Does POMALIDOMIDE Cause Intentional product use issue? 393 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 393 reports of Intentional product use issue have been filed in association with POMALIDOMIDE (Pomalyst). This represents 0.4% of all adverse event reports for POMALIDOMIDE.
393
Reports of Intentional product use issue with POMALIDOMIDE
0.4%
of all POMALIDOMIDE reports
28
Deaths
32
Hospitalizations
How Dangerous Is Intentional product use issue From POMALIDOMIDE?
Of the 393 reports, 28 (7.1%) resulted in death, 32 (8.1%) required hospitalization, and 4 (1.0%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POMALIDOMIDE. However, 393 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which POMALIDOMIDE Alternatives Have Lower Intentional product use issue Risk?
POMALIDOMIDE vs POMALYST
POMALIDOMIDE vs PONATINIB
POMALIDOMIDE vs PONATINIB\PONATINIB
POMALIDOMIDE vs PONESIMOD
POMALIDOMIDE vs PORACTANT ALFA