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Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group.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)
Hyperaesthesia23.03.03.080; 17.02.06.004--Not Available
Hyperbilirubinaemia14.11.01.010; 09.01.01.003; 01.06.04.003--Not Available
Hyperhidrosis23.02.03.004; 08.01.03.028--
Hyperlactacidaemia14.01.01.0060.006631%Not Available
Hypertriglyceridaemia14.08.02.0010.004421%
Hyporeflexia17.02.01.003--
Hypotension24.06.03.0020.004421%
Hypotonia17.05.02.002; 15.05.04.0080.006631%Not Available
Hypoxia22.02.02.003--
Influenza22.07.02.001; 11.05.03.001--Not Available
Influenza like illness08.01.03.010--
Insomnia19.02.01.002; 17.15.03.002--
Intestinal perforation07.04.06.0020.004421%Not Available
Irritability19.04.02.013; 08.01.03.011--
Jaundice23.03.03.030; 09.01.01.004; 01.06.04.004--Not Available
Lactic acidosis14.01.01.0020.006631%Not Available
Leukopenia01.02.02.0010.004421%Not Available
Liver disorder09.01.08.001--Not Available
Local reaction08.01.03.012--Not Available
Loss of consciousness17.02.04.004--Not Available
Lymphadenopathy01.09.01.0020.006631%Not Available
Lymphopenia01.02.02.0020.004421%Not Available
Macrocytosis01.07.02.003--Not Available
Macular oedema06.04.06.005--Not Available
Malaise08.01.01.003--
Mania19.16.02.002--
Mental impairment19.21.02.003; 17.03.03.002--Not Available
Metabolic acidosis14.01.01.0030.006631%Not Available
Mood swings19.04.03.001--Not Available
Mouth ulceration07.05.06.004--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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