Mounjaro®
Starting from £179.99/mo
Start journey Learn moreMounjaro pens are labelled with letters (Y, G, R, P and others) that identify the dose strength inside each KwikPen. The Y on your Mounjaro pen simply marks the 2.5 mg starter strength, the first pen in the licensed titration schedule. It is a prescription-only medicine, so a clinical assessment by a qualified prescriber comes before any treatment begins. Here is how that labelling system works in practice, and why it matters.
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Eli Lilly designed the Mounjaro KwikPen range with a colour-and-letter system so that patients and pharmacists can distinguish doses at a glance without relying on reading fine print. Y is the letter assigned to the 2.5 mg strength. Each pen contains four weekly doses, so one Y pen covers the first four weeks of treatment.
The letter does not tell you anything about efficacy on its own. It is simply a packaging identifier, the same way a traffic light uses colour as a quick reference. If you have ever wondered why your pen does not read "2.5 mg" on the front in large text, the letter system is the reason: it keeps dose selection deliberate and prescriber-led rather than something a patient self-selects by scanning a number.
A practical habit worth building: before every injection, read the letter on the pen label and cross-check it against your prescription or the instructions your prescriber gave you. That takes under a minute and is one of the simplest ways to catch a dispensing mix-up before it happens. The full Mounjaro overview has a complete breakdown of all pen strengths and their corresponding letters.
Tirzepatide's most common side effects are gastrointestinal, nausea, loose stools, indigestion, that heavy feeling after small meals. Starting at 2.5 mg keeps those effects manageable while your gut adapts to a medicine that slows how quickly food leaves your stomach and changes hunger signalling in the brain.
Clinical trials published in the New England Journal of Medicine (SURMOUNT-1) showed average body-weight reductions of around 20–21% at the 15 mg maintenance dose over 72 weeks, but participants spent weeks at lower doses first. The Y pen is the foundation that makes those outcomes achievable without unnecessary early dropout.
This is also why the dose is not titrated upward the moment it feels tolerable: prescribers typically hold each strength for around four weeks before considering an increase. Your body's response at 2.5 mg genuinely informs what the prescriber recommends next, and our Mounjaro 2 page goes into further detail about what to expect during those first weeks at this starting strength. For context on how the 5 mg step follows, the Mounjaro 5 mg page explains what that transition looks like.
After the Y pen, the licensed UK strengths continue through 5, 7.5, 10, 12.5 and 15 mg, each with its own pen letter. Titration is guided by the prescriber based on how well each dose is tolerated and whether weight loss is progressing as expected. There is no fixed schedule that applies to everyone; the prescriber reads the whole clinical picture.
NICE's appraisal of tirzepatide (TA1026) notes that continuing treatment is reviewed if less than 5% weight loss has occurred after six months at the highest tolerated dose. That review is a clinical conversation, not an automatic stop, which is why having an accessible prescriber matters throughout, not just at the start.
If you are thinking about what private treatment involves in terms of cost, the Mounjaro cost context page covers UK pricing honestly, including what a legitimate prescription-inclusive price should contain. And if you want to understand tirzepatide's mechanism more deeply before starting, the tirzepatide information page goes into how the dual-agonist pathway differs from a standard GLP-1 medicine.
Mounjaro is a Prescription-Only Medicine. Every step of the titration (starting at Y, moving up, pausing, switching) requires a prescriber's assessment. This is not bureaucracy for its own sake: dose changes carry real physiological effects, and the prescriber's review before each repeat is the mechanism that catches problems early.
At nume, a GPhC-registered Independent Prescriber reads every consultation personally. No automated approval system makes that call. The clinical team page gives more detail about how clinical oversight is structured. Transfer patients who are already established on a dose (including the Y pen) provide evidence of current treatment so the prescriber can review the full picture before continuing, and if you are exploring how our electronic prescribing process works you can find a full explanation on the e-Mounjaro page.
Patients can also report any unexpected reactions through the MHRA's Yellow Card scheme, which is open to patients directly, not just healthcare professionals. If you have questions about the process before starting, our FAQs cover the most common ones, and the team is reachable via the contact page if something needs a direct answer.
When you feel ready to talk it through with a prescriber, you can start a free consultation and have your answers reviewed 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.