ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL and PRODUCT DOSE OMISSION ISSUE

16 reports of this reaction

2.1% of all ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL reports

#9 most reported adverse reaction

Overview

PRODUCT DOSE OMISSION ISSUE is the #9 most commonly reported adverse reaction for ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, manufactured by Dolgencorp, Inc. (DOLLAR GENERAL & REXALL). There are 16 FDA adverse event reports linking ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL to PRODUCT DOSE OMISSION ISSUE. This represents approximately 2.1% of all 769 adverse event reports for this drug.

Patients taking ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL who experience product dose omission issue 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 DOSE OMISSION ISSUE16 of 769 reports

PRODUCT DOSE OMISSION ISSUE is a less commonly reported adverse event for ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, but still significant enough to appear in the safety profile.

Other Side Effects of ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL

In addition to product dose omission issue, the following adverse reactions have been reported for ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL:

Other Drugs Associated with PRODUCT DOSE OMISSION ISSUE

The following drugs have also been linked to product dose omission issue in FDA adverse event reports:

ABALOPARATIDEACALABRUTINIBACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCLACETAMINOPHEN, IBUPROFENACETAMINOPHEN, PHENYLEPHRINE HCLACTIVATED CHARCOALADRENALINUMAFLIBERCEPTALIROCUMABALLERGY RELIEFALUMINUM CHLORIDEALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, DIMETHICONEAMIKACINANAKINRAANTACID TABLETSAPALUTAMIDEAPREMILASTARTHRITIS PAIN RELIEFAVAPRITINIBAZELASTINE

Frequently Asked Questions

Does ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL cause PRODUCT DOSE OMISSION ISSUE?

PRODUCT DOSE OMISSION ISSUE has been reported as an adverse event in 16 FDA reports for ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.

How common is PRODUCT DOSE OMISSION ISSUE with ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL?

PRODUCT DOSE OMISSION ISSUE accounts for approximately 2.1% of all adverse event reports for ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL, making it a notable side effect.

What should I do if I experience PRODUCT DOSE OMISSION ISSUE while taking ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL?

If you experience product dose omission issue while taking ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE 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

ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL Full ProfileAll Drugs Causing PRODUCT DOSE OMISSION ISSUEDolgencorp, Inc. (DOLLAR GENERAL & REXALL) 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.