Does SODIUM ASCORBATE Cause Intentional product misuse? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Intentional product misuse have been filed in association with SODIUM ASCORBATE. This represents 18.2% of all adverse event reports for SODIUM ASCORBATE.
12
Reports of Intentional product misuse with SODIUM ASCORBATE
18.2%
of all SODIUM ASCORBATE reports
12
Deaths
9
Hospitalizations
How Dangerous Is Intentional product misuse From SODIUM ASCORBATE?
Of the 12 reports, 12 (100.0%) resulted in death, 9 (75.0%) required hospitalization, and 9 (75.0%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for SODIUM ASCORBATE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does SODIUM ASCORBATE Cause?
Nausea (31)
Off label use (29)
Abdominal pain (26)
Constipation (26)
Drug ineffective (24)
Anaemia (22)
Death (22)
Pyrexia (21)
Abdominal distension (19)
Vomiting (18)
What Other Drugs Cause Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)