Does DASATINIB Cause Product dose omission? 96 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 96 reports of Product dose omission have been filed in association with DASATINIB (dasatinib). This represents 0.3% of all adverse event reports for DASATINIB.
96
Reports of Product dose omission with DASATINIB
0.3%
of all DASATINIB reports
1
Deaths
11
Hospitalizations
How Dangerous Is Product dose omission From DASATINIB?
Of the 96 reports, 1 (1.0%) resulted in death, 11 (11.5%) 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 DASATINIB. However, 96 reports have been filed with the FAERS database.
What Other Side Effects Does DASATINIB Cause?
Pleural effusion (2,424)
Fatigue (2,173)
Death (1,741)
Nausea (1,740)
Diarrhoea (1,728)
Headache (1,625)
Adverse event (1,382)
Rash (1,300)
Drug ineffective (1,271)
Hospitalisation (1,181)
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 DASATINIB Alternatives Have Lower Product dose omission Risk?
DASATINIB vs DATOPOTAMAB DERUXTECAN-DLNK
DASATINIB vs DAUNORUBICIN
DASATINIB vs DAXIBOTULINUMTOXIN A-LANM
DASATINIB vs DAYTRANA
DASATINIB vs DECITABINE