Mounjaro®
Starting from £179.99/mo
Start journey Learn moreTirzepatide activates two gut-hormone receptors simultaneously — GIP and GLP-1 — making it the only dual-agonist peptide licensed for weight management in the UK. In clinical trials involving thousands of adults, average body-weight reductions of around 20% were recorded at the highest dose over 72 weeks. As a prescription-only medicine, whether it's right for you depends on a clinical assessment, not a self-referral. The sections below explain what the peptide actually does, and why the dual mechanism matters.
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If you've been reading about weight-loss medicines for any length of time, GLP-1 agonists have probably come up repeatedly. Semaglutide, the active ingredient in Wegovy, works on that single receptor and produces meaningful results. Tirzepatide does something structurally distinct: it also activates the GIP receptor, a second gut-hormone pathway that regulates fat storage and insulin sensitivity through mechanisms that don't fully overlap with GLP-1. The two pathways are complementary rather than redundant.
There's a common assumption that adding a second receptor just means more side effects rather than more benefit. The clinical evidence doesn't support that. In the SURMOUNT programme, participants on tirzepatide at higher doses saw greater average weight loss than those on licensed doses of semaglutide in the SURMOUNT-5 head-to-head trial, results published in the New England Journal of Medicine in 2025. What the dual action appears to do is create appetite suppression and metabolic change through two distinct signalling channels, which may explain why the effect is stronger at comparable doses. The NHS medicines page on tirzepatide describes the mechanism clearly for anyone who wants the patient-level summary.
Understanding the mechanism matters because it shapes realistic expectations. This isn't a stimulant. It doesn't speed up your metabolism in the way some people imagine. It changes the hormonal signals that drive hunger and fullness, and does so through two separate routes at once.
Each weekly injection maintains a sustained level of the peptide in the bloodstream for around seven days. During that window, tirzepatide slows gastric emptying, food moves through the stomach more slowly, so fullness lasts longer. It also acts on receptors in the brain involved in appetite regulation, reducing the drive to eat beyond energy needs. The GIP component adds influence over fat-cell metabolism and insulin release in ways that remain an active area of research.
The practical result, for many people, is that the relationship with food changes. Portion sizes that once felt insufficient begin to feel adequate. The impulse to snack between meals quietens. This isn't willpower, it's the peptide altering the hormonal context in which food decisions happen. That reframing is something our prescribers at nume find patients find genuinely useful: understanding that the medicine is changing the biological signal, not just asking you to try harder.
Treatment starts at 2.5mg, a dose chosen for tolerability rather than effect. The prescriber titrates upward, typically in four-week steps, to find the dose that balances benefit and tolerability for each individual. Dosing decisions stay with the prescriber throughout, the SmPC and your Patient Information Leaflet carry the full detail. You can read more about what tirzepatide as a peptide compound means structurally if the science interests you further.
The UK licence for tirzepatide as a weight-management medicine covers adults with a BMI of 30 or above, or 27 and above if at least one weight-related condition is present, for example, high blood pressure, type 2 diabetes, high cholesterol or obstructive sleep apnoea. Lower BMI thresholds apply for some ethnic backgrounds under UK guidance. BMI alone doesn't determine suitability; a prescriber considers the full picture, including any conditions that might make tirzepatide unsuitable.
NICE's appraisal of tirzepatide (TA1026, published in December 2024) sets out the NHS eligibility criteria, which are narrower than the licensed criteria and phased by comorbidity count. Private routes, like the consultation service at Mounjaro through nume, follow the licensed criteria with a full clinical assessment. The peptide benefits are the same either way; what differs is the access pathway. People who don't meet the current NHS thresholds, or who prefer not to wait, sometimes use a regulated private service instead.
Tirzepatide is not licensed for people under 18, and it isn't recommended during pregnancy, breastfeeding, or for anyone actively trying to conceive. Certain conditions (including a personal or family history of medullary thyroid carcinoma) require prescriber discussion before it's considered. These aren't caveats to skip past; they're part of why a clinical assessment exists. If you're weighing the broader benefits of Mounjaro against your own health profile, a consultation is where that conversation belongs.
The most frequently reported effects are gastrointestinal: nausea, loose stools, constipation, indigestion and occasional vomiting. These tend to be most noticeable in the first few weeks or after a dose increase, and they often ease as the body adjusts. They're not trivial for everyone, but they're also not a sign that something has gone wrong, they reflect the medicine doing what it's designed to do in the gut.
A small number of people experience more significant reactions. Acute pancreatitis is a known but infrequent risk; the MHRA highlighted this in a Drug Safety Update in January 2026, advising that severe stomach pain (particularly pain that spreads toward the back) warrants prompt medical attention. Other signs to act on quickly include symptoms of a serious allergic reaction, gallbladder discomfort or significant dehydration from persistent vomiting or diarrhoea. The MHRA's Yellow Card scheme allows anyone to report suspected side effects, and it's worth knowing that route exists. The fuller picture of what to watch for, and when to contact a doctor, is on the GLP-1 and tirzepatide page. If you're curious about lower-dose approaches, the microdosing discussion covers that angle separately.
For anyone weighing up whether to take the first step, the free consultation at nume is reviewed the same day by a named, GPhC-registered prescriber. No algorithm makes the call. You can also browse the FAQs if you have questions before you start.
The people
Superintendent Pharmacist (GPhC No. 2217101)
Accountable for the safe running of our registered pharmacy, from every dispensing check to every dispatch.
Clinical Lead (GPhC No. 2231744)
Sets our clinical standards and checks everything we publish against current MHRA guidance.
Independent Prescriber (GPhC No. 2084501)
Personally reviews consultations and assesses whether treatment is clinically appropriate, and leads dose adjustments and follow-up checks.
Independent Prescriber (GPhC No. 2083426)
Personally reviews consultations and assesses whether treatment is clinically appropriate, and leads dose adjustments and follow-up checks.