5 drug(s) with this reaction
7,639 total reports
Tremor has been reported as an adverse reaction across 5 drug(s) manufactured by Abbvie Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 7,639 adverse event reports mention tremor in connection with Abbvie Inc products.
This page provides a breakdown of which Abbvie Inc drugs are most commonly associated with tremor, 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 Abbvie Inc drugs have tremor listed in their FDA adverse event reports, sorted by report count:
In addition to tremor, the following adverse reactions have been reported across Abbvie Inc's drug portfolio:
5 drug(s) manufactured by Abbvie Inc have tremor listed in their FDA adverse event reports: LEVOTHYROXINE SODIUM, DIVALPROEX SODIUM, FENOFIBRATE, ATOGEPANT, GLECAPREVIR AND PIBRENTASVIR.
There are a combined 7,639 reports of tremor across 5 Abbvie Inc drug(s) in the FDA adverse event database.