Does DARATUMUMAB Cause Intentional product misuse? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Intentional product misuse have been filed in association with DARATUMUMAB (DARZALEX). This represents 0.0% of all adverse event reports for DARATUMUMAB.
8
Reports of Intentional product misuse with DARATUMUMAB
0.0%
of all DARATUMUMAB reports
4
Deaths
1
Hospitalizations
How Dangerous Is Intentional product misuse From DARATUMUMAB?
Of the 8 reports, 4 (50.0%) resulted in death, 1 (12.5%) required hospitalization.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DARATUMUMAB. However, 8 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 Intentional product misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which DARATUMUMAB Alternatives Have Lower Intentional product misuse Risk?
DARATUMUMAB vs DARATUMUMAB\HYALURONIDASE-FIHJ
DARATUMUMAB vs DARBEPOETIN ALFA
DARATUMUMAB vs DARIDOREXANT
DARATUMUMAB vs DARIFENACIN HYDROBROMIDE
DARATUMUMAB vs DAROLUTAMIDE