Abdominal Pain Upper in Haleon Us Holdings Llc Drugs
19 drug(s) with this reaction
15,288 total reports
Overview
Abdominal Pain Upper has been reported as an adverse reaction across 19 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 15,288 adverse event reports mention abdominal pain upper 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 pain upper, 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 Pain Upper
The following Haleon Us Holdings Llc drugs have abdominal pain upper listed in their FDA adverse event reports, sorted by report count:
Which Haleon Us Holdings Llc drugs cause Abdominal Pain Upper?
19 drug(s) manufactured by Haleon Us Holdings Llc have abdominal pain upper listed in their FDA adverse event reports: DICLOFENAC SODIUM, CALCIUM CARBONATE, FLUTICASONE PROPIONATE, ORLISTAT, IBUPROFEN SODIUM, and others.
How many Abdominal Pain Upper reports are there for Haleon Us Holdings Llc drugs?
There are a combined 15,288 reports of abdominal pain upper across 19 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.