Sinusitis in Haleon Us Holdings Llc Drugs

15 drug(s) with this reaction

11,542 total reports

Overview

Sinusitis has been reported as an adverse reaction across 15 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 11,542 adverse event reports mention sinusitis 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 sinusitis, 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 Sinusitis

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

Other Reactions Reported for Haleon Us Holdings Llc Drugs

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

COVID 19DISEASE RECURRENCEDRUG INEFFECTIVEPRODUCT USE IN UNAPPROVED INDICATIONDRUG EFFECTIVE FOR UNAPPROVED INDICATIONHEADACHENAUSEAFATIGUEDIZZINESSMIGRAINEPAINVOMITINGABDOMINAL PAIN UPPERINSOMNIAOVERDOSEINCORRECT DOSE ADMINISTEREDDIARRHOEAMALAISEFEELING ABNORMALABDOMINAL DISCOMFORT

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Sinusitis?

15 drug(s) manufactured by Haleon Us Holdings Llc have sinusitis listed in their FDA adverse event reports: DICLOFENAC SODIUM, FLUTICASONE PROPIONATE, CALCIUM CARBONATE, ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL, IBUPROFEN SODIUM, and others.

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

There are a combined 11,542 reports of sinusitis across 15 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Sinusitis
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.