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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 administration error? 13 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product administration error have been filed in association with RANIBIZUMAB-EQRN. This represents 13.4% of all adverse event reports for RANIBIZUMAB-EQRN.

13
Reports of Product administration error with RANIBIZUMAB-EQRN
13.4%
of all RANIBIZUMAB-EQRN reports
0
Deaths
0
Hospitalizations

How Dangerous Is Product administration error From RANIBIZUMAB-EQRN?

Of the 13 reports.

Is Product administration error Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RANIBIZUMAB-EQRN. However, 13 reports have been filed with the FAERS database.

What Other Side Effects Does RANIBIZUMAB-EQRN Cause?

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) Product use issue (6) Vision blurred (5)

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)

Related Pages

RANIBIZUMAB-EQRN Full Profile All Product administration error Reports All Drugs Causing Product administration error RANIBIZUMAB-EQRN Demographics