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Description A piperidinyl isoindole originally introduced as a non-barbiturate hypnotic, but withdrawn from the market due to teratogenic effects.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Marketing Status approved; investigational; withdrawn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)
Mental status changes19.07.01.001--Not Available
Musculoskeletal disorder15.03.05.0250.000844%Not Available
Hypoacusis04.02.01.0060.002266%
Seasonal allergy22.04.04.008; 10.01.04.001; 06.04.01.0130.000820%Not Available
Peripheral swelling08.01.03.053; 02.05.04.0150.020543%Not Available
Red blood cell sedimentation rate decreased13.01.03.003--Not Available
General physical health deterioration08.01.03.0180.003086%Not Available
Blood phosphorus decreased13.11.01.015--Not Available
Muscle tightness15.05.03.0070.000820%Not Available
Balance disorder17.02.02.007; 08.01.03.0810.005256%Not Available
Lung cancer metastatic22.08.01.004; 16.19.02.0030.000241%Not Available
Deep vein thrombosis24.01.02.0030.006872%Not Available
Cardiopulmonary failure22.02.06.004; 02.05.01.0040.000362%Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.0150.000241%Not Available
Respiratory tract congestion22.02.07.0030.000940%Not Available
Lymphatic disorder01.09.01.003--Not Available
Foetor hepaticus09.01.05.006; 07.01.06.026--Not Available
Musculoskeletal stiffness15.03.05.027--Not Available
Protein urine present13.13.02.006--Not Available
Musculoskeletal discomfort15.03.04.0010.000530%Not Available
Inappropriate antidiuretic hormone secretion14.05.07.001; 05.03.03.001--Not Available
Tracheal disorder22.04.07.0050.000241%Not Available
Bronchopneumopathy22.02.07.010--Not Available
Affect lability19.04.01.001--Not Available
Pulmonary mass22.02.07.0040.000241%Not Available
Cutaneous lupus erythematosus23.03.02.008; 15.06.02.007; 10.04.03.0070.000820%Not Available
Hypoaesthesia oral17.02.06.021; 07.05.05.0030.000651%Not Available
Paraesthesia oral07.05.05.035; 17.02.06.0080.001230%Not Available
Spleen palpable13.15.01.011--Not Available
Toxic skin eruption12.03.01.073; 23.03.05.003; 10.01.01.008--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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