Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Dulaglutide
Drug ID BADD_D00733
Description Dulaglutide, marketed by Eli Lilly as Trulicity, is a once-weekly subcutaneous glucagon-like peptide-1 (GLP-1) receptor agonist designed using recombinant DNA technology; it has been approved as an adjunct therapy to diet and exercise in the management of 2 diabetes (T2DM).[A236070] Dulaglutide was initially approved by the FDA in 2014, and in February 2020 was approved for use in patients with T2DM and multiple cardiovascular risk factors for the prevention of cardiovascular events. It is the first T2DM drug approved to reduce major adverse cardiovascular events (MACE) risk in primary and secondary prevention populations.[L34665]
Indications and Usage Indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Marketing Status Prescription
ATC Code A10BJ05
DrugBank ID DB09045
KEGG ID D09889
MeSH ID C555680
PubChem ID Not Available
TTD Drug ID D03NAW
NDC Product Code 0002-1434; 62195-433; 54568-001; 0002-1402; 0002-2236; 0002-1433; 50090-5467; 62381-1434; 0002-1401; 62381-1433; 63419-0525; 0002-3182; 62195-434; 50090-3484; 50090-3483
Synonyms dulaglutide | LY 2189265 | LY-2189265 | LY2189265 | Trulicity
Chemical Information
Molecular Formula Not Available
CAS Registry Number 923950-08-7
SMILES Not Available
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal discomfort07.01.06.001--Not Available
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Abdominal pain lower07.01.05.010--Not Available
Abdominal pain upper07.01.05.003--
Abdominal tenderness07.01.05.004--Not Available
Amylase increased13.05.01.009--
Asthenia08.01.01.001--Not Available
Atrioventricular block first degree02.03.01.004--
Constipation07.02.02.001--
Diarrhoea07.02.01.001--
Dyspepsia07.01.02.001--
Eructation07.01.02.003--
Face oedema08.01.07.003; 23.04.01.004; 10.01.05.002--
Fatigue08.01.01.002--
Flatulence07.01.04.002--
Frequent bowel movements07.02.04.002--Not Available
Gastrooesophageal reflux disease07.02.02.003--
Gastrointestinal disorder07.11.01.001--Not Available
Gastrointestinal pain07.01.05.005--
Heart rate increased13.14.04.002--Not Available
Hypoglycaemia14.06.03.001; 05.06.03.001--
Injection site reaction12.07.03.015; 08.02.03.014--
Lip swelling23.04.01.007; 10.01.05.005; 07.05.04.005--Not Available
Lipase increased13.05.01.003--
Malaise08.01.01.003--
Nausea07.01.07.001--
Retching07.01.07.002--Not Available
Sinus tachycardia02.03.03.010--
Systemic lupus erythematosus rash10.04.03.005; 23.03.13.007; 15.06.02.005--Not Available
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