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Description A dideoxynucleoside compound in which the 3'-hydroxy group on the sugar moiety has been replaced by a hydrogen.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)
Abdominal pain07.01.05.002--
Abdominal pain upper07.01.05.003--
Acquired immunodeficiency syndrome11.05.17.007; 10.03.03.001--Not Available
Agranulocytosis01.02.03.001--Not Available
Alanine aminotransferase increased13.03.04.005--
Alopecia23.02.02.001--
Amylase increased13.05.01.009--
Anaemia01.03.02.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction10.01.07.003; 24.06.03.007--Not Available
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.001--Not Available
Blood bilirubin increased13.03.04.018--
Blood uric acid increased13.02.04.001--Not Available
Body temperature increased13.15.01.001--Not Available
Breast feeding26.05.01.001--Not Available
Chills15.05.03.016; 08.01.09.001--
Dermatitis23.03.04.002--Not Available
Diabetes mellitus14.06.01.001; 05.06.01.001--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Drug interaction08.06.03.001--Not Available
Dry eye06.08.02.001--
Dry mouth07.06.01.002--
Dyspepsia07.01.02.001--
Flatulence07.01.04.002--
Gamma-glutamyltransferase increased13.03.04.024--
Gastrointestinal pain07.01.05.005--
Haemodialysis25.07.02.002--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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