Does DARATUMUMAB Cause Product use issue? 412 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 412 reports of Product use issue have been filed in association with DARATUMUMAB (DARZALEX). This represents 1.5% of all adverse event reports for DARATUMUMAB.
412
Reports of Product use issue with DARATUMUMAB
1.5%
of all DARATUMUMAB reports
58
Deaths
66
Hospitalizations
How Dangerous Is Product use issue From DARATUMUMAB?
Of the 412 reports, 58 (14.1%) resulted in death, 66 (16.0%) required hospitalization, and 20 (4.9%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARATUMUMAB. However, 412 reports have been filed with the FAERS database.
What Other Side Effects Does DARATUMUMAB Cause?
Plasma cell myeloma (2,980)
Infusion related reaction (2,557)
Off label use (2,494)
Pneumonia (1,450)
Neutropenia (1,351)
Drug ineffective (1,110)
Thrombocytopenia (1,089)
Death (1,088)
Pyrexia (1,032)
Dyspnoea (996)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which DARATUMUMAB Alternatives Have Lower Product use issue Risk?
DARATUMUMAB vs DARATUMUMAB\HYALURONIDASE-FIHJ
DARATUMUMAB vs DARBEPOETIN ALFA
DARATUMUMAB vs DARIDOREXANT
DARATUMUMAB vs DARIFENACIN HYDROBROMIDE
DARATUMUMAB vs DAROLUTAMIDE