Does RITUXIMAB-ARRX Cause Condition aggravated? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Condition aggravated have been filed in association with RITUXIMAB-ARRX. This represents 1.4% of all adverse event reports for RITUXIMAB-ARRX.
5
Reports of Condition aggravated with RITUXIMAB-ARRX
1.4%
of all RITUXIMAB-ARRX reports
4
Deaths
5
Hospitalizations
How Dangerous Is Condition aggravated From RITUXIMAB-ARRX?
Of the 5 reports, 4 (80.0%) resulted in death, 5 (100.0%) required hospitalization, and 4 (80.0%) 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-ARRX. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB-ARRX Cause?
Product storage error (165)
Circumstance or information capable of leading to medication error (116)
Off label use (56)
Intercepted product administration error (51)
Accidental exposure to product (17)
Intercepted product preparation error (16)
Fatigue (14)
Infusion related reaction (14)
Drug ineffective (12)
Dyspnoea (12)
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-ARRX Alternatives Have Lower Condition aggravated Risk?
RITUXIMAB-ARRX vs RITUXIMAB-PVVR
RITUXIMAB-ARRX vs RIVAROXABAN
RITUXIMAB-ARRX vs RIVASTIGMINE
RITUXIMAB-ARRX vs RIVOTRIL
RITUXIMAB-ARRX vs RIZATRIPTAN