Does SODIUM OXYBATE Cause Product prescribing issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product prescribing issue have been filed in association with SODIUM OXYBATE (sodium oxybate). This represents 0.0% of all adverse event reports for SODIUM OXYBATE.
21
Reports of Product prescribing issue with SODIUM OXYBATE
0.0%
of all SODIUM OXYBATE reports
0
Deaths
4
Hospitalizations
How Dangerous Is Product prescribing issue From SODIUM OXYBATE?
Of the 21 reports, 4 (19.0%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM OXYBATE. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM OXYBATE Cause?
Nausea (4,528)
Anxiety (3,678)
Somnolence (3,642)
Feeling abnormal (3,018)
Insomnia (2,993)
Depression (2,937)
Fatigue (2,923)
Headache (2,916)
Dizziness (2,699)
Weight decreased (2,618)
What Other Drugs Cause Product prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which SODIUM OXYBATE Alternatives Have Lower Product prescribing issue Risk?
SODIUM OXYBATE vs SODIUM PHENYLBUTYRATE
SODIUM OXYBATE vs SODIUM PHENYLBUTYRATE\TAURURSODIOL
SODIUM OXYBATE vs SODIUM PICOSULFATE
SODIUM OXYBATE vs SODIUM POLYSTYRENE SULFONATE
SODIUM OXYBATE vs SODIUM SALICYLATE