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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-EQRN Cause Product use issue? 6 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 6 reports of Product use issue have been filed in association with RANIBIZUMAB-EQRN. This represents 6.2% of all adverse event reports for RANIBIZUMAB-EQRN.

6
Reports of Product use issue with RANIBIZUMAB-EQRN
6.2%
of all RANIBIZUMAB-EQRN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product use issue From RANIBIZUMAB-EQRN?

Of the 6 reports.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RANIBIZUMAB-EQRN. However, 6 reports have been filed with the FAERS database.

What Other Side Effects Does RANIBIZUMAB-EQRN Cause?

Product administration error (13) Product contamination (9) Product storage error (8) Circumstance or information capable of leading to medication error (7) Visual impairment (7) Death (6) Drug ineffective (6) Vision blurred (5)

What Other Drugs Cause Product use issue?

INFLIXIMAB (12,752) DUPILUMAB (10,575) POLYETHYLENE GLYCOL 3350 (9,432) METHOTREXATE (8,185) DICLOFENAC (8,009) RITUXIMAB (6,948) ADALIMUMAB (6,379) ETANERCEPT (6,062) TOCILIZUMAB (5,944) ABATACEPT (5,915)

Related Pages

RANIBIZUMAB-EQRN Full Profile All Product use issue Reports All Drugs Causing Product use issue RANIBIZUMAB-EQRN Demographics