Does BREXANOLONE Cause Incorrect product administration duration? 12 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Incorrect product administration duration have been filed in association with BREXANOLONE. This represents 4.6% of all adverse event reports for BREXANOLONE.
12
Reports of Incorrect product administration duration with BREXANOLONE
4.6%
of all BREXANOLONE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Incorrect product administration duration From BREXANOLONE?
Of the 12 reports, 1 (8.3%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BREXANOLONE. However, 12 reports have been filed with the FAERS database.
What Other Side Effects Does BREXANOLONE Cause?
Product administration error (36)
Anxiety (34)
Drug ineffective (26)
Off label use (24)
Drug monitoring procedure incorrectly performed (19)
Fatigue (17)
Dizziness (16)
Perinatal depression (15)
Crying (14)
Product administration interrupted (14)
What Other Drugs Cause Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which BREXANOLONE Alternatives Have Lower Incorrect product administration duration Risk?
BREXANOLONE vs BREXPIPRAZOLE
BREXANOLONE vs BREXUCABTAGENE AUTOLEUCEL
BREXANOLONE vs BRIGATINIB
BREXANOLONE vs BRILINTA
BREXANOLONE vs BRILIQUE