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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does RITUXIMAB Cause Performance status decreased? 45 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 45 reports of Performance status decreased have been filed in association with RITUXIMAB (Rituxan). This represents 0.0% of all adverse event reports for RITUXIMAB.

45
Reports of Performance status decreased with RITUXIMAB
0.0%
of all RITUXIMAB reports
11
Deaths
21
Hospitalizations

How Dangerous Is Performance status decreased From RITUXIMAB?

Of the 45 reports, 11 (24.4%) resulted in death, 21 (46.7%) required hospitalization, and 1 (2.2%) were considered life-threatening.

Is Performance status decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RITUXIMAB. However, 45 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 Performance status decreased?

BACLOFEN (156) LENALIDOMIDE (118) PACLITAXEL (112) BEVACIZUMAB (103) SODIUM OXYBATE (103) CARBOPLATIN (100) DEXAMETHASONE (80) CAPECITABINE (75) NIRAPARIB (75) LUMATEPERONE (68)

Which RITUXIMAB Alternatives Have Lower Performance status decreased Risk?

RITUXIMAB vs RITUXIMAB-ABBS RITUXIMAB vs RITUXIMAB-ARRX RITUXIMAB vs RITUXIMAB-PVVR RITUXIMAB vs RIVAROXABAN RITUXIMAB vs RIVASTIGMINE

Related Pages

RITUXIMAB Full Profile All Performance status decreased Reports All Drugs Causing Performance status decreased RITUXIMAB Demographics