Does OFATUMUMAB Cause Wrong technique in product usage process? 153 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 153 reports of Wrong technique in product usage process have been filed in association with OFATUMUMAB (ARZERRA). This represents 0.5% of all adverse event reports for OFATUMUMAB.
153
Reports of Wrong technique in product usage process with OFATUMUMAB
0.5%
of all OFATUMUMAB reports
0
Deaths
4
Hospitalizations
How Dangerous Is Wrong technique in product usage process From OFATUMUMAB?
Of the 153 reports, 4 (2.6%) required hospitalization, and 1 (0.7%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for OFATUMUMAB. However, 153 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 Wrong technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which OFATUMUMAB Alternatives Have Lower Wrong technique in product usage process Risk?
OFATUMUMAB vs OFLOXACIN
OFATUMUMAB vs OLANZAPINE
OFATUMUMAB vs OLANZAPINE\SAMIDORPHAN L-MALATE
OFATUMUMAB vs OLAPARIB
OFATUMUMAB vs OLARATUMAB