Does RITUXIMAB-PVVR Cause Product administration error? 11 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 11 reports of Product administration error have been filed in association with RITUXIMAB-PVVR. This represents 0.3% of all adverse event reports for RITUXIMAB-PVVR.
11
Reports of Product administration error with RITUXIMAB-PVVR
0.3%
of all RITUXIMAB-PVVR reports
2
Deaths
2
Hospitalizations
How Dangerous Is Product administration error From RITUXIMAB-PVVR?
Of the 11 reports, 2 (18.2%) resulted in death, 2 (18.2%) required hospitalization.
Is Product administration error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-PVVR. However, 11 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)
Condition aggravated (514)
Death (338)
Covid-19 (322)
Fatigue (318)
Dyspnoea (314)
Inappropriate schedule of product administration (311)
Headache (291)
Pruritus (288)
What Other Drugs Cause Product administration error?
HYDROXYPROGESTERONE CAPROATE (972)
ACETAMINOPHEN (666)
CENEGERMIN-BKBJ (613)
LEUPROLIDE (595)
EVOLOCUMAB (565)
ADALIMUMAB (543)
METHYLPHENIDATE (414)
OLMESARTAN MEDOXOMIL (314)
ASPIRIN (241)
SECUKINUMAB (225)
Which RITUXIMAB-PVVR Alternatives Have Lower Product administration error Risk?
RITUXIMAB-PVVR vs RIVAROXABAN
RITUXIMAB-PVVR vs RIVASTIGMINE
RITUXIMAB-PVVR vs RIVOTRIL
RITUXIMAB-PVVR vs RIZATRIPTAN
RITUXIMAB-PVVR vs ROACTEMRA