Does OFATUMUMAB Cause Incorrect dose administered by device? 339 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 339 reports of Incorrect dose administered by device have been filed in association with OFATUMUMAB (ARZERRA). This represents 1.1% of all adverse event reports for OFATUMUMAB.
339
Reports of Incorrect dose administered by device with OFATUMUMAB
1.1%
of all OFATUMUMAB reports
0
Deaths
2
Hospitalizations
How Dangerous Is Incorrect dose administered by device From OFATUMUMAB?
Of the 339 reports, 2 (0.6%) required hospitalization.
Is Incorrect dose administered by device Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OFATUMUMAB. However, 339 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 Incorrect dose administered by device?
EXENATIDE (3,332)
EVOLOCUMAB (2,840)
SOMATROPIN (2,486)
ALBUTEROL (1,236)
ETANERCEPT (1,032)
SECUKINUMAB (996)
ERENUMAB-AOOE (973)
BUDESONIDE\FORMOTEROL (753)
INSULIN GLARGINE (753)
BUDESONIDE\FORMOTEROL\GLYCOPYRROLATE (674)
Which OFATUMUMAB Alternatives Have Lower Incorrect dose administered by device Risk?
OFATUMUMAB vs OFLOXACIN
OFATUMUMAB vs OLANZAPINE
OFATUMUMAB vs OLANZAPINE\SAMIDORPHAN L-MALATE
OFATUMUMAB vs OLAPARIB
OFATUMUMAB vs OLARATUMAB