Swelling Face in Haleon Us Holdings Llc Drugs

8 drug(s) with this reaction

1,304 total reports

Overview

Swelling Face has been reported as an adverse reaction across 8 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 1,304 adverse event reports mention swelling face 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 swelling face, 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 Swelling Face

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

Other Reactions Reported for Haleon Us Holdings Llc Drugs

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

DRUG INEFFECTIVEPRODUCT USE IN UNAPPROVED INDICATIONDRUG EFFECTIVE FOR UNAPPROVED INDICATIONHEADACHENAUSEAFATIGUEDIZZINESSMIGRAINEPAINVOMITINGABDOMINAL PAIN UPPERINSOMNIAOVERDOSEINCORRECT DOSE ADMINISTEREDDIARRHOEAMALAISEFEELING ABNORMALABDOMINAL DISCOMFORTOFF LABEL USEDYSPNOEA

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Swelling Face?

8 drug(s) manufactured by Haleon Us Holdings Llc have swelling face listed in their FDA adverse event reports: IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, DOCOSANOL, GLYCERIN, LIDOCAINE, IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE, and others.

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

There are a combined 1,304 reports of swelling face across 8 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Swelling Face
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.