4 drug(s) with this reaction
9,365 total reports
Adverse Drug Reaction has been reported as an adverse reaction across 4 drug(s) manufactured by Amgen Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 9,365 adverse event reports mention adverse drug reaction in connection with Amgen Inc products.
This page provides a breakdown of which Amgen Inc drugs are most commonly associated with adverse drug reaction, 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 adverse drug reaction listed in their FDA adverse event reports, sorted by report count:
In addition to adverse drug reaction, the following adverse reactions have been reported across Amgen Inc's drug portfolio:
4 drug(s) manufactured by Amgen Inc have adverse drug reaction listed in their FDA adverse event reports: Otezla, APREMILAST, CINACALCET HYDROCHLORIDE, DENOSUMAB.
There are a combined 9,365 reports of adverse drug reaction across 4 Amgen Inc drug(s) in the FDA adverse event database.