Does RITUXIMAB Cause Product quality issue? 669 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 669 reports of Product quality issue have been filed in association with RITUXIMAB (Rituxan). This represents 0.4% of all adverse event reports for RITUXIMAB.
669
Reports of Product quality issue with RITUXIMAB
0.4%
of all RITUXIMAB reports
561
Deaths
508
Hospitalizations
How Dangerous Is Product quality issue From RITUXIMAB?
Of the 669 reports, 561 (83.9%) resulted in death, 508 (75.9%) required hospitalization, and 506 (75.6%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 669 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB Cause?
Off label use (39,751)
Drug ineffective (32,186)
Rheumatoid arthritis (19,850)
Pain (16,675)
Fatigue (15,602)
Arthralgia (12,529)
Rash (12,102)
Drug intolerance (11,876)
Infusion related reaction (11,871)
Joint swelling (11,170)
What Other Drugs Cause Product quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which RITUXIMAB Alternatives Have Lower Product quality issue Risk?
RITUXIMAB vs RITUXIMAB-ABBS
RITUXIMAB vs RITUXIMAB-ARRX
RITUXIMAB vs RITUXIMAB-PVVR
RITUXIMAB vs RIVAROXABAN
RITUXIMAB vs RIVASTIGMINE