Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Penicillamine
Drug ID BADD_D01709
Description Penicillamine is a pharmaceutical of the chelator class. The pharmaceutical form is D-penicillamine, as L-penicillamine is toxic (it inhibits the action of pyridoxine). It is an α-amino acid metabolite of penicillin, although it has no antibiotic properties.
Indications and Usage For treatment of Wilson's disease, cystinuria and active rheumatoid arthritis.
Marketing Status approved
ATC Code M01CC01
DrugBank ID DB00859
KEGG ID D00496
MeSH ID D010396
PubChem ID 5852
TTD Drug ID D08HZC
NDC Product Code 59285-014; 76339-159; 0254-2000; 68682-020; 70010-907; 0591-4171; 68022-7041; 72640-012; 25010-705; 60505-4696; 62559-970; 71205-916; 0037-4401; 62207-013; 71052-491; 43598-634; 51991-974; 70748-153; 42973-230; 51552-1096; 49884-146; 68475-201; 59651-245; 70159-004; 76003-0870
UNII GNN1DV99GX
Synonyms Penicillamine | Mercaptovaline | D-Penicillamine | D Penicillamine | Dimethylcysteine | beta,beta-Dimethylcysteine | beta,beta Dimethylcysteine | D-3-Mercaptovaline | D 3 Mercaptovaline | Metalcaptase | Cuprimine | Copper Penicillaminate | Penicillaminate, Copper | Cuprenil
Chemical Information
Molecular Formula C5H11NO2S
CAS Registry Number 771431-20-0
SMILES CC(C)(C(C(=O)O)N)S
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)
Drug eruption23.03.05.001; 10.01.01.005; 08.01.06.015--Not Available
Drug hypersensitivity10.01.01.0010.000986%Not Available
Drug ineffective08.06.01.0060.000190%Not Available
Dysgeusia17.02.07.003; 07.14.03.001--
Dystonia17.01.03.0010.000051%Not Available
Elastosis perforans23.03.02.0100.000051%Not Available
Eosinophilia01.02.04.001--
Extravasation08.01.03.008--Not Available
Febrile neutropenia08.05.02.004; 01.02.03.0020.000077%
Glomerulonephritis20.05.01.001; 10.02.01.006--Not Available
Glomerulonephritis membranous20.05.01.007--Not Available
Glomerulonephritis rapidly progressive20.05.01.004; 10.04.04.0080.000051%Not Available
Glossitis07.14.01.001--Not Available
Goodpasture's syndrome22.01.01.010; 20.05.01.009; 10.04.04.006--Not Available
Guillain-Barre syndrome17.09.01.001; 11.07.01.001; 10.04.10.005--
Haematuria20.02.01.006; 21.10.01.018; 24.07.01.047--
Haemoglobin13.01.05.018--Not Available
Haemolytic anaemia01.06.03.002--Not Available
Hepatic failure09.01.03.002--
Hepatic function abnormal09.01.02.001--Not Available
Hepatitis toxic09.01.07.017; 12.03.01.016--Not Available
Hyperplasia08.03.04.008--Not Available
Hyperpyrexia08.05.02.002--Not Available
Hypersensitivity10.01.03.0030.000175%
Hypogeusia07.14.03.002; 17.02.07.004--Not Available
Hypoglycaemia14.06.03.001; 05.06.03.001--
Injury12.01.08.004--Not Available
Interstitial lung disease22.01.02.003; 10.02.01.033--Not Available
Iron deficiency14.13.02.002--Not Available
Leukaemia01.10.03.001; 16.01.03.001--
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ADReCS-Target
Drug Name ADR Term Target
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