Does RITUXIMAB-PVVR Cause Condition aggravated? 514 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 514 reports of Condition aggravated have been filed in association with RITUXIMAB-PVVR. This represents 12.2% of all adverse event reports for RITUXIMAB-PVVR.
514
Reports of Condition aggravated with RITUXIMAB-PVVR
12.2%
of all RITUXIMAB-PVVR reports
26
Deaths
147
Hospitalizations
How Dangerous Is Condition aggravated From RITUXIMAB-PVVR?
Of the 514 reports, 26 (5.1%) resulted in death, 147 (28.6%) required hospitalization, and 9 (1.8%) 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-PVVR. However, 514 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB-PVVR Cause?
Off label use (2,079)
Intentional product use issue (627)
Death (338)
Covid-19 (322)
Fatigue (318)
Dyspnoea (314)
Inappropriate schedule of product administration (311)
Headache (291)
Pruritus (288)
Nausea (286)
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-PVVR Alternatives Have Lower Condition aggravated Risk?
RITUXIMAB-PVVR vs RIVAROXABAN
RITUXIMAB-PVVR vs RIVASTIGMINE
RITUXIMAB-PVVR vs RIVOTRIL
RITUXIMAB-PVVR vs RIZATRIPTAN
RITUXIMAB-PVVR vs ROACTEMRA