ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE and WRONG TECHNIQUE IN PRODUCT USAGE PROCESS

Overview

WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is the #4 most commonly reported adverse reaction for ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, manufactured by Kenvue Brands LLC. There are 125 FDA adverse event reports linking ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE to WRONG TECHNIQUE IN PRODUCT USAGE PROCESS. This represents approximately 4.1% of all 3,027 adverse event reports for this drug.

Patients taking ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE who experience wrong technique in product usage process should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.

Reporting Frequency

WRONG TECHNIQUE IN PRODUCT USAGE PROCESS is moderately reported among ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE users, representing a notable but not dominant share of adverse events.

Other Side Effects of ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE

In addition to wrong technique in product usage process, the following adverse reactions have been reported for ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE:

• OFF LABEL USE — 180 reports
• VOMITING — 141 reports
• DRUG ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE — 132 reports
• INCORRECT DOSE ADMINISTERED — 123 reports
• PRODUCT USE ISSUE — 107 reports
• DRUG INEFFECTIVE — 106 reports
• PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE — 94 reports
• ACCIDENTAL EXPOSURE TO PRODUCT BY CHILD — 88 reports
• PRODUCT USE IN UNAPPROVED INDICATION — 76 reports
• ACCIDENTAL EXPOSURE TO PRODUCT — 71 reports

Other Drugs Associated with WRONG TECHNIQUE IN PRODUCT USAGE PROCESS

The following drugs have also been linked to wrong technique in product usage process in FDA adverse event reports:

Does ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE cause WRONG TECHNIQUE IN PRODUCT USAGE PROCESS?

WRONG TECHNIQUE IN PRODUCT USAGE PROCESS has been reported as an adverse event in 125 FDA reports for ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is WRONG TECHNIQUE IN PRODUCT USAGE PROCESS with ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE?

WRONG TECHNIQUE IN PRODUCT USAGE PROCESS accounts for approximately 4.1% of all adverse event reports for ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, making it a notable side effect.

What should I do if I experience WRONG TECHNIQUE IN PRODUCT USAGE PROCESS while taking ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE?

If you experience wrong technique in product usage process while taking ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.

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