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 Prescription
ATC Code A04AD12
DrugBank ID DB00673
KEGG ID D02968
MeSH ID D000077608
PubChem ID 135413536
TTD Drug ID D0GU4K
NDC Product Code 65372-1169; 0006-0461; 56125-632; 72643-020; 55111-892; 68462-583; 66039-851; 0781-2323; 50370-0038; 13668-593; 0781-4063; 50370-0048; 13668-592; 0006-3066; 0006-0464; 13668-594; 0781-2321; 50370-0022; 68462-585; 13668-591; 68462-584; 73309-380; 13612-0024; 59285-015; 0006-0462; 68462-112; 0781-2322; 65977-0024; 56125-634; 65085-0043; 47426-201; 64567-0021; 0006-3862; 66039-880; 56125-633
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
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)
Vomiting07.01.07.0030.001310%
Weight decreased13.15.01.005--
Weight increased13.15.01.006--
Wheezing22.03.01.009--
White blood cell count decreased13.01.06.012--
White blood cell count increased13.01.06.013--Not Available
White blood cells urine positive13.13.02.004--Not Available
Wound dehiscence12.02.05.003--
Infusion site erythema23.03.06.016; 12.07.05.009; 08.02.05.008--Not Available
Neutropenic sepsis01.02.03.007; 11.01.11.006--Not Available
Subileus07.13.01.004--Not Available
Leukocyturia20.02.01.014--Not Available
Deep vein thrombosis24.01.02.003--Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
Lymphatic disorder01.09.01.003--Not Available
Thoracic operation25.13.05.001--Not Available
Protein urine present13.13.02.006--Not Available
Epigastric discomfort07.01.02.004--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Inappropriate antidiuretic hormone secretion14.05.07.001; 05.03.03.001--Not Available
Infusion site induration12.07.05.010; 08.02.05.009--Not Available
Infusion site pain12.07.05.002; 08.02.05.014--Not Available
Infusion site pruritus08.02.05.004; 23.03.12.006; 12.07.05.005--Not Available
Infusion site reaction12.07.05.006; 08.02.05.005--Not Available
Anxiety disorder19.06.01.002--Not Available
Cognitive disorder19.21.02.001; 17.03.03.003--
Post procedural complication12.02.05.018--Not Available
Staphylococcal infection11.02.05.002--Not Available
Angiopathy24.03.02.007--Not Available
Blood alkaline phosphatase increased13.04.02.004--
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