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Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by an azido group.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)
Tenderness08.01.08.0050.004421%Not Available
Tension19.06.02.005--Not Available
Thrombocytopenia01.08.01.0020.004421%Not Available
Thrombosis24.01.01.0060.004421%Not Available
Tongue disorder07.14.01.002--Not Available
Tongue oedema10.01.05.008; 23.04.01.009; 07.14.02.007--Not Available
Toxic epidermal necrolysis23.03.01.008; 12.03.01.015; 11.07.01.006; 10.01.01.006--
Tremor17.01.06.002--
Urethral disorder20.07.01.002--Not Available
Urinary hesitation20.02.02.009--Not Available
Urinary tract disorder20.08.01.001--Not Available
Urticaria23.04.02.001; 10.01.06.001--
Varicose vein24.10.04.0010.004421%Not Available
Vasculitis24.12.04.027; 10.02.02.006--
Vertigo04.04.01.003; 17.02.12.002--
Vomiting07.01.07.0030.017682%
Weight decreased13.15.01.005--
Wheezing22.03.01.009--
Fat redistribution14.08.04.002--Not Available
Hypoacusis04.02.01.006--
Retinal toxicity12.03.01.036; 06.09.03.0130.006631%Not Available
Peripheral swelling08.01.03.053; 02.05.04.0150.004421%Not Available
Localised oedema14.05.06.009; 08.01.07.011; 02.05.04.006--
Psychomotor skills impaired19.22.01.002; 17.02.10.0050.004421%Not Available
Lipodystrophy acquired14.08.04.008; 23.07.01.0030.011051%Not Available
Left ventricular hypertrophy02.04.02.014--Not Available
Lipase13.05.01.011--Not Available
Deep vein thrombosis24.01.02.0030.004421%Not Available
Necrotising colitis07.08.01.0130.006631%Not Available
Lymphatic disorder01.09.01.003--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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