Mounjaro®
Starting from £179.99/mo
Start journey Learn moreMoving up to 5mg Mounjaro is the first scheduled dose increase in the licensed treatment plan — it follows four weeks at 2.5mg and marks the point where tirzepatide begins working at a genuinely therapeutic level. The 2.5mg starting dose exists to let your body adapt; 5mg is where the clinical programme starts in earnest. According to the SmPC published on the Electronic Medicines Compendium, titration happens in approximately four-week steps, and the prescriber decides whether the increase is appropriate for you based on how you've tolerated the starter dose. These are prescription-only medicines, so every dose change requires clinical sign-off — not just a request.
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The SURMOUNT-1 study (published in the New England Journal of Medicine and the evidence base behind NICE's appraisal of tirzepatide) built titration into its methodology from the start. Participants didn't begin at a maintenance dose; they stepped up at regular intervals, with the lower early doses specifically designed to give the body time to adjust to tirzepatide's dual action on GIP and GLP-1 receptors. The 2.5mg pen is essentially a settling-in period. Some people feel a noticeable drop in appetite even at that stage; others feel very little. Either is normal. The 5mg dose is where the licensed schedule begins to deliver consistent appetite regulation and the slowing of gastric emptying that underpins the weight-management effect. That's why Mounjaro 5mg is sometimes described as the true starting point, even though it comes second in the schedule.
If you found the first four weeks straightforward (manageable side effects, no significant nausea) your prescriber will typically confirm the step up. If you had a rougher start, they may recommend staying at 2.5mg a little longer. That call is clinical, not administrative.
At 5mg, most people begin to notice a more consistent reduction in hunger between meals and a lower appetite overall. The hormone signals that tell your brain you've eaten enough start to register more reliably. For many patients this is also where gastrointestinal effects reassert themselves briefly, the pattern after moving from 2.5mg to 5mg often mirrors the first week at 2.5mg, with nausea or looser stools possible in the days following injection. This is a recognised feature of dose titration, not a sign something has gone wrong. It's worth being honest: the step-up can feel like going back to square one for a week. Most people find it settles faster the second time.
Practical strategies that consistently help include injecting in the evening so peak nausea (if it arrives) happens during sleep, eating smaller meals rather than forcing normal portions, staying hydrated, and leaning on protein-rich foods to protect lean mass. Your prescriber's guidance and the Patient Information Leaflet should be your first reference for managing specific symptoms, not general online advice, which varies in quality considerably.
The NHS tirzepatide patient information page lists the common side effects across the treatment programme, which helps set realistic expectations before any increase.
A question the clinical team at nume hears regularly: do I just move up automatically after four weeks? The answer is no. The four-week interval is a minimum, not a trigger. What matters is whether your tolerance at 2.5mg has been acceptable. Persistent significant nausea, frequent vomiting, or other poorly managed side effects are reasons to pause the increase and review, not override it. Conversely, if you've had no side effects at all and appetite suppression has been minimal, your prescriber may want to confirm your tolerance is genuine before stepping up.
At Mounjaro's higher doses, the weight-loss results in trials were substantially greater than at 5mg alone, the full SURMOUNT programme points to cumulative benefit across the titration schedule. That context matters: there's no shortcut through the earlier steps that reliably improves outcomes. The schedule exists because the data supports it. For anyone thinking about the longer journey, our guide to going from 5mg to 7.5mg Mounjaro explains what that next clinical step involves, and the same review logic applies there too.
If you're considering treatment and want to understand how the consultation process works, or if you're already on treatment and have questions about your next increase, a prescriber review is the right place to start, not a forum, and not a general dose guide.
It helps to see 5mg not as a destination but as confirmation that the programme is under way. The SURMOUNT-1 data showed that meaningful weight reduction builds across the titration schedule, with the largest effects at 10mg and 15mg over 72 weeks. Reaching 5mg successfully (tolerating it and beginning to see appetite change) is the first real clinical checkpoint. Some patients do plateau at 5mg or 7.5mg and find those doses sufficient; others need to continue stepping up to see the results the trials reported at higher levels, and our guide to going up to 7.5mg Mounjaro covers what that progression typically involves. That's a clinical conversation, and it depends on individual response, not a preset plan.
For context on how cost works across the different dose pens (something people reasonably want to understand before committing) the weight-loss treatment overview sets out how private treatment is structured and what the transparent price covers. Understanding the concept of the maintenance dose can also help frame what the titration schedule is ultimately working towards.
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.