Overdose in Haleon Us Holdings Llc Drugs

9 drug(s) with this reaction

4,194 total reports

Overview

Overdose has been reported as an adverse reaction across 9 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 4,194 adverse event reports mention overdose in connection with Haleon Us Holdings Llc products.

This page provides a breakdown of which Haleon Us Holdings Llc drugs are most commonly associated with overdose, 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.

Haleon Us Holdings Llc Drugs Reporting Overdose

The following Haleon Us Holdings Llc drugs have overdose listed in their FDA adverse event reports, sorted by report count:

Other Reactions Reported for Haleon Us Holdings Llc Drugs

In addition to overdose, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:

DRUG INEFFECTIVEPRODUCT USE IN UNAPPROVED INDICATIONDRUG EFFECTIVE FOR UNAPPROVED INDICATIONHEADACHENAUSEAFATIGUEDIZZINESSPAINMIGRAINEVOMITINGABDOMINAL PAIN UPPERINCORRECT DOSE ADMINISTEREDINSOMNIAOFF LABEL USEDIARRHOEAFEELING ABNORMALABDOMINAL DISCOMFORTMALAISETHERAPEUTIC RESPONSE UNEXPECTEDDYSPNOEA

Frequently Asked Questions

Which Haleon Us Holdings Llc drugs cause Overdose?

9 drug(s) manufactured by Haleon Us Holdings Llc have overdose listed in their FDA adverse event reports: NICOTINE POLACRILEX, NICOTINE, IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, ACETAMINOPHEN, ASPIRIN, AND CAFFEINE, and others.

How many Overdose reports are there for Haleon Us Holdings Llc drugs?

There are a combined 4,194 reports of overdose across 9 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.

Related Pages

All Haleon Us Holdings Llc DrugsAll Drugs Causing Overdose
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.