Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Rifaximin
Drug ID BADD_D01938
Description Rifaximin is a semisynthetic, rifamycin-based non-systemic antibiotic, meaning that the drug will not pass the gastrointestinal wall into the circulation as is common for other types of orally administered antibiotics. It has multiple indications and is used in treatment of traveller's diarrhea caused by E. coli; reduction in risk of overt hepatic encephalopathy recurrence; as well as diarrhea-predominant irritable bowel syndrome (IBS-D) in adult women and men. It is marketed under the brand name Xifaxan by Salix Pharmaceuticals.
Indications and Usage Rifaximin has multiple indications by the FDA: for the treatment of patients (≥12 years of age) with traveller's diarrhea caused by noninvasive strains of Escherichia coli; for the reduction of overt hepatic encephalopathy recurrence in patients ≥18 years of age; and in May 2015 it was approved for irritable bowel syndrome with diarrhea (IBS-D) treatment in adult men and women.
Marketing Status Prescription
ATC Code A07AA11; D06AX11
DrugBank ID DB01220
KEGG ID D02554
MeSH ID D000078262
PubChem ID 6436173
TTD Drug ID D04ITO
NDC Product Code 50090-2445; 10695-011; 14501-0082; 57297-029; 70799-000; 65649-301; 14501-0093; 17337-0043; 55154-6777; 62756-693; 65649-303; 14501-0021; 59285-008; 62207-017; 76278-1109; 62207-014; 12828-0089; 17337-0044; 17337-0032; 73309-232
Synonyms Rifaximin | 4-Deoxy-4'-methylpyrido(1',2'-1,2)imidazo(5,4C)rifamycin | L 105 | L-105 | L105 | Redactiv | Xifaxan
Chemical Information
Molecular Formula C43H51N3O11
CAS Registry Number 80621-81-4
SMILES CC1C=CC=C(C(=O)NC2=C(C3=C(C4=C(C(=C3O)C)OC(C4=O)(OC=CC(C(C(C(C(C(C1O)C)O)C)OC(=O )C)C)OC)C)C5=C2N6C=CC(=CC6=N5)C)O)C
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)
Abdominal discomfort07.01.06.001--Not Available
Abdominal distension07.01.04.0010.006631%
Abdominal pain07.01.05.0020.013999%
Abdominal pain lower07.01.05.010--Not Available
Abdominal pain upper07.01.05.003--
Abdominal tenderness07.01.05.004--Not Available
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Ageusia17.02.07.001; 07.14.03.003--Not Available
Alanine aminotransferase increased13.03.01.003--
Ammonia increased13.03.01.0230.013999%Not Available
Amnesia19.20.01.001; 17.03.02.001--
Anaemia01.03.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Angioedema10.01.05.009; 23.04.01.001--Not Available
Anxiety19.06.02.002--
Arthralgia15.01.02.001--
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.009578%
Aspartate aminotransferase increased13.03.01.006--
Asthenia08.01.01.0010.008841%Not Available
Back pain15.03.04.005--
Bacteraemia11.01.11.0010.000577%
Blister23.03.01.001; 12.01.06.0020.001474%Not Available
Blood bilirubin increased13.03.01.0080.001474%
Blood creatine phosphokinase increased13.04.01.001--
Blood glucose decreased13.02.02.0010.002210%Not Available
Blood pressure increased13.14.03.005--Not Available
Blood sodium decreased13.11.01.0120.001474%Not Available
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.004--Not Available
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