Does POMALIDOMIDE Cause Product prescribing issue? 236 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 236 reports of Product prescribing issue have been filed in association with POMALIDOMIDE (Pomalyst). This represents 0.3% of all adverse event reports for POMALIDOMIDE.
236
Reports of Product prescribing issue with POMALIDOMIDE
0.3%
of all POMALIDOMIDE reports
1
Deaths
5
Hospitalizations
How Dangerous Is Product prescribing issue From POMALIDOMIDE?
Of the 236 reports, 1 (0.4%) resulted in death, 5 (2.1%) required hospitalization.
Is Product prescribing issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POMALIDOMIDE. However, 236 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 prescribing issue?
DUPILUMAB (1,715)
POLYETHYLENE GLYCOL 3350 (1,439)
LENALIDOMIDE (948)
OXYCODONE (646)
RIVAROXABAN (359)
ACETAMINOPHEN\OXYCODONE (347)
ETONOGESTREL (311)
ACETAMINOPHEN\HYDROCODONE (298)
CERTOLIZUMAB PEGOL (297)
CABOZANTINIB S-MALATE (294)
Which POMALIDOMIDE Alternatives Have Lower Product prescribing issue Risk?
POMALIDOMIDE vs POMALYST
POMALIDOMIDE vs PONATINIB
POMALIDOMIDE vs PONATINIB\PONATINIB
POMALIDOMIDE vs PONESIMOD
POMALIDOMIDE vs PORACTANT ALFA