Mounjaro®
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Start journey Learn moreTirzepatide has been through one of the most extensive regulatory assessments of any weight-loss medicine in recent UK history, and the short answer is: for most eligible adults, taking it under clinical supervision is considered safe. The MHRA licensed it for weight management after reviewing substantial trial data, and NICE's appraisal of tirzepatide (TA1026) concluded the benefit-risk balance supports its use in adults with obesity or excess weight alongside certain health conditions. That does not mean risk-free — no medicine is — and honest safety education matters more than reassurance for its own sake. Tirzepatide is a prescription-only medicine, which means a prescriber assesses whether it is right for you personally before any treatment begins.
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The SURMOUNT clinical programme enrolled thousands of adults with obesity or overweight, and the tolerability data from those trials forms the basis of what regulators now know about tirzepatide's safety in this population. In SURMOUNT-1, the most common reason participants reduced or paused their dose was gastrointestinal discomfort, not any serious organ-level problem. The NHS medicines page for tirzepatide lists the typical side effects as nausea, vomiting, diarrhoea, constipation, indigestion, burping, fatigue, and headache, a list that looks alarming in print but, in practice, most people experience only some of these, usually mildly and mostly in the early weeks. The medicine slows gastric emptying as part of how it works, and that mechanism is largely responsible for the gut-related symptoms. Starting at 2.5mg (the lowest strength) gives your digestive system time to adjust before the dose moves upward, which is precisely why that graduated approach exists. One misconception worth setting aside gently: many people assume that because tirzepatide is a newer medicine, the safety record is thin. In fact, if you are weighing up whether tirzepatide is safe, it helps to know that it was studied across the SURPASS diabetes trials and the SURMOUNT weight-management programme combined, involving well over ten thousand participants, giving regulators a substantial evidence base before the UK licence was granted.
Balanced safety education means naming rarer but more serious concerns clearly. On 29 January 2026, the MHRA issued a Drug Safety Update for GLP-1 receptor agonist medicines highlighting acute pancreatitis: a rare, potentially serious condition whose warning signs include severe stomach pain that persists and may radiate toward the back, sometimes accompanied by vomiting. If you experience that symptom pattern, seek urgent medical help and tell the clinician which medicine you are taking. Separately, gallbladder problems have been reported with this drug class. People who become significantly dehydrated through repeated vomiting or diarrhoea face a secondary risk of kidney strain, so staying hydrated matters and persistent symptoms should prompt contact with your prescriber. Allergic reactions are uncommon but possible; signs include swelling, rash, or difficulty breathing. People with a personal or family history of medullary thyroid carcinoma or multiple endocrine neoplasia type 2 should not take tirzepatide, and those with a history of pancreatitis should discuss this with a prescriber before starting. These are also reasons why tirzepatide is prescription-only: the prescriber's job, at every stage, is to weigh your individual picture against these known risks, and our page on whether tirzepatide is safe to use explores how that clinical judgement works in practice. Our clinical team at nume reviews every consultation with this in mind.
The trial populations that generated this evidence were adults, predominantly without active severe GI disease, not pregnant, and not breastfeeding. Tirzepatide is not licensed for anyone under 18, and it is not recommended during pregnancy or breastfeeding, or for those actively trying to conceive, if your circumstances change while on treatment, contact your prescriber promptly. Oral contraceptive absorption may be reduced during the first four weeks of tirzepatide and for four weeks after each dose increase, because the medicine slows how quickly the gut processes things; NHS England's guidance on weight-management injections recommends adding a barrier method during those windows. If you take HRT in tablet form, your prescriber may suggest switching to a transdermal option for the same reason. Always tell any healthcare professional (including an anaesthetist before surgery) that you are taking tirzepatide. These are not reasons to avoid the medicine; they are reasons to take it with proper clinical oversight, which is the only setting in which it should be used. You can read more about the broader safety question from a slightly different angle on our page covering whether tirzepatide is safe to take.
Most people taking tirzepatide do not experience a medical emergency. But knowing when to act quickly matters. Seek same-day or emergency medical help if you develop: severe stomach pain lasting more than a few hours, especially if it reaches into your back; signs of a serious allergic reaction such as swelling around the face or throat; sudden, significant changes in vision; or symptoms of severe dehydration such as dizziness, very dark urine, or inability to keep any fluids down. Contact your prescriber or GP (rather than waiting) for persistent vomiting that lasts more than two or three days, any mood changes or thoughts of self-harm, or injection-site reactions that worsen rather than settle. For less urgent questions about how the medicine is affecting you day to day, our aftercare team is available seven days a week. If you suspect you have experienced a side effect, reporting it to the MHRA through the Yellow Card scheme helps build the ongoing safety record for tirzepatide in the UK population, patient reports genuinely matter to that process. For a fuller breakdown of individual side effects and how common each one is, the detailed tirzepatide side-effects page covers this systematically. Our prescribers discuss suitability and the full side-effect picture as a normal part of the consultation, and if you are also considering Mounjaro specifically, our page on Mounjaro side effects and our guide to whether taking Mounjaro is safe are worth reading alongside this one. Start your free consultation to have that conversation with a real clinician.
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.