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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 administration interrupted? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration interrupted have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 0.1% of all adverse event reports for DIVALPROEX.

9
Reports of Product administration interrupted with DIVALPROEX
0.1%
of all DIVALPROEX reports
0
Deaths
6
Hospitalizations

How Dangerous Is Product administration interrupted From DIVALPROEX?

Of the 9 reports, 6 (66.7%) required hospitalization.

Is Product administration interrupted Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 9 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 administration interrupted?

CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446) SODIUM OXYBATE (1,272) CANNABIDIOL (511) ISOTRETINOIN (503) APREMILAST (314) TREPROSTINIL (295) EPOPROSTENOL (205) LENALIDOMIDE (146) ETANERCEPT (142) INTERFERON BETA-1A (115)

Which DIVALPROEX Alternatives Have Lower Product administration interrupted 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 administration interrupted Reports All Drugs Causing Product administration interrupted DIVALPROEX Demographics