NSTK · 01.2026Independent supplement reference
NutriStack
Edition 1.0Updated July 13, 2026

Dulaglutide

Prescription ·Exploratory record · not publication-reviewed ·Updated July 13, 2026

Dulaglutide is an FDA-approved once-weekly GLP-1 receptor agonist peptide drug available as prescription Trulicity for type 2 diabetes in adults and pediatric patients 10 years and older, and for reducing major adverse cardiovascular events in labeled adults with type 2 diabetes and cardiovascular disease or multiple risk factors. This app supports FDA-approved prescription Trulicity only; compounded, research-use, vial-based, or non-prescribed dulaglutide products are unsupported.

Publication status

Exploratory record, not a reviewed medical publication.

See the editorial and medical-review policies for the publication gate.

This generated database record has not completed a claim-level review by a qualified human medical reviewer. Bibliography links and evidence labels are not approval. The page remains available for reference and is excluded from search indexing.

In short

What the research says.

A quick, data-only summary. The full evidence, dosing, and sources are below.

Dulaglutide is an FDA-approved once-weekly GLP-1 receptor agonist peptide drug available as prescription Trulicity for type 2 diabetes in adults and pediatric patients 10 years and older, and for reducing major adverse cardiovascular events in labeled adults with type 2 diabetes and cardiovascular disease or multiple risk factors. NutriStack rates the supporting evidence as strong. Common adult dosing is Product-specific titration only: adults 0.75-4.5 mg once weekly; pediatric patients 10 years and older 0.75-1.5 mg once weekly (as prescribed by your clinician), though a prescriber sets the actual dose. This profile indexes 12 sources.

What it's good for
  • Improves glycemic control in adults and pediatric patients 10 years and older with type 2 diabetes2,3
  • Reduces major adverse cardiovascular events in labeled adults with type 2 diabetes11,6
  • Once-weekly subcutaneous administration9,3
  • Ready-to-use single-dose pen format2
  • Low hypoglycemia risk when not combined with insulin or insulin secretagogues6
What to watch for
  • Nausea, vomiting, diarrhea, abdominal pain, decreased appetite, dyspepsia, and fatigue
  • Injection-site reactions
  • Hypoglycemia risk increases when combined with insulin or insulin secretagogues
  • Personal or family history of medullary thyroid carcinoma (MTC)
  • Multiple endocrine neoplasia syndrome type 2 (MEN 2)4

The bottom line

Evidence rating strong. Most-documented uses: improves glycemic control in adults and pediatric patients 10 years and older with type 2 diabetes, reduces major adverse cardiovascular events in labeled adults with type 2 diabetes, once-weekly subcutaneous administration. 12 sources indexed (2021–2026), with 0 interaction records on file.

The science

How it works, mechanistically.

Core mechanism

A GLP-1 receptor agonist consisting of a modified GLP-1 analogue covalently linked to a modified Fc fragment of human IgG4, which slows clearance and extends the half-life to approximately 5 days. Activates GLP-1 receptors to enhance glucose-dependent insulin secretion, suppress glucagon, slow gastric emptying, and reduce appetite.10

Class
GLP-1 Receptor Agonist
Dosing

Dosing & protocol.

Common range
Product-specific titration only: adults 0.75-4.5 mg once weekly; pediatric patients 10 years and older 0.75-1.5 mg once weekly (as prescribed by your clinician)
Recommended form
FDA-approved prescription Trulicity single-dose pen selected by the prescriber. Do not use compounded, research-use-only, or unverified vial/syringe dulaglutide.

Dulaglutide is injected subcutaneously once weekly without regard to meals. It delays gastric emptying and may affect absorption of concomitant oral medications, so narrow-therapeutic-index oral drugs may need clinical monitoring.2

Safety

Full safety detail.

Side effects

  • Nausea, vomiting, diarrhea, abdominal pain, decreased appetite, dyspepsia, and fatigue
  • Injection-site reactions
  • Hypoglycemia risk increases when combined with insulin or insulin secretagogues
  • Acute pancreatitis has been reported with GLP-1 receptor agonists
  • Acute gallbladder disease
  • Acute kidney injury due to volume depletion from severe gastrointestinal adverse reactions
  • Severe gastrointestinal adverse reactions; not recommended in severe gastroparesis
  • Diabetic retinopathy complications in patients with a history of diabetic retinopathy
  • Serious hypersensitivity reactions including anaphylaxis or angioedema
  • Pulmonary aspiration during general anesthesia or deep sedation has been reported postmarketing

Contraindications

  • Personal or family history of medullary thyroid carcinoma (MTC)
  • Multiple endocrine neoplasia syndrome type 2 (MEN 2)4
  • Prior serious hypersensitivity reaction to dulaglutide or product excipients6
Sources

Sources, by evidence tier.

Numbered references. Citations throughout the page link here.

Meta-analyses & systematic reviews

1

Randomized controlled trials

4

Reference material

7
FAQ

Common questions.

Quick answers about Dulaglutide, drawn from the data on this page.

What is Dulaglutide?

Dulaglutide is an FDA-approved once-weekly GLP-1 receptor agonist peptide drug available as prescription Trulicity for type 2 diabetes in adults and pediatric patients 10 years and older, and for reducing major adverse cardiovascular events in labeled adults with type 2 diabetes and cardiovascular disease or multiple risk factors. This app supports FDA-approved prescription Trulicity only; compounded, research-use, vial-based, or non-prescribed dulaglutide products are unsupported.

What is Dulaglutide used for?

Commonly cited benefits of Dulaglutide include: Improves glycemic control in adults and pediatric patients 10 years and older with type 2 diabetes; Reduces major adverse cardiovascular events in labeled adults with type 2 diabetes; Once-weekly subcutaneous administration; Ready-to-use single-dose pen format; Low hypoglycemia risk when not combined with insulin or insulin secretagogues. NutriStack rates the overall evidence as strong.

What is a typical dose of Dulaglutide?

A typical adult dose of Dulaglutide is Product-specific titration only: adults 0.75-4.5 mg once weekly; pediatric patients 10 years and older 0.75-1.5 mg once weekly (as prescribed by your clinician). The commonly recommended form is FDA-approved prescription Trulicity single-dose pen selected by the prescriber. Do not use compounded, research-use-only, or unverified vial/syringe dulaglutide.. These are general ranges, not personalized advice; confirm the right dose with a clinician.

What are the side effects of Dulaglutide?

Reported side effects include nausea, vomiting, diarrhea, abdominal pain, decreased appetite, dyspepsia, and fatigue, injection-site reactions, hypoglycemia risk increases when combined with insulin or insulin secretagogues, acute pancreatitis has been reported with glp-1 receptor agonists, acute gallbladder disease, acute kidney injury due to volume depletion from severe gastrointestinal adverse reactions. This is educational information; check with a healthcare professional before use.

How strong is the evidence for Dulaglutide?

NutriStack rates this as Strong, meaning multiple high-quality meta-analyses or systematic reviews converge on the same finding. Full tier criteria are at https://nutristackapp.com/methodology/evidence-tiers.

Use this with your stack

Dulaglutide in NutriStack.

Add it to your stack, see how it interacts with everything else you take, and get a Stack Score that updates the moment it does.

NutriStack is an informational and organizational tool, not a medical service, and not a substitute for professional advice. Always consult a qualified healthcare professional before starting, stopping, or changing any supplement or medication.