Does OFATUMUMAB Cause Device malfunction? 525 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 525 reports of Device malfunction have been filed in association with OFATUMUMAB (ARZERRA). This represents 1.8% of all adverse event reports for OFATUMUMAB.
525
Reports of Device malfunction with OFATUMUMAB
1.8%
of all OFATUMUMAB reports
1
Deaths
23
Hospitalizations
How Dangerous Is Device malfunction From OFATUMUMAB?
Of the 525 reports, 1 (0.2%) resulted in death, 23 (4.4%) required hospitalization, and 3 (0.6%) were considered life-threatening.
Is Device malfunction Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OFATUMUMAB. However, 525 reports have been filed with the FAERS database.
What Other Side Effects Does OFATUMUMAB Cause?
Fatigue (5,202)
Headache (4,430)
Pain (3,382)
Chills (3,372)
Pyrexia (3,370)
Influenza like illness (2,727)
Nausea (1,688)
Multiple sclerosis relapse (1,525)
Covid-19 (1,435)
Asthenia (1,393)
What Other Drugs Cause Device malfunction?
PEGFILGRASTIM (6,818)
EXENATIDE (3,273)
BUDESONIDE\FORMOTEROL (2,771)
ABATACEPT (2,459)
SOMATROPIN (2,311)
GOLIMUMAB (2,293)
SECUKINUMAB (2,259)
ALBUTEROL (2,257)
GUSELKUMAB (1,410)
MOMETASONE FUROATE (1,332)
Which OFATUMUMAB Alternatives Have Lower Device malfunction Risk?
OFATUMUMAB vs OFLOXACIN
OFATUMUMAB vs OLANZAPINE
OFATUMUMAB vs OLANZAPINE\SAMIDORPHAN L-MALATE
OFATUMUMAB vs OLAPARIB
OFATUMUMAB vs OLARATUMAB