Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sitagliptin
Drug ID BADD_D02029
Description Sitagliptin is an oral dipeptidyl peptidase-4 (DPP-4) inhibitor used in conjunction with diet and exercise to improve glycemic control in patients with type 2 diabetes mellitus[Label,A2260,A2255,A2256]. The effect of this medication leads to glucose dependent increases in insulin and decreases in glucagon to improve control of blood sugar[Label,A2255]. Sitagliptin was granted FDA approval on October 16, 2006[L6061].
Indications and Usage For use as an adjunct to diet and exercise to improve glycemic control in patients with type 2 diabetes mellitus. Also for use in patients with type 2 diabetes mellitus to improve glycemic control in combination with metformin or a PPARγ agonist (e.g., thiazolidinediones) when the single agent alone, with diet and exercise, does not provide adequate glycemic control.
Marketing Status Prescription
ATC Code A10BH01
DrugBank ID DB01261
KEGG ID D08516
MeSH ID D000068900
PubChem ID 4369359
TTD Drug ID D0U2JP
NDC Product Code 55154-5042; 50090-3527; 0006-0221; 50090-3472; 0006-0112; 50090-4084; 50090-4087; 50090-5517; 50090-4086; 59285-042; 55154-5040; 50090-5547; 50090-5585; 0006-0277
Synonyms Sitagliptin Phosphate | Phosphate, Sitagliptin | Sitagliptin Phosphate Monohydrate | Monohydrate, Sitagliptin Phosphate | Phosphate Monohydrate, Sitagliptin | Sitagliptin Monophosphate Monohydrate | Monohydrate, Sitagliptin Monophosphate | Monophosphate Monohydrate, Sitagliptin | MK 0431 | 0431, MK | MK0431 | MK-0431 | Sitagliptin Phosphate Anhydrous | Anhydrous, Sitagliptin Phosphate | Phosphate Anhydrous, Sitagliptin | Sitagliptin | 4-Oxo-4-(3-(trifluoromethyl)-5,6-dihydro(1,2,4)triazolo(4,3-a)pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl)butan-2-amine | Januvia
Chemical Information
Molecular Formula C16H15F6N5O
CAS Registry Number 486460-32-6
SMILES C1CN2C(=NN=C2C(F)(F)F)CN1C(=O)CC(CC3=CC(=C(C=C3F)F)F)N
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)
Cutaneous vasculitis24.05.02.004; 23.06.02.001; 10.02.02.003--Not Available
Cyanosis24.03.01.007; 22.02.02.007; 02.01.02.0020.000250%
Cyst16.02.02.002; 08.03.05.0010.000375%Not Available
Deafness04.02.01.0010.000375%Not Available
Death08.04.01.001--
Decreased activity19.11.01.002; 08.01.01.0060.000250%Not Available
Decubitus ulcer23.03.11.0060.000375%Not Available
Dehydration14.05.05.0010.004126%
Delirium19.13.02.0010.000625%
Dementia19.20.02.001; 17.03.01.0010.001375%Not Available
Depressed level of consciousness17.02.04.002--
Depressed mood19.15.02.0010.000500%Not Available
Depression19.15.01.0010.003376%
Dermatitis23.03.04.002--Not Available
Dermatitis acneiform23.02.01.0040.000250%
Dermatitis allergic10.01.03.014; 23.03.04.0030.000375%Not Available
Dermatitis bullous23.03.01.0020.000375%
Dermatitis exfoliative10.01.01.004; 23.03.07.0010.000250%
Dermatomyositis23.03.02.001; 15.05.01.002; 10.04.02.0010.000250%Not Available
Diabetes mellitus14.06.01.001; 05.06.01.0010.001500%Not Available
Diabetes mellitus inadequate control05.06.01.004; 14.06.01.0040.007252%Not Available
Diabetic ketoacidosis14.07.03.001; 05.07.03.0010.001000%Not Available
Diabetic neuropathy17.09.04.002; 14.07.04.003; 05.07.04.0030.000375%Not Available
Diabetic retinopathy06.10.02.002; 05.07.01.002; 24.03.07.004; 14.07.01.0020.000250%Not Available
Diarrhoea07.02.01.001--
Dilatation ventricular02.04.02.0260.000250%Not Available
Diplopia17.17.01.005; 06.02.06.002--Not Available
Discomfort08.01.08.003--Not Available
Disorientation19.13.01.002; 17.02.05.015--Not Available
Diverticulitis11.01.07.003; 07.10.02.0010.000875%Not Available
The 5th Page    First    Pre   5 6 7 8 9    Next   Last    Total 24 Pages