Does SODIUM OXYBATE Cause Product administration interrupted? 1,272 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,272 reports of Product administration interrupted have been filed in association with SODIUM OXYBATE (sodium oxybate). This represents 2.1% of all adverse event reports for SODIUM OXYBATE.
1,272
Reports of Product administration interrupted with SODIUM OXYBATE
2.1%
of all SODIUM OXYBATE reports
7
Deaths
321
Hospitalizations
How Dangerous Is Product administration interrupted From SODIUM OXYBATE?
Of the 1,272 reports, 7 (0.6%) resulted in death, 321 (25.2%) required hospitalization, and 2 (0.2%) were considered life-threatening.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM OXYBATE. However, 1,272 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 administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
ADALIMUMAB (86)
Which SODIUM OXYBATE Alternatives Have Lower Product administration interrupted 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