Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Leflunomide
Drug ID BADD_D01252
Description Leflunomide is a pyrimidine synthesis inhibitor belonging to the DMARD (disease-modifying antirheumatic drug) class of drugs, which are chemically and pharmacologically very heterogeneous. Leflunomide was approved by FDA and in many other countries (e.g., Canada, Europe) in 1999.
Indications and Usage For the management of the signs and symptoms of active rheumatoid arthritis (RA) to improve physical function and to slow the progression of structural damage associated with the disease. Has also been used for the prevention of acute and chronic rejection in recipients of solid organ trasnplants and is designated by the FDA as an orphan drug for this use.
Marketing Status approved; investigational
ATC Code L04AA13
DrugBank ID DB01097
KEGG ID D00749
MeSH ID D000077339
PubChem ID 3899
TTD Drug ID D08ROP
NDC Product Code 23155-044; 35573-447; 59651-349; 35573-448; 12579-510; 0088-2161; 59651-348; 60505-2502; 70748-130; 72266-133; 60505-2503; 0088-2160; 23155-043; 50268-478; 62332-061; 70771-1491; 70771-1492; 12579-509; 0955-1737; 71052-260; 10702-278; 46708-437; 0955-1735; 51927-4520; 10702-277; 0088-2162; 50268-477; 62332-062; 70518-3240; 70748-129; 14593-911; 46708-436; 70710-1157; 70710-1158; 72266-132; 53104-7557; 57741-3600; 66499-0001; 42291-420; 42291-421; 50090-5992
UNII G162GK9U4W
Synonyms Leflunomide | N-(4-Trifluoromethyphenyl)-5-methylisoxazole-4-carboxamide | HWA 486 | HWA-486 | HWA486 | SU101 | Arava
Chemical Information
Molecular Formula C12H9F3N2O2
CAS Registry Number 75706-12-6
SMILES CC1=C(C=NO1)C(=O)NC2=CC=C(C=C2)C(F)(F)F
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)
Panniculitis10.01.03.024; 23.07.02.0020.000428%Not Available
Papule23.03.03.0380.000428%Not Available
Paraesthesia23.03.03.094; 17.02.06.0050.004456%
Parkinsonism17.01.05.0030.000428%Not Available
Pelvic pain21.10.01.001; 20.02.03.007; 07.01.06.012--
Pericardial effusion02.06.01.0020.000643%
Pericarditis02.06.02.0010.001285%
Peripheral coldness23.06.04.008; 24.04.03.006; 08.01.09.0100.000943%Not Available
Pharyngeal oedema23.04.01.016; 22.04.05.003; 10.01.05.0160.001371%Not Available
Pharyngitis22.07.03.004; 07.05.07.004; 11.01.13.003--
Photosensitivity reaction23.03.09.003--
Pleural effusion22.05.02.002--
Pleurisy22.05.01.0010.000643%Not Available
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Pneumonitis22.01.01.0060.002656%
Pneumothorax22.05.02.0030.000643%
Pollakiuria20.02.02.007--
Polyneuropathy17.09.03.0120.002999%Not Available
Pregnancy18.08.02.0040.000943%Not Available
Premature baby18.04.02.0010.000857%Not Available
Premature rupture of membranes18.07.01.0030.000428%Not Available
Productive cough22.02.03.005--
Prostatic disorder21.04.01.001--Not Available
Proteinuria20.02.01.0110.000857%
Prurigo23.03.04.0170.000428%Not Available
Pruritus23.03.12.0010.008355%
Psoriasis23.03.14.002; 10.02.01.0360.003599%Not Available
Psoriatic arthropathy23.03.14.005; 15.01.10.001; 10.02.01.0310.001500%Not Available
Pulmonary fibrosis22.01.02.0060.000643%
Pulmonary granuloma22.01.01.0140.000428%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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