Does POMALIDOMIDE Cause Subdural haematoma? 43 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 43 reports of Subdural haematoma have been filed in association with POMALIDOMIDE (Pomalyst). This represents 0.1% of all adverse event reports for POMALIDOMIDE.
43
Reports of Subdural haematoma with POMALIDOMIDE
0.1%
of all POMALIDOMIDE reports
26
Deaths
32
Hospitalizations
How Dangerous Is Subdural haematoma From POMALIDOMIDE?
Of the 43 reports, 26 (60.5%) resulted in death, 32 (74.4%) required hospitalization, and 8 (18.6%) were considered life-threatening.
Is Subdural haematoma Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for POMALIDOMIDE. However, 43 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 Subdural haematoma?
RIVAROXABAN (1,423)
ASPIRIN (1,181)
APIXABAN (1,025)
WARFARIN (1,012)
CLOPIDOGREL BISULFATE (809)
DABIGATRAN ETEXILATE (648)
IBRUTINIB (342)
HEPARIN (201)
ENOXAPARIN (156)
CYCLOPHOSPHAMIDE (146)
Which POMALIDOMIDE Alternatives Have Lower Subdural haematoma Risk?
POMALIDOMIDE vs POMALYST
POMALIDOMIDE vs PONATINIB
POMALIDOMIDE vs PONATINIB\PONATINIB
POMALIDOMIDE vs PONESIMOD
POMALIDOMIDE vs PORACTANT ALFA