Does DIVALPROEX Cause Condition aggravated? 353 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 353 reports of Condition aggravated have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 3.1% of all adverse event reports for DIVALPROEX.
353
Reports of Condition aggravated with DIVALPROEX
3.1%
of all DIVALPROEX reports
3
Deaths
246
Hospitalizations
How Dangerous Is Condition aggravated From DIVALPROEX?
Of the 353 reports, 3 (0.8%) resulted in death, 246 (69.7%) required hospitalization, and 10 (2.8%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 353 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which DIVALPROEX Alternatives Have Lower Condition aggravated Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS