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Mounjaro vs Trulicity

Last reviewed against the current FDA prescribing information for both products. Not medical advice.

Short answer

Mounjaro (tirzepatide) and Trulicity (dulaglutide) are different medicines: Mounjaro is taken once weekly and Trulicity once weekly.

Mounjaro is not FDA-approved for weight management; Trulicity is not FDA-approved for weight management. The table below lists each product's approved uses, doses and most common side effects from its FDA label. Your prescriber can tell you which, if either, fits your situation.

This pairing isn't one of our reviewed comparison guides. For the comparisons people ask about most, see all GLP-1 comparisons.

Mounjaro and Trulicity side by side

Mounjaro vs Trulicity, from each product's FDA prescribing information
From the FDA labelMounjaroTrulicity
Active ingredienttirzepatidedulaglutide
Drug classGIP receptor and GLP-1 receptor agonistGLP-1 receptor agonist
ManufacturerEli LillyEli Lilly
FDA-approved uses
  • Improving blood sugar control in adults and children 10 and older with type 2 diabetes, alongside diet and exercise
  • Lowering the risk of major cardiovascular events (cardiovascular death, heart attack or stroke) in adults with type 2 diabetes who are at high risk of these events
  • Improving blood sugar control in adults and children 10 and older with type 2 diabetes, alongside diet and exercise
  • Lowering the risk of major cardiovascular events in adults with type 2 diabetes who have established cardiovascular disease or multiple cardiovascular risk factors
Approved for weight management?NoNo
How it's takenInjection under the skin (subcutaneous)Injection under the skin (subcutaneous)
How oftenOnce weeklyOnce weekly
Starting dose2.5 mg once weekly0.75 mg once weekly (adults)
Dose increasesIf more blood sugar control is needed, increase in 2.5 mg steps after at least 4 weeks on the current doseAdults: after 4 weeks, may increase to 1.5 mg, then in 1.5 mg steps after at least 4 weeks on each dose if more blood sugar control is needed. Children: may increase to 1.5 mg after at least 4 weeks
Maintenance doseNo single maintenance dose in the label; the dose is raised in 2.5 mg steps only if more blood sugar control is neededSet by your prescriber based on blood sugar control, within the dose range above
Maximum dose15 mg once weekly in adults; 10 mg once weekly in children4.5 mg once weekly in adults; 1.5 mg once weekly in children
When to take itAny time of day, with or without meals. The injection day can be changed if doses are at least 3 days (72 hours) apartAny time of day, with or without food. The injection day can be changed if the last dose was 3 or more days earlier
Pens and devicesSingle-dose pens, single-dose vials, 4-dose vials and 4-dose KwikPens, each in 2.5, 5, 7.5, 10, 12.5 and 15 mg strengthsSingle-dose pens: 0.75 mg, 1.5 mg, 3 mg and 4.5 mg
StorageRefrigerate. Single-dose pens and vials can be kept unrefrigerated (up to 86°F) for a total of 21 days. KwikPens and multi-dose vials: throw away after 30 days at room temperature, 30 days after first use or 4 weekly doses, whichever comes first. Do not freezeRefrigerate. Each pen can be kept at room temperature (up to 86°F) for a total of 14 days. Do not freeze
Weight results in the labelNone: not a weight-management productNone: not a weight-management product
Most common side effects (≥5%)Nausea, Diarrhea, Decreased appetite, Vomiting, Constipation, Indigestion (dyspepsia), Abdominal painNausea, Diarrhea, Vomiting, Abdominal pain, Decreased appetite
Boxed warningRisk of thyroid C-cell tumors. Do not use if you or a family member have had medullary thyroid carcinoma (MTC) or if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).Risk of thyroid C-cell tumors. Do not use if you or a family member have had medullary thyroid carcinoma (MTC) or if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
First FDA approvalMay 13, 2022September 18, 2014

Side effects listed are the label's “most common adverse reactions”; the full label also covers serious risks such as pancreatitis, gallbladder problems and low blood sugar. Weight results come from separate placebo-controlled trials and are not a head-to-head comparison unless stated.

Good to know

  • Mounjaro is not FDA-approved for weight management. The weight-management tirzepatide product is Zepbound.
  • Trulicity is not FDA-approved for weight management.

Questions to ask your prescriber

  • Which of these is approved for my diagnosis, and is it covered by my plan?
  • How should I step up the dose, and what should I do if the side effects are hard to tolerate?
  • Do any of my other medicines, or my personal or family history, rule one of these out?
  • If I switch from one to the other, what dose should I start on and when?

Sources

  1. Mounjaro (tirzepatide) injection — FDA prescribing information, DailyMed (label effective August 27, 2026, version 40) (Sections 1, 2, 3, 6, 12.1, 16, boxed warning; checked September 24, 2026)
  2. Drugs@FDA: NDA 215866 (Mounjaro) (Original approval date; checked September 24, 2026)
  3. Trulicity (dulaglutide) injection — FDA prescribing information, DailyMed (label effective June 16, 2026, version 62) (Sections 1, 2.1, 3, 6, 16, boxed warning; checked September 24, 2026)
  4. Drugs@FDA: BLA 125469 (Trulicity) (Original approval date; checked September 24, 2026)

How we review: every fact on this page is taken from the current FDA prescribing information on DailyMed or from Drugs@FDA, and re-checked on the date shown. This page was reviewed against FDA labeling, not by a named clinician.

Medical disclaimer: This page is general information, not medical advice, diagnosis or treatment, and it doesn't cover every use, dose, warning or side effect. Always follow the advice of your doctor, pharmacist or other prescriber and read the Medication Guide that comes with your medicine. If you think you are having a medical emergency, call your local emergency number. ShotWise is a tracking app and does not prescribe, sell or recommend any medication.

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