Does DIVALPROEX Cause Wrong technique in product usage process? 104 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 104 reports of Wrong technique in product usage process have been filed in association with DIVALPROEX (Divalproex Sodium). This represents 0.9% of all adverse event reports for DIVALPROEX.
104
Reports of Wrong technique in product usage process with DIVALPROEX
0.9%
of all DIVALPROEX reports
1
Deaths
39
Hospitalizations
How Dangerous Is Wrong technique in product usage process From DIVALPROEX?
Of the 104 reports, 1 (1.0%) resulted in death, 39 (37.5%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DIVALPROEX. However, 104 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which DIVALPROEX Alternatives Have Lower Wrong technique in product usage process Risk?
DIVALPROEX vs DOBUTAMINE
DIVALPROEX vs DOBUTAMINE\DOBUTAMINE
DIVALPROEX vs DOCETAXEL
DIVALPROEX vs DOCETAXEL ANHYDROUS
DIVALPROEX vs DOCETAXEL\DOCETAXEL ANHYDROUS