1,783 reports of this reaction
3.5% of all IBUPROFEN AND DIPHENHYDRAMINE CITRATE reports
#3 most reported adverse reaction
NAUSEA is the #3 most commonly reported adverse reaction for IBUPROFEN AND DIPHENHYDRAMINE CITRATE, manufactured by Kenvue Brands LLC. There are 1,783 FDA adverse event reports linking IBUPROFEN AND DIPHENHYDRAMINE CITRATE to NAUSEA. This represents approximately 3.5% of all 50,486 adverse event reports for this drug.
Patients taking IBUPROFEN AND DIPHENHYDRAMINE CITRATE who experience nausea should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
NAUSEA is moderately reported among IBUPROFEN AND DIPHENHYDRAMINE CITRATE users, representing a notable but not dominant share of adverse events.
In addition to nausea, the following adverse reactions have been reported for IBUPROFEN AND DIPHENHYDRAMINE CITRATE:
The following drugs have also been linked to nausea in FDA adverse event reports:
NAUSEA has been reported as an adverse event in 1,783 FDA reports for IBUPROFEN AND DIPHENHYDRAMINE CITRATE. This does not prove causation, but indicates an association observed in post-market surveillance data.
NAUSEA accounts for approximately 3.5% of all adverse event reports for IBUPROFEN AND DIPHENHYDRAMINE CITRATE, making it one of the most commonly reported side effect.
If you experience nausea while taking IBUPROFEN AND DIPHENHYDRAMINE CITRATE, 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.