Does SODIUM OXYBATE Cause Product preparation error? 222 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 222 reports of Product preparation error have been filed in association with SODIUM OXYBATE (sodium oxybate). This represents 0.4% of all adverse event reports for SODIUM OXYBATE.
222
Reports of Product preparation error with SODIUM OXYBATE
0.4%
of all SODIUM OXYBATE reports
0
Deaths
33
Hospitalizations
How Dangerous Is Product preparation error From SODIUM OXYBATE?
Of the 222 reports, 33 (14.9%) required hospitalization.
Is Product preparation error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM OXYBATE. However, 222 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 preparation error?
ONABOTULINUMTOXINA (3,593)
EVOLOCUMAB (2,785)
DUPILUMAB (2,707)
BUPRENORPHINE\NALOXONE (777)
ABOBOTULINUMTOXINA (751)
ALBIGLUTIDE (691)
ALBUTEROL (520)
PEGFILGRASTIM (473)
ALIROCUMAB (402)
LEUPROLIDE (400)
Which SODIUM OXYBATE Alternatives Have Lower Product preparation error 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