Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Naloxegol oxalate
Drug ID BADD_D01524
Description Naloxegol, for "PEGylated naloxol" is a peripherally-selective opioid antagonist developed by AstraZeneca. It was approved by the FDA in September 2014 and is indicated for the treatment of opioid-induced constipation (OIC) in adult patients with chronic non‑cancer pain. The advantage of naloxegol over the opioid antagonist naloxone is that its PEGylated structure allows for high selectivity for peripheral opioid receptors and lack of entry into the central nervous system through the blood-brain barrier.
Indications and Usage Indicated for the treatment of opioid-induced constipation (OIC) in adult patients with chronic non-cancer pain.
Marketing Status approved
ATC Code A06AH03
DrugBank ID DB09049
KEGG ID D10375
MeSH ID C000589308
PubChem ID 56959086
TTD Drug ID D07LCF
NDC Product Code 17228-1970; 17228-1969; 59116-4290; 69766-046; 57841-1301; 82625-8802; 55700-988; 57841-1300; 82625-8801
UNII 65I14TNM33
Synonyms naloxegol | Movantik | NKTR-118
Chemical Information
Molecular Formula C36H55NO15
CAS Registry Number 1354744-91-4
SMILES COCCOCCOCCOCCOCCOCCOCCOC1CCC2(C3CC4=C5C2(C1OC5=C(C=C4)O)CCN3CC=C)O.C(=O)(C(=O)O) 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--
Diarrhoea07.02.01.001--
Flatulence07.01.04.002--
Gastrointestinal disorder07.11.01.001---
Gastrointestinal perforation07.04.04.001---
Headache17.14.01.001--
Hyperhidrosis08.01.03.028; 23.02.03.004--
Nausea07.01.07.001--
Vomiting07.01.07.003--
Opiates13.17.02.008---
The 1th Page    1    Total 1 Pages