Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Fingolimod hydrochloride
Drug ID BADD_D00899
Description Multiple sclerosis or MS is a devastating inflammatory disease that often progresses and causes severe neurological, physical, and cognitive effects.[A176474] Fingolimod is a sphingosine 1-phosphate receptor modulator for the treatment of relapsing-remitting multiple sclerosis. It was developed by Novartis and initially approved by the FDA in 2010.[L12651] Fingolimod is currently being studied for the treatment of COVID-19, the disease caused by infection with the SARS-CoV-2 virus. Phase 2 clinical trials are currently underway and completion is expected in July 2020.[L12654]
Indications and Usage Fingolimod is indicated for the treatment of patients aged 10 and above with relapsing forms of multiple sclerosis, which may include clinically isolated syndrome, relapsing-remitting disease, as well as active secondary progressive disease.[L12651] This drug is being studied for administration in patients infected with COVID-19 with a high risk for acute respiratory distress syndrome, or ARDS.[L12654] As of April 3 2020, this is currently not an approved indication and clinical trials are underway.[L12657]
Marketing Status approved; investigational
ATC Code L04AA27
DrugBank ID DB08868
KEGG ID D04187
MeSH ID D000068876
PubChem ID 107969
TTD Drug ID D0HI1K
NDC Product Code 57741-3100; 16729-342; 67877-476; 54893-0025; 65015-834; 69037-0006; 65035-138; 66039-886; 82920-019; 65727-036; 82245-0106
UNII G926EC510T
Synonyms Fingolimod Hydrochloride | 2-Amino-2-(2-(4-octylphenyl)ethyl)-1,3-propanediol hydrochloride | FTY-720 | FTY 720 | FTY720 | Gilenya | Gilenia | Fingolimod
Chemical Information
Molecular Formula C19H34ClNO2
CAS Registry Number 162359-56-0
SMILES CCCCCCCCC1=CC=C(C=C1)CCC(CO)(CO)N.Cl
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)
Acute disseminated encephalomyelitis17.16.02.003; 10.04.10.010--Not Available
Alanine aminotransferase increased13.03.04.005--
Alopecia23.02.02.001--
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.001--Not Available
Atrioventricular block02.03.01.002--Not Available
Atrioventricular block complete02.03.01.003--
Atrioventricular block first degree02.03.01.004--
Atrioventricular block second degree02.03.01.005--
B-cell lymphoma16.28.01.001; 01.15.01.001--Not Available
Back pain15.03.04.005--
Blood triglycerides increased13.12.03.001--Not Available
Bradycardia02.03.02.002--Not Available
Bronchitis22.07.01.001; 11.01.09.001--
Cardiac arrest02.03.04.001--
Cerebral haemorrhage24.07.04.001; 17.08.01.003--Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Cough22.02.03.001--
Death08.04.01.001--
Depressed mood19.15.02.001--Not Available
Depression19.15.01.001--
Diarrhoea07.02.01.001--
Diffuse large B-cell lymphoma16.28.02.001; 01.15.02.001--Not Available
Dizziness24.06.02.007; 17.02.05.003; 02.11.04.006--
Dyspnoea02.11.05.003; 22.02.01.004--
Eczema23.03.04.006--
Eye disorder06.08.03.001--Not Available
Eye pain06.08.03.002--
Fatigue08.01.01.002--
Gamma-glutamyltransferase increased13.03.04.024--
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