Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Edaravone
Drug ID BADD_D02508
Description Edaravone is a free radical scavenger approved in May, 2017 for the treatment of amyotrophic lateral scleorosis (ALS). Clinical studies showed that the treatment attenuated deterioration of the disease when compared to placebo. It has been previously investigated for the treatment of ischemic stroke, reperfusion Injury, and myocardial Infarction as it possesses antioxidant and anti-apoptotic properties. Being a low molecular weight molecule with good water and lipid-soluble properies, it is therapeutically advantageous in crossing the blood-brain barrier to mediate nootropic and neuroprotective effects. Oral formulation of edaravone is currently under development.
Indications and Usage Indicated for improving neurological symptoms and damage from acute ischemic stroke and delaying disease progression of ALS.
Marketing Status approved; investigational
ATC Code N07XX14
DrugBank ID DB12243
KEGG ID D01552
MeSH ID D000077553
PubChem ID 4021
TTD Drug ID D06DLI
NDC Product Code 53296-0120; 70510-2171; 53069-1070; 72643-034; 70510-2322; 70510-2191; 16436-0120; 69037-0060; 70510-2321; 64552-4098; 14501-0100; 71796-017; 73435-008
UNII S798V6YJRP
Synonyms Edaravone | Norantipyrine | Norphenazone | Edarabone | 1-Phenyl-3-methyl-5-pyrazolone | 1 Phenyl 3 methyl 5 pyrazolone | 3-Methyl-1-phenyl-2-pyrazolin-5-one | 3 Methyl 1 phenyl 2 pyrazolin 5 one | MCI 186 | MCI-186 | MCI186 | Radicava | Phenylmethylpyrazolone
Chemical Information
Molecular Formula C10H10N2O
CAS Registry Number 89-25-8; 19735-89-8
SMILES CC1=NN(C(=O)C1)C2=CC=CC=C2
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)
Respiratory disorder22.02.07.0020.001077%Not Available
Respiratory failure22.02.06.002; 14.01.04.0030.002692%
Speech disorder22.12.03.027; 19.19.02.002; 17.02.08.0030.002746%Not Available
Subarachnoid haemorrhage17.08.01.010; 12.01.10.011; 24.07.04.0040.000808%Not Available
Therapeutic response unexpected08.06.01.0010.004845%Not Available
Transient ischaemic attack17.08.04.001; 24.04.06.0050.000538%
Tremor17.01.06.0020.002100%
Mobility decreased15.03.05.023; 17.02.05.018; 08.01.03.0300.004845%Not Available
Poor venous access24.03.02.0170.001184%Not Available
General physical health deterioration08.01.03.0180.003015%Not Available
Balance disorder08.01.03.081; 17.02.02.0070.001184%Not Available
Deep vein thrombosis24.01.02.0030.000808%Not Available
Musculoskeletal stiffness15.03.05.0270.002100%Not Available
Infusion site pain12.07.05.002; 08.02.05.0140.001830%Not Available
Limb discomfort15.03.04.0140.000538%Not Available
Disease progression08.01.03.0380.028209%
Infusion site extravasation12.07.05.008; 08.02.05.0070.001830%
Acute kidney injury20.01.03.0160.002423%
Haemorrhagic cerebral infarction24.07.04.026; 17.08.01.0500.000538%Not Available
Haemorrhagic infarction24.04.02.0080.000808%Not Available
Gastric fistula07.11.05.011; 12.02.03.0180.000538%
Catheter site thrombosis24.01.01.038; 12.07.02.029; 08.02.02.0290.001184%Not Available
Illness08.01.03.0910.001184%Not Available
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