Does IXAZOMIB Cause Product dose omission in error? 17 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 17 reports of Product dose omission in error have been filed in association with IXAZOMIB (NINLARO). This represents 0.1% of all adverse event reports for IXAZOMIB.
17
Reports of Product dose omission in error with IXAZOMIB
0.1%
of all IXAZOMIB reports
3
Deaths
10
Hospitalizations
How Dangerous Is Product dose omission in error From IXAZOMIB?
Of the 17 reports, 3 (17.6%) resulted in death, 10 (58.8%) required hospitalization, and 1 (5.9%) were considered life-threatening.
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 IXAZOMIB. However, 17 reports have been filed with the FAERS database.
What Other Side Effects Does IXAZOMIB Cause?
Plasma cell myeloma (3,249)
Death (2,845)
Off label use (2,841)
Diarrhoea (2,560)
Pneumonia (1,583)
Nausea (1,568)
Fatigue (1,456)
Neuropathy peripheral (1,162)
Vomiting (977)
Thrombocytopenia (964)
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 IXAZOMIB Alternatives Have Lower Product dose omission in error Risk?
IXAZOMIB vs IXEKIZUMAB
IXAZOMIB vs JAKAFI
IXAZOMIB vs JAKAVI
IXAZOMIB vs JANUMET
IXAZOMIB vs JANUVIA