Does DIVALPROEX Cause Product quality issue? 107 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 107 reports of Product quality issue have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 0.9% of all adverse event reports for DIVALPROEX.
107
Reports of Product quality issue with DIVALPROEX
0.9%
of all DIVALPROEX reports
1
Deaths
17
Hospitalizations
How Dangerous Is Product quality issue From DIVALPROEX?
Of the 107 reports, 1 (0.9%) resulted in death, 17 (15.9%) required hospitalization, and 8 (7.5%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 107 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which DIVALPROEX Alternatives Have Lower Product quality issue Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS