255 reports of this reaction
2.7% of all ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE reports
#4 most reported adverse reaction
DIZZINESS is the #4 most commonly reported adverse reaction for ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, manufactured by Kenvue Brands LLC. There are 255 FDA adverse event reports linking ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE to DIZZINESS. This represents approximately 2.7% of all 9,511 adverse event reports for this drug.
Patients taking ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE who experience dizziness should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
DIZZINESS is a less commonly reported adverse event for ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, but still significant enough to appear in the safety profile.
In addition to dizziness, the following adverse reactions have been reported for ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE:
The following drugs have also been linked to dizziness in FDA adverse event reports:
DIZZINESS has been reported as an adverse event in 255 FDA reports for ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE. This does not prove causation, but indicates an association observed in post-market surveillance data.
DIZZINESS accounts for approximately 2.7% of all adverse event reports for ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, making it a notable side effect.
If you experience dizziness while taking ACETAMINOPHEN, DIPHENHYDRAMINE 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.