Mounjaro®
Starting from £179.99/mo
Start journey Learn moreIn clinical trials, adults taking tirzepatide (Mounjaro) at the highest dose lost an average of around 20–21% of their body weight over 72 weeks, compared with roughly 3% on placebo. That is the headline figure from SURMOUNT-1, the landmark trial published in the New England Journal of Medicine involving 2,539 adults with obesity and no diabetes. For many people, the before-and-after difference represented the most significant sustained weight change of their adult lives. Mounjaro is a prescription-only medicine, so what any individual experiences depends on their clinical profile, starting weight and how well the treatment is tolerated — a prescriber, not a trial average, is the right person to set expectations for you personally.
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The question behind every "before and after" search is a fair one: what can this treatment realistically do? SURMOUNT-1 gives the most rigorous answer available. Over 72 weeks, participants who reached the 15mg maintenance dose lost an average of around 20–21% of their body weight. At 10mg the average was around 19.5%, and at 5mg approximately 15%. The placebo group, also following lifestyle guidance, lost roughly 3%.
Those are averages. The distribution matters. Some participants lost considerably more; some lost less. A handful responded minimally. No published data can tell you in advance which group you will fall into, which is one reason NICE guidance includes a review point at six months: if weight loss is under 5% at the highest tolerated dose, continuing is assessed afresh.
What the trial did not measure, because it cannot, is the before-and-after that patients describe as qualitative: how food noise quietens, how the relationship with eating shifts, how clothes fit differently before the scale moves much at all. Those experiences are reported consistently but are individual. They are not clinical claims.
If you want a sense of the broader tirzepatide evidence base, the SURMOUNT programme also covered people with type 2 diabetes, cardiovascular risk and sleep apnoea, showing effects beyond weight alone.
The trajectory matters as much as the end point. Treatment starts at 2.5mg, a dose calibrated to help your system adjust rather than to produce rapid loss. Most people notice the appetite shift before they notice much on the scales. Nausea, if it occurs, tends to peak in the first fortnight after a dose increase and then settle.
By weeks 12–16, once titration has reached 5mg or 7.5mg for many patients, weight change tends to become more visible. The steepest phase of loss in SURMOUNT-1 occurred between months 3 and 9. After that, loss continued but more gradually, and a new set-point begins to establish.
Practically: one patient described keeping their pen in the fridge door and setting a reminder on their phone for the same day each week, consistency with injection timing matters. Whether you take your dose in the morning or evening does not affect efficacy, but picking the same window each week builds a rhythm that supports adherence.
Understanding what to expect in the weeks immediately after starting helps too. How quickly the appetite effect arrives after the first injection is one of the most common questions our prescribers hear.
"Before and after" on tirzepatide is not just a number on a scale. SURMOUNT-1 participants showed measurable reductions in waist circumference (an average of around 14–18 cm across dose groups), improvements in blood pressure, and meaningful changes in fasting glucose, insulin resistance and lipid profiles. These cardiometabolic shifts are part of why NICE recommended the medicine for weight management in adults with a qualifying weight-related condition, not simply as a cosmetic intervention.
The NICE appraisal of tirzepatide (TA1026) notes that the clinical-trial results represent a step change from earlier weight-management medicines. SURMOUNT-5 (a head-to-head trial published in the New England Journal of Medicine in 2025) found greater average weight loss with tirzepatide than with semaglutide 2.4mg (Wegovy) over 72 weeks, though both produced clinically significant outcomes.
Side effects are part of the before-and-after story too. The gastrointestinal profile (nausea, loose stools, reduced appetite) is real and predictable. Serious effects are less common but include pancreatitis, gallbladder issues and, in people with diabetes, hypoglycaemia when combined with insulin. There are practical things that help manage tolerability during the early weeks. And knowing what to watch for matters: report anything unexpected to your prescriber, and use the Yellow Card service at yellowcard.mhra.gov.uk for any suspected side effects.
Trial averages describe a population, not a person. Your before-and-after will depend on your starting BMI, whether you have conditions such as type 2 diabetes or insulin resistance, how your body tolerates titration, and how closely treatment is combined with changes to diet and activity. Mounjaro's licence covers adults with a BMI of 30 or above, or 27 or above alongside at least one weight-related health condition. Lower BMI thresholds apply for some ethnic backgrounds under UK guidance.
The honest truth is that the tirzepatide before-and-after evidence is among the strongest in the history of pharmaceutical weight management. It is also not a guarantee. Knowing what to do before taking Mounjaro is an important part of that review, covering the health checks and disclosures that help a prescriber match the treatment to your circumstances safely.
If you are weighing up private treatment costs alongside what the NHS offers, the Mounjaro price comparison page sets out the UK private market context clearly. What is important is that any route you take involves genuine clinical oversight. That is the part the trial data never varies on: all SURMOUNT participants were under close medical supervision throughout.
Ready to talk to a prescriber about whether Mounjaro is right for you? Check your eligibility with our free consultation, reviewed the same day by a real clinician, not a bot.
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.