Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Fingolimod
Drug ID BADD_D02464
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 D10001
MeSH ID D000068876
PubChem ID 107970
TTD Drug ID D07UHS
NDC Product Code 54893-0026; 60505-4332; 70771-1603; 68462-166; 64380-776; 65035-201; 31722-889; 62756-064; 68382-912; 43598-285; 43547-003; 0378-4525
UNII 3QN8BYN5QF
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 C19H33NO2
CAS Registry Number 162359-55-9
SMILES CCCCCCCCC1=CC=C(C=C1)CCC(CO)(CO)N
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)
Vitiligo23.05.02.004; 10.04.02.0040.000940%Not Available
Vitreous detachment06.09.01.002; 12.01.04.0050.001326%Not Available
Vitreous floaters06.09.01.0050.008174%
Vitreous haemorrhage24.07.05.005; 06.10.03.0010.000241%
Vulval disorder21.08.01.0070.000241%Not Available
Vulvovaginal discomfort21.08.02.0050.000651%Not Available
Vulvovaginal dryness21.08.02.0030.000362%
Wandering pacemaker02.03.03.0180.000241%Not Available
Wheezing22.03.01.0090.005521%
Xerosis08.01.03.0160.001423%Not Available
Yellow skin23.03.03.042; 09.01.01.009; 08.01.03.0460.001013%Not Available
Zinc deficiency14.13.01.0010.000241%Not Available
Mental status changes19.07.01.001--Not Available
Mobility decreased15.03.05.023; 17.02.05.018; 08.01.03.0300.020253%Not Available
Multiple sclerosis relapse17.16.01.0030.194554%Not Available
Fibromyalgia15.05.02.0020.002146%Not Available
Lip disorder07.05.01.0080.000530%Not Available
Musculoskeletal disorder15.03.05.0250.001543%Not Available
Coronary artery dissection12.02.01.035; 24.02.02.001; 02.02.01.0040.000362%Not Available
Agnosia17.02.03.012; 19.21.01.0060.000362%Not Available
Postictal state19.13.01.005; 17.02.04.0140.000362%Not Available
Axillary pain08.01.08.0150.000241%Not Available
Energy increased08.01.03.0170.000892%Not Available
Breast calcifications21.05.04.0090.000892%Not Available
Sebaceous hyperplasia23.02.07.0050.001133%Not Available
Deafness unilateral04.02.01.0110.000723%Not Available
Ischaemic cardiomyopathy02.04.01.004; 24.04.04.0190.000482%Not Available
Hypoacusis04.02.01.0060.006510%
Onychoclasis23.02.05.0050.001591%Not Available
Seasonal allergy06.04.01.013; 22.04.04.008; 10.01.04.0010.002773%Not Available
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