Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Alogliptin
Drug ID BADD_D00079
Description Alogliptin is a selective, orally-bioavailable inhibitor of enzymatic activity of dipeptidyl peptidase-4 (DPP-4). Chemically, alogliptin is prepared as a benzoate salt and exists predominantly as the R-enantiomer (>99%). It undergoes little or no chiral conversion in vivo to the (S)-enantiomer. FDA approved January 25, 2013.
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 A10BH04
DrugBank ID DB06203
KEGG ID D06553
MeSH ID C520853
PubChem ID 11450633
TTD Drug ID D0NJ5H
NDC Product Code 64764-250; 45802-087; 66332-7001; 66332-7003; 45802-103; 11532-7001; 71610-300; 64764-125; 64764-625; 11532-7002; 45802-150; 71610-661; 65392-2813; 50090-5574; 66332-7002; 11532-7003
UNII JHC049LO86
Synonyms alogliptin | 2-((6-((3R)-3-aminopiperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)methyl) benzonitrile | nesina | SYR 322 | SYR322 | SYR-322
Chemical Information
Molecular Formula C18H21N5O2
CAS Registry Number 850649-61-5
SMILES CN1C(=O)C=C(N(C1=O)CC2=CC=CC=C2C#N)N3CCCC(C3)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)
Pemphigoid23.03.01.004; 10.04.02.0020.006541%Not Available
Pemphigus23.03.01.005; 10.04.02.0030.000399%Not Available
Photosensitivity reaction23.03.09.0030.001555%
Pruritus23.03.12.0010.003988%
Pyrexia08.05.02.0030.001396%
Rash23.03.13.0010.008176%Not Available
Rash papular23.03.13.0170.001356%Not Available
Retinopathy24.03.07.003; 06.10.02.0010.000399%
Rhabdomyolysis15.05.05.0020.001396%
Serum sickness12.02.08.004; 10.01.03.004--
Skin exfoliation23.03.07.0030.000399%Not Available
Stevens-Johnson syndrome10.01.01.045; 23.03.01.007; 12.03.01.014; 11.07.01.0050.000997%
Sudden death02.03.04.013; 08.04.01.0030.000399%
Suicide attempt19.12.01.0040.000399%
Swollen tongue23.04.01.014; 10.01.05.015; 07.14.02.0030.000399%Not Available
Upper respiratory tract infection22.07.03.011; 11.01.13.009--
Urticaria23.04.02.001; 10.01.06.0010.004188%
Vertigo17.02.12.002; 04.04.01.0030.000399%
Vomiting07.01.07.0030.004507%
Tubulointerstitial nephritis20.05.02.0020.000399%Not Available
Lung neoplasm malignant22.08.01.001; 16.19.02.0010.001196%Not Available
Prostate cancer16.25.01.001; 21.04.02.0020.000598%Not Available
Hyperinsulinism14.06.03.007; 05.06.03.0070.000399%Not Available
Renal impairment20.01.03.0100.000598%Not Available
Hyperamylasaemia14.11.01.0030.000399%Not Available
Chronic kidney disease20.01.03.0170.000877%
Bone marrow failure01.03.03.0050.000399%
Drug-induced liver injury12.03.01.044; 09.01.07.0230.000798%Not Available
Biliary obstruction09.02.02.0050.000399%Not Available
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ADReCS-Target
Drug Name ADR Term Target
Tip:  Drug Name  ADR Term  Protein  Variation  Gene