Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ondansetron
Drug ID BADD_D01617
Description A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties. Having been developed in the 1980s by GlaxoSmithKline and approved by the US FDA since January 1991, ondansetron has demonstrated a long history of use and efficacy. Commonly formulated as oral tablets, orally disintegrating tablets (ODT), and injections, and available as generic products as well, ondansetron continues to see contemporary innovations in its formulation and use, including the development of orally soluble films that are both discreet in administration and less of a burden in comparison to having patients attempt to swallow pills during emesis [L5221].
Indications and Usage For the prevention of nausea and vomiting associated with emetogenic cancer chemotherapy, postoperation, and radiation. Also used for the treatment of postoperative nausea and vomiting.
Marketing Status Prescription; Discontinued
ATC Code A04AA01
DrugBank ID DB00904
KEGG ID D00456
MeSH ID D017294
PubChem ID 4595
TTD Drug ID D0K7WK
NDC Product Code 68788-7565; 65862-391; 63850-2706; 72572-520; 63187-670; 72266-123; 71872-7068; 62135-122; 0143-9890; 57237-077; 16729-298; 63187-002; 55111-050; 0404-9930; 51662-1469; 68071-5021; 16714-159; 43063-770; 71335-1314; 68071-2284; 68071-4570; 68071-3028; 61919-545; 23155-547; 71872-7107; 63629-7951; 60760-277; 0378-7734; 68788-7705; 63629-4306; 71872-7162; 52584-069; 71335-0496; 68071-4834; 71930-018; 61919-087; 61919-986; 71335-0650; 55154-4567; 68071-5230; 16714-160; 63187-483; 23155-549; 0409-4759; 68083-113; 71335-1731; 63187-526; 67296-1294; 68462-158; 71335-0657; 55154-2876; 16714-201; 63187-693; 70518-2895; 71930-017; 71872-7140; 43063-870; 45865-598; 51662-1246; 55700-952; 68071-4566; 50436-0390; 0904-7073; 68071-4190; 68462-106; 63629-4014; 55700-672; 16714-200; 50090-4632; 71872-7138; 80425-0113; 63187-256; 68071-4513; 68071-1804; 52482-019; 68071-4717; 53002-0570; 76420-056; 62756-356; 51662-1539; 63187-379; 70518-2650; 61919-565; 50090-1201; 50090-1200; 17856-0691; 80425-0073; 51662-1377; 0641-6080; 55154-3680; 68071-4409; 43063-857; 53002-0590; 67184-0507; 50090-1658; 63739-333; 63187-266; 50090-1659; 63629-5083; 68788-9559; 68083-114; 51662-1366; 0143-9891; 0641-6078; 71335-1071; 68462-157; 53002-0580; 60760-313; 23155-550; 68071-1987; 65162-691; 68071-2584; 0409-4755; 68071-4810; 23155-548; 63187-236; 65862-390; 60760-305; 68788-9670; 54348-819; 68071-2652; 51662-1245; 68071-4594; 60760-306; 62135-121; 70518-0829; 45963-539; 50090-4935; 43063-273; 68788-7644; 72266-124; 62756-240; 63304-458; 53002-0582; 60505-6130; 57237-078; 45963-538; 0641-6079; 0378-7732; 55154-2877; 70518-3075; 68071-5167; 50090-1660; 50090-1128; 70166-486; 71335-0132; 63187-065; 66651-904; 63304-459; 45865-105; 67457-440; 68462-105; 70934-809; 51846-1033; 45865-563; 68071-1904; 68071-4426; 68001-247; 70518-1551; 68001-246; 63187-199; 68071-1730; 65129-2118; 50090-5346; 16729-297; 60687-252; 51662-1514; 89141-444; 68071-4881; 57451-1191; 53002-0591
Synonyms Ondansetron | Ondansetron, (+,-)-Isomer | 4H-Carbazol-4-one, 1,2,3,9-tetrahydro-9-methyl-3-((2-methyl-1H-imidazol-1-yl)methyl)- | Ondansetron Hydrochloride | Hydrochloride, Ondansetron | Ondansetron Monohydrochloride | Monohydrochloride, Ondansetron | Ondansetron Monohydrochloride Dihydrate | Dihydrate, Ondansetron Monohydrochloride | Monohydrochloride Dihydrate, Ondansetron | GR38032F | GR-38032F | GR 38032F | Ondansetron, (S)-Isomer | SN-307 | SN 307 | SN307 | Zofran | Ondansetron, (R)-Isomer
Chemical Information
Molecular Formula C18H19N3O
CAS Registry Number 99614-02-5
SMILES CC1=NC=CN1CC2CCC3=C(C2=O)C4=CC=CC=C4N3C
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)
Aortic valve incompetence02.07.03.0010.000449%Not Available
Aphasia19.21.01.001; 17.02.03.0010.000100%
Aphthous ulcer07.05.06.0020.000150%Not Available
Apnoea22.02.01.0010.000599%
Appendicitis11.01.07.001; 07.19.01.0010.000150%
Arrhythmia02.03.02.0010.000699%Not Available
Arthralgia15.01.02.0010.000699%
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.000300%
Aspartate aminotransferase increased13.03.01.0060.000100%
Aspiration22.02.07.0070.000026%
Asthenia08.01.01.0010.000799%Not Available
Asthma22.03.01.002; 10.01.03.0100.001698%Not Available
Ataxia17.02.02.001; 08.01.02.0040.000100%
Atelectasis22.01.02.0010.000549%
Atrial fibrillation02.03.03.002--
Atrial septal defect03.07.02.002; 02.04.02.0090.001133%Not Available
Atrial tachycardia02.03.03.0040.000250%
Atrioventricular block02.03.01.0020.000100%Not Available
Atrioventricular block complete02.03.01.0030.000150%
Atrioventricular block second degree02.03.01.005--
Attention deficit/hyperactivity disorder19.21.04.0010.000949%Not Available
Atypical pneumonia22.07.01.010; 11.01.09.0120.000150%Not Available
Back pain15.03.04.0050.000949%
Bacteraemia11.01.11.0010.000499%
Blepharitis23.03.04.012; 06.04.04.0010.000100%Not Available
Blindness17.17.01.003; 06.02.02.0010.000100%Not Available
Blindness transient17.17.01.004; 06.02.02.002--Not Available
Blood cholesterol increased13.12.01.0020.000100%
Blood pressure increased13.14.03.0050.000250%Not Available
Body temperature increased13.15.01.001--Not Available
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