3 drug(s) with this reaction
9,401 total reports
Arthropathy has been reported as an adverse reaction across 3 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 9,401 adverse event reports mention arthropathy 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 arthropathy, 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.
The following Haleon Us Holdings Llc drugs have arthropathy listed in their FDA adverse event reports, sorted by report count:
In addition to arthropathy, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
3 drug(s) manufactured by Haleon Us Holdings Llc have arthropathy listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE.
There are a combined 9,401 reports of arthropathy across 3 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.