7 drug(s) with this reaction
2,695 total reports
Incorrect Drug Administration Duration 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 2,695 adverse event reports mention incorrect drug administration duration 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 incorrect drug administration duration, 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 incorrect drug administration duration listed in their FDA adverse event reports, sorted by report count:
In addition to incorrect drug administration duration, 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 incorrect drug administration duration listed in their FDA adverse event reports: GLYCERIN, LIDOCAINE, DOCOSANOL, NICOTINE POLACRILEX, NICOTINE, ACETAMINOPHEN, ASPIRIN, AND CAFFEINE, and others.
There are a combined 2,695 reports of incorrect drug administration duration across 7 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.