3 drug(s) with this reaction
127 total reports
Hyperaesthesia Teeth has been reported as an adverse reaction across 3 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 127 adverse event reports mention hyperaesthesia teeth 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 hyperaesthesia teeth, 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 hyperaesthesia teeth listed in their FDA adverse event reports, sorted by report count:
In addition to hyperaesthesia teeth, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
3 drug(s) manufactured by Haleon Us Holdings Llc have hyperaesthesia teeth listed in their FDA adverse event reports: POTASSIUM NITRATE, SODIUM FLUORIDE, POTASSIUM NITRATE AND SODIUM FLUORIDE, STANNOUS FLUORIDE.
There are a combined 127 reports of hyperaesthesia teeth across 3 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.