22,200 reports of this reaction
2.0% of all ACETAMINOPHEN reports
#9 most reported adverse reaction
ARTHRALGIA is the #9 most commonly reported adverse reaction for ACETAMINOPHEN, manufactured by Kenvue Brands LLC. There are 22,200 FDA adverse event reports linking ACETAMINOPHEN to ARTHRALGIA. This represents approximately 2.0% of all 1,089,938 adverse event reports for this drug.
Patients taking ACETAMINOPHEN who experience arthralgia should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
ARTHRALGIA is a less commonly reported adverse event for ACETAMINOPHEN, but still significant enough to appear in the safety profile.
In addition to arthralgia, the following adverse reactions have been reported for ACETAMINOPHEN:
The following drugs have also been linked to arthralgia in FDA adverse event reports:
ARTHRALGIA has been reported as an adverse event in 22,200 FDA reports for ACETAMINOPHEN. This does not prove causation, but indicates an association observed in post-market surveillance data.
ARTHRALGIA accounts for approximately 2.0% of all adverse event reports for ACETAMINOPHEN, making it a notable side effect.
If you experience arthralgia while taking ACETAMINOPHEN, 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.