Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Zidovudine
Drug ID BADD_D02383
Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. The compound is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA during reverse transcription. It improves immunologic function, partially reverses the HIV-induced neurological dysfunction, and improves certain other clinical abnormalities associated with AIDS. Its principal toxic effect is dose-dependent suppression of bone marrow, resulting in anemia and leukopenia. [PubChem]
Indications and Usage Used in combination with other antiretroviral agents for the treatment of human immunovirus (HIV) infections.
Marketing Status approved
ATC Code J05AF01
DrugBank ID DB00495
KEGG ID D00413
MeSH ID D015215
PubChem ID 35370
TTD Drug ID D01XYJ
NDC Product Code 65015-765; 31722-509; 49702-212; 53104-7545; 68554-0047; 65862-107; 65015-703; 65862-024; 53873-070; 58326-2172; 65862-258; 49702-213; 65862-048; 70518-1656; 49587-101; 49702-211; 65862-321; 68554-0017; 70159-003
UNII 4B9XT59T7S
Synonyms Zidovudine | Azidothymidine | AZT Antiviral | 3'-Azido-3'-deoxythymidine | 3' Azido 3' deoxythymidine | AZT (Antiviral) | 3'-Azido-2',3'-Dideoxythymidine | 3' Azido 2',3' Dideoxythymidine | AZT, Antiviral | Antiviral AZT | Retrovir | BW A509U | BWA-509U | BWA 509U | BWA509U
Chemical Information
Molecular Formula C10H13N5O4
CAS Registry Number 30516-87-1
SMILES CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)N=[N+]=[N-]
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)
Low birth weight baby18.04.02.0030.008841%Not Available
Type 2 diabetes mellitus14.06.01.003; 05.06.01.0030.004421%Not Available
Mucosal pigmentation08.01.06.006--Not Available
Intellectual disability19.21.06.001; 17.03.07.0010.004421%Not Available
Acute kidney injury20.01.03.0160.011051%
Foetal growth restriction18.03.01.0020.008841%
Sensitisation10.02.01.012; 08.01.05.009--Not Available
Anaplastic large-cell lymphoma16.20.01.003; 01.12.01.0030.006631%Not Available
Antiphospholipid syndrome10.04.01.009; 01.01.02.016; 24.01.01.029; 18.02.04.0020.004421%Not Available
Small for dates baby18.04.02.0020.004421%Not Available
Non-cirrhotic portal hypertension24.08.06.003; 09.01.06.0190.004421%Not Available
Astrocytoma malignant17.20.02.007; 16.30.02.0070.006631%Not Available
Immune thrombocytopenia10.02.01.083; 01.08.01.0130.004421%Not Available
Lymphangiectasia24.09.02.009; 01.09.01.0340.004421%Not Available
Neutropenia neonatal01.02.03.016; 18.04.03.0070.004421%Not Available
Post streptococcal glomerulonephritis20.05.01.023; 11.07.01.0290.013262%Not Available
Treatment noncompliance08.06.01.067; 12.09.02.0060.004421%Not Available
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ADReCS-Target
Drug Name ADR Term Target
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