Glossodynia in Haleon Us Holdings Llc Drugs

6 drug(s) with this reaction

9,469 total reports

Overview

Glossodynia has been reported as an adverse reaction across 6 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 9,469 adverse event reports mention glossodynia 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 glossodynia, 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.

Haleon Us Holdings Llc Drugs Reporting Glossodynia

The following Haleon Us Holdings Llc drugs have glossodynia listed in their FDA adverse event reports, sorted by report count:

Other Reactions Reported for Haleon Us Holdings Llc Drugs

In addition to glossodynia, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:

DRUG INEFFECTIVEPRODUCT USE IN UNAPPROVED INDICATIONDRUG EFFECTIVE FOR UNAPPROVED INDICATIONHEADACHENAUSEAFATIGUEDIZZINESSPAINMIGRAINEVOMITINGABDOMINAL PAIN UPPERINCORRECT DOSE ADMINISTEREDINSOMNIAOFF LABEL USEDIARRHOEAFEELING ABNORMALABDOMINAL DISCOMFORTMALAISEOVERDOSETHERAPEUTIC RESPONSE UNEXPECTED

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Glossodynia?

6 drug(s) manufactured by Haleon Us Holdings Llc have glossodynia listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, STANNOUS FLUORIDE, POTASSIUM NITRATE, SODIUM FLUORIDE, SODIUM MONOFLUOROPHOSPHATE, and others.

How many Glossodynia reports are there for Haleon Us Holdings Llc drugs?

There are a combined 9,469 reports of glossodynia across 6 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Glossodynia
Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.