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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does UBLITUXIMAB Cause Adverse event? 12 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 12 reports of Adverse event have been filed in association with UBLITUXIMAB (BRIUMVI). This represents 0.8% of all adverse event reports for UBLITUXIMAB.

12
Reports of Adverse event with UBLITUXIMAB
0.8%
of all UBLITUXIMAB reports
0
Deaths
0
Hospitalizations

How Dangerous Is Adverse event From UBLITUXIMAB?

Of the 12 reports.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UBLITUXIMAB. However, 12 reports have been filed with the FAERS database.

What Other Side Effects Does UBLITUXIMAB Cause?

Infusion related reaction (538) Fatigue (110) Headache (55) Inappropriate schedule of product administration (53) Malaise (49) Multiple sclerosis relapse (48) Asthenia (45) Pain (45) Illness (43) Urinary tract infection (42)

What Other Drugs Cause Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which UBLITUXIMAB Alternatives Have Lower Adverse event Risk?

UBLITUXIMAB vs UBLITUXIMAB-XIIY UBLITUXIMAB vs UBROGEPANT UBLITUXIMAB vs ULIPRISTAL UBLITUXIMAB vs UMBRALISIB UBLITUXIMAB vs UMECLIDINIUM

Related Pages

UBLITUXIMAB Full Profile All Adverse event Reports All Drugs Causing Adverse event UBLITUXIMAB Demographics