Joint Swelling in Haleon Us Holdings Llc Drugs

8 drug(s) with this reaction

12,953 total reports

Overview

Joint Swelling 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 12,953 adverse event reports mention joint swelling 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 joint swelling, 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 Joint Swelling

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

Other Reactions Reported for Haleon Us Holdings Llc Drugs

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

COVID 19DISEASE RECURRENCEDRUG INEFFECTIVEFATIGUENAUSEAHEADACHEPAINDIARRHOEADIZZINESSPRODUCT USE IN UNAPPROVED INDICATIONARTHRALGIADYSPNOEAVOMITINGOFF LABEL USEMALAISEABDOMINAL DISCOMFORTRASHPAIN IN EXTREMITYABDOMINAL PAIN UPPERPRURITUS

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Joint Swelling?

8 drug(s) manufactured by Haleon Us Holdings Llc have joint swelling listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, FLUTICASONE PROPIONATE, IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, and others.

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

There are a combined 12,953 reports of joint swelling across 8 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Joint Swelling
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.