Does RITUXIMAB-ABBS Cause Therapy interrupted? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Therapy interrupted have been filed in association with RITUXIMAB-ABBS. This represents 1.2% of all adverse event reports for RITUXIMAB-ABBS.
52
Reports of Therapy interrupted with RITUXIMAB-ABBS
1.2%
of all RITUXIMAB-ABBS reports
4
Deaths
7
Hospitalizations
How Dangerous Is Therapy interrupted From RITUXIMAB-ABBS?
Of the 52 reports, 4 (7.7%) resulted in death, 7 (13.5%) required hospitalization, and 1 (1.9%) were considered life-threatening.
Is Therapy interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 52 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 Therapy interrupted?
ADALIMUMAB (5,755)
ETANERCEPT (3,397)
RELUGOLIX (3,251)
CERTOLIZUMAB PEGOL (3,209)
LENALIDOMIDE (2,724)
UPADACITINIB (1,741)
ABATACEPT (1,726)
CLOZAPINE (1,722)
AMIKACIN (1,283)
TOFACITINIB (1,182)
Which RITUXIMAB-ABBS Alternatives Have Lower Therapy interrupted Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL