Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Deflazacort
Drug ID BADD_D02492
Description Deflazacort, also known as Emflaza, is a corticosteroid prodrug used as an agent to manage Duchenne Muscular Dystrophy (DMD). It is marketed by Marathon Pharmaceuticals and was approved in February 2017 by the FDA.[L6694,FDA label] Duchenne Muscular Dystrophy is an inherited disorder resulting from mutations of the dystrophin gene, which is important for muscle function. This disease can cause serious muscle weakness and progressive breathing and cardiovascular disability, severely impacting patient quality of life and survival.[A179446,A179449,L6697] This disease usually manifests by muscle weakness in early childhood followed by loss of the ability to walk (ambulation) as early as age 7.[A179449] Deflazacort delays the onset of muscle related complications resulting from DMD[A179455], prolonging the lives of children diagnosed with this disease and exerting less harmful effects on the bone health and weight than other steroid medications.[A179452,A25340]
Indications and Usage Deflazacort is indicated for the treatment of Duchenne Muscular Dystrophy (DMD) in patients 2 years of age and older.[FDA label]
Marketing Status approved; investigational
ATC Code H02AB13
DrugBank ID DB11921
KEGG ID D03671
MeSH ID C021988
PubChem ID 189821
TTD Drug ID D09WYX
NDC Product Code 52128-135; 24002-0036; 52856-503; 52856-501; 64918-1111; 57582-040; 64918-1901; 52856-502; 52856-504; 22552-0027; 52856-505
UNII KR5YZ6AE4B
Synonyms deflazacort | Dezacor | Emflaza | Calcort | Zamene
Chemical Information
Molecular Formula C25H31NO6
CAS Registry Number 14484-47-0
SMILES CC1=NC2(C(O1)CC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)C)C(=O)COC(=O)C
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)
Pyrexia08.05.02.0030.003069%
Rash23.03.13.0010.003676%Not Available
Rash erythematous23.03.13.0290.000175%Not Available
Rash macular23.03.13.0030.000250%Not Available
Rectal prolapse07.03.01.0050.000034%Not Available
Respiratory disorder22.02.07.0020.000168%Not Available
Restlessness19.11.02.002; 17.02.05.0210.000233%
Retching07.01.07.0020.000350%Not Available
Rhinorrhoea22.12.03.0210.000525%
Scoliosis15.10.04.0010.000219%
Screaming19.04.02.020; 08.01.03.0990.000309%Not Available
Skin discolouration23.03.03.0050.000250%Not Available
Skin disorder23.03.03.0070.000134%Not Available
Skin papilloma23.10.01.002; 16.26.01.002; 11.05.07.0010.000117%
Skin striae23.01.05.0020.000425%Not Available
Sleep apnoea syndrome22.02.01.013; 19.02.05.002; 17.15.05.0010.000175%
Speech disorder22.12.03.027; 19.19.02.002; 17.02.08.0030.000250%Not Available
Strabismus17.17.01.009; 06.05.02.0040.000117%Not Available
Swelling08.01.03.0150.000384%Not Available
Swelling face08.01.03.100; 23.04.01.018; 10.01.05.0180.002709%Not Available
Tearfulness19.15.02.0050.000117%Not Available
Thirst14.03.02.007; 08.01.09.0210.000175%Not Available
Throat irritation07.05.05.037; 22.12.03.0290.000075%Not Available
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.0060.000034%
Urinary incontinence20.02.02.010; 17.05.01.0080.000175%
Vitamin D deficiency14.12.03.0030.000117%Not Available
Vomiting07.01.07.0030.004012%
Wheezing22.03.01.0090.000175%
Mobility decreased15.03.05.023; 17.02.05.018; 08.01.03.0300.000809%Not Available
Energy increased08.01.03.0170.000233%Not Available
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