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)
Cellulitis23.09.01.001; 11.02.01.0010.000625%Not Available
Cellulitis staphylococcal23.09.01.013; 11.02.05.0060.000250%Not Available
Cerebral haemorrhage17.08.01.003; 24.07.04.001--Not Available
Cerebral infarction24.04.06.002; 17.08.01.0040.000750%Not Available
Cerebrovascular accident17.08.01.007; 24.03.05.0010.005627%
Cerebrovascular disorder24.03.05.002; 17.08.02.0020.000098%Not Available
Chest discomfort02.02.02.009; 22.02.08.001; 08.01.08.019--Not Available
Chest pain22.02.08.003; 08.01.08.002; 02.02.02.0110.002501%Not Available
Chills15.05.03.016; 08.01.09.0010.000875%
Cholangiocarcinoma09.04.02.009; 16.07.01.0020.000098%Not Available
Cholangitis09.02.01.0020.001000%Not Available
Cholecystitis09.03.01.0010.000625%
Cholecystitis acute09.03.01.0030.000375%Not Available
Cholelithiasis09.03.01.0020.004251%Not Available
Cholestasis09.01.01.0010.001625%Not Available
Chromaturia20.02.01.0020.000375%
Chronic obstructive pulmonary disease22.03.01.0070.000587%Not Available
Circulatory collapse24.06.02.0010.000250%Not Available
Clostridium difficile colitis07.19.01.004; 11.02.02.0040.000375%Not Available
Clubbing22.02.08.013; 15.03.02.006; 02.01.02.0120.000065%Not Available
Coagulopathy01.01.02.0010.000750%Not Available
Cold sweat08.01.03.024; 23.02.03.0020.000250%Not Available
Colitis07.08.01.001--
Colon cancer16.13.01.001; 07.21.01.0010.000065%Not Available
Completed suicide19.12.01.001; 08.04.01.010--Not Available
Confusional state17.02.03.005; 19.13.01.0010.002501%
Constipation07.02.02.0010.005001%
Coordination abnormal17.02.02.0040.000250%Not Available
Coronary artery disease24.04.04.006; 02.02.01.0010.002376%Not Available
Cough22.02.03.0010.002501%
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