1 reports of this reaction
2.0% of all ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE reports
#19 most reported adverse reaction
EXPIRED PRODUCT ADMINISTERED is the #19 most commonly reported adverse reaction for ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE, manufactured by Kenvue Brands LLC. There are 1 FDA adverse event reports linking ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE to EXPIRED PRODUCT ADMINISTERED. This represents approximately 2.0% of all 51 adverse event reports for this drug.
Patients taking ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE who experience expired product administered should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
EXPIRED PRODUCT ADMINISTERED is a less commonly reported adverse event for ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to expired product administered, the following adverse reactions have been reported for ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE:
The following drugs have also been linked to expired product administered in FDA adverse event reports:
EXPIRED PRODUCT ADMINISTERED has been reported as an adverse event in 1 FDA reports for ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
EXPIRED PRODUCT ADMINISTERED accounts for approximately 2.0% of all adverse event reports for ACETAMINOPHEN AND PHENYLEPHRINE HYDROCHLORIDE, making it a notable side effect.
If you experience expired product administered while taking ACETAMINOPHEN 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.