Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sodium oxybate
Drug ID BADD_D02047
Description Sodium oxybate (Xyrem) is a central nervous system depressant used for the treatment of cataplexy and extreme daytime sleepiness (EDS) associated with narcolepsy. It is the sodium salt of gamma hydroxybutyric acid (GHB) which is an endogenous compound and a metabolite of the neurotransmitter GABA. The exact mechanism of action for treating EDS and cataplexy is not known but is is hypothesised that its therapeutic effects are due to GABA(B) effects on noradrenergic, dopaminaergic and thalamocorticol neurons. The drug follows non-linear pharmacokinetics. As it has been associated with misuse/abuse it is strictly controlled and all patients and prescribers must enroll in the sodium oxybate REMs program in order to gain access to the medication.
Indications and Usage For the treatment of cataplexy and excessive daytime sleepiness (EDS) associated with narcolepsy.
Marketing Status approved
ATC Code N01AX11; N07XX04
DrugBank ID DB09072
KEGG ID D05866
MeSH ID D012978
PubChem ID 23663870
TTD Drug ID Not Available
NDC Product Code 13551-001; 49812-0207; 0054-9628; 69238-2391; 0792-4356; 13551-002; 13551-003; 68727-100; 61960-0221; 13551-004; 59116-5950
UNII 7G33012534
Synonyms Sodium Oxybate | Oxybate, Sodium | Sodium Oxybutyrate | Oxybutyrate, Sodium | Sodium gamma-Hydroxybutyrate | Sodium gamma Hydroxybutyrate | 4-Hydroxybutyrate Sodium | 4 Hydroxybutyrate Sodium | Oxybate Sodium | gamma-Hydroxybutyrate | gamma Hydroxybutyrate | Somsanit | Xyrem
Chemical Information
Molecular Formula C4H7NaO3
CAS Registry Number 502-85-2
SMILES C(CC(=O)[O-])CO.[Na+]
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)
Daydreaming19.21.02.0050.000912%Not Available
Hypoaesthesia oral17.02.06.021; 07.05.05.0030.002361%Not Available
Paraesthesia oral07.05.05.035; 17.02.06.0080.001368%Not Available
Breast cancer female21.05.01.011; 16.10.01.0040.000536%Not Available
Anxiety disorder19.06.01.0020.000858%Not Available
Bipolar disorder19.16.01.0030.004346%Not Available
Major depression19.15.01.0030.002548%Not Available
Dyslipidaemia14.08.04.0150.001046%Not Available
Thyroid mass05.02.01.0030.000268%Not Available
Restless legs syndrome17.02.07.008; 15.05.03.0120.012098%Not Available
Appetite disorder19.09.01.002; 14.03.01.0040.000268%Not Available
Bladder disorder20.03.01.0020.001449%Not Available
Cardiac disorder02.11.01.003--Not Available
Connective tissue disorder10.04.04.026; 15.06.01.0060.000268%Not Available
Eye movement disorder17.02.05.025; 06.05.02.0080.000590%Not Available
Impulse-control disorder19.18.01.0020.000912%Not Available
Inflammation08.01.05.007; 10.02.01.0890.002226%Not Available
Limb discomfort15.03.04.0140.006277%Not Available
Intervertebral disc degeneration15.10.01.0020.002843%Not Available
Jaw disorder15.02.04.0090.001502%Not Available
Joint lock15.01.08.0040.000912%Not Available
Malnutrition14.03.02.0040.000268%Not Available
Mental disorder19.07.01.0020.004346%Not Available
Spinal disorder15.02.04.0230.000536%Not Available
Spondylitis15.01.09.0020.000590%Not Available
Abnormal behaviour19.01.01.0010.005848%Not Available
Decreased appetite14.03.01.005; 08.01.09.0280.021862%
Feeling of body temperature change08.01.09.0120.002870%Not Available
Gastrointestinal ulcer07.04.04.0020.000402%Not Available
Erectile dysfunction21.03.01.007; 19.08.04.0010.002629%
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