Does RITUXIMAB-ABBS Cause Hypersensitivity? 148 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 148 reports of Hypersensitivity have been filed in association with RITUXIMAB-ABBS. This represents 3.4% of all adverse event reports for RITUXIMAB-ABBS.
148
Reports of Hypersensitivity with RITUXIMAB-ABBS
3.4%
of all RITUXIMAB-ABBS reports
71
Deaths
94
Hospitalizations
How Dangerous Is Hypersensitivity From RITUXIMAB-ABBS?
Of the 148 reports, 71 (48.0%) resulted in death, 94 (63.5%) required hospitalization, and 86 (58.1%) were considered life-threatening.
Is Hypersensitivity Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 148 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB-ABBS Cause?
Off label use (2,167)
Intentional product use issue (273)
Dyspnoea (208)
Pain (205)
Rheumatoid arthritis (202)
Intentional dose omission (196)
Fatigue (195)
Drug ineffective (186)
Hypertension (183)
Infusion related reaction (183)
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 RITUXIMAB-ABBS Alternatives Have Lower Hypersensitivity Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL