9 drug(s) with this reaction
1,820 total reports
Product Complaint has been reported as an adverse reaction across 9 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 1,820 adverse event reports mention product complaint 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 product complaint, 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 product complaint listed in their FDA adverse event reports, sorted by report count:
In addition to product complaint, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
9 drug(s) manufactured by Haleon Us Holdings Llc have product complaint listed in their FDA adverse event reports: NICOTINE, DOCOSANOL, GLYCERIN, LIDOCAINE, NICOTINE POLACRILEX, ORLISTAT, and others.
There are a combined 1,820 reports of product complaint across 9 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.