3 reports of this reaction
1.7% of all IBUPROFEN, DIPHENHYDRAMINE HCL reports
#11 most reported adverse reaction
ARTHROPATHY is the #11 most commonly reported adverse reaction for IBUPROFEN, DIPHENHYDRAMINE HCL, manufactured by CVS Pharmacy. There are 3 FDA adverse event reports linking IBUPROFEN, DIPHENHYDRAMINE HCL to ARTHROPATHY. This represents approximately 1.7% of all 180 adverse event reports for this drug.
Patients taking IBUPROFEN, DIPHENHYDRAMINE HCL who experience arthropathy should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ARTHROPATHY is a less commonly reported adverse event for IBUPROFEN, DIPHENHYDRAMINE HCL, but still significant enough to appear in the safety profile.
In addition to arthropathy, the following adverse reactions have been reported for IBUPROFEN, DIPHENHYDRAMINE HCL:
The following drugs have also been linked to arthropathy in FDA adverse event reports:
ARTHROPATHY has been reported as an adverse event in 3 FDA reports for IBUPROFEN, DIPHENHYDRAMINE HCL. This does not prove causation, but indicates an association observed in post-market surveillance data.
ARTHROPATHY accounts for approximately 1.7% of all adverse event reports for IBUPROFEN, DIPHENHYDRAMINE HCL, making it a notable side effect.
If you experience arthropathy while taking IBUPROFEN, DIPHENHYDRAMINE 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.