Does BOSUTINIB Cause Product dose omission? 26 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 26 reports of Product dose omission have been filed in association with BOSUTINIB (BOSULIF). This represents 0.3% of all adverse event reports for BOSUTINIB.
26
Reports of Product dose omission with BOSUTINIB
0.3%
of all BOSUTINIB reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product dose omission From BOSUTINIB?
Of the 26 reports, 1 (3.8%) resulted in death, 5 (19.2%) required hospitalization, and 1 (3.8%) were considered life-threatening.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for BOSUTINIB. However, 26 reports have been filed with the FAERS database.
What Other Side Effects Does BOSUTINIB Cause?
Diarrhoea (1,820)
Nausea (886)
Fatigue (626)
Vomiting (469)
Death (465)
Rash (426)
Pleural effusion (398)
Neoplasm progression (376)
Dyspnoea (319)
Headache (283)
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 BOSUTINIB Alternatives Have Lower Product dose omission Risk?
BOSUTINIB vs BOTOX
BOSUTINIB vs BOTOX COSMETIC
BOSUTINIB vs BOTULINUM TOXIN NOS
BOSUTINIB vs BOTULINUM TOXIN TYPE A
BOSUTINIB vs BREMELANOTIDE