Does DIVALPROEX Cause Product dose omission issue? 84 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 84 reports of Product dose omission issue have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 0.7% of all adverse event reports for DIVALPROEX.
84
Reports of Product dose omission issue with DIVALPROEX
0.7%
of all DIVALPROEX reports
1
Deaths
58
Hospitalizations
How Dangerous Is Product dose omission issue From DIVALPROEX?
Of the 84 reports, 1 (1.2%) resulted in death, 58 (69.0%) required hospitalization.
Is Product dose omission issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 84 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 dose omission issue?
DUPILUMAB (18,189)
USTEKINUMAB (9,405)
GUSELKUMAB (9,267)
LENALIDOMIDE (8,145)
MEPOLIZUMAB (5,873)
TOFACITINIB (5,646)
VOXELOTOR (5,122)
BELIMUMAB (4,671)
SECUKINUMAB (4,572)
APREMILAST (4,460)
Which DIVALPROEX Alternatives Have Lower Product dose omission issue Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS