Does DIVALPROEX Cause Product use in unapproved indication? 326 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 326 reports of Product use in unapproved indication have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 2.8% of all adverse event reports for DIVALPROEX.
326
Reports of Product use in unapproved indication with DIVALPROEX
2.8%
of all DIVALPROEX reports
10
Deaths
149
Hospitalizations
How Dangerous Is Product use in unapproved indication From DIVALPROEX?
Of the 326 reports, 10 (3.1%) resulted in death, 149 (45.7%) required hospitalization, and 14 (4.3%) were considered life-threatening.
Is Product use in unapproved indication Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 326 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 Product use in unapproved indication?
DUPILUMAB (33,452)
DICLOFENAC (12,197)
METHOTREXATE (8,930)
PREDNISONE (7,625)
RITUXIMAB (7,519)
MYCOPHENOLATE MOFETIL (5,910)
ACETAMINOPHEN (5,819)
CYCLOPHOSPHAMIDE (5,750)
RISPERIDONE (5,551)
TACROLIMUS (5,057)
Which DIVALPROEX Alternatives Have Lower Product use in unapproved indication Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS