Dizziness in Haleon Us Holdings Llc Drugs

23 drug(s) with this reaction

25,021 total reports

Overview

Dizziness has been reported as an adverse reaction across 23 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 25,021 adverse event reports mention dizziness 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 dizziness, 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 Dizziness

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

Other Reactions Reported for Haleon Us Holdings Llc Drugs

In addition to dizziness, 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 INDICATIONHEADACHENAUSEAFATIGUEMIGRAINEPAINVOMITINGABDOMINAL PAIN UPPERINSOMNIAOVERDOSEINCORRECT DOSE ADMINISTEREDDIARRHOEAMALAISEFEELING ABNORMALABDOMINAL DISCOMFORTOFF LABEL USE

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Dizziness?

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

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

There are a combined 25,021 reports of dizziness across 23 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Dizziness
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.