7 drug(s) with this reaction
6,214 total reports
Stomatitis 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 6,214 adverse event reports mention stomatitis 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 stomatitis, 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 stomatitis listed in their FDA adverse event reports, sorted by report count:
In addition to stomatitis, 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 stomatitis listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, NICOTINE POLACRILEX, STANNOUS FLUORIDE, POTASSIUM NITRATE AND SODIUM FLUORIDE, and others.
There are a combined 6,214 reports of stomatitis across 7 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.