Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ethambutol
Drug ID BADD_D00841
Description Ethambutol is a bacteriostatic agent indicated alongside medications such as [isoniazid], [rifampin], and [pyrazinamide] in the treatment of pulmonary tuberculosis.[L31743] Ethambutol was first described in the literature in 1961.[A229048] It was developed out of a need for therapies active against isoniazid resistant strains of _Mycobacterium tuberculosis_.[A229048] Ethambutol was granted FDA approval on 6 November 1967.[L31663]
Indications and Usage Ethambutol is indicated in combination with other anti-tuberculosis drugs in the treatment of pulmonary tuberculosis.[L31663] Ethambutol is commonly used in combination with [isoniazid], [rifampin], and [pyrazinamide].[L31743]
Marketing Status approved
ATC Code J04AK02
DrugBank ID DB00330
KEGG ID D07925
MeSH ID D004977
PubChem ID 14052
TTD Drug ID D08QME
NDC Product Code 60592-243
UNII 8G167061QZ
Synonyms Ethambutol | Dexambutol | Etibi | EMB-Fatol | EMB Fatol | Etambutol Llorente | Llorente, Etambutol | Ethambutol Hydrochloride | Hydrochloride, Ethambutol | Myambutol | Miambutol | EMB-Hefa | EMB Hefa
Chemical Information
Molecular Formula C10H24N2O2
CAS Registry Number 74-55-5
SMILES CCC(CO)NCCNC(CC)CO
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)
Abdominal discomfort07.01.06.0010.001027%Not Available
Abdominal pain07.01.05.0020.001027%
Alopecia23.02.02.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Arthralgia15.01.02.0010.001027%
Asthenia08.01.01.0010.001540%Not Available
Blindness06.02.10.003; 17.17.01.003--Not Available
Body temperature increased13.15.01.001--Not Available
Cardio-respiratory arrest22.02.06.007; 02.03.04.0020.001027%Not Available
Chills08.01.09.001; 15.05.03.016--
Cholestasis09.01.01.0010.001027%Not Available
Chromaturia20.02.01.0020.002259%
Coagulopathy01.01.02.0010.001027%Not Available
Colour blindness06.02.09.001; 03.01.01.001--Not Available
Condition aggravated08.01.03.0040.001027%Not Available
Confusional state19.13.01.001; 17.02.03.005--
Dermatitis23.03.04.002--Not Available
Dermatitis exfoliative23.03.07.001; 10.01.01.004--
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Disorientation19.13.01.002; 17.02.05.015--Not Available
Dizziness17.02.05.003; 02.11.04.006; 24.06.02.0070.001027%
Drug interaction08.06.03.0010.003081%Not Available
Dysaesthesia23.03.03.077; 17.02.06.0030.001027%
Dysgeusia17.02.07.003; 07.14.03.0010.001027%
Dyspnoea02.11.05.003; 22.02.01.0040.001540%
Eosinophilia01.02.04.001--
Erythema multiforme10.01.03.015; 23.03.01.003--
Feeling abnormal08.01.09.014--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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