Does RITUXIMAB-ABBS Cause Dyspnoea? 208 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 208 reports of Dyspnoea have been filed in association with RITUXIMAB-ABBS. This represents 4.8% of all adverse event reports for RITUXIMAB-ABBS.
208
Reports of Dyspnoea with RITUXIMAB-ABBS
4.8%
of all RITUXIMAB-ABBS reports
65
Deaths
104
Hospitalizations
How Dangerous Is Dyspnoea From RITUXIMAB-ABBS?
Of the 208 reports, 65 (31.3%) resulted in death, 104 (50.0%) required hospitalization, and 77 (37.0%) were considered life-threatening.
Is Dyspnoea Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 208 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)
Pain (205)
Rheumatoid arthritis (202)
Intentional dose omission (196)
Fatigue (195)
Drug ineffective (186)
Hypertension (183)
Infusion related reaction (183)
Rash (183)
What Other Drugs Cause Dyspnoea?
ALBUTEROL (21,856)
TREPROSTINIL (16,348)
AMBRISENTAN (13,367)
PREDNISONE (12,830)
BUDESONIDE\FORMOTEROL (11,158)
TIOTROPIUM (10,863)
ADALIMUMAB (10,547)
DUPILUMAB (10,310)
FLUTICASONE\SALMETEROL (9,783)
MEPOLIZUMAB (9,192)
Which RITUXIMAB-ABBS Alternatives Have Lower Dyspnoea Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL