ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE and DYSGEUSIA

28 reports of this reaction

1.6% of all ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE reports

#13 most reported adverse reaction

Overview

DYSGEUSIA is the #13 most commonly reported adverse reaction for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, manufactured by The Procter & Gamble Manufacturing Company. There are 28 FDA adverse event reports linking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE to DYSGEUSIA. This represents approximately 1.6% of all 1,750 adverse event reports for this drug.

Patients taking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE who experience dysgeusia 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

DYSGEUSIA28 of 1,750 reports

DYSGEUSIA is a less commonly reported adverse event for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.

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

In addition to dysgeusia, the following adverse reactions have been reported for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE:

Other Drugs Associated with DYSGEUSIA

The following drugs have also been linked to dysgeusia in FDA adverse event reports:

ACETAMINOPHEN, DEXTROMETHORPHAN HBRACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEASENAPINE MALEATECETYLPYRIDINIUM CHLORIDECHILDRENS ACETAMINOPHENESZOPICLONEFAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDEIPRATROPIUM BROMIDE AND ALBUTEROL SULFATELIFITEGRASTMICONAZOLE NITRATE 2%NIRMATRELVIR AND RITONAVIRPOTASSIUM NITRATEPOTASSIUM NITRATE AND SODIUM FLUORIDEPOTASSIUM NITRATE, SODIUM FLUORIDERUCAPARIBSTANNOUS FLUORIDESUNITINIB MALATETERBINAFINE HYDROCHLORIDETETRAHYDROZOLINE HCL

Frequently Asked Questions

Does ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE cause DYSGEUSIA?

DYSGEUSIA has been reported as an adverse event in 28 FDA reports for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is DYSGEUSIA with ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE?

DYSGEUSIA accounts for approximately 1.6% of all adverse event reports for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE, making it a notable side effect.

What should I do if I experience DYSGEUSIA while taking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE?

If you experience dysgeusia while taking ACETAMINOPHEN, 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.

Related Pages

ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE Full ProfileAll Drugs Causing DYSGEUSIAThe Procter & Gamble Manufacturing Company Drugs
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.