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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 Product administration error? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product administration error have been filed in association with RITUXIMAB-ABBS. This represents 0.2% of all adverse event reports for RITUXIMAB-ABBS.

9
Reports of Product administration error with RITUXIMAB-ABBS
0.2%
of all RITUXIMAB-ABBS reports
1
Deaths
0
Hospitalizations

How Dangerous Is Product administration error From RITUXIMAB-ABBS?

Of the 9 reports, 1 (11.1%) resulted in death, and 1 (11.1%) were considered life-threatening.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RITUXIMAB-ABBS. However, 9 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 administration error?

HYDROXYPROGESTERONE CAPROATE (972) ACETAMINOPHEN (666) CENEGERMIN-BKBJ (613) LEUPROLIDE (595) EVOLOCUMAB (565) ADALIMUMAB (543) METHYLPHENIDATE (414) OLMESARTAN MEDOXOMIL (314) ASPIRIN (241) SECUKINUMAB (225)

Which RITUXIMAB-ABBS Alternatives Have Lower Product administration error 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 Product administration error Reports All Drugs Causing Product administration error RITUXIMAB-ABBS Demographics