Does SODIUM OXYBATE Cause Intentional product use issue? 1,706 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 1,706 reports of Intentional product use issue have been filed in association with SODIUM OXYBATE (sodium oxybate). This represents 2.8% of all adverse event reports for SODIUM OXYBATE.
1,706
Reports of Intentional product use issue with SODIUM OXYBATE
2.8%
of all SODIUM OXYBATE reports
5
Deaths
164
Hospitalizations
How Dangerous Is Intentional product use issue From SODIUM OXYBATE?
Of the 1,706 reports, 5 (0.3%) resulted in death, 164 (9.6%) required hospitalization.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM OXYBATE. However, 1,706 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which SODIUM OXYBATE Alternatives Have Lower Intentional product use 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