Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Adefovir dipivoxil
Drug ID BADD_D00044
Description Adefovir dipivoxil, previously called bis-POM PMEA, with trade names Preveon and Hepsera, is an orally-administered acyclic nucleotide analog reverse transcriptase inhibitor (ntRTI) used for treatment of hepatitis B. It is ineffective against HIV-1. Adefovir dipivoxil is the diester prodrug of adefovir.
Indications and Usage Indicated for the treatment of chronic hepatitis B in adult patients with evidence of active viral replication and either evidence of persistent elevations in serum aminotransferases (ALT or AST) or histologically active disease; this is based on histological, virological, biochemical, and serological responses in adult patients with HBeAg+ and HBeAg- chronic hepatitis B with compensated liver function, and in adult patients with clinical evidence of lamivudine-resistant hepatitis B virus with either compensated or decompensated liver function.
Marketing Status approved; investigational
ATC Code J05AF08
DrugBank ID DB00718
KEGG ID D01655
MeSH ID C106812
PubChem ID 60871
TTD Drug ID D0ML1F
NDC Product Code 53104-7602; 42794-003; 60505-3947; 61958-0501
UNII U6Q8Z01514
Synonyms adefovir dipivoxil | adefovir depivoxil | 9-(2-((-bis((pivaloyloxy)methoxy)phosphinyl)methoxy)ethyl)adenine | Hepsera | Preveon | GS 840 | GS-0840
Chemical Information
Molecular Formula C20H32N5O8P
CAS Registry Number 142340-99-6
SMILES CC(C)(C)C(=O)OCOP(=O)(COCCN1C=NC2=C(N=CN=C21)N)OCOC(=O)C(C)(C)C
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 distension07.01.04.0010.000423%
Abdominal pain07.01.05.002--
Acidosis14.01.03.0020.000565%
Acidosis hyperchloraemic14.01.01.0070.000282%Not Available
Alanine aminotransferase increased13.03.04.005--
Albuminuria20.02.01.0010.000847%Not Available
Anaemia01.03.02.001--
Arthralgia15.01.02.0010.011911%
Arthritis15.01.01.0010.000282%
Ascites09.01.05.003; 07.07.01.001; 02.05.04.0020.000282%
Asthenia08.01.01.0010.003302%Not Available
Autonomic nervous system imbalance24.06.01.005; 17.05.01.011; 08.01.01.0100.000282%Not Available
Azotaemia20.01.01.0010.000988%Not Available
Back pain15.03.04.0050.007677%
Benign hepatic neoplasm16.06.01.001; 09.04.01.0010.000706%Not Available
Blood creatinine increased13.13.01.004--
Body temperature increased13.15.01.001--Not Available
Bone disorder15.02.04.0040.001976%Not Available
Bone pain15.02.01.0010.015242%
Chest discomfort22.12.02.002; 08.01.08.019; 02.02.02.0090.000706%Not Available
Chest pain22.12.02.003; 08.01.08.002; 02.02.02.0110.003302%Not Available
Chromaturia20.02.01.0020.000282%
Condition aggravated08.01.03.0040.002117%Not Available
Cough22.02.03.0010.001129%
Delirium tremens19.13.02.002; 12.03.01.037; 08.06.02.0060.000706%Not Available
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.0030.000706%Not Available
Dyskinesia17.01.02.0060.000282%
Dyspepsia07.01.02.001--
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