Does BINIMETINIB Cause Product dose omission? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Product dose omission have been filed in association with BINIMETINIB (MEKTOVI). This represents 0.9% of all adverse event reports for BINIMETINIB.
65
Reports of Product dose omission with BINIMETINIB
0.9%
of all BINIMETINIB reports
3
Deaths
18
Hospitalizations
How Dangerous Is Product dose omission From BINIMETINIB?
Of the 65 reports, 3 (4.6%) resulted in death, 18 (27.7%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BINIMETINIB. However, 65 reports have been filed with the FAERS database.
What Other Side Effects Does BINIMETINIB Cause?
Off label use (902)
Death (719)
Nausea (657)
Fatigue (562)
Diarrhoea (521)
Product use in unapproved indication (508)
Pyrexia (490)
Neoplasm progression (387)
Vomiting (375)
Rash (360)
What Other Drugs Cause Product dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which BINIMETINIB Alternatives Have Lower Product dose omission Risk?
BINIMETINIB vs BIOFLAVONOIDS
BINIMETINIB vs BIOTIN
BINIMETINIB vs BIPERIDEN
BINIMETINIB vs BIRCH TRITERPENES
BINIMETINIB vs BISACODYL