1 drug(s) with this reaction
8,931 total reports
Unintentional Medical Device Removal 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 8,931 adverse event reports mention unintentional medical device removal in connection with Amgen Inc products.
This page provides a breakdown of which Amgen Inc drugs are most commonly associated with unintentional medical device removal, 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 unintentional medical device removal listed in their FDA adverse event reports, sorted by report count:
In addition to unintentional medical device removal, the following adverse reactions have been reported across Amgen Inc's drug portfolio:
1 drug(s) manufactured by Amgen Inc have unintentional medical device removal listed in their FDA adverse event reports: PEGFILGRASTIM.
There are a combined 8,931 reports of unintentional medical device removal across 1 Amgen Inc drug(s) in the FDA adverse event database.