Does DIVALPROEX Cause Intentional product misuse? 36 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 36 reports of Intentional product misuse have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 0.3% of all adverse event reports for DIVALPROEX.
36
Reports of Intentional product misuse with DIVALPROEX
0.3%
of all DIVALPROEX reports
3
Deaths
10
Hospitalizations
How Dangerous Is Intentional product misuse From DIVALPROEX?
Of the 36 reports, 3 (8.3%) resulted in death, 10 (27.8%) required hospitalization, and 1 (2.8%) 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 DIVALPROEX. However, 36 reports have been filed with the FAERS database.
What Other Side Effects Does DIVALPROEX Cause?
Drug ineffective (1,121)
Seizure (1,095)
Off label use (576)
Somnolence (545)
Drug interaction (540)
Nausea (526)
Weight increased (509)
Tremor (461)
Toxicity to various agents (452)
Vomiting (436)
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)
Which DIVALPROEX Alternatives Have Lower Intentional product misuse Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS