Pneumonia in Abbvie Inc Drugs

15 drug(s) with this reaction

49,502 total reports

Overview

Pneumonia has been reported as an adverse reaction across 15 drug(s) manufactured by Abbvie Inc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 49,502 adverse event reports mention pneumonia in connection with Abbvie Inc products.

This page provides a breakdown of which Abbvie Inc drugs are most commonly associated with pneumonia, 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.

Abbvie Inc Drugs Reporting Pneumonia

The following Abbvie Inc drugs have pneumonia listed in their FDA adverse event reports, sorted by report count:

Other Reactions Reported for Abbvie Inc Drugs

In addition to pneumonia, the following adverse reactions have been reported across Abbvie Inc's drug portfolio:

DRUG INEFFECTIVESEIZUREWEIGHT INCREASEDNAUSEAOFF LABEL USEFATIGUEPAINSOMNOLENCETREMORFALLANXIETYVOMITINGCONVULSIONHEADACHEDEPRESSIONINSOMNIADIZZINESSDIARRHOEADRUG INTERACTIONDIABETES MELLITUS

Frequently Asked Questions

Which Abbvie Inc drugs cause Pneumonia?

15 drug(s) manufactured by Abbvie Inc have pneumonia listed in their FDA adverse event reports: Humira, ADALIMUMAB, LEVOTHYROXINE SODIUM, VENETOCLAX, UPADACITINIB, and others.

How many Pneumonia reports are there for Abbvie Inc drugs?

There are a combined 49,502 reports of pneumonia across 15 Abbvie Inc drug(s) in the FDA adverse event database.

Disclaimer: This analysis is based on FDA adverse event reports and is for informational purposes only. Reports do not prove causation. Always consult your healthcare provider.