12 drug(s) with this reaction
3,164 total reports
Dry Mouth has been reported as an adverse reaction across 12 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 3,164 adverse event reports mention dry mouth 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 dry mouth, 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 dry mouth listed in their FDA adverse event reports, sorted by report count:
In addition to dry mouth, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
12 drug(s) manufactured by Haleon Us Holdings Llc have dry mouth listed in their FDA adverse event reports: CALCIUM CARBONATE, FLUTICASONE PROPIONATE, IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, SIMETHICONE, and others.
There are a combined 3,164 reports of dry mouth across 12 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.