1 drug(s) with this reaction
4,222 total reports
Laboratory Test Abnormal 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 4,222 adverse event reports mention laboratory test abnormal in connection with Amgen Inc products.
This page provides a breakdown of which Amgen Inc drugs are most commonly associated with laboratory test abnormal, 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 laboratory test abnormal listed in their FDA adverse event reports, sorted by report count:
In addition to laboratory test abnormal, the following adverse reactions have been reported across Amgen Inc's drug portfolio:
1 drug(s) manufactured by Amgen Inc have laboratory test abnormal listed in their FDA adverse event reports: CINACALCET HYDROCHLORIDE.
There are a combined 4,222 reports of laboratory test abnormal across 1 Amgen Inc drug(s) in the FDA adverse event database.