Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Teriflunomide
Drug ID BADD_D02165
Description Teriflunomide is the active metabolite of leflunomide, and it acts as an immunomodulatory agent by inhibiting pyrimidine synthesis. It is marketed under the name Aubagio® and is indicated for the treatment of multiple sclerosis, specifically relapsing forms. The FDA label states an important warning about the risk of hepatoxicity and teratogenicity for patients using teriflunomide.
Indications and Usage Used in the treatment of relapsing forms of multiple sclerosis (MS).
Marketing Status approved
ATC Code L04AA31
DrugBank ID DB08880
KEGG ID D10172
MeSH ID C527525
PubChem ID 54684141
TTD Drug ID Not Available
NDC Product Code 47621-049; 51991-882; 58468-0211; 59651-054; 62332-314; 69339-169; 70377-017; 70710-1114; 12579-185; 12579-190; 59651-036; 65727-058; 0378-0628; 69238-1303; 69238-1304; 51991-881; 0480-3157; 69539-315; 69539-316; 70512-851; 66499-0059; 16729-400; 70710-1115; 70771-1011; 53747-061; 66039-916; 59651-055; 0378-0627; 70771-1010; 59285-001; 63850-8081; 69037-0016; 16729-399; 46708-314; 0480-3156; 69339-170; 69539-033; 70377-018; 12579-191; 42291-831; 60505-4478; 69025-129; 69025-130; 69539-032; 31722-247; 46708-313; 62332-313; 12579-186; 14501-0086; 17337-0070; 43598-281; 43598-282; 60505-4477; 68462-423; 68462-424; 0781-5747; 0781-5755; 31722-246; 42291-830; 58468-0210
UNII 1C058IKG3B
Synonyms teriflunomide | (Z)-2-cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)-2-butenamide | (2Z)-2-cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)-2-butenamide | 2-cyano-3-hydroxy-N-(4-(trifluoromethyl)phenyl)-2-butenamide | 2-hydroxyethylidene-cyanoacetic acid-4-trifluoromethyl anilide | RS 61980 | Aubagio | HMR1726 | HMR-1726 | A 771726 | A 1726 | A771726 | A-771726 | A77 1726
Chemical Information
Molecular Formula C12H9F3N2O2
CAS Registry Number 163451-81-8
SMILES CC(=C(C#N)C(=O)NC1=CC=C(C=C1)C(F)(F)F)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)
Tremor17.01.06.0020.024449%
Trichorrhexis23.02.06.0070.000940%Not Available
Trigeminal neuralgia17.04.08.0010.003303%Not Available
Ulcer08.03.06.0010.002049%Not Available
Upper gastrointestinal haemorrhage24.07.02.024; 07.12.02.006--
Upper respiratory tract infection22.07.03.011; 11.01.13.009--
Urethral disorder20.07.01.002--Not Available
Urge incontinence20.02.02.0080.000530%Not Available
Urinary incontinence20.02.02.010; 17.05.01.0080.009114%
Urinary retention20.02.02.011--
Urinary tract disorder20.08.01.0010.000651%Not Available
Urinary tract infection20.08.02.001; 11.01.14.004--
Urine abnormality20.02.01.0130.000820%Not Available
Urine flow decreased20.02.02.0120.000530%Not Available
Uterine leiomyoma21.07.02.004; 16.04.02.0010.000482%Not Available
Uveitis10.02.01.023; 06.04.03.0030.001567%
Vein disorder24.03.02.0150.000241%Not Available
Vertigo17.02.12.002; 04.04.01.0030.012586%
Vision blurred17.17.01.010; 06.02.06.0070.019289%
Visual field defect17.17.01.001; 06.02.07.0030.000603%Not Available
Visual impairment06.02.10.0130.040772%Not Available
Vitamin B12 deficiency14.12.02.0040.000241%Not Available
Vitiligo23.05.02.004; 10.04.02.0040.001881%Not Available
Vitreous floaters06.09.01.0050.000772%
Vomiting07.01.07.003--
Vulval ulceration23.07.03.013; 21.08.01.0130.000651%Not Available
Weight decreased13.15.01.005--
White blood cell count decreased13.01.06.012--
Yellow skin23.03.03.042; 09.01.01.009; 08.01.03.0460.000772%Not Available
Mobility decreased15.03.05.023; 17.02.05.018; 08.01.03.0300.066812%Not Available
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