Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Albiglutide
Drug ID BADD_D00053
Description Albiglutide is a glucagon-like peptide-1 agonist (GLP-1) biologic drug indicated in the treatment of type 2 diabetes. It is marketed under the brands Eperzan and Tanzeum by GSK (GlaxoSmithKline). It is a dipeptidyl peptidase-4-resistant glucagon-like peptide-1 dimer fused to human albumin. Albiglutide was approved on April 15, 2014 by the FDA.
Indications and Usage Indicated as an adjunct to diet and exercise to improve glycemic control in adults with type 2 diabetes mellitus.
Marketing Status approved
ATC Code A10BJ04
DrugBank ID DB09043
KEGG ID D08843
MeSH ID C534611
PubChem ID 145994868
TTD Drug ID Not Available
NDC Product Code Not Available
UNII 5E7U48495E
Synonyms rGLP-1 protein | Eperzan | Tanzeum | albiglutide
Chemical Information
Molecular Formula C148H224N40O45
CAS Registry Number 782500-75-8
SMILES CCC(C)C(C(=O)NC(C)C(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)NC(CC(C)C)C(=O)NC(C(C)C)C(=O)N C(CCCCN)C(=O)NCC(=O)NC(CCCNC(=N)N)C(=O)N)NC(=O)C(CC3=CC=CC=C3)NC(=O)C(CCC(=O)O)N C(=O)C(CCCCN)NC(=O)C(C)NC(=O)C(C)NC(=O)C(CCC(=O)N)NC(=O)CNC(=O)C(CCC(=O)O)NC(=O) C(CC(C)C)NC(=O)C(CC4=CC=C(C=C4)O)NC(=O)C(CO)NC(=O)C(CO)NC(=O)C(C(C)C)NC(=O)C(CC( =O)O)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C(CC5=CC=CC=C5)NC(=O)C(C(C)O)NC(=O)CNC(=O)C( CCC(=O)O)NC(=O)CNC(=O)C(CC6=CN=CN6)N
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice..
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Appendicitis11.01.07.001; 07.19.01.001--
Arthralgia15.01.02.001--
Atrial fibrillation02.03.03.002--
Atrial flutter02.03.03.003--
Back pain15.03.04.005--
Cough22.02.03.001--
Diarrhoea07.02.01.001--
Dyspepsia07.01.02.001--
Gamma-glutamyltransferase increased13.03.04.024--
Gastrooesophageal reflux disease07.02.02.003--
Heart rate increased13.14.04.002--Not Available
Hypoglycaemia14.06.03.001; 05.06.03.001--
Influenza22.07.02.001; 11.05.03.001--Not Available
Injection site erythema12.07.03.001; 08.02.03.001; 23.03.06.015--Not Available
Injection site haematoma24.07.01.009; 12.07.03.004; 08.02.03.004--Not Available
Injection site haemorrhage24.07.01.010; 12.07.03.005; 08.02.03.005--Not Available
Injection site hypersensitivity08.02.03.006; 12.07.03.006; 10.01.03.017--Not Available
Injection site rash23.03.13.010; 12.07.03.032; 08.02.03.032--Not Available
Injection site reaction12.07.03.015; 08.02.03.014--
Nausea07.01.07.001--
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Sinusitis22.07.03.007; 11.01.13.005--
Upper respiratory tract infection22.07.03.011; 11.01.13.009--
Vomiting07.01.07.003--
Immunology test13.06.03.007--Not Available
Hepatic enzyme abnormal13.03.04.026--Not Available
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