OXYMETAZOLINE HCL and ANOSMIA

30 reports of this reaction

2.8% of all OXYMETAZOLINE HCL reports

#2 most reported adverse reaction

Overview

ANOSMIA is the #2 most commonly reported adverse reaction for OXYMETAZOLINE HCL, manufactured by Wal-Mart Stores Inc. There are 30 FDA adverse event reports linking OXYMETAZOLINE HCL to ANOSMIA. This represents approximately 2.8% of all 1,077 adverse event reports for this drug.

Patients taking OXYMETAZOLINE HCL who experience anosmia 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

ANOSMIA30 of 1,077 reports

ANOSMIA is a less commonly reported adverse event for OXYMETAZOLINE HCL, but still significant enough to appear in the safety profile.

Other Side Effects of OXYMETAZOLINE HCL

In addition to anosmia, the following adverse reactions have been reported for OXYMETAZOLINE HCL:

Other Drugs Associated with ANOSMIA

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

OXYMETAZOLINE HYDROCHLORIDE

Frequently Asked Questions

Does OXYMETAZOLINE HCL cause ANOSMIA?

ANOSMIA has been reported as an adverse event in 30 FDA reports for OXYMETAZOLINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is ANOSMIA with OXYMETAZOLINE HCL?

ANOSMIA accounts for approximately 2.8% of all adverse event reports for OXYMETAZOLINE HCL, making it one of the most commonly reported side effect.

What should I do if I experience ANOSMIA while taking OXYMETAZOLINE HCL?

If you experience anosmia while taking OXYMETAZOLINE HCL, 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

OXYMETAZOLINE HCL Full ProfileAll Drugs Causing ANOSMIAWal-Mart Stores Inc 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.