and Concerns About Data Suppression

The major concern is subclinical, asymptomatic inflammation of the pancreas, which can predispose individuals to pancreatic cancer. Some rats showed potentially premalignant changes in their pancreases while on these drugs. The pro-proliferative actions of GLP-1 could accelerate the progression of premalignant lesions towards cancer. GLP-1 drugs are modeled after a compound found in Gila monster saliva, which the lizard uses to rapidly proliferate its tissues after long periods without food. A British Medical Journal investigation revealed unpublished data from animal and human studies indicating pathological changes in the pancreas, with drug companies allegedly suppressing scientific debate by withholding safety data. Companies may be incentivized to avoid monitoring the safety of their products to avoid legal liability, a concept referred to as the "three monkey paradigm." A professor at the Mayo Clinic suggested that most patients and clinicians might opt to avoid GLP-1 based drugs or limit their use to a short period. A study of transplant-quality pancreases from accident victims who had been taking GLP-1 drugs for at least a year showed abnormalities in every pancreas, including enlargement, dysplasia, and small tumors.

Current Understanding and the Broader Context of Cancer Risk

It remains unclear whether the use of GLP-1 drugs is linked to an increased risk of pancreatic cancer, and trials would need to be enormous to exclude such a risk. Most data may remain hidden from independent scrutiny. Thousands of pancreatic cancer cases have been reportedly tied to GLP-1 drugs via the FDA's Adverse Events Reporting System, but these databases are limited by potential reporting bias. If there is even a remote chance that certain drugs can impact cancer development and progression, such risks should not be taken lightly. Being overweight increases the risk of 18 different kinds of cancer. Weight loss achieved through these drugs could potentially lower overall cancer risk. A meta-analysis of bariatric surgery studies found that significant weight loss can lower the risk of getting and dying from cancer. Widespread use of new-generation weight-loss drugs like Ozempic could prevent more than 1 out of 100 cancers over the next 25 years. The cardiovascular benefits of significant weight loss may outweigh any potential risks.

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Transcript

Full transcript of “Podcast: Is Ozempic (Semaglutide) Safe? Does It Increase Cancer Risk?”. Click a timestamp to open the video at that moment. Need another video? Use the YouTube transcript generator.

0:01 Have you ever wondered if there are more natural ways to lower your high blood pressure, guard against Alzheimer's, lose weight, and feel better? Well, it turns out there is! Welcome to the Nutrition Facts Podcast. I’m your host, Dr. Michael Greger. Today we continue our series on Ozempic as we look at the potential side effects of GLP-1 weight-loss drugs, such as suicide, pancreatitis, bowel obstruction, thyroid cancer, and pancreatic cancer. GLP-1 weight-loss drugs. How safe are they? Regulatory authorities have expressed concerns about the potential risk of acute pancreatitis, thyroid cancer, and kidney failure, warnings that are appropriately conveyed in every box of drugs handed to a patient.

0:48 Here’s the actual package insert for high-dose Ozempic, sold for weight loss as Wegovy. Warnings and precautions include thyroid tumors, acute inflammation of the pancreas, acute gallbladder disease, heightened risk of low blood sugars if you’re on blood sugar-lowering medications, acute kidney injury, allergic reactions, worsening eye disease for those with type 2 diabetes, an increase in heart rate that should be monitored, and suicidal thoughts and behaviors. And the package insert for the other major GLP-1 weight loss drug, tirzepatide, sold as Zepbound, reads almost word for word the same. Let’s start with the good news, suicide. The possibility of an adverse psychiatric event on GLP-1 drugs is biologically plausible because GLP-1 receptors are widely expressed in the central nervous system, including our brain.

1:35 So, what does the science show? This meta-analysis of randomized controlled trials did not highlight any detrimental effect on these drugs on mental health, including suicide. Now, this meta-analysis only covered studies up through the end of 2023 and only clinical trials, and those with mental illnesses are usually excluded from such studies. But there have been newer studies done with subjects out in the real world, and again, no clear increased risk. And this study, on the association of the Ozempic drug semaglutide with risk of suicidal ideation in another cohort found that the drug was associated with a lower risk for incident and recurrent suicidal ideation, apparently cutting suicidal thoughts by more than half, compared to those on the older, less effective weight-loss drugs. After all, a weight-reducing treatment

2:22 that limits the burden of obesity could improve mood. I told you suicide was the good news! Now, on to cancer. Both Wegovy, high-dose Ozempic, and Zepbound (tirzepatide), carry so-called black box warnings for thyroid cancer risk. Black box warnings are the U.S. Food and Drug Administration’s strictest caution about potentially life-threatening hazards. In rodents, these drugs cause dose-dependent and duration-dependent thyroid tumors at clinically relevant exposures, meaning the kind of doses prescribed to humans. Now, we don’t know yet whether these drugs cause a thyroid cancer called medullary thyroid carcinoma, which is a cancer of the thyroid C cells in humans. To be on the safe side, the drugs shouldn’t be prescribed

3:07 for high-risk individuals, like those with a personal or family history of thyroid cancer, but it’s not like the rats had thyroid cancer running in their families. Doctors should counsel their patients to remain alert for symptoms of thyroid tumors, like a lump or swelling in the neck, trouble swallowing, shortness of breath, or persistent hoarseness. I’d be curious in the comments to see if any viewers who’ve been prescribed these drugs were told any of this by their prescribing physicians. Can’t we just ultrasound people’s necks to see if they develop thyroid tumors on these drugs? That’s considered to be of uncertain value, since no such studies have been done. Now, there have been studies done on GLP-1 drugs, like Ozempic, and the risk of thyroid cancer in people. Researchers found increased risk of all thyroid cancers

3:54 and specifically, medullary thyroid cancer in people using these drugs, particularly after taking them for a few years. A commentary citing the study asked, "Is it the time to be concerned?" Maybe that one study was just a fluke? No, after putting together all the best studies, a systematic review and meta-analysis of randomized controlled trials found, again, a significant increase in the risk of overall thyroid cancer, about 52 percent greater odds. That sounds bad, until you realize just how rare the cancer is overall. The incidence of thyroid cancer in this kind of population is 0.285 cases per 1,000 patient years. This means that over a span of 10 years, we’d only expect about three people out of 1,000

4:39 to get that cancer. So, even if you bump up that risk by 50 percent, you’re still only talking about four in 1,000 getting it over a decade, compared to three in 1,000 if you hadn’t started taking the drugs. That translates to a five-year "number needed to harm" of 1,349. That means that even if this were truly cause-and-effect, it would take treating 1,349 people for five years to cause a single additional case of thyroid cancer. And even if you’re the unlucky soul who gets it, it’s pretty mild, as cancers go. The five-year relative survival rate, meaning the likelihood you’ll still be alive five years after diagnosis compared to people without the cancer is 98.4 percent. Okay, but what about the risk of pancreatic cancer

5:27 with the use of these drugs? That has a relative five-year survival rate of only 12.8 percent. For thyroid cancer, a bunch of people are diagnosed with it, but very few die from it, whereas for pancreatic cancer, almost everyone who gets it dies from it. So, do these drugs cause pancreatic cancer? That’s exactly the question I’ll address next. The most common adverse side effects of Ozempic-type weight-loss drugs are gastrointestinal issues, including nausea, vomiting, diarrhea, and constipation, but Ozempic may also heighten the risk of pancreatitis, kidney failure, and thyroid cancer. Many of the kidney issues may stem from dehydration due to excessive vomiting or diarrhea caused by the drugs,

6:12 but what about the pancreas inflammation? Analyzing the prescription records of 16 million Americans, compared to taking an older class of weight-loss drugs, the use of GLP-1 drugs like Ozempic was associated with nine times more pancreatitis, as well as four times higher risk of bowel obstruction. Remember, GLP-1 slows down your digestive tract. That’s part of the reason people get nauseous and barfy, but that’s also part of why you feel fuller for longer and lose weight. But sometimes, it can make your gut so sluggish, it stops working, and you get a blockage that could become a surgical emergency. It’s super rare, though. The number needed to harm after one year of use is 1,223, meaning that more than 1,000 people

6:57 would have to take the drug for a year to cause a single extra case of bowel obstruction. So, even after 10 years of treatment, your cumulative risk would be less than one percent. But what about this 800 percent increased risk of pancreatitis? Digestive hormones like GLP-1 act on multiple targets within the body, with multiple effects, perhaps more "magic shotgun" than "magic bullet," but maybe not so magical for the pancreas. GLP-1 receptors are expressed abundantly throughout the pancreas, and in response to GLP-1 therapy, the cells of the pancreas proliferate, swelling the organ and potentially squeezing off ducts, causing inflammation, at least in rats, but that led to human studies like this, suggesting that GLP-1 drugs

7:42 may increase the odds of pancreatitis as much as six-fold. This led some investigators to conclude that the balance of evidence suggests an association between the use of GLP-1 based therapies and acute pancreatitis. The major concern is not pancreatitis, though. Acute pancreatitis is unpleasant enough, but the major concern is subclinical, asymptomatic inflammation of the pancreas, because inflammation of the pancreas is well known to predispose to pancreatic cancer, which is one of the deadliest forms of cancer. And some of the rats did show potentially premalignant changes in their pancreases on these drugs. The concern is that the pro-proliferative actions of GLP-1 could take premalignant lesions and accelerate their progression towards cancer.

8:30 Remember how these drugs were modeled off a compound found in Gila monster saliva? Few have paused to wonder why they would produce it. The answer is that the Gila monster is a desert lizard that goes for weeks or even months between meals and conserves energy during those intervals by shrinking its digestive tract, including its pancreas. So, when it finally does eat, it needs a way to rapidly proliferate its tissues. After reviewing thousands of pages of documents obtained through freedom of information requests, a British Medical Journal investigation unearthed unpublished data from animal and human studies that point to pathological changes in the pancreas, including attempts by drug companies to suppress scientific debate by withholding important safety data

9:15 from the public. Why have the companies been so slow to respond to this threat? Because of the "three monkey paradigm," which operates as follows. Companies are legally responsible for monitoring the safety of their own products, but obviously can’t be held responsible for tackling a safety concern that does not exist. A concern that can be plausibly doubted or denied carries no legal liability, whereas one that gives rise to serious consideration leaves the door wide open to lawsuits. Thus, inviting companies to monitor the safety of their own products provides them with the strongest possible incentive for failing to do so, an instance of the law of unintended consequences. The three monkeys, who neither hear nor see nor speak,

10:02 have been allowed to flourish at the heart of our system for protecting the public. "After careful reflection," wrote a professor of medicine at the Mayo Clinic, "most patients and clinicians may opt to avoid GLP-1 based drugs or at least avoid using them for a prolonged period of time." And this was all before this pivotal study came out, where researchers obtained transplant-quality pancreases from, like, accident victims who had been taking GLP-1 drugs for at least a year before they died, and every single pancreas showed abnormalities, marked enlargement, dysplasia, and even a few little tumors. This was all discovered more than a decade ago, though. Where are we now? It remains unclear whether the use of GLP-1 drugs

10:48 is linked to an increased risk of pancreatic cancer. But trials would have to be enormous to exclude an increased risk, and unless the rules change radically by the time they are to be reported, most of the data will remain hidden from independent scrutiny. And as one Johns Hopkins drug safety researcher asked, "The fundamental question is who bears the burden of the passage of time while these debates are settled?" Thousands of pancreatic cancer cases have been reportedly tied to GLP-1 drugs, like Ozempic, based on the U.S. Food and Drug Administration’s Adverse Events Reporting System, but adverse event databases that rely on voluntary reporting are limited by the potential for reporting bias. That’s like the Centers for Disease Control’s VAERS database,

11:34 the Vaccine Adverse Events Reporting System. During COVID, the more states were inclined to vote Republican, the more likely their vaccine recipients or clinicians were to report COVID vaccine side effects; so, maybe there was some kind of similar reporting bias among those who submit their pancreatic cancer to the FDA? Either way, if there is even a remote chance that certain drugs can have an impact on cancer development and progression, then such risks should not be taken lightly. But if you really don’t want to get cancer, then you really don’t want to be overweight. Based on a study following millions of people, the longer you’re overweight or obese, the higher your apparent risk of 18 different kinds of cancer. So, even if you cared only about cancer,

12:22 might these drugs actually lower your overall cancer risk if they caused enough weight loss? A meta-analysis of bariatric surgery studies found that those going under the knife tend to lose so much weight that they have a significantly lower risk of getting cancer and appear to cut their risk of dying from cancer nearly in half. This modeling study suggests that widespread usage of these new-generation weight-loss drugs, like Ozempic, could prevent more than, like, 1 out of 100 cancers over the next 25 years. And that’s just cancer. Wouldn’t just the cardiovascular benefits of losing a lot of weight alone outweigh any potential risks? Visit nutritionfacts.org/audio to see all of the podcast episodes with descriptions that include links to their associated videos.

13:10 Sources cited and other details are available on each video's page. Information about my books— How Not to Die, How Not to Diet, and How Not to Age— is at nutritionfacts.org/books. All proceeds from book sales go to charity. And sign up for our free newsletter at nutritionfacts.org/subscribe to stay updated on the latest bite-sized videos and articles. NutritionFacts.org is a science-based non-profit, and everything on the website is free. There are no ads, no corporate sponsorships, no kickbacks. Strictly non-commercial, not selling anything. I just put up as a public service, as a labor of love, as a tribute to my grandmother whose own life was saved with evidence-based nutrition. Thanks for listening.

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