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Wellness Exchange: Health Discussions

"Oral Ozempic: The New Weight Loss Craze?"

Duration:
6m
Broadcast on:
20 Nov 2024
Audio Format:
other

This is Ted. The news was published on Wednesday, November 20th. Today, we've got Eric and Kate joining us for a lively discussion about a hot topic, the surge in off-brand oral ozempic available online. Eric, can you start by explaining the key details from the article? Sure, Ted. First off, injectable GLP1 drugs like ozempic are a big deal, because they're super effective at treating diabetes and obesity, plus they've got some nice cardiovascular benefits. But the major downside is they require a weekly shot, and let's be real, nobody likes getting poked with needles all the time. Yeah, but now there are oral versions sold online, mainly on social media platforms like Instagram and Facebook. These come as lozenges, tablets, gels, drops, and even dissolving strips, much easier than getting a shot every week, if you ask me. Correct. These off-brand oral meds come from compounding pharmacies and telehealth clinics. They sprang up after a shortage of the brand name injectables in 2022. They market themselves by promising the same active ingredients, but in a form you swallow, which understandably many people find a lot more appealing. And they're way cheaper. For instance, you can get a month's supply of semaglutide lozenges for like $149, whereas the brand name "Wegavi" costs over a whopping $1,000. That's a massive price difference and makes it more accessible for a lot of people. True. But let's not forget these oral versions aren't approved by the FDA and haven't been put through rigorous clinical trials like the injectable ones have. There's no concrete evidence they work as effectively, so we're basically taking a gamble here. But people want convenience and affordability. These oral versions don't need refrigeration and are easier to ship and store. Isn't that a big plus? Not to mention they avoid the whole... It's not just about convenience. Without proper clinical testing, we can't be sure of their efficiency. They might not deliver the same results as injectables. We've got to consider the safety and real effectiveness here, right? Come on. Even pharmacists are excited about these oral versions because they're easier for patients to take. Isn't that somewhat reassuring? I mean, if the pros in the field see some potential, that counts for something. Sure. Melinda Lee, a pharmacist, does see the appeal, but she's also skeptical until we have more proof. Just because it's easier doesn't mean it's effective or safe, we need to make sure we're not jumping the gun. So is the convenience and low cost of these oral versions enough to offset the lack of proven efficacy and FDA approval? Let's dive into a past event with a similar shadow of uncertainty. Eric, any thoughts on a related historical precedent? Definitely. This reminds me of the early days of off-brand opioids in the 1990s. They were touted as being less addictive and safer than their standard counterparts, but as we all know, that didn't end well. The opioid crisis blew up, becoming a massive public health disaster. That's a bit extreme, Eric. I get where you're coming from, though. Historical lessons can be valuable. But it's not like these oral GLP1 drugs are addictive, or at least we hope not. It's more about making medication more accessible to... The point is about safety and unapproved alternatives. Just like with the opioids, we're dealing with unknown risks here. We can't afford to gamble with public health like this. But don't forget, the opioid crisis also happened because of malpractice and mismanagement by big pharma. Here, we're talking about smaller, focused businesses trying to fill a gap... Filling a gap without proper oversight and clinical trials is dicey. These smaller operations might be flying by the seat of their pants. We can't just ignore the lessons history has taught us... Maybe. But consider the accessibility angle. Think back to the AIDS crisis in the 1980s. People demanded access to experimental drugs because their lives depended on it. Sometimes waiting for full approval isn't an option when there's an urgent need. Urgency doesn't justify skipping crucial safety steps. The AIDS crisis led to fast tracking, sure, but it still involved proper trials and regulatory oversight. We need a balanced approach, not reckless abandon. True. But innovation often sparks a lot of debate. For those who urgently need solutions, the potential benefits might outweigh... Pain cautious is crucial. Past failure show us the importance of prioritizing safety and efficacy over convenience and immediacy. Interesting points from both sides. Moving on, let's speculate on how this trend might unfold. What are your predictions? Eric, paint us a picture of one possible future. If these oral drugs keep flooding the market without proper regulation, we might see a wave of ineffective treatments. People hoping for results might not get them, leading to widespread disappointment and public mistrust in these medications. Or we could see these oral versions revolutionizing the treatment of diabetes and obesity. Affordable alternatives might push big pharma to drop prices, making effective treatment more accessible for everyone. That's an optimistic scenario, but it's unlikely without proper oversight. If these unapproved meds cause any adverse effects, it could outweigh the cost benefits. Regulators might then call for stricter policies, potentially stifling future innovation. But what if regulators adapt and establish clear guidelines for these oral versions? Then we could have a balanced marketplace where approved alternatives coexist. Fostering innovation... It's a delicate balance. We can't rely on what ifs. The potential for harm due to lack of testing could far outweigh any benefits from cheaper drugs. Proven treatments should come first. People need options now, though. Waiting for the lengthy approval process might cause more suffering in the meantime. A regulated but fast tracking with the right oversight might work. However, without robust trials, it's still a dangerous game. We need solid proof these oral versions are both effective and safe. True. But we can design flexible and dynamic regulation that ensures safety while providing much-needed accessibility. Flexibility needs a solid framework where trial evidence is key. Without that, we're risking another health crisis. I think there's room for more innovative management. Modern tracking systems could quickly identify and address adverse effects, balancing risk and... Thank you both. This debate highlights the complexity of ensuring safe, affordable and effective treatments. We'll be following this topic closely as it develops.