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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-ABBS Cause Hypoxia? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Hypoxia have been filed in association with RITUXIMAB-ABBS. This represents 0.6% of all adverse event reports for RITUXIMAB-ABBS.

24
Reports of Hypoxia with RITUXIMAB-ABBS
0.6%
of all RITUXIMAB-ABBS reports
2
Deaths
11
Hospitalizations

How Dangerous Is Hypoxia From RITUXIMAB-ABBS?

Of the 24 reports, 2 (8.3%) resulted in death, 11 (45.8%) required hospitalization, and 4 (16.7%) were considered life-threatening.

Is Hypoxia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 24 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 Hypoxia?

TREPROSTINIL (1,322) PREDNISONE (898) MACITENTAN (845) ALBUTEROL (763) CYCLOPHOSPHAMIDE (749) PACLITAXEL (684) DEXAMETHASONE (628) AMBRISENTAN (613) TIOTROPIUM (582) ACETAMINOPHEN (545)

Which RITUXIMAB-ABBS Alternatives Have Lower Hypoxia Risk?

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

Related Pages

RITUXIMAB-ABBS Full Profile All Hypoxia Reports All Drugs Causing Hypoxia RITUXIMAB-ABBS Demographics