Does RITUXIMAB-ABBS Cause Condition aggravated? 141 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 141 reports of Condition aggravated have been filed in association with RITUXIMAB-ABBS. This represents 3.2% of all adverse event reports for RITUXIMAB-ABBS.
141
Reports of Condition aggravated with RITUXIMAB-ABBS
3.2%
of all RITUXIMAB-ABBS reports
61
Deaths
86
Hospitalizations
How Dangerous Is Condition aggravated From RITUXIMAB-ABBS?
Of the 141 reports, 61 (43.3%) resulted in death, 86 (61.0%) required hospitalization, and 62 (44.0%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 141 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which RITUXIMAB-ABBS Alternatives Have Lower Condition aggravated Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL