7 drug(s) with this reaction
5,760 total reports
Drug Administration Error has been reported as an adverse reaction across 7 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 5,760 adverse event reports mention drug administration error in connection with Haleon Us Holdings Llc products.
This page provides a breakdown of which Haleon Us Holdings Llc drugs are most commonly associated with drug administration error, along with report counts and links to detailed safety analyses for each medication. Understanding which drugs from a single manufacturer share a common adverse reaction can help patients and healthcare providers identify potential class-wide safety patterns.
The following Haleon Us Holdings Llc drugs have drug administration error listed in their FDA adverse event reports, sorted by report count:
In addition to drug administration error, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
7 drug(s) manufactured by Haleon Us Holdings Llc have drug administration error listed in their FDA adverse event reports: GLYCERIN, LIDOCAINE, DOCOSANOL, NICOTINE POLACRILEX, NICOTINE, ORLISTAT, and others.
There are a combined 5,760 reports of drug administration error across 7 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.