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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 RANIBIZUMAB Cause Sepsis? 27 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 27 reports of Sepsis have been filed in association with RANIBIZUMAB (CIMERLI). This represents 0.2% of all adverse event reports for RANIBIZUMAB.

27
Reports of Sepsis with RANIBIZUMAB
0.2%
of all RANIBIZUMAB reports
14
Deaths
23
Hospitalizations

How Dangerous Is Sepsis From RANIBIZUMAB?

Of the 27 reports, 14 (51.9%) resulted in death, 23 (85.2%) required hospitalization, and 2 (7.4%) were considered life-threatening.

Is Sepsis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RANIBIZUMAB. However, 27 reports have been filed with the FAERS database.

What Other Side Effects Does RANIBIZUMAB Cause?

Death (2,250) Off label use (1,467) Visual acuity reduced (1,342) Visual impairment (1,185) No adverse event (1,012) Drug ineffective (831) Blindness (760) Vision blurred (711 503 Service Unavailable

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