Does RITUXIMAB-ABBS Cause Product quality issue? 21 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 21 reports of Product quality issue have been filed in association with RITUXIMAB-ABBS. This represents 0.5% of all adverse event reports for RITUXIMAB-ABBS.
21
Reports of Product quality issue with RITUXIMAB-ABBS
0.5%
of all RITUXIMAB-ABBS reports
10
Deaths
10
Hospitalizations
How Dangerous Is Product quality issue From RITUXIMAB-ABBS?
Of the 21 reports, 10 (47.6%) resulted in death, 10 (47.6%) required hospitalization, and 14 (66.7%) 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-ABBS. However, 21 reports have been filed with the FAERS database.
What Other Side Effects Does RITUXIMAB-ABBS Cause?
Off label use (2,167)
Intentional product use issue (273)
Dyspnoea (208)
Pain (205)
Rheumatoid arthritis (202)
Intentional dose omission (196)
Fatigue (195)
Drug ineffective (186)
Hypertension (183)
Infusion related reaction (183)
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-ABBS Alternatives Have Lower Product quality issue Risk?
RITUXIMAB-ABBS vs RITUXIMAB-ARRX
RITUXIMAB-ABBS vs RITUXIMAB-PVVR
RITUXIMAB-ABBS vs RIVAROXABAN
RITUXIMAB-ABBS vs RIVASTIGMINE
RITUXIMAB-ABBS vs RIVOTRIL