Does ALECTINIB Cause Intentional product use issue? 79 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 79 reports of Intentional product use issue have been filed in association with ALECTINIB (ALECENSA). This represents 0.9% of all adverse event reports for ALECTINIB.
79
Reports of Intentional product use issue with ALECTINIB
0.9%
of all ALECTINIB reports
10
Deaths
8
Hospitalizations
How Dangerous Is Intentional product use issue From ALECTINIB?
Of the 79 reports, 10 (12.7%) resulted in death, 8 (10.1%) required hospitalization, and 1 (1.3%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ALECTINIB. However, 79 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ALECTINIB Alternatives Have Lower Intentional product use issue Risk?
ALECTINIB vs ALEMTUZUMAB
ALECTINIB vs ALENDRONATE
ALECTINIB vs ALENDRONATE\CHOLECALCIFEROL
ALECTINIB vs ALENDRONIC ACID
ALECTINIB vs ALEVE