Does DINUTUXIMAB BETA Cause Off label use? 82 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 82 reports of Off label use have been filed in association with DINUTUXIMAB BETA. This represents 52.2% of all adverse event reports for DINUTUXIMAB BETA.
82
Reports of Off label use with DINUTUXIMAB BETA
52.2%
of all DINUTUXIMAB BETA reports
22
Deaths
7
Hospitalizations
How Dangerous Is Off label use From DINUTUXIMAB BETA?
Of the 82 reports, 22 (26.8%) resulted in death, 7 (8.5%) required hospitalization, and 5 (6.1%) were considered life-threatening.
Is Off label use Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DINUTUXIMAB BETA. However, 82 reports have been filed with the FAERS database.
What Other Side Effects Does DINUTUXIMAB BETA Cause?
Pyrexia (57)
Pain (46)
Death (20)
Neoplasm progression (20)
Device related bacteraemia (17)
Device related infection (16)
Diarrhoea (11)
Therapy partial responder (11)
Cough (10)
Rash (10)
What Other Drugs Cause Off label use?
RITUXIMAB (39,751)
INFLIXIMAB (34,801)
DENOSUMAB (34,612)
METHOTREXATE (24,020)
VEDOLIZUMAB (21,017)
ETANERCEPT (20,178)
TOCILIZUMAB (18,256)
PREDNISONE (17,867)
LENALIDOMIDE (17,017)
ADALIMUMAB (16,417)
Which DINUTUXIMAB BETA Alternatives Have Lower Off label use Risk?
DINUTUXIMAB BETA vs DIOSMIN
DINUTUXIMAB BETA vs DIOSMIN\HESPERIDIN
DINUTUXIMAB BETA vs DIOVAN
DINUTUXIMAB BETA vs DIPHENHYDRAMINE
DINUTUXIMAB BETA vs DIPHENHYDRAMINE\IBUPROFEN