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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 PROPARACAINE Cause Product use issue? 5 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product use issue have been filed in association with PROPARACAINE (Proparacaine hydrochloride). This represents 1.6% of all adverse event reports for PROPARACAINE.

5
Reports of Product use issue with PROPARACAINE
1.6%
of all PROPARACAINE reports
0
Deaths
3
Hospitalizations

How Dangerous Is Product use issue From PROPARACAINE?

Of the 5 reports, 3 (60.0%) required hospitalization.

Is Product use issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PROPARACAINE. However, 5 reports have been filed with the FAERS database.

What Other Side Effects Does PROPARACAINE Cause?

Corneal oedema (43) Eye pain (42) Vision blurred (37) Conjunctival hyperaemia (29) Eye irritation (26) Persistent corneal epithelial defect (24) Corneal epithelium defect (23) Hypopyon (22) Keratopathy (20) Ocular hyperaemia (19)

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)

Which PROPARACAINE Alternatives Have Lower Product use issue Risk?

PROPARACAINE vs PROPECIA PROPARACAINE vs PROPIOMAZINE PROPARACAINE vs PROPOFOL PROPARACAINE vs PROPOXYPHENE PROPARACAINE vs PROPOXYPHENE/ACETAMINOPHEN

Related Pages

PROPARACAINE Full Profile All Product use issue Reports All Drugs Causing Product use issue PROPARACAINE Demographics