7 drug(s) with this reaction
4,134 total reports
Disease Progression has been reported as an adverse reaction across 7 drug(s) manufactured by Amgen Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 4,134 adverse event reports mention disease progression in connection with Amgen Inc products.
This page provides a breakdown of which Amgen Inc drugs are most commonly associated with disease progression, 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 Amgen Inc drugs have disease progression listed in their FDA adverse event reports, sorted by report count:
In addition to disease progression, the following adverse reactions have been reported across Amgen Inc's drug portfolio:
7 drug(s) manufactured by Amgen Inc have disease progression listed in their FDA adverse event reports: DENOSUMAB, FILGRASTIM, PANITUMUMAB, PEGFILGRASTIM, DARBEPOETIN ALFA, and others.
There are a combined 4,134 reports of disease progression across 7 Amgen Inc drug(s) in the FDA adverse event database.