Mounjaro®
Starting from £179.99/mo
Start journey Learn moreMost people notice changes on Mounjaro within the first two to four weeks, though meaningful weight progress typically builds over several months as the dose increases. Results vary by individual (clinical trials reported average reductions of around 20–21% of body weight at the highest dose over 72 weeks) and the pattern of progress is rarely a straight line. Mounjaro is a prescription-only medicine; a GPhC-registered prescriber assesses whether it is right for you before any treatment begins.
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The 2.5mg starting dose has one job: getting your body accustomed to tirzepatide without overwhelming it. It is the settling-in dose, not the dose that drives the headline results you may have read about. For most people, the most noticeable shift in the early weeks is appetite, meals feel more satisfying, the pull towards snacking fades, and portion sizes shrink naturally.
Weight change at this stage is real but modest. That is by design. The SURMOUNT-1 trial (which followed 2,539 adults with obesity across 72 weeks) showed that the steeper losses came as doses increased, not from the starting pen alone. A question our prescribers hear most weeks at this stage is whether something has gone wrong because the scale has barely moved. It hasn't. The biology is still shifting.
Gastrointestinal effects such as nausea or loose stools are most common in this first month, particularly in the days after an injection. They tend to ease as the body adapts. If they feel unmanageable, the right move is to contact your prescribing team rather than skip doses, dropping a dose unilaterally can disrupt the whole titration schedule. The Mounjaro overview covers the full picture of what the medicine is and how it works, and if you're sourcing your treatment through us, the Mounjaro MediExpress page explains how that process works in practice.
At each four-weekly titration step) 2.5mg to 5mg, then 7.5mg if clinically appropriate, appetite suppression deepens noticeably. Most people find months two through four feel meaningfully different from the first few weeks. Energy improves as food noise quiets. The weight change on the scale becomes more consistent.
Progress still varies. Factors that shape this phase include how closely a reduced-calorie diet is maintained, activity levels, sleep quality, and individual metabolic differences. Tirzepatide activates both GLP-1 and GIP receptors (a dual mechanism that no other licensed UK weight-loss injection shares) and the GIP pathway in particular influences fat tissue directly, not only through appetite. The tirzepatide page covers the mechanism in more detail.
Keeping a simple record during this phase pays off: weekly weigh-ins at the same time of day, photos if you find them useful, and notes on hunger and energy. These data points matter clinically. A prescriber reviewing your repeat will want to see that progress is happening at the appropriate rate for your current dose. That clinical re-review happens before every repeat at nume, no automatic renewals, no skipped checks.
By month five most people on optimised doses are well into consistent loss, but plateaus still happen. They are a normal feature of weight physiology, not a sign that the medicine has stopped working. The body defends its set point; even with effective treatment, there are weeks where the scale stalls before moving again.
The SURMOUNT-1 data, published in the New England Journal of Medicine, show that weight loss continued to accumulate throughout the 72-week trial at the higher doses. The steepest rate of loss was not the last word, sustained effort compounds over time. Protein intake, resistance exercise and adequate hydration all help preserve muscle during this phase, which matters for long-term metabolic health.
It is also worth understanding what your personal target looks like. NICE's appraisal of tirzepatide (TA1026) recommends reviewing continuation if less than 5% weight loss has occurred after six months at the highest tolerated dose, a clinically grounded benchmark. A prescriber can discuss whether your trajectory is on track. If you're thinking about what the treatment costs relative to the value it delivers, the Mounjaro cost page sets out the honest picture.
Weight is the metric most people focus on, and it matters. But progress on Mounjaro often shows up elsewhere first: blood pressure improving, HbA1c coming down in those with prediabetes, sleep becoming less disrupted in people with obstructive sleep apnoea. These are not side benefits, they are part of why the medicine is licensed in the first place.
Tracking non-scale markers helps sustain motivation during the weeks the scale is stubborn. Clothing fit, resting heart rate, how far you walk without fatigue, these shifts are real data. If you take oral contraception, it is worth knowing that tirzepatide's slowing effect on gastric emptying can reduce pill absorption in the first four weeks of treatment and after each dose increase; using a non-oral backup during those windows is recommended. The progesterone-only pill page and the broader progesterone page cover the detail.
Progress also means staying safe. Severe or persistent stomach pain that radiates to the back needs prompt medical attention, the MHRA highlighted acute pancreatitis as a recognised, if infrequent, risk in its January 2026 Drug Safety Update for GLP-1 medicines. For questions about your individual trajectory, or if you're considering starting, speak to our prescribers, a clinician, not a form, reviews every consultation the same day it arrives.
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.