1 drug(s) with this reaction
6,023 total reports
Device Use Error has been reported as an adverse reaction across 1 drug(s) manufactured by Amgen Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 6,023 adverse event reports mention device use error in connection with Amgen Inc products.
This page provides a breakdown of which Amgen Inc drugs are most commonly associated with device use error, 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 device use error listed in their FDA adverse event reports, sorted by report count:
In addition to device use error, the following adverse reactions have been reported across Amgen Inc's drug portfolio:
1 drug(s) manufactured by Amgen Inc have device use error listed in their FDA adverse event reports: PEGFILGRASTIM.
There are a combined 6,023 reports of device use error across 1 Amgen Inc drug(s) in the FDA adverse event database.