Does ALECTINIB Cause Product dose omission in error? 10 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 10 reports of Product dose omission in error have been filed in association with ALECTINIB (ALECENSA). This represents 0.1% of all adverse event reports for ALECTINIB.
10
Reports of Product dose omission in error with ALECTINIB
0.1%
of all ALECTINIB reports
1
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From ALECTINIB?
Of the 10 reports, 1 (10.0%) resulted in death, 1 (10.0%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALECTINIB. However, 10 reports have been filed with the FAERS database.
What Other Side Effects Does ALECTINIB Cause?
Death (702)
Fatigue (618)
Constipation (525)
Off label use (495)
No adverse event (488)
Disease progression (366)
Rash (312)
Dyspnoea (296)
Drug ineffective (269)
Myalgia (268)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which ALECTINIB Alternatives Have Lower Product dose omission in error Risk?
ALECTINIB vs ALEMTUZUMAB
ALECTINIB vs ALENDRONATE
ALECTINIB vs ALENDRONATE\CHOLECALCIFEROL
ALECTINIB vs ALENDRONIC ACID
ALECTINIB vs ALEVE