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Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group.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)
Blood creatine phosphokinase increased13.04.01.001--
Blood lactate dehydrogenase increased13.04.02.002--
Body temperature increased13.15.01.001--Not Available
Cardiac failure02.05.01.0010.008841%
Cardiac failure congestive02.05.01.002--Not Available
Cardiomyopathy02.04.01.001--Not Available
Cerebellar syndrome17.02.02.0020.004421%Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.011--Not Available
Chills15.05.03.016; 08.01.09.001--
Cholestasis09.01.01.0010.004421%Not Available
Condition aggravated08.01.03.0040.006631%Not Available
Confusional state19.13.01.001; 17.02.03.005--
Congenital anomaly03.02.01.001--Not Available
Constipation07.02.02.001--
Cough22.02.03.001--
Cystitis20.03.02.002; 11.01.14.001--
Deafness04.02.01.001--Not Available
Dehydration14.05.05.0010.004421%
Depression19.15.01.001--
Dermatitis23.03.04.002--Not Available
Developmental delay19.07.05.003; 08.01.03.0370.004421%Not Available
Diabetes mellitus14.06.01.001; 05.06.01.0010.006631%Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness17.02.05.003; 02.11.04.006; 24.06.02.007--
Drug interaction08.06.03.001--Not Available
Dysgeusia17.02.07.003; 07.14.03.001--
Dyskinesia17.01.02.0060.008841%
Dyspepsia07.01.02.001--
Dysphagia07.01.06.003--
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ADReCS-Target
Drug Name ADR Term Target
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