Depression in Haleon Us Holdings Llc Drugs

18 drug(s) with this reaction

12,249 total reports

Overview

Depression has been reported as an adverse reaction across 18 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 12,249 adverse event reports mention depression 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 depression, 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 Depression

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

Other Reactions Reported for Haleon Us Holdings Llc Drugs

In addition to depression, 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 Depression?

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

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

There are a combined 12,249 reports of depression across 18 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Depression
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.