13 drug(s) with this reaction
4,464 total reports
Incorrect Dose Administered has been reported as an adverse reaction across 13 drug(s) manufactured by Haleon Us Holdings Llc in the FDA Adverse Event Reporting System (FAERS) database. A combined total of 4,464 adverse event reports mention incorrect dose administered 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 incorrect dose administered, 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 Haleon Us Holdings Llc drugs have incorrect dose administered listed in their FDA adverse event reports, sorted by report count:
In addition to incorrect dose administered, the following adverse reactions have been reported across Haleon Us Holdings Llc's drug portfolio:
13 drug(s) manufactured by Haleon Us Holdings Llc have incorrect dose administered listed in their FDA adverse event reports: FLUTICASONE PROPIONATE, ACETAMINOPHEN, ASPIRIN, AND CAFFEINE, IBUPROFEN SODIUM, IBUPROFEN TABLETS, COATED, ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL, and others.
There are a combined 4,464 reports of incorrect dose administered across 13 Haleon Us Holdings Llc drug(s) in the FDA adverse event database.