Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Didanosine
Drug ID BADD_D00661
Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen. This modification prevents the formation of phosphodiester linkages which are needed for the completion of nucleic acid chains. Didanosine is a potent inhibitor of HIV replication, acting as a chain-terminator of viral DNA by binding to reverse transcriptase; ddI is then metabolized to dideoxyadenosine triphosphate, its putative active metabolite.
Indications and Usage For use, in combination with other antiretroviral agents, in the treatment of HIV-1 infection in adults.
Marketing Status approved
ATC Code J05AF02
DrugBank ID DB00900
KEGG ID D00296
MeSH ID D016049
PubChem ID 135398739
TTD Drug ID D06FDR
NDC Product Code 65015-794; 65862-400; 65862-322; 68554-0012
UNII K3GDH6OH08
Synonyms Didanosine | Dideoxyinosine | 2',3'-Dideoxyinosine | 2',3' Dideoxyinosine | ddI (Antiviral) | Videx | NSC-612049 | NSC 612049 | NSC612049
Chemical Information
Molecular Formula C10H12N4O3
CAS Registry Number 69655-05-6
SMILES C1CC(OC1CO)N2C=NC3=C2N=CNC3=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)
Parotid gland enlargement07.06.03.001--Not Available
Portal hypertension24.08.06.001; 09.01.06.006--
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Retinal anomaly congenital06.13.01.001; 03.01.03.002--Not Available
Retinal degeneration06.09.03.002--Not Available
Retinal depigmentation06.09.03.004--Not Available
Retinal disorder06.08.03.005--Not Available
Rhabdomyolysis15.05.05.002--
Sensory loss17.02.07.007--Not Available
Sialoadenitis11.01.04.002; 07.06.04.002--
Thrombocytopenia01.08.01.002--Not Available
Vomiting07.01.07.003--
Fat redistribution14.08.04.002--Not Available
Musculoskeletal disorder15.03.05.025--Not Available
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Metabolic disorder14.11.01.001--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Neurological symptom17.02.05.010--Not Available
Inflammation10.02.01.089; 08.01.05.007--Not Available
Decreased appetite08.01.09.028; 14.03.01.005--
Blood disorder01.05.01.004--Not Available
Autoimmune disorder10.04.04.003--
Hepatobiliary disease09.01.08.003--Not Available
Renal impairment20.01.03.010--Not Available
Lipohypertrophy23.07.01.005; 14.08.04.009--
Liver injury12.01.17.012; 09.01.07.022--Not Available
Acute kidney injury20.01.03.016--
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ADReCS-Target
Drug Name ADR Term Target
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