Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Anidulafungin
Drug ID BADD_D00143
Description Anidulafungin or Eraxis is an anti-fungal drug manufactured by Pfizer that gained approval by the Food and Drug Administration (FDA) in February 21, 2006; it was previously known as LY303366. There is preliminary evidence that it has a similar safety profile to caspofungin.
Indications and Usage For use in the treatment of the following fungal infections: Candidemia and other forms of Candida infections (intra-abdominal abscess, and peritonitis), Aspergillus infections, and esophageal candidiasis. Also considered an alternative treatment for oropharyngeal canaidiasis.
Marketing Status approved; investigational
ATC Code J02AX06
DrugBank ID DB00362
KEGG ID D03211
MeSH ID D000077612
PubChem ID 166548
TTD Drug ID D0F9BY
NDC Product Code 0009-0043; 11722-054; 0049-0114; 62227-007; 65727-072; 68254-0013; 0049-0116
UNII 9HLM53094I
Synonyms Anidulafungin | 1-((4R,5R)-4,5-Dihydroxy-N2-((4''-(pentyloxy)(1,1':4',1''-terphenyl)-4-yl)carbonyl)-L-ornithine)-echinocandin B | LY 303366 | LY303366 | LY-303366 | Eraxis
Chemical Information
Molecular Formula C58H73N7O17
CAS Registry Number 166663-25-8
SMILES CCCCCOC1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=C(C=C3)C(=O)NC4CC(C(NC(=O)C5C(C(CN5C(=O)C( NC(=O)C(NC(=O)C6CC(CN6C(=O)C(NC4=O)C(C)O)O)C(C(C7=CC=C(C=C7)O)O)O)C(C)O)C)O)O)O
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)
Pruritus23.03.12.0010.000150%
Pyrexia08.05.02.0030.000299%
Rash23.03.13.0010.000224%Not Available
Rash maculo-papular23.03.13.004--
Rash papular23.03.13.017--Not Available
Respiratory distress22.02.01.012--Not Available
Seizure17.12.03.0010.000150%
Sepsis11.01.11.003--
Sinus arrhythmia02.03.03.008--Not Available
Skin disorder23.03.03.007--Not Available
Status epilepticus17.12.03.0050.000150%Not Available
Systemic candida11.03.03.016--Not Available
Tachycardia02.03.02.0070.000150%Not Available
Thrombocytopenia01.08.01.002--Not Available
Thrombocytosis01.08.02.001--Not Available
Urethral disorder20.07.01.002--Not Available
Urinary tract disorder20.08.01.001--Not Available
Urinary tract infection20.08.02.001; 11.01.14.004--
Urticaria10.01.06.001; 23.04.02.001--
Ventricular extrasystoles02.03.04.007--Not Available
Vision blurred17.17.01.010; 06.02.06.007--
Visual impairment06.02.10.013--Not Available
Vomiting07.01.07.003--
White blood cell count decreased13.01.06.012--
White blood cell count increased13.01.06.013--Not Available
Deep vein thrombosis24.01.02.003--Not Available
Platelet count increased13.01.04.002--Not Available
Infusion related reaction12.02.05.009; 10.01.01.017; 08.01.03.002--
Lymphatic disorder01.09.01.003--Not Available
Infusion site pain12.07.05.002; 08.02.05.014--Not Available
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