Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Aprepitant
Drug ID BADD_D00157
Description Aprepitant, an antiemetic, is a substance P/neurokinin 1 (NK1) receptor antagonist which, in combination with other antiemetic agents, is indicated for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy. Aprepitant is a selective high-affinity antagonist of human substance P/neurokinin 1 (NK1) receptors. Aprepitant has little or no affinity for serotonin (5-HT3), dopamine, and corticosteroid receptors, the targets of existing therapies for chemotherapy-induced nausea and vomiting (CI NV).
Indications and Usage For the prevention of nausea and vomiting associated with highly emetogenic cancer chemotherapy, including high-dose cisplatin (in combination with other antiemetic agents).
Marketing Status approved; investigational
ATC Code A04AD12
DrugBank ID DB00673
KEGG ID D02968
MeSH ID D000077608
PubChem ID 135413536
TTD Drug ID D0GU4K
NDC Product Code 50370-0048; 59285-015; 66039-851; 73005-0009; 47426-201; 68462-112; 55111-892; 56125-634; 65085-0043; 66039-880; 13668-593; 0006-0461; 0006-3066; 0006-3862; 47426-401; 13612-0024; 50370-0022; 68462-584; 68462-585; 56125-632; 64567-0021; 0006-0464; 68462-583; 0781-2321; 0781-2322; 0781-2323; 56125-633; 73309-380; 0781-4063; 0006-0462; 50370-0038; 65372-1169; 13668-591; 13668-592; 65977-0024; 72643-020; 13668-594
UNII 1NF15YR6UY
Synonyms Aprepitant | MK 869 | MK 0869 | MK-0869 | MK0869 | MK-869 | MK869 | (2R)-(1R)-3,5-bis(Trifluoromethylphenyl)ethoxy)-(3S)-(4-fluoro)phenyl-4-(3-(5-oxo-1H,4H-1,2,4-triazole)methyl-morpholine | MK 0517 | MK0517 | MK-0517 | (1-(3,5-bis(Trifluoromethyl)phenyl)ethoxy)-3-(fluoro)phenyl-4-(3-oxo-1,2,4-triazol-5-yl)methylmorpholine | Emend | L 754030 | L-754030 | L754030 | L 754,030 | L-754,030 | L754,030
Chemical Information
Molecular Formula C23H21F7N4O3
CAS Registry Number 170729-80-3
SMILES CC(C1=CC(=CC(=C1)C(F)(F)F)C(F)(F)F)OC2C(N(CCO2)CC3=NNC(=O)N3)C4=CC=C(C=C4)F
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)
Bronchospasm10.01.03.012; 22.03.01.0040.000121%
Cardiovascular disorder02.11.01.010; 24.03.02.009--Not Available
Chest discomfort22.12.02.002; 08.01.08.019; 02.02.02.0090.000218%Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.0110.000218%Not Available
Chills15.05.03.016; 08.01.09.0010.000081%
Confusional state19.13.01.001; 17.02.03.005--
Conjunctivitis11.01.06.012; 06.04.01.002--
Constipation07.02.02.001--
Cough22.02.03.001--
Cyst16.02.02.002; 08.03.05.001--Not Available
Death08.04.01.001--
Dehydration14.05.05.001--
Depressed level of consciousness17.02.04.002--
Depression19.15.01.001--
Dermatitis23.03.04.002--Not Available
Diabetes mellitus14.06.01.001; 05.06.01.001--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Disorientation17.02.05.015; 19.13.01.002--Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.003--
Dry mouth07.06.01.002--
Duodenal ulcer07.04.02.002--
Duodenal ulcer perforation07.04.02.003--Not Available
Dysarthria19.19.03.001; 17.02.08.001--
Dysgeusia07.14.03.001; 17.02.07.003--
Dyspepsia07.01.02.001--
Dysphagia07.01.06.003--
Dysphonia22.12.03.006; 19.19.03.002; 17.02.08.004--
Dyspnoea02.11.05.003; 22.02.01.0040.000978%
Dysuria20.02.02.002--
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ADReCS-Target
Drug Name ADR Term Target
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