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Trulicity ® (dulaglutide) injection0.75 mg/0.5 mL, 1.5 mg/0.5 mL, 3mg/0.5mL, 4.5mg/0.5mL
This information is provided in response to your request. Resources may contain information about doses, uses, formulations and populations different from product labeling. See Prescribing Information above, if applicable.
Have hypersensitivity reactions been reported with Trulicity® (dulaglutide)?
Serious hypersensitivity reactions including anaphylactic reactions and angioedema have been reported with Trulicity (dulaglutide).
Dulaglutide is contraindicated in patients who have had a prior serious hypersensitivity reaction to dulaglutide or to any of its product components.1
Serious hypersensitivity reactions, including anaphylactic reactions and angioedema, have been reported in patients treated with dulaglutide and other GLP-1 RAs.1
Use caution in patients with a history of angioedema or anaphylaxis with a GLP-1 RA other than dulaglutide because it is unknown whether these patients will be predisposed to anaphylaxis when receiving dulaglutide.1
If a hypersensitivity reaction occurs, discontinue dulaglutide, treat promptly per standard of care, and monitor until signs and symptoms resolve. Do not use in patients with a previous hypersensitivity reaction to dulaglutide.1
Clinical Study Experience
Systemic hypersensitivity adverse reactions were experienced by 0.5% of patients who received dulaglutide in 4 phase 2 and 5 phase 3 studies that included
facial edema, and
There have been reports of anaphylactic reactions and angioedema during postapproval use of dulaglutide.1
Because these events are reported voluntarily from a population of uncertain size, it is generally not possible to reliably estimate their frequency or establish a causal relationship to drug exposure.1
Enclosed Prescribing Information
GLP-1 RA = glucagon-like peptide-1 receptor agonist
Date of Last Review: April 06, 2020