Mounjaro®
Starting from £179.99/mo
Start journey Learn moreMounjaro (tirzepatide) follows a structured dosage schedule for weight loss, starting at 2.5 mg once weekly and rising in steps — typically every four weeks — up to a maximum of 15 mg. That graduated approach is not arbitrary: the SURMOUNT-1 trial, published in the New England Journal of Medicine, showed that adults on tirzepatide at the highest dose achieved an average body-weight reduction of around 20–21% over 72 weeks. Mounjaro is a prescription-only medicine, and a prescriber decides which dose is right for you, based on how your body responds and your individual health picture. The schedule below reflects the licensed UK framework, not a self-dosing guide.
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The standard Mounjaro titration runs through six strengths: 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg and 15 mg. Patients begin at 2.5 mg for the first four weeks. This is a tolerability dose, its purpose is to let your digestive system adapt to tirzepatide's mechanism (slowing gastric emptying, reducing appetite through dual GIP and GLP-1 receptor activity) before the dose climbs. Expecting meaningful weight loss during the first pen is one of the most common misconceptions people bring to their first consultation, and it is worth letting that expectation go early.
After four weeks, a prescriber will typically move the dose to 5 mg, then onward in similar four-weekly steps toward the highest dose the patient tolerates well. The NHS medicines page for tirzepatide confirms this schedule and notes that 15 mg is the maximum licensed dose. Reaching it is not mandatory, some people find an intermediate dose gives them adequate results with better tolerability, and the prescriber's job is to find that balance.
Every dose step should be guided by a clinician. Skipping steps or self-adjusting timing is not safe practice. If you are considering starting or reviewing your Mounjaro injection dosage, that conversation starts with a qualified prescriber, not an online calculator.
The SURMOUNT-1 trial is the foundational evidence base for Mounjaro's weight-loss dosage. Over 72 weeks, adults with obesity who received tirzepatide at 15 mg lost an average of around 20–21% of their body weight, some analyses put the figure closer to 22.5% in certain participant subgroups. Results at 10 mg and 12.5 mg were also substantial, though slightly lower on average. This dose-response relationship is why prescribers aim to reach the highest dose a patient tolerates: the evidence consistently shows more average loss at higher strengths.
That said, averages conceal real variation. Some people respond well at 7.5 mg; others need the full 15 mg and still see more modest results. The NICE appraisal of tirzepatide (Technology Appraisal TA1026) built this variability into its guidance, noting that continuing treatment at the highest tolerated dose should be reviewed if less than 5% weight loss has been achieved after six months.
These figures come from controlled clinical trials alongside reduced-calorie diet and increased physical activity. Treatment alone, without those lifestyle elements, is unlikely to replicate trial outcomes. You can read more about tirzepatide's evidence base on our Mounjaro overview page.
Dose increases in clinical practice are not automatic. A prescriber looks at how you are tolerating the current pen before recommending the next strength. Persistent nausea, vomiting or significant gastrointestinal discomfort at 5 mg, for instance, would normally prompt a longer stay at that level rather than an immediate move to 7.5 mg. Rushing titration tends to worsen side effects and can lead people to stop treatment prematurely.
At nume, every repeat order receives a fresh clinical review before dispatch. That means a GPhC-registered prescriber reads your check-in responses before authorising a dose increase, a real clinician considers your update, not an automated system. If you have questions about how titration decisions are made, our FAQs cover the most common ones, and you can always reach the team through aftercare support.
For anyone weighing up how the different strengths compare in terms of expected outcomes, our dosage and weight-loss outcomes guide goes into detail on what the data shows at each level. A closer look at the 5 mg pen specifically is useful if you are approaching your first dose increase and want to know what to expect. Private treatment prices (which vary by dose) are covered honestly on our Mounjaro prices page.
Mounjaro is injected once weekly, subcutaneously, into the abdomen, thigh or upper arm. Sites should be rotated. Each KwikPen contains four doses, so one pen lasts the month. Storage is refrigerated at 2–8°C; there is a limited window during which the pen can be kept at room temperature, but for the exact duration always refer to the Patient Information Leaflet inside the pack rather than any third-party summary, that detail can vary by formulation and the leaflet is authoritative.
Missed doses and what to do about them are a question our prescribers hear regularly. The consistent clinical advice is to follow the guidance in the Patient Information Leaflet and, if in doubt, contact your prescriber. Decisions about catching up or adjusting timing should not come from a forum or a search result. If you have recently transferred to Mounjaro and want to understand how the tirzepatide injection dosage compares with other formulations, a detailed guide to tirzepatide dosage may help. Ready to discuss your suitability? Start your free consultation and a prescriber will review your answers the same day.
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.