Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Thalidomide
Drug ID BADD_D02192
Description A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects. It has been reintroduced and used for a number of immunological and inflammatory disorders. Thalidomide displays immunosuppresive and anti-angiogenic activity. It inhibits release of tumor necrosis factor-alpha from monocytes, and modulates other cytokine action. [PubChem]
Indications and Usage For the acute treatment of the cutaneous manifestations of moderate to severe erythema nodosum leprosum (ENL). Also for use as maintenance therapy for prevention and suppression of the cutaneous manifestations of ENL recurrence.
Marketing Status approved; investigational; withdrawn
ATC Code L04AX02
DrugBank ID DB01041
KEGG ID D00754
MeSH ID D013792
PubChem ID 5426
TTD Drug ID D0U7GK
NDC Product Code 17205-205; 59572-215; 68554-0011; 82991-205; 59572-220; 17337-0301; 59572-210; 59572-205; 63818-0424
UNII 4Z8R6ORS6L
Synonyms Thalidomide | Sedoval | Thalomid
Chemical Information
Molecular Formula C13H10N2O4
CAS Registry Number 50-35-1
SMILES C1CC(=O)NC(=O)C1N2C(=O)C3=CC=CC=C3C2=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)
Graft versus host disease10.02.01.027; 12.02.09.0010.000241%Not Available
Granulocytopenia01.02.03.003--Not Available
Gynaecomastia21.05.04.003; 05.05.02.003--
Haematuria21.10.01.018; 24.07.01.047; 20.02.01.006--
Haemolytic anaemia01.06.03.0020.000241%Not Available
Hangover08.01.09.018--Not Available
Headache17.14.01.001--
Hepatic cirrhosis09.01.04.0010.001085%Not Available
Hepatic encephalopathy17.13.01.003; 09.01.03.0060.000482%Not Available
Hepatic failure09.01.03.0020.000964%
Hepatitis09.01.07.004--Not Available
Hepatocellular injury09.01.07.008--Not Available
Hepatomegaly09.01.05.0010.000530%Not Available
Hernia08.01.04.0010.000241%Not Available
Herpes simplex23.11.05.004; 11.05.02.001--Not Available
Hiccups22.12.01.001; 07.01.06.0090.000530%
Hodgkin's disease16.31.01.001; 01.16.01.001--Not Available
Hodgkin's disease lymphocyte depletion type stage unspecified16.31.03.001; 01.16.03.001--Not Available
Hodgkin's disease lymphocyte predominance type stage unspecified16.31.04.001; 01.16.04.001--Not Available
Hodgkin's disease nodular sclerosis16.31.02.002; 01.16.02.002--Not Available
Hostility19.05.01.003--Not Available
Hydrocephalus17.07.01.0010.000482%
Hyperaesthesia23.03.03.080; 17.02.06.004--Not Available
Hyperbilirubinaemia14.11.01.010; 09.01.01.003; 01.06.04.003--Not Available
Hypercalcaemia14.04.01.003; 05.04.01.0020.000482%
Hypercholesterolaemia14.08.01.001--Not Available
Hyperglycaemia05.06.02.002; 14.06.02.002--
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hyperkalaemia14.05.03.0010.000844%
Hyperkinesia17.01.02.008--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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