Abdominal Discomfort in Haleon Us Holdings Llc Drugs
21 drug(s) with this reaction
19,036 total reports
Overview
Abdominal Discomfort has been reported as an adverse reaction across 21 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 19,036 adverse event reports mention abdominal discomfort 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 abdominal discomfort, 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 Abdominal Discomfort
The following Haleon Us Holdings Llc drugs have abdominal discomfort listed in their FDA adverse event reports, sorted by report count:
Which Haleon Us Holdings Llc drugs cause Abdominal Discomfort?
21 drug(s) manufactured by Haleon Us Holdings Llc have abdominal discomfort listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, FLUTICASONE PROPIONATE, IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, and others.
How many Abdominal Discomfort reports are there for Haleon Us Holdings Llc drugs?
There are a combined 19,036 reports of abdominal discomfort across 21 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.
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.