Does RITUXIMAB-PVVR Cause Inappropriate schedule of product administration? 311 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 311 reports of Inappropriate schedule of product administration have been filed in association with RITUXIMAB-PVVR. This represents 7.4% of all adverse event reports for RITUXIMAB-PVVR.
311
Reports of Inappropriate schedule of product administration with RITUXIMAB-PVVR
7.4%
of all RITUXIMAB-PVVR reports
21
Deaths
77
Hospitalizations
How Dangerous Is Inappropriate schedule of product administration From RITUXIMAB-PVVR?
Of the 311 reports, 21 (6.8%) resulted in death, 77 (24.8%) required hospitalization, and 4 (1.3%) were considered life-threatening.
Is Inappropriate schedule of product administration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-PVVR. However, 311 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)
Headache (291)
Pruritus (288)
Nausea (286)
What Other Drugs Cause Inappropriate schedule of product administration?
ADAPALENE (16,473)
DUPILUMAB (14,927)
AVOBENZONE\OCTISALATE\OCTOCRYLENE (12,546)
INSULIN GLARGINE (8,982)
INFLIXIMAB (6,847)
INFLIXIMAB-DYYB (5,977)
SECUKINUMAB (4,817)
DULAGLUTIDE (3,606)
VEDOLIZUMAB (3,259)
SACUBITRIL\VALSARTAN (2,870)
Which RITUXIMAB-PVVR Alternatives Have Lower Inappropriate schedule of product administration Risk?
RITUXIMAB-PVVR vs RIVAROXABAN
RITUXIMAB-PVVR vs RIVASTIGMINE
RITUXIMAB-PVVR vs RIVOTRIL
RITUXIMAB-PVVR vs RIZATRIPTAN
RITUXIMAB-PVVR vs ROACTEMRA