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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-XIIY Cause Hypersensitivity? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Hypersensitivity have been filed in association with UBLITUXIMAB-XIIY. This represents 0.7% of all adverse event reports for UBLITUXIMAB-XIIY.

6
Reports of Hypersensitivity with UBLITUXIMAB-XIIY
0.7%
of all UBLITUXIMAB-XIIY reports
0
Deaths
0
Hospitalizations

How Dangerous Is Hypersensitivity From UBLITUXIMAB-XIIY?

Of the 6 reports.

Is Hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for UBLITUXIMAB-XIIY. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does UBLITUXIMAB-XIIY Cause?

Infusion related reaction (481) Fatigue (48) Headache (34) Malaise (22) Inappropriate schedule of product administration (21) Product dose omission issue (19) Asthenia (18) Drug ineffective (18) Nausea (18) Dizziness (17)

What Other Drugs Cause Hypersensitivity?

ETANERCEPT (10,846) ADALIMUMAB (10,641) METHOTREXATE (9,799) TOCILIZUMAB (9,076) ABATACEPT (8,945) INFLIXIMAB (8,519) RITUXIMAB (8,408) ADAPALENE (8,356) LEFLUNOMIDE (7,926) CERTOLIZUMAB PEGOL (7,353)

Which UBLITUXIMAB-XIIY Alternatives Have Lower Hypersensitivity Risk?

UBLITUXIMAB-XIIY vs UBROGEPANT UBLITUXIMAB-XIIY vs ULIPRISTAL UBLITUXIMAB-XIIY vs UMBRALISIB UBLITUXIMAB-XIIY vs UMECLIDINIUM UBLITUXIMAB-XIIY vs UMECLIDINIUM\VILANTEROL TRIFENATATE

Related Pages

UBLITUXIMAB-XIIY Full Profile All Hypersensitivity Reports All Drugs Causing Hypersensitivity UBLITUXIMAB-XIIY Demographics