Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Pegloticase
Drug ID BADD_D01698
Description Pegloticase is a recombinant porcine-like uricase drug indicated for the treatment of severe, treatment-refractory, chronic gout. Similarly to rasburicase, pegloticase metabolises the conversion of uric acid to allantoin. This reduces the risk of precipitate formation and development of gout, since allantoin is five to ten times more soluble than uric acid. Pegloticase is a pegylated form of uricase which offers an extended half-life of ten-12 days compared to rasburicase's 8 hours. It also offers reduced immunogenicity due to the bulky PEG group. The longer haf-life allows for less frequent dosing at once every 2-4 weeks making pegloticase more convenient for chronic use.
Indications and Usage For the treatment of chronic gout in adult patients refractory to conventional therapy.
Marketing Status approved; investigational
ATC Code M04AX02
DrugBank ID DB09208
KEGG ID D09316
MeSH ID C031545
PubChem ID Not Available
TTD Drug ID D06ZIT
NDC Product Code 75987-080
UNII R581OT55EA
Synonyms Pegloticase | polyethylene glycol-uricase | PEG-uricase | methoxypolyethylene glycol uricase | Krystexxa | Puricase
Chemical Information
Molecular Formula Not Available
CAS Registry Number 885051-90-1
SMILES Not Available
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)
Anaphylactic reaction10.01.07.001; 24.06.03.006--
Arrhythmia02.03.02.001--Not Available
Cardiac failure02.05.01.001--
Cardiac failure congestive02.05.01.002--Not Available
Chest discomfort22.12.02.002; 08.01.08.019; 02.02.02.009--Not Available
Chest pain02.02.02.011; 22.12.02.003; 08.01.08.002--Not Available
Constipation07.02.02.001--
Coronary artery disease24.04.04.006; 02.02.01.001--Not Available
Diabetes mellitus14.06.01.001; 05.06.01.001--Not Available
Dyspnoea02.11.05.003; 22.02.01.004--
Ecchymosis01.01.03.001; 24.07.06.002; 23.06.01.001--Not Available
Erythema23.03.06.001--Not Available
Eye disorder06.08.03.001--Not Available
Gout14.09.01.001; 15.01.06.001--Not Available
Hypertension24.08.02.001--
Nasopharyngitis22.07.03.002; 11.01.13.002--Not Available
Nausea07.01.07.001--
Pruritus23.03.12.001--
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
Left ventricular dysfunction02.04.02.011--
Contusion15.03.05.007; 24.07.06.001; 23.03.11.002; 12.01.06.001--
Infusion related reaction12.02.05.009; 10.01.01.017; 08.01.03.002--
Dyslipidaemia14.08.04.015--Not Available
Chronic kidney disease20.01.03.017--
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