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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 Condition aggravated? 195 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 195 reports of Condition aggravated have been filed in association with RANIBIZUMAB (CIMERLI). This represents 1.3% of all adverse event reports for RANIBIZUMAB.

195
Reports of Condition aggravated with RANIBIZUMAB
1.3%
of all RANIBIZUMAB reports
2
Deaths
18
Hospitalizations

How Dangerous Is Condition aggravated From RANIBIZUMAB?

Of the 195 reports, 2 (1.0%) resulted in death, 18 (9.2%) required hospitalization.

Is Condition aggravated Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RANIBIZUMAB. However, 195 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) Eye pain (632) Cerebrovascular accident (543)

What Other Drugs Cause Condition aggravated?

TOFACITINIB (16,925) INFLIXIMAB (16,616) DUPILUMAB (16,459) ETANERCEPT (15,897) METHOTREXATE (14,938) ADALIMUMAB (13,527) PREDNISONE (10,751) INFLIXIMAB-DYYB (10,275) HYDROXYCHLOROQUINE (8,848) RITUXIMAB (8,627)

Which RANIBIZUMAB Alternatives Have Lower Condition aggravated Risk?

RANIBIZUMAB vs RANIMUSTINE RANIBIZUMAB vs RANITIDINE RANIBIZUMAB vs RANITIDINE\RANITIDINE RANIBIZUMAB vs RANOLAZINE RANIBIZUMAB vs RAPAMUNE

Related Pages

RANIBIZUMAB Full Profile All Condition aggravated Reports All Drugs Causing Condition aggravated RANIBIZUMAB Demographics