9 drug(s) with this reaction
35,599 total reports
Abdominal Discomfort has been reported as an adverse reaction across 9 drug(s) manufactured by Abbvie Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 35,599 adverse event reports mention abdominal discomfort in connection with Abbvie Inc products.
This page provides a breakdown of which Abbvie Inc 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.
The following Abbvie Inc drugs have abdominal discomfort listed in their FDA adverse event reports, sorted by report count:
In addition to abdominal discomfort, the following adverse reactions have been reported across Abbvie Inc's drug portfolio:
9 drug(s) manufactured by Abbvie Inc have abdominal discomfort listed in their FDA adverse event reports: Humira, ADALIMUMAB, LEVOTHYROXINE SODIUM, FENOFIBRATE, UPADACITINIB, and others.
There are a combined 35,599 reports of abdominal discomfort across 9 Abbvie Inc drug(s) in the FDA adverse event database.