Does POMALIDOMIDE Cause Product dose omission in error? 147 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 147 reports of Product dose omission in error have been filed in association with POMALIDOMIDE (Pomalyst). This represents 0.2% of all adverse event reports for POMALIDOMIDE.
147
Reports of Product dose omission in error with POMALIDOMIDE
0.2%
of all POMALIDOMIDE reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product dose omission in error From POMALIDOMIDE?
Of the 147 reports, 13 (8.8%) required hospitalization, and 1 (0.7%) 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 POMALIDOMIDE. However, 147 reports have been filed with the FAERS database.
What Other Side Effects Does POMALIDOMIDE Cause?
Plasma cell myeloma (7,023)
Death (6,795)
Fatigue (6,530)
Pneumonia (5,792)
Off label use (3,845)
Diarrhoea (3,351)
White blood cell count decreased (3,328)
Neutropenia (3,029)
Rash (2,715)
Dyspnoea (2,543)
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 POMALIDOMIDE Alternatives Have Lower Product dose omission in error Risk?
POMALIDOMIDE vs POMALYST
POMALIDOMIDE vs PONATINIB
POMALIDOMIDE vs PONATINIB\PONATINIB
POMALIDOMIDE vs PONESIMOD
POMALIDOMIDE vs PORACTANT ALFA