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 Sitagliptin is indicated for the management of glycemic control in type 2 diabetes mellitus along with diet and exercise[Label].
Marketing Status approved; investigational
ATC Code A10BH01
DrugBank ID DB01261
KEGG ID D08516
MeSH ID D000068900
PubChem ID 4369359
TTD Drug ID D0U2JP
NDC Product Code 50090-4084; 0006-0277; 50090-4086; 50090-5517; 55154-5040; 50090-5547; 55154-5042; 50090-5585; 0006-0221; 50090-3527; 59285-042; 0006-0112; 50090-4087; 50090-3472
UNII QFP0P1DV7Z
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
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)
Diverticulum intestinal07.10.01.0020.000425%Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.0030.002680%
Dizziness postural02.11.04.008; 24.06.02.008; 17.02.05.0040.000180%Not Available
Drug eruption23.03.05.001; 10.01.01.005; 08.01.06.0150.000186%Not Available
Drug interaction08.06.03.0010.000876%Not Available
Dry mouth07.06.01.002--
Duodenal ulcer07.04.02.0020.000212%
Duodenitis07.08.03.0010.000053%Not Available
Dysmenorrhoea21.01.01.002--
Dyspepsia07.01.02.0010.000589%
Dysphagia07.01.06.0030.002563%
Dyspnoea02.11.05.003; 22.02.01.004--
Dyspnoea at rest22.02.01.025; 02.11.05.0040.000053%Not Available
Dyspnoea exertional02.11.05.005; 22.02.01.0050.000292%Not Available
Dysuria20.02.02.0020.000610%
Ear disorder04.03.01.001--Not Available
Eczema23.03.04.0060.000053%
Electrolyte imbalance14.05.01.0020.000080%Not Available
Embolism venous24.01.01.0030.000053%Not Available
Emphysema22.01.02.0020.000212%Not Available
Enterocolitis07.08.03.0030.000053%
Eructation07.01.02.0030.000080%
Erythema23.03.06.0010.001141%Not Available
Erythema multiforme23.03.01.003; 10.01.03.0150.000053%
Essential hypertension24.08.02.0080.000212%Not Available
Extrasystoles02.03.02.0030.000053%Not Available
Eye disorder06.08.03.0010.000260%Not Available
Eye pain06.08.03.0020.000143%
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.003--
Faeces discoloured07.01.03.0020.000080%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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