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Start journey Learn moreUsing expired Wegovy is not recommended. The expiry date on a Wegovy pen is the manufacturer's guarantee that the semaglutide inside meets its full potency and safety specification up to that point — not a day beyond. Once a pen is past its date, you may be injecting a degraded medicine, with unknown effectiveness and unpredictable risk. If you have a pen that has passed its printed date, the practical answer is: do not use it. Semaglutide is a prescription-only medicine; your prescriber or pharmacist is the right person to advise on your next step.
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Pharmaceutical expiry dates are not conservative guesses. They reflect the end-point of rigorous real-time and accelerated stability testing carried out under controlled temperature and humidity conditions. For Wegovy, Novo Nordisk's stability programme demonstrated that semaglutide retains its potency and purity up to the printed date when stored correctly. Beyond that point, the data simply stops, which is the problem. The degradation of a GLP-1 peptide like semaglutide is not a cliff-edge moment; it is a gradual process of chemical breakdown. But without post-date stability data, nobody can tell you how fast that process is running in your specific pen.
What we do know is that semaglutide is sensitive to both temperature and light. A pen that has also been stored incorrectly (left out of the fridge for longer than the Patient Information Leaflet permits, for instance) will degrade faster still. The result of injecting a meaningfully degraded solution could range from reduced therapeutic effect (so you get less appetite suppression than expected) to unpredictable reactions. Neither outcome is worth the risk, especially when you are using a medicine to actively manage your weight under clinical oversight.
For a fuller look at what happens inside a pen that is past its date, our page on what happens if you take expired semaglutide covers the degradation mechanism in more detail. The NHS semaglutide medicine guide also notes that storage and handling instructions should be followed precisely at all times.
A question our prescribers hear most weeks, particularly from patients who have missed a dose and discovered an old pen at the back of the fridge: is it actually dangerous, or just ineffective? The honest answer is that the risk profile is genuinely uncertain, and that uncertainty itself is clinically significant.
On the mild end, the peptide may simply be too degraded to produce meaningful GLP-1 receptor activation, so you lose a week of treatment without benefit. On the more serious end, protein degradation in injectable medicines can produce immunogenic fragments, molecules that trigger an immune response. This is not specific to semaglutide; it is a general principle of injectable biologics, and one reason why expiry dates on injectables are treated with greater seriousness than expiry dates on many oral medicines.
There is also a practical point about injection safety. If degradation has affected the pen's solution in ways that are not visible to the naked eye, you have no reliable way to detect it. Clear does not mean intact. Our overview of expired semaglutide side effects covers what has been reported when patients have administered out-of-date pens.
If you are managing your treatment through a regulated service and have concerns about a specific pen, the safest route is to contact your prescriber before injecting. At nume, the clinical team is reachable seven days a week specifically for situations like this.
An expired pen should go into a sharps disposal container, not a household bin. The needle remains hazardous regardless of whether the pen was used, and the Wegovy cartridge contains a residual biological product that needs appropriate containment. A 1-litre sharps container meets standard UK household requirements. Full pens go in whole; do not attempt to disassemble, and if you are unsure how the pen works before disposal, our guide on splitting a Wegovy pen explains the device mechanics in useful detail. Once the container is full, your local authority or pharmacy will accept it for disposal.
The more pressing question after discarding the pen is what to do about the missed dose. Missing a single injection is not a catastrophe, but the timing of your next dose matters. The Wegovy treatment guide has practical detail on the licensed schedule, but the specific decision (whether to inject on the original day, shift the schedule, or skip entirely) should come from your prescriber, not a general article. That is especially true if you are partway through a titration.
Replacing the pen itself depends on where you obtain your treatment. If you are on a private prescription through an online pharmacy, check whether same-day dispatch is available for your current dose. The guide to sourcing Wegovy in the UK explains legitimate supply routes, including what to look for when verifying a pharmacy on the GPhC register. One thing worth knowing: a legitimate UK pharmacy will never supply Wegovy (a prescription-only medicine) without a valid, current prescription issued following a clinical assessment. If you see a service offering pens without that process, treat it as a warning sign.
For context on how refrigeration conditions affect shelf life in the first place, does Wegovy expire in the fridge covers storage requirements and what happens when cold chain is disrupted. And if you are reviewing whether your current treatment is working as expected, our overview of weight-loss treatment options gives a broader picture of what regulated private treatment looks like.
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.