ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE and PRODUCT ADMINISTRATION INTERRUPTED

3 reports of this reaction

1.8% of all ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE reports

#16 most reported adverse reaction

Overview

PRODUCT ADMINISTRATION INTERRUPTED is the #16 most commonly reported adverse reaction for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, manufactured by Rite Aid Corporation. There are 3 FDA adverse event reports linking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE to PRODUCT ADMINISTRATION INTERRUPTED. This represents approximately 1.8% of all 171 adverse event reports for this drug.

Patients taking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE who experience product administration interrupted 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

PRODUCT ADMINISTRATION INTERRUPTED3 of 171 reports

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

Other Side Effects of ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE

In addition to product administration interrupted, the following adverse reactions have been reported for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE:

Other Drugs Associated with PRODUCT ADMINISTRATION INTERRUPTED

The following drugs have also been linked to product administration interrupted in FDA adverse event reports:

ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDECALCIUM, MAGNESIUM, POTASSIUM, AND SODIUM OXYBATES

Frequently Asked Questions

Does ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE cause PRODUCT ADMINISTRATION INTERRUPTED?

PRODUCT ADMINISTRATION INTERRUPTED has been reported as an adverse event in 3 FDA reports for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is PRODUCT ADMINISTRATION INTERRUPTED with ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE?

PRODUCT ADMINISTRATION INTERRUPTED accounts for approximately 1.8% of all adverse event reports for ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE, making it a notable side effect.

What should I do if I experience PRODUCT ADMINISTRATION INTERRUPTED while taking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE?

If you experience product administration interrupted while taking ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, 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, PHENYLEPHRINE HYDROCHLORIDE Full ProfileAll Drugs Causing PRODUCT ADMINISTRATION INTERRUPTEDRite Aid Corporation 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.