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)
Urine output increased13.13.03.002--Not Available
Hot flush24.03.01.005; 21.02.02.001; 08.01.03.027--
Benign neoplasm16.02.02.007--Not Available
Breast disorder21.05.04.004--Not Available
Cardiac disorder02.01.01.003--Not Available
Connective tissue disorder15.06.01.006--Not Available
Embolism24.01.01.009--
Infestation23.09.05.001; 11.09.01.001--Not Available
Malnutrition14.03.02.004--Not Available
Mediastinal disorder22.09.03.001--Not Available
Mental disorder19.07.01.002--Not Available
Poisoning12.03.01.004--Not Available
Decreased appetite08.01.09.028; 14.03.01.005--
Ill-defined disorder08.01.03.049--Not Available
Inner ear disorder04.04.02.002--Not Available
Polyp16.02.02.005; 08.01.06.010--Not Available
Blood disorder01.05.01.004--Not Available
Non-small cell lung cancer22.08.01.002; 16.19.01.001--Not Available
Pulmonary function test decreased13.19.01.001--Not Available
Renal impairment20.01.03.010--Not Available
Respiratory tract infection22.07.07.001; 11.01.08.017--Not Available
Neutropenic colitis07.08.01.014; 01.02.03.010--Not Available
Infusion site thrombosis12.07.05.007; 08.02.05.006; 24.01.01.022--Not Available
Procedural nausea12.02.03.003; 07.01.07.005--Not Available
Procedural vomiting12.02.03.004; 07.01.07.006--Not Available
Post procedural infection12.02.05.010; 11.01.08.019--Not Available
Gastrointestinal sounds abnormal07.01.01.002--Not Available
Fasting26.01.02.001--Not Available
Oropharyngeal pain07.05.05.004; 22.02.05.022--
Upper-airway cough syndrome22.02.05.030--
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