Does SODIUM OXYBATE Cause Wrong product administered? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Wrong product administered have been filed in association with SODIUM OXYBATE (sodium oxybate). This represents 0.0% of all adverse event reports for SODIUM OXYBATE.
5
Reports of Wrong product administered with SODIUM OXYBATE
0.0%
of all SODIUM OXYBATE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Wrong product administered From SODIUM OXYBATE?
Of the 5 reports.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM OXYBATE. However, 5 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which SODIUM OXYBATE Alternatives Have Lower Wrong product administered 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