Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Flucaonazole
Drug ID BADD_D00909
Description Not Available
Indications and Usage Not Available
Marketing Status Not Available
ATC Code Not Available
DrugBank ID Not Available
KEGG ID Not Available
MeSH ID Not Available
PubChem ID Not Available
TTD Drug ID Not Available
NDC Product Code Not Available
UNII Not Available
Synonyms Not Available
Chemical Information
Molecular Formula Not Available
CAS Registry Number Not Available
SMILES Not Available
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)
Malaise08.01.01.003--
Myalgia15.05.02.001--
Nausea07.01.07.001--
Neutropenia01.02.03.004--Not Available
Paraesthesia17.02.06.005; 23.03.03.094--
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Seizure17.12.03.001--
Somnolence19.02.05.003; 17.02.04.006--
Stevens-Johnson syndrome23.03.01.007; 12.03.01.014; 11.07.01.005; 10.01.01.045--
Thrombocytopenia01.08.01.002--Not Available
Torsade de pointes02.03.04.005--Not Available
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.006--
Tremor17.01.06.002--
Vertigo17.02.12.002; 04.04.01.003--
Vomiting07.01.07.003--
Acute generalised exanthematous pustulosis10.01.01.034; 23.03.10.002; 12.03.01.005; 11.07.01.018--Not Available
Transaminases increased13.03.04.036--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Blood test abnormal13.18.01.003--Not Available
Renal function test abnormal13.13.01.012--Not Available
Exfoliative rash23.03.07.006--Not Available
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