Tirzepatide · Dose evidence · updated 8 October 2026
Tirzepatide dosage: what studies actually used
The short answer
The Zepbound label starts tirzepatide at 2.5 mg once a week for 4 weeks, then raises it in 2.5 mg steps at least 4 weeks apart to a maintenance dose of 5, 10 or 15 mg a week; 15 mg is the maximum4. The large trials behind the label used the same 5 to 15 mg weekly range56. This page reports those doses and is not dosing advice. Vials sold online as tirzepatide are another matter: as of 30 September 2026, 59 of Finnrick’s latest 196 completed tests failed7.
Not dosing advice. This page reports doses that studies and approved labels used, with their sources. It does not recommend a dose, and we do not give mixing, injection or unit-conversion instructions. Gray-market vials often do not contain what their label says. How we report doses.
Every dose studied in people
| Study | Who | People | Dose and route | What happened |
|---|---|---|---|---|
| SURPASS-CVOT (Nicholls 2025), randomized trial | Adults with type 2 diabetes and heart or blood-vessel disease | 13,299 | Up to 15 mg once a week, versus dulaglutide 1.5 mg Injection under the skin · Median follow-up 210.1 weeks (about 4 years) |
Heart attack, stroke or cardiovascular death in 12.2% versus 13.1% on dulaglutide, an older GLP-1 drug: as good as, but not shown to be better89. |
| SURMOUNT-1 (Jastreboff 2022), randomized trial | Adults with obesity, or overweight with a weight-related condition, without diabetes | 2,539 | 5, 10 or 15 mg once a week Injection under the skin · 72 weeks, including 20 weeks of dose increases |
Weight fell 15.0%, 19.5% and 20.9% on 5, 10 and 15 mg, versus 3.1% on placebo; 4.3%, 7.1% and 6.2% stopped because of side effects, versus 2.6%5. |
| SURPASS-2 (Frías 2021), open-label randomized trial | Adults with type 2 diabetes | 1,879 | 5, 10 or 15 mg once a week, versus semaglutide 1 mg Injection under the skin · 40 weeks |
HbA1c, a measure of average blood sugar, fell 2.01, 2.24 and 2.30 percentage points, versus 1.86 on semaglutide; nausea affected 17% to 22%, versus 18%1. |
| SURMOUNT-2 (Garvey 2023), randomized trial | Adults with obesity or overweight and type 2 diabetes | 938 | 10 or 15 mg once a week Injection under the skin · 72 weeks |
Weight fell 12.8% and 14.7%, versus 3.2% on placebo; digestive side effects were mostly mild to moderate, and few led people to stop (under 5%)2. |
| SURMOUNT-5 (Aronne 2025), open-label randomized trial | Adults with obesity, without type 2 diabetes | 751 | Highest tolerated dose, 10 or 15 mg once a week, versus semaglutide 1.7 or 2.4 mg Injection under the skin · 72 weeks |
Weight fell 20.2% on tirzepatide versus 13.7% on semaglutide; digestive side effects came mainly while the dose was being raised10. |
| SUMMIT (Packer 2025), randomized trial | Adults with obesity and heart failure with preserved ejection fraction | 731 | Up to 15 mg once a week Injection under the skin · At least 52 weeks; median follow-up 104 weeks |
Cardiovascular death or worsening heart failure in 9.9% versus 15.3% on placebo; 6.3% versus 1.4% stopped because of side effects11. |
| SURMOUNT-4 (Aronne 2024), randomized withdrawal trial | Adults with obesity or overweight, without diabetes, after a 36-week lead-in on tirzepatide | 670 | Highest tolerated dose, 10 or 15 mg once a week, or a switch to placebo Injection under the skin · 36-week lead-in, then 52 weeks |
Weight fell a further 5.5% on tirzepatide and rose 14.0% after the switch to placebo12. |
| SURMOUNT-OSA (Malhotra 2024), two randomized trials | Adults with obesity and moderate to severe obstructive sleep apnea | 469 | Highest tolerated dose, 10 or 15 mg once a week Injection under the skin · 52 weeks |
Breathing pauses during sleep fell by 25.3 and 29.3 events an hour in the two trials, versus 5.3 and 5.5 on placebo6. |
| Phase 2 trial (Frías 2018), randomized trial | Adults with type 2 diabetes | 318 | 1, 5, 10 or 15 mg once a week, versus dulaglutide 1.5 mg or placebo Injection under the skin · 26 weeks |
HbA1c fell 1.06 to 1.94 percentage points across the doses; weight, counted only while people stayed on treatment, fell 0.9 to 11.3 kg; digestive side effects rose with dose, from 23.1% on 1 mg to 66.0% on 15 mg3. |
The approved schedule (Zepbound (FDA label))
The Zepbound label (version 40, effective 28 August 2026) sets one schedule for all its uses: weight reduction and long-term weight maintenance in adults, and moderate to severe obstructive sleep apnea in adults with obesity4. It says to raise the dose this way to reduce the risk of digestive side effects, and to consider a lower maintenance dose if one is not tolerated4.
| When | Dose on the label | Note |
|---|---|---|
| Weeks 1 to 4 | 2.5 mg once a week | Starting dose only; not approved as a maintenance dose |
| Week 5 onward | 5 mg once a week | The lowest maintenance dose |
| After at least 4 weeks on each dose | Increases of 2.5 mg: 7.5, 10, 12.5, then 15 mg once a week | Only until the chosen maintenance dose is reached |
| Maintenance, weight reduction | 5, 10 or 15 mg once a week | Chosen by response and tolerability |
| Maintenance, sleep apnea | 10 or 15 mg once a week | |
| Maximum, all uses | 15 mg once a week |
Studies, animals and users: kept apart
Doses below are what studies used or what a label says. They are not advice, and gray-market products may not contain what their label says.
In human studies
Zepbound label (weight loss and sleep apnea): start at 2.5 mg injected under the skin once weekly for 4 weeks, then increase in 2.5 mg steps, at least 4 weeks apart, until the maintenance dose is reached. Maintenance is 5, 10 or 15 mg weekly for weight (10 or 15 mg for sleep apnea); 2.5 mg is for starting only, and the maximum is 15 mg weekly4. Mounjaro label (type 2 diabetes): start at 2.5 mg weekly and increase in 2.5 mg steps after at least 4 weeks if needed; maximum 15 mg weekly in adults and 10 mg in children 10 and older14. Since 27 August 2026 the Mounjaro label allows 2.5 mg for ongoing blood sugar control15. The trials used the same range: fixed 5, 10 or 15 mg weekly in SURMOUNT-1, and the maximum tolerated dose of 10 or 15 mg, or up to 15 mg, in the sleep apnea, heart and heart-failure trials56811. Phase 1 tested single doses of 0.25 to 8 mg, 4-week courses of 0.5 to 10 mg in healthy volunteers and 0.5 to 15 mg in people with type 2 diabetes, with doses above 5 mg reached by stepping up16.
In animal studies
Rats: 0.15, 0.50 and 1.5 mg/kg injected under the skin twice weekly for 2 years; thyroid C-cell adenomas and carcinomas combined rose at all doses4. rasH2 transgenic mice: 1, 3 and 10 mg/kg twice weekly for 6 months; it did not cause tumors4. Rat fertility studies: 0.5, 1.5 and 3 mg/kg twice weekly; no effect on mating, fertility or conception, but female rats had fewer implantation sites and viable embryos at all doses, which the label attributes to lower food intake and body weight4. These are animal safety-study doses, not human doses.
What users report Anecdotal · not validated · not a recommendation
A 2026 journal commentary says “microdosing” of single- and dual-receptor GLP-1 drugs (tirzepatide is a dual agonist) is typically defined as 25% to 50% of the manufacturer’s recommended starting dose, or longer intervals between doses. It says the practice spread through patient communities, telehealth weight-loss programs and clinician anecdotes, and that high-quality evidence is essentially absent13.
Half-life and how it is taken
- Half-life
- About 5 to 6 days4Adults with overweight or obesity, including those with sleep apnea, after subcutaneous injection (Zepbound label, clinical pharmacology section); the same label’s overdose section rounds it to about 5 days. Tirzepatide is 99% bound to albumin.
- Routes
- Subcutaneous injection, once weekly (the only approved route and the route used in all trials cited here)
Why the dose goes up slowly
The label says the dose goes up in steps to reduce the risk of digestive side effects such as nausea, vomiting and diarrhea4. In the two main weight-loss trials behind the label, digestive side effects affected 56% of people on each dose versus 30% on placebo, and most nausea, vomiting and diarrhea came while the dose was being raised and eased over time4. Most people who stopped because of side effects did so in the first few months4.
Tirzepatide slows the emptying of the stomach, an effect that is largest after the first dose and fades over time4. Blood levels settle at a steady level after 4 weeks of weekly doses4. In SURMOUNT-1, the 72-week trial included a 20-week period of dose increases5.
In a 26-week phase 2 trial in type 2 diabetes, digestive side effects rose with the dose: 23.1% of people on 1 mg, 32.7% on 5 mg, 51.0% on 10 mg and 66.0% on 15 mg, versus 9.8% on placebo3. In the two weight-loss trials behind the label, stopping for digestive side effects rose with the dose even though the side effects were equally common4. It went from 1.9% of people on 5 mg to 3.3% on 10 mg and 4.3% on 15 mg, versus 0.5% on placebo4. The label also advises anyone taking birth-control pills to switch to a non-oral method or add a barrier method for 4 weeks after starting and after each dose increase, because the slower stomach emptying may make the pills less effective4.
What happens if you miss a dose (per the label)
The Zepbound label says to take a missed dose as soon as possible within 4 days (96 hours)4. If more than 4 days have passed, it says to skip that dose, take the next one on the usual day and carry on once a week4. The weekly dose day can be changed as long as doses are at least 3 days (72 hours) apart4.
The Mounjaro label gives the same rules14. Neither label has a separate rule for several missed doses in a row, unlike the Wegovy label for semaglutide, which says to restart the dose increases from a lower dose after 2 or more missed doses in a row41417.
The Mounjaro schedule for type 2 diabetes
Mounjaro is tirzepatide approved for type 2 diabetes in adults and children 10 and older, and for lowering the risk of heart attack, stroke and cardiovascular death in adults with type 2 diabetes at high risk14. Its label (version 40, effective 27 August 2026) also starts at 2.5 mg once a week, and allows increases of 2.5 mg after at least 4 weeks on the current dose if more blood-sugar control is needed14.
The maximum is 15 mg once a week for adults and 10 mg for children 10 and older14. Unlike Zepbound, whose label calls 2.5 mg a starting dose only, Mounjaro’s label has allowed 2.5 mg as an ongoing dose since 27 August 202641415.
Why gray-market vials make doses unreliable
Every dose on this page comes from trials and labels of Lilly’s approved medicine45. Online sellers also offer “research use only” tirzepatide vials, which FDA says are sold for human use with dosing instructions18. FDA has also found fraudulent compounded tirzepatide whose labels name pharmacies that do not exist or did not make the product18.
Independent tests show how far such products can drift719. Of Finnrick’s latest 196 completed tirzepatide tests, 59 failed (30.1%) as of 30 September 20267. Its default pass mark allows the measured amount to differ from the label by up to 35%, so a vial can pass while holding about a third more or less than it says719. Finnrick’s results come from users who chose to send samples, not from a random sample of the market720.
Some fakes hold a different drug: lab tests on two counterfeit tirzepatide pens detained in Ireland in 2025 found insulin instead of tirzepatide, which can cause severe low blood sugar (hypoglycemia)21.
Questions people ask
How much tirzepatide should I take?
For the approved medicine, the Zepbound label starts at 2.5 mg once a week for 4 weeks and sets a maintenance dose of 5, 10 or 15 mg once a week, with 15 mg as the maximum4. The main weight-loss trials used the same range510. Ask your prescriber which dose, if any, fits you.
What is the maximum dose of tirzepatide?
15 mg once a week, on both the Zepbound label and the Mounjaro label for adults414. For children 10 and older with type 2 diabetes, the Mounjaro maximum is 10 mg once a week14.
How long do you stay on each tirzepatide dose?
At least 4 weeks: the Zepbound label starts with 4 weeks at 2.5 mg, and each 2.5 mg increase comes after at least 4 weeks on the current dose4. At that pace, reaching 15 mg takes at least 20 weeks, matching the 20-week period of dose increases in SURMOUNT-145.
Is 2.5 mg of tirzepatide enough to lose weight?
It is not approved for that: the Zepbound label uses 2.5 mg only to start treatment, not as a maintenance dose4. The lowest maintenance dose, 5 mg, cut weight by 15.0% at 72 weeks in SURMOUNT-1, versus 3.1% on placebo5. The Mounjaro label, which is for type 2 diabetes, has allowed 2.5 mg as an ongoing dose since 27 August 202615.
What happens when you stop taking tirzepatide?
In SURMOUNT-4, people switched to placebo after 36 weeks on tirzepatide saw their weight rise 14.0% over the next 52 weeks, while those who stayed on it lost a further 5.5%12. At the end, 89.5% of those who stayed on it had kept at least 80% of their earlier weight loss, versus 16.6% of those switched to placebo12.
Go deeper
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- Compounded semaglutide, tirzepatide and microdosing: what the evidence says
Sources
- 1Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes New England Journal of Medicine, 5 Aug 2021. pubmed.ncbi.nlm.nih.gov
- 2Tirzepatide once weekly for the treatment of obesity in people with type 2 diabetes (SURMOUNT-2): a double-blind, randomised, multicentre, placebo-controlled, phase 3 trial The Lancet, 19 Aug 2023. pubmed.ncbi.nlm.nih.gov
- 3Efficacy and safety of LY3298176, a novel dual GIP and GLP-1 receptor agonist, in patients with type 2 diabetes: a randomised, placebo-controlled and active comparator-controlled phase 2 trial The Lancet, 17 Nov 2018. pubmed.ncbi.nlm.nih.gov
- 4ZEPBOUND (tirzepatide) injection, for subcutaneous use: prescribing information Eli Lilly and Company via DailyMed (U.S. National Library of Medicine), 28 Aug 2026. dailymed.nlm.nih.gov
- 5Tirzepatide Once Weekly for the Treatment of Obesity New England Journal of Medicine, 21 Jul 2022. pubmed.ncbi.nlm.nih.gov
- 6Tirzepatide for the Treatment of Obstructive Sleep Apnea and Obesity New England Journal of Medicine, 3 Oct 2024. pubmed.ncbi.nlm.nih.gov
- 7Tirzepatide: vendor test results Finnrick, 29 Sep 2026. finnrick.com
- 8Cardiovascular Outcomes with Tirzepatide versus Dulaglutide in Type 2 Diabetes New England Journal of Medicine, 18 Dec 2025. pubmed.ncbi.nlm.nih.gov
- 9FDA approves Lilly’s Mounjaro (tirzepatide) to reduce cardiovascular risk in adults with type 2 diabetes Eli Lilly and Company (PR Newswire), 28 Aug 2026. prnewswire.com
- 10Tirzepatide as Compared with Semaglutide for the Treatment of Obesity New England Journal of Medicine, 3 Jul 2025. pubmed.ncbi.nlm.nih.gov
- 11Tirzepatide for Heart Failure with Preserved Ejection Fraction and Obesity New England Journal of Medicine, 30 Jan 2025. pubmed.ncbi.nlm.nih.gov
- 12Continued Treatment With Tirzepatide for Maintenance of Weight Reduction in Adults With Obesity: The SURMOUNT-4 Randomized Clinical Trial JAMA, 2 Jan 2024. pubmed.ncbi.nlm.nih.gov
- 13Considerations and challenges in microdosing of GLP-1-based receptor agonists Expert Opinion on Pharmacotherapy, 5 Oct 2026. pubmed.ncbi.nlm.nih.gov
- 14MOUNJARO (tirzepatide) injection, for subcutaneous use: prescribing information Eli Lilly and Company via DailyMed (U.S. National Library of Medicine), 27 Aug 2026. dailymed.nlm.nih.gov
- 15Supplement approval letter, NDA 215866/S-044 and S-045 (Mounjaro) U.S. Food and Drug Administration, 27 Aug 2026. accessdata.fda.gov
- 16LY3298176, a novel dual GIP and GLP-1 receptor agonist for the treatment of type 2 diabetes mellitus: From discovery to clinical proof of concept Molecular Metabolism, Dec 2018. pubmed.ncbi.nlm.nih.gov
- 17WEGOVY (semaglutide) injection and tablets: prescribing information (SPL version 19) Novo Nordisk via DailyMed (U.S. National Library of Medicine), 30 Jun 2026. dailymed.nlm.nih.gov
- 18FDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight Loss U.S. Food and Drug Administration, 1 Oct 2026. fda.gov
- 19Methodology Finnrick, accessed 30 Sep 2026. finnrick.com
- 20We’d Rather Buy the Future Than Wait For It Finnrick, 10 Jun 2026. finnrick.com
- 21HPRA health warning after detention of counterfeit tirzepatide pens containing insulin Health Products Regulatory Authority (Ireland), 10 Oct 2025. hpra.ie
Not medical advice. Talk to a licensed clinician before using any drug. Report an error.