Does RITUXIMAB-ABBS Cause Product use issue? 119 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Product use issue have been filed in association with RITUXIMAB-ABBS. This represents 2.7% of all adverse event reports for RITUXIMAB-ABBS.
119
Reports of Product use issue with RITUXIMAB-ABBS
2.7%
of all RITUXIMAB-ABBS reports
62
Deaths
82
Hospitalizations
How Dangerous Is Product use issue From RITUXIMAB-ABBS?
Of the 119 reports, 62 (52.1%) resulted in death, 82 (68.9%) required hospitalization, and 61 (51.3%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 119 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 Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which RITUXIMAB-ABBS Alternatives Have Lower Product use issue Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL