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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does DIVALPROEX Cause Product use issue? 210 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Product use issue have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 1.8% of all adverse event reports for DIVALPROEX.

210
Reports of Product use issue with DIVALPROEX
1.8%
of all DIVALPROEX reports
8
Deaths
39
Hospitalizations

How Dangerous Is Product use issue From DIVALPROEX?

Of the 210 reports, 8 (3.8%) resulted in death, 39 (18.6%) required hospitalization, and 2 (1.0%) were considered life-threatening.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 210 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 issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Which DIVALPROEX Alternatives Have Lower Product use issue Risk?

DIVALPROEX vs DOBUTAMINE DIVALPROEX vs DOBUTAMINE\DOBUTAMINE DIVALPROEX vs DOCETAXEL DIVALPROEX vs DOCETAXEL ANHYDROUS DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS

Related Pages

DIVALPROEX Full Profile All Product use issue Reports All Drugs Causing Product use issue DIVALPROEX Demographics