Women on blockbuster weight loss drugs warned to use effective contraception
The UK Medicines and Healthcare products Regulatory Agency (MHRA) also said women should not take weight loss drugs if they are breastfeeding or trying to get pregnant, because there isn't enough safety data to know whether the medicine could affect their baby.
'Anyone who gets pregnant while using them should speak to their healthcare professional and stop the medicine as soon as possible,' the agency said.
Meanwhile, all women taking the jabs should ensure they are using a form of contraception that works, the MHRA said.
Related
Weight-loss drugs like Wegovy could help serious liver condition that has no cure-all treatment
One of the drugs, Mounjaro, may make birth control pills less effective, so the agency says women taking the jab should also use a non-oral form of contraception, like an implant or intrauterine device (IUD).
'Obesity reduces fertility in women. So, women with obesity taking GLP-1 drugs are more likely to get pregnant than before they lost weight,' Dr Channa Jayasena, a reproductive endocrinology researcher at Imperial College London, said in a statement.
'Women are advised to do all they can to prevent pregnancy while taking [these] drugs,' Jayasena added.
Related
France won't pay for weight loss drug Wegovy. What about other European countries?
In the UK, women already receive these warnings when they get their prescriptions for the blockbuster jabs, which include Ozempic, Wegovy, Saxenda, and Victoza as well as Mounjaro.
The drugs, known as GLP-1 receptor agonists, work by mimicking hormones that help regulate appetites and make people feel full for longer. They have been approved to treat type 2 diabetes and obesity.
Related
Why are 1 in 10 French women still smoking during pregnancy despite the health risks?
But the MHRA issued the reminder Thursday due to concerns that the drugs' growing popularity means women are buying them illegally online or at beauty salons, without seeing a doctor.
'Skinny jabs are medicines licensed to treat specific medical conditions and should not be used as aesthetic or cosmetic treatments,' Dr Alison Cave, MHRA's chief safety officer, said in a statement.
'They are not a quick fix to lose weight and have not been assessed to be safe when used in this way,' she added.
Hashtags

Try Our AI Features
Explore what Daily8 AI can do for you:
Comments
No comments yet...
Related Articles


Axios
2 hours ago
- Axios
"Fibermaxxing" is trending, but don't overdo it
On TikTok, users are eating a ton of dietary fiber, but making it sound cool: They're " fibermaxxing." Why it matters: Most Americans fall short of their daily fiber needs, so a viral push to increase intake could help close the gap. That said, "you can get too much of a good thing," says registered dietitian nutritionist Janet Helm. What's happening: Content creators are suggesting ways to add fibrous foods like beans and chia seeds to meals, in order to be fuller, more regular and manage weight. State of play: " Fiber is beginning to have a moment," say Sherry Frey, VP of total wellness at consumer intelligence firm NielsenIQ. Along with being good for your bowels, blood sugar and heart — fiber lowers the risk of colorectal cancer, a disease that's seeing more early-stage diagnoses. And it's the latest topic in the gut health conversation, popular among wellness influencers and GLP-1 users changing their diets. (See also: protein and probiotics.) By the numbers: Supplements and powders containing fiber are an $8.8 billion industry, up more than 15% today compared to two years ago, according to NielsenIQ. Yes, but: "Where the trend has gone too far for me" is when people are consuming more than the recommended 25 to 38 grams for adults, Helm says. Eating too much too fast could cause bloat, gas and diarrhea, she says. To healthfully introduce more fiber into your life, start slowly, stay hydrated and look for both soluble and insoluble fiber sources in whole foods.


Medscape
4 hours ago
- Medscape
Do Women With Acute ACS Face Unnecessary Bleeding Risk?
A consensus statement from two European cardiology organizations contends antithrombotic treatment for myocardial infarction and angina overlooks sex differences that heighten bleeding risk in women. Compared with men, women treated for acute coronary syndromes (ACS) are at a greater risk for in-hospital bleeding related to invasive cardiac procedures and more long-term outpatient bleeding events, according to the statement from the European Association of Percutaneous Cardiovascular Interventions and the European Society of Cardiology Working Group on Thrombosis. Antithrombotic therapies such as heparin and fondaparinux used in invasive ACS procedures typically have a similar efficacy in women and men, but women have a higher bleeding risk of these agents, said Davide Capodanno, MD, PhD, professor of cardiology at the University of Catania, Catania, Italy, and co-author of the consensus statement. Some ways to reduce bleeding risk in women are to adjust antithrombotic dosing for body weight and kidney function, Capodanno told Medscape Medical News , and to opt for radial access over femoral access for percutaneous coronary intervention (PCI). 'Our paper shows that women still experience delays in diagnosis and treatment, receive excessive antithrombotic doses more often, and remain underrepresented in trials,' Capodanno said. 'All of this creates the need for clear, pragmatic, sex-informed recommendations.' Physiologic Differences Hormonal differences between men and women play an important role in bleeding risk. Estrogen promotes the production of prostacyclin, increases the availability of nitric oxide, and reduces platelet aggregation. These features might protect against the earlier onset of coronary artery disease, but fluctuations in hormonal status due to the menstrual cycle, use of oral contraceptives, menopause, and hormone replacement therapy can also influence thrombotic and bleeding risks. Sex differences in protease-activated receptor signaling pathways, smaller coronary artery sizes, and a cascade of other factors contribute to the greater risk for bleeding associated with ACS treatment (Figure). Although ACS typically affects postmenopausal women, the incidence is increasing in premenopausal women, whose bleeding risk is even more elevated because of lower platelet reactivity due to estrogen receptors on the platelet surface. Data from nearly 4000 women and 10,000 men undergoing PCI showed women younger than 50 years were four times more likely than men of the same age to experience major and minor bleeding events associated with stenting. Wanted: More Sex-Specific Data Women also often experience delays in the diagnosis of ACS and referral for invasive treatments, such as PCI, for their condition. Clinicians still lack strong evidence to help them address sex differences in clotting and response to anticoagulation, Capodanno suggested. Awareness is improving, but there's still work to be done. 'We simply don't have enough sex-powered data to guide all our decisions. Women remain underrepresented in clinical trials, which limits the strength of sex-specific evidence,' Capodanno said. 'We need to push for more equitable research by enrolling and retaining more women in clinical studies and ensuring that results are analyzed and published separately for men and women.' Sunil V. Rao, MD, lead author of the 2025 joint clinical practice guidelines on ACS from the American College of Cardiology and the American Heart Association, agreed. 'There are very few clinical trials of bleeding reduction that have strong female representation,' said Rao, deputy director of the Leon H. Charney Division of Cardiology and director of interventional cardiology at NYU Langone Heart in New York City. One such study, the SAFE-PCI for Women randomized trial Rao led, compared radial access and femoral access in women undergoing stenting. The research showed using radial instead of femoral access for the intervention reduces the risk for bleeding in women. 'We need more trials like this to help guide the clinical community on how to mitigate the risks of antithrombotic therapy in women,' Rao said. Take-Home: Male Isn't Norm How can individual clinicians adjust their practice? 'We recommend actively reducing bleeding risk — for example, using radial access whenever possible, using ultrasound guidance if femoral access is needed, and always avoiding overdosing by adjusting for weight and kidney function,' Capodanno said. Prompt treatment is key to avoid sex-related delays in starting antithrombotic medications. 'Also, be mindful of sex-specific presentations in ACS,' he added. Among these is myocardial infarction with nonobstructive coronary arteries, which includes spontaneous coronary artery dissection, responsible for 25%-35% of myocardial infarctions in women younger than 50 years. According to Rao, European guidelines are generally consistent with North American recommendations with respect to antithrombotic strategies for ACS. 'I don't think we can make strong recommendations to change practice just yet,' he said. 'The message really is to counsel patients, especially female patients, on the benefit-risk balance of antithrombotic therapy, to use evidence-based approaches to reduce bleeding risk — such as radial access — and to refer female patients for clinical trials when possible.' Capodanno reported payment for speaker fees and advisory board participation from Bristol Myers Squibb, Daiichi Sankyo, Novo Nordisk, Sanofi, and Terumo. Rao reported no relevant financial conflicts of interest.


Business Wire
5 hours ago
- Business Wire
ieso Sharpens Focus on AI-Powered Mental Healthcare with Sale of UK Telecare Services Business
CAMBRIDGE, England & BOSTON--(BUSINESS WIRE)-- ieso, a global leader in evidence-based digital mental health, today announced the sale of its UK telecare services business to Mindler, a leading pan-European digital therapy provider. The acquisition is specific to ieso's NHS-facing care operations in the UK, including delivery of typed and video therapy services. Mindler's press release is available here. "As AI adoption accelerates, mental health is emerging as one of its most urgent and natural use cases. The market is moving fast, and so are we." - Kent Tangen, CEO, ieso Share The parent company, ieso Digital Health Limited, remains fully independent and continues to operate under the ieso brand. With the sale now complete, ieso is entirely focused on scaling its clinical-grade generative AI platform, Velora, to deliver safe, effective, personalized mental health support via SaaS integration into clinical workflows. 'We're proud to have supported thousands of lives through ieso's UK telecare services. That legacy will always be a part of who we are,' said Kent Tangen, CEO at ieso. 'With those operations now in excellent hands at Mindler, ieso is committed to building the future we've long envisioned: delivering safe, effective AI-powered mental healthcare at scale. Our immediate focus is in the US, but our mission is global. As AI adoption accelerates, mental health is emerging as one of its most urgent and natural use cases. The market is moving fast, and so are we.' ieso was advised on the transaction by Cooley LLP and Artis Finance. About ieso ieso is a pioneer in AI-powered mental healthcare, combining clinical expertise with advanced technology to help more people feel better, faster. Its latest product, Velora, is a next-generation generative AI-based program that delivers outcomes on par with human-delivered care and is designed to integrate seamlessly into existing clinical workflows. Backed by over a decade of research and real-world data, ieso is focused on increasing access to safe, effective, and scalable mental health support in the US and beyond. To learn more or request a demo, visit